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CYRX

CryoPortC
Nasdaq / Pharmaceuticals, Biotechnology & Life Sciences
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2026-06-02
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2026-05-05
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Earnings documents stored for CYRX.

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Investor releaseQuarter not tagged2026-05-05

Cryoport (CYRX) Q2 2025 Earnings Transcript

Motley Fool

Image source: The Motley Fool. Tuesday, August 5, 2025 at 5 p.m. ET Chief Executive Officer — Jerrell W. Shelton Chief Financial Officer — Robert S. Stefanovich Chief Scientific Officer — Mark W. Sawicki Vice President, Corporate Development & Investor Relations — Thomas J. Heinzen Managing Director (Moderator) — Todd Fromer Todd Fromer: Thank you, operator. Before we begin today, I would like to remind everyone that this conference call contains certain forward- looking statements. All statements that address our operating performance, events or developments that we expect or anticipate occurring in the future are forward-looking statements. These forward-looking statements are based on management's beliefs and assumptions and not on information currently available to our management team. Our management team believes that these forward-looking statements are reasonable as and when made. However, you should not place undue reliance on any such forward-looking statements because such statements speak only as of the date when made. We do not undertake any obligation to publicly update or revise any forward-looking statements, whether as a result of new information or future events or otherwise, except as required by law. In addition, forward-looking statements are subject to certain risks and uncertainties that could cause actual results, events and developments to differ materially from our historical experience and our present expectations or projections. These risks and uncertainties include, but are not limited to, those described in Item 1A, Risk Factors and elsewhere in our Annual Report on Form 10- K to be filed with the Securities and Exchange Commission and those described from time to time in the other reports, which we file with the Securities and Exchange Commission. As a reminder, Cryoport has uploaded their second quarter 2025 in review document to the main page of the Cryoport website. These documents provide a review of Cryoport's financial and operational performance and a general business outlook. Before I turn the call over to Jerry, please note that because of the strategic partnership that has been established with DHL Group and the related sale of CRYOPDP to DHL, CRYOPDP's financials, which were previously a part of Cryoport's Life Science Services reportable segment are now presented as discontinued operations. Cryoport previously provid...

Investor releaseQuarter not tagged2026-05-05

Cryoport (CYRX) Q3 2025 Earnings Transcript

Motley Fool

Image source: The Motley Fool. Tuesday, Nov. 4, 2025 at 5 p.m. ET Chief Executive Officer — Jerrell Shelton Chief Financial Officer — Robert Stefanovich Chief Scientific Officer — Mark W. Sawicki Vice President of Corporate Development and Investor Relations — Thomas Heinzen Todd Fromer: Thank you, operator. Before we begin today, I would like to remind everyone that this conference call contains certain forward-looking statements. All statements that address our operating performance, events or developments that we expect or anticipate occurring in the future are forward-looking statements. These forward-looking statements are based on management's beliefs and assumptions and not on information currently available to our management team. Our management team believes that these forward-looking statements are reasonable as and when made. However, you should not place undue reliance on any such forward-looking statements because such statements speak only as of the date when made. We do not undertake any obligation to publicly update or revise any forward-looking statements, whether as a result of new information or future events or otherwise, except as required by law. In addition, forward-looking statements are subject to certain risks and uncertainties that could cause actual results, events and developments to differ materially from our historical experience and our present expectations or projections. These risks and uncertainties include, but are not limited to, those described in Item 1A, Risk Factors and elsewhere in our annual report on Form 10-K to be filed with the Securities and Exchange Commission and those described from time to time in the other reports which we file with the Securities and Exchange Commission. As a reminder, Cryoport has uploaded their third quarter 2025 in review document to the main page of the Cryoport Inc. website. This document provides a review of Cryoport's financial and operational performance and a general business outlook. Before I turn the call over to Jerry, please note that because of the strategic partnership that has been established with DHL Group and related sale of CRYOPDP to DHL, CRYOPDP's financials, which were previously a part of Cryoport's Life Sciences Services reportable segment are now presented as discontinued operations. Cryoport previously provided quarterly historical information on this basis for...

Investor releaseQuarter not tagged2026-05-05

Cryoport (CYRX) Q1 2025 Earnings Transcript

Motley Fool

Image source: The Motley Fool. Wednesday, May 7, 2025 at 5 p.m. ET Chief Executive Officer — Jerrell Shelton Chief Financial Officer — Robert Stefanovich Chief Scientific Officer — Mark Sawicki Vice President, Corporate Development & Investor Relations — Thomas Heinzen Need a quote from a Motley Fool analyst? Email [email protected] Jerrell Shelton, Chief Executive Officer of Cryoport. Jerry, the floor is yours. Jerrell Shelton: Thank you, Todd. Good afternoon, ladies and gentlemen. With us this afternoon is our Chief Financial Officer, Robert Stefanovich; our Chief Scientific Officer, Dr. Mark Sawicki; and our Vice President of Corporate Development and Investor Relations, Thomas Heinzen. As a reminder, we have uploaded our first quarter 2025 in review document to our website. It can be found on the main page of the Cryoport, Inc. website. This document provides a review of our financial and operational performance and a general business outlook. If you do not have a chance to read it, I would encourage you to go to the website and download it. Before I review our results, I would like to highlight that, due to our recently announced strategic partnership with DHL and the related sale of CryoPDP to DHL, CryoPDP's financials, which were previously a part of Cryoport's Life Sciences Services reportable segment, are now presented as discontinued operations. Accordingly, we have provided quarterly historical information on this basis for 2024 in our first quarter 2025 in review document. This information is intended to support financial modeling efforts for those needing this information. Please note that unless indicated, all revenue figures discussed today will refer to continuing operations. This includes our fiscal year 2025 revenue guidance, first shared alongside our DHL transaction announcement. Now I'll provide a brief update on our business and then we will take your questions. Cryoport had a solid start to the year with $41 million of revenue from continuing operations for the first quarter, which represented 10% year-over-year growth and helped to drive meaningful adjusted EBITDA improvement. Three things that excited us about the first quarter were: First, client engagement and life sciences services grew substantially, highlighting a new momentum in our business. Second, order patterns for our Life Sciences products continued to show signs of stabilizati...

Investor releaseQuarter not tagged2026-05-05

Cryoport, Inc. Q1 2026 Earnings Call Summary

Moby

Revenue growth of 16% was driven by a 26% surge in commercial cell and gene therapy support and an 18% increase in clinical trial revenue, reflecting Cryoport's market-leading position. The Life Sciences Services segment benefited from a 21% increase in biostorage and bioservices, as clients increasingly adopt the full-service portfolio for complex cell therapy programs. Life Sciences Products saw 15% growth due to stabilized global demand for MVE cryogenic systems, particularly in animal health and life sciences across all geographies. The launch of the Fusion 800 series cryogenic freezer represents a strategic move to access previously unreachable markets by eliminating the need for continuous liquid nitrogen supply. Management attributes the $2.2 million improvement in adjusted EBITDA to top-line growth combined with operational discipline and the use of generative AI to automate internal workflows. The IntegraCell platform reached a milestone by shipping its first cryopreserved clinical trial materials, validating the strategic shift toward a fully integrated supply chain model. Full-year 2026 revenue guidance was raised to $192 million to $196 million, reflecting increased visibility despite continued global macroeconomic uncertainty. Management expects to achieve positive adjusted EBITDA in the second half of 2026, supported by organic revenue growth and the completion of key facility investments. The pipeline for 2026 includes 10 expected BLA or MAA filings and up to eight additional new therapy approvals, which are anticipated to drive future commercial revenue. New supply chain centers in Paris and Santa Ana are expected to contribute more significantly to revenue in 2027 following client audits and full operational ramp-up. The Life Sciences Products market is projected to maintain high single-digit growth as global demand for cryogenic storage solutions continues to solidify. Cryo PDP financials are now presented as discontinued operations following the strategic sale to DHL Group in June 2025, shifting focus to core continuing operations. The company is aggressively implementing generative AI tools to manage risk and accelerate decision-making, viewing digitization as a long-term driver of efficiency. Gross margins in the services segment outperformed initial expectations in Q1, though management anticipates some pressure before a more significan...

Investor releaseQuarter not tagged2026-05-05

CryoPort Q1 Earnings Call Highlights

MarketBeat

Q1 revenue was $47.8 million, up 16% year-over-year with double-digit growth in both segments, and management raised full-year fiscal 2026 revenue guidance to $192 million–$196 million. Cryoport supported a record 766 global clinical trials (a net +55 year-over-year), including 357 Phase II and 91 Phase III trials, currently supports 21 commercial therapies, and expects about 10 BLA/MAA filings and up to 8 additional approvals in fiscal 2026. Adjusted EBITDA improved by $2.2 million year-over-year (Q1 adjusted EBITDA was negative $0.6 million), with management targeting positive adjusted EBITDA in H2 FY2026 while citing IntegriCell milestone shipments and planned facility expansions as drivers of future margin and revenue expansion. Interested in CryoPort, Inc.? Here are five stocks we like better. CryoPort (NASDAQ:CYRX) reported first-quarter fiscal 2026 results that management said reflected continued momentum across its integrated services and products platform, highlighted by double-digit revenue growth in both reporting segments and improved profitability metrics. On the call, CEO Jerrell Shelton was joined by CFO Robert Stefanovich, Chief Scientific Officer Dr. Mark Sawicki, and Vice President of Corporate Development and Investor Relations Thomas Heinzen. The company also reiterated that, following the sale of CRYOPDP to DHL Group in June 2025, CRYOPDP is presented as discontinued operations; management noted that revenue figures discussed on the call refer to continuing operations unless otherwise indicated. → Roblox Stock Slides to New Low as Safety Changes Weigh on Outlook Shelton said Cryoport generated first-quarter revenue of $47.8 million, an increase of 16% year over year. He attributed the growth to momentum “over the past several quarters across our integrated services and products platform.” Within that total, Shelton highlighted growth tied to cell and gene therapy activity: Commercial cell and gene therapy support revenue grew 26% to $9.1 million. Clinical trial-related revenue increased 18% to $12.9 million. → The Real SpaceX Play: 5 Chip Stocks Powering the IPO Before It Launches The Life Sciences Services segment posted revenue growth of 18% year over year, including 21% growth in BioStorage/BioServices. Shelton said the quarter reflected “increasing adaptation of our full service portfolio” as programs become more complex. The Life Sc...

Investor releaseQuarter not tagged2026-05-05

Cryoport (CYRX) Q1 2026 Earnings Transcript

Motley Fool

Image source: The Motley Fool. Monday, May 4, 2026 at 5 p.m. ET Chief Executive Officer — Jerrell W. Shelton Chief Financial Officer — Robert S. Stefanovich Chief Scientific Officer — Mark W. Sawicki Vice President of Corporate Development and Investor Relations — Thomas J. Heinzen Need a quote from a Motley Fool analyst? Email [email protected] As a reminder, Cryoport, Inc. has uploaded their first quarter 2026 in review document to the main page of the Cryoport, Inc. website. This document provides a review of Cryoport, Inc.'s financial and operational performance and the general business outlook. Before I turn the call over to Jerry, please note that because of the strategic partnership that has been established with DHL Group, and the related sale of Cryo PDP to DHL in June 2025, Cryo PDP's financials, which were previously a part of Cryoport, Inc.'s Life Sciences Services reportable segment, are now presented as discontinued operations. Please note that unless otherwise indicated, all revenue figures discussed today will refer to continuing operations. This includes Cryoport, Inc.'s fiscal year 2026 revenue guidance. It is now my pleasure to turn the call over to Mr. Jerrell W. Shelton, Chief Executive Officer of Cryoport, Inc. Jerry, the floor is yours. Jerrell W. Shelton: Thank you, Todd, and good afternoon, ladies and gentlemen. With me today is our Chief Financial Officer, Robert S. Stefanovich; our Chief Scientific Officer, Mark W. Sawicki; and our Vice President of Corporate Development and Investor Relations, Thomas J. Heinzen. Our first quarter results continue to demonstrate our market-leading position, as revenue was $47.8 million, up 16% year over year, which puts us off to a very strong start for the year. This growth is a combination of our momentum over the past several quarters across our integrated services and products platform. Revenue in support of our commercial cell and gene therapy grew 26% to $9.1 million, while revenue from clinical trials grew 18% to $12.9 million. We continue to support one of the industry's broadest cell and gene therapy pipelines, and our leadership across both commercial and clinical programs positions us well for future sustainable growth. As of March 31, we supported a record total of 766 global clinical trials, a net increase of 55 clinical trials over the prior year, with 91 of these clinical trials in Phase I...

Investor releaseQuarter not tagged2026-05-05

Cryoport Reports First Quarter 2026 Financial Results

PR Newswire

First quarter revenue grew 16% year-over-year to $47.8 million Commercial cell and gene therapy (CGT) revenue grew 26% year-over-year to $9.1 million, reflecting continued expansion in approved CGT programs Life Sciences Services revenue increased 18% year-over-year, led by 21% growth in BioStorage/BioServices Life Sciences Products revenue increased 15% year-over-year, driven by strong demand for cryogenic systems Supporting a record 766 global clinical trials and 21 commercially approved CGTs as of March 31, 2026 Company raises full-year revenue guidance to $192 million - $196 million NASHVILLE, Tenn., May 4, 2026 /PRNewswire/ -- Cryoport, Inc. (NASDAQ: CYRX) ("Cryoport" or the "Company"), a leading global provider of integrated temperature-controlled supply chain solutions for the life sciences, today announced financial results for its first quarter (Q1) of 2026. Jerrell Shelton, CEO of Cryoport, commented, "Cryoport delivered a strong start to 2026 with first-quarter revenue of $47.8 million, up 16% year-over-year, reflecting a continuation of our momentum over the past several quarters across our integrated services and products platform. Revenue in support of commercial Cell and Gene Therapies (CGT) grew 26% to $9.1 million, while clinical trial support revenue grew 18% to $12.9 million. We continue to support one of the industry's broadest CGT pipelines, and our leadership across both clinical and commercial programs positions us well for sustainable growth. "Our Life Sciences Services segment delivered another strong quarter, with revenue increasing 18% year-over-year, including 21% growth in BioStorage/BioServices. This performance reflects the increasing scope and complexity of the Cell & Gene Therapy programs we support and underscores the critical role we play in supporting our clients with our integrated, temperature-controlled supply chain services. "Our Life Sciences Products segment also performed very well, generating 15% revenue growth, driven by global demand for MVE Biological Solutions' cryogenic systems. MVE continues to innovate and further solidify its position as the global leader in high-quality cryogenic systems. "This growth across both our reporting segments, combined with solid gross margins and continued operational discipline, drove a $2.2 million year-over-year improvement in adjusted EBITDA from continuing operations, advan...

TranscriptFY2026 Q12026-05-04

FY2026 Q1 earnings call transcript

Earnings source - 96 paragraphs
Operator

As a reminder, this call is being recorded. I will now turn the call over to your host, Todd Fromer from KCSA Strategic Communications. Please go ahead.

Todd Fromer

Thank you, operator. Before we begin today, I would like to remind everyone that this conference call contains certain forward-looking statements. All statements that address our operating performance, events or developments that we expect or anticipate occurring in the future are forward-looking statements. These forward-looking statements are based on management's beliefs and assumptions and not on information currently available to our management team. Our management team believes that these forward-looking statements are reasonable as and when made. However, you should not place undue reliance on any such forward-looking statements because such statements speak only as of the date when made. We do not undertake any obligation to publicly update or revise any forward-looking statements, whether as a result of new information or future events or otherwise, except as required by law.

Todd Fromer

Forward-looking statements are subject to certain risks and uncertainties that could cause actual results, events and developments to differ materially from our historical experience and our present expectations or projections. These risks and uncertainties include, but are not limited to, those described in Item 1A, Risk factors and elsewhere in our annual report on Form 10-K to be filed with the Securities and Exchange Commission, and those described from time to time in the other reports which we file with the Securities and Exchange Commission. As a reminder, Cryoport has uploaded their first quarter 2026 in review document to the main page of the Cryoport, Inc. website. This document provides a review of Cryoport's financial and operational performance and a general business outlook.

Todd Fromer

Before I turn the call over to Jerry, please note that because of the strategic partnership that has been established with DHL Group and the related sale of CRYOPDP to DHL in June 2025, CRYOPDP's financials, which were previously a part of Cryoport's Life Sciences Services reportable segment, are now presented as discontinued operations. Please note that unless otherwise indicated, all revenue figures discussed today will refer to continuing operations. This includes Cryoport's fiscal year 2026 revenue guidance. It is now my pleasure to turn the call over to Mr. Jerrell Shelton, chief executive officer of Cryoport. Jerry, the floor is yours.

Jerry Shelton

Thank you, Todd, and good afternoon, ladies and gentlemen. With me today is our Chief Financial Officer, Robert Stefanovich, our Chief Scientific Officer, Dr. Mark Sawicki, and our Vice President of Corporate Development and Investor Relations, Thomas Heinzen. Our first quarter results continue to demonstrate our market-leading position as revenue was $47.8 million, up 16% year-over-year, which puts us off to a very strong start for the year. This growth is a combination of our momentum over the past several quarters across our integrated services and products platform. Revenue in support of our commercial cell and gene therapy grew 26% to $9.1 million, while revenue from clinical trials grew 18% to $12.9 million.

Jerry Shelton

We continue to support one of the industry's broadest cell and gene therapy pipelines, and our leadership across both commercial and clinical programs positions us well for future sustainable growth. As of March 31st, we supported a record total of 766 global clinical trials, a net increase of 55 clinical trials over the prior year, with 91 of these clinical trials in phase III. From this market-leading base, we believe we will continue to drive robust growth in our commercial revenue in both the near and the longer term. During the first quarter, I'm happy to report that our client, Rocket Pharmaceuticals, received an accelerated approval from the FDA for their gene therapy, Carvykti. With this approval, the number of commercial therapies we are supporting has increased to 21.

Jerry Shelton

For the remainder of 2026, based on current information, we expect another 10 BLA or MAA application filings and up to 8 additional new therapy approvals. Our Life Sciences Services segment delivered a strong quarter, with revenue increasing 18% year-over-year, including 21% growth in BioStorage Bioservices. This performance reflects increasing adaptation of our full service portfolio in conjunction with the increasing scope and complexity of the cell therapy programs we support. It also underscores the critical role we play in supporting our clients with our extensive array of integrated temperature control supply chain services and solutions. Our Life Sciences Products segment also performed well, generating a 15% revenue growth driven by global demand for MVE Biological Solutions cryogenic systems.

Jerry Shelton

For over 60 years, MVE has provided high quality, reliable cryogenic systems to the market, and every day it continues to further reinforce its position as the global leader. For example, during the first quarter, MVE introduced its new Fusion 800 Series, which is a self-sustaining cryogenic freezer that eliminates the need for a continuous liquid nitrogen supply feed, delivering exceptional reliability, safety and sustainability in a compact footprint designed for space-constrained environments where a source of liquid nitrogen is not readily available.

Jerry Shelton

This is quite an accomplished engineering feat which will pay dividends for years to come as we open up new markets that were heretofore inaccessible. Growth across both our reporting segments, Life Sciences Services and Life Sciences Products, combined with the solid gross margins and continued operational discipline, drove a $2.2 million year-over-year improvement in adjusted EBITDA from continuing operations, advancing us meaningfully along our pathway to profitability. We also reached a milestone moment during the 1st quarter as our IntegriCell team shipped its first cryopreserved clinical trial patient materials from both our Houston, Texas, and Liège, Belgium facilities for two separate clients. This achievement highlights IntegriCell's progress as it continues to develop and moves us a step further toward being a meaningful contributor to the cell and gene therapy industry and Cryoport's future revenue and profitability.

Jerry Shelton

In parallel, we continued to advance our digital and information strategy, including initiatives in digitization and generative AI to support complex internal workflows and improving our effectiveness and efficiency in day-to-day operations. Our focus is currently on enabling employees to use secure enterprise-approved generative AI tools to automate repetitive tasks, analyze data in real time, manage risk, and accelerate decision-making and execution. We are already seeing tangible benefits and believe AI will play an increasingly important role in our future. Reflecting on our strong performance for the first quarter and our increased visibility into the remainder of the year, we're raising our full year 2026 revenue guidance to $192 million-$196 million. We continue to review our guidance on a quarterly basis, and we will make any further adjustments as warranted.

Jerry Shelton

We also believe that based on our progress year to date, we will achieve positive adjusted EBITDA in the second half of this year. This concludes my remarks for today. I'll ask the operator to open the floor for your questions.

Operator

Your first question comes from the line of Puneet Souda from Leerink Partners. Please go ahead.

Puneet Souda

Yeah. Hi, guys. Thanks for the questions here. You had a $3 million beat versus the consensus, but just you're raising the guide by $2 million. Just wondering how much of it is prudence being sort of early in the year, any other considerations, and how should we think about, you know, 2Q, if you can provide some context there, just given the momentum you're seeing on the business and versus the, you know, core clinical trials?

Jerry Shelton

Well, Puneet, thank you for the question. We think that, you know, Q2, of course, was an outstanding quarter, but we think it's a responsible guide given the given the continued uncertainty on a global macroeconomic basis. You know, we'll continue to evaluate this on a quarterly basis, and of course, we'll adjust the guidance if it's warranted in the future.

Puneet Souda

Okay. maybe if I could switch gears to MVE Life Sciences Products. You had 15% growth. That was against an easier comp. just, you know, trying to understand, how should we think about growth for Life Sciences Products MVE overall with the new product introduction there as well this year? wondering if Robert can comment on that too.

Jerry Shelton

Well, Robert can comment on it, but I'll start. You know, all products in life sciences, as you know very well, take time to ramp up, whether it's products or it's facilities. It'll take time for those products to ramp up in the marketplace and to have any kind of an impact. We do think the markets are solid and have been, you know, they've solidified, and we see continued indications to that, to that, to support that. We think that we will have a high single-digit growth market going forward. Now, we may exceed that from time to time, but that's kind of our assessment. Robert, you may want to add some things there.

Robert Stefanovich

Yeah. Just to further amplify, look, the outperformance in MVE, you know, during Q1, you know, was really driven by strong demand across all geographies and in solid performance, particularly in the animal health but also the life science overall. You know, MVE is the number 1 leader in the market worldwide. We already saw stability in 2025 in terms of return of product demand for cryogenic systems, and we continue to see that improvement, you know, as demonstrated in our Q1 performance.

Puneet Souda

Okay. Super. If I could ask one more on, obviously, we've seen improvement in biotech funding in the fourth quarter that is continued so far in the first quarter. Just wondering if you're seeing some higher momentum from that for RFP volumes or other contract volumes in, you know, here in the first quarter or the second quarter so far. Your clinical trials was up only, net trial adds were only, you know, 6, but just wondering if you are seeing any momentum from or hearing further momentum from your customers given the funding environment.

Jerry Shelton

Mark will take that.

Mark Sawicki

Yeah, happy to. Hey, Puneet, how are you? Yeah, I mean, what we're seeing is a definitive continued investment into phase II and phase III programs. If you take a look, obviously, at our numbers, you know, the phase II data itself and phase III data are increasing very, very nicely. I mean, phase III data was up 5 trials sequentially, which is very unusual, and we haven't seen that in a, in a long time. You know, phase II continues. Year over year, phase II is up, you know, almost 30 programs. A lot of that money is going into that and really is being invested in pushing these late-stage clinical assets over the finish line. So yes, we do see some very positive signs from that.

Robert Stefanovich

Yeah. Puneet Souda, maybe just to add to it, you know, it's less about, you know, the number of increase in clinical trials. It's really looking at the 766 clinical trials we're supporting. That's a very, very strong number. Looking at, like as Mark Sawicki mentioned, the maturation of those trials moving into phase II and phase III. You'll remember that, you know, the majority of cell therapies that are approved to date went directly from phase II to commercial launch, and they're conducting their phase III in parallel. You really have to look at, you know, the 357 phase II clinical trials and the now 91 phase III as, you know, potential for commercial launches.

Puneet Souda

Got it. That's super helpful. Congrats on the quarter. Thank you.

Robert Stefanovich

Thank you.

Operator

Thank you. Your next question comes from the line of Anna Snopkowski from KeyBanc Capital Markets. Please go ahead.

Anna Snopkowski

Hi, this is Anna on for Paul Knight. Thanks for taking my question, and congrats on a great quarter. I have two questions, but maybe to start, you mentioned you shipped your first clinical trial patient material for IntegriCell, which is very exciting. Maybe could you just walk us through your initial learnings from this rollout, and what your expectations are for IntegriCell in 2026?

Mark Sawicki

Yeah, happy to.

Jerry Shelton

Yeah.

Mark Sawicki

Yeah, we're really pleased about the fact that we're now supporting actual clinical processes in both locations, both the site in Belgium and the site in Houston. You know, it's, it's a very nice achievement and, you know, it's, it's something that, you know, we've been working towards for a long period of time. You know, so, we talked a lot about this over the last couple of quarters, but IntegriCell is, it's, you know, as an organization and as an asset is gonna be a very important driver for long-term revenue and margin expansion. It's a long cycle time for onboarding.

Mark Sawicki

You know, it typically takes, you know, it could take 12 to 18 months in some cases to onboard. We do have active projects ongoing. We have additional clients that are coming on board now, and so you know, our overall outlook is extremely positive. From a learning standpoint, you know, it's been extremely well-received. I think one of the key elements here is the fully integrated platform, right? Our fully integrated service platform, which includes our biologistics bioservices, our initial clients are using all of our service competencies. I think that's a very important learning for our team as we harmonize and optimize those processes to really drive efficiency for our clients.

Anna Snopkowski

Great. Thank you. Maybe switching to the EBITDA side, do you think you could walk us through some of the assumptions to get to that 2H positivity? It seems like there's some facilities ramping, so that should help. Also the commercial therapies mix. If you could just walk through some variables there and, if there's any areas of upside, that would be helpful. Thank you.

Robert Stefanovich

Yeah, certainly. I think if you look at our Q1 performance, obviously we're very close to break even on the adjusted EBITDA side with a negative $0.6 million. We certainly can reiterate, yeah, reaching positive EBITDA in the second half of the year. This is obviously gonna be driven, you know, by the revenue growth that we see. You mentioned, you know, some of the initiatives, the investments we have. Those are really gonna drive operating leverage in 2027. The achievements for Q2 of this year are really driven by the current organic revenue growth. The new facilities, you know, those are investments we've begun in 2025 and we're completing now in 2026. They're really gonna drive further enhancement of our profitability and adjusted EBITDA in 2026 and beyond.

Anna Snopkowski

Great. Thank you. Congrats again.

Robert Stefanovich

Thank you.

Operator

Thank you. Your next question comes from the line of David Saxon from Needham. Please go ahead.

David Saxon

Great. Good afternoon, everyone. Thanks for taking my questions, and I'll echo, you know, my congrats on the quarter. Really strong start to the year. In the script this quarter and last quarter, you talked about AI initiatives that are helping reduce OpEx. Would love to understand just how durable that is and, you know, whether that can be applied to, I guess, more of the business, or are we kinda seeing the full extent of the savings potential?

Jerry Shelton

Yeah, David, all of our AI initiatives are durable, and they're focused on internally to enhance our efficiency and our effectiveness within the company. It's another tool. It's a very powerful tool. It will reshape our business, I'm sure, over time as it will most other businesses as it has an impact on business and an impact on society.

Jerry Shelton

We're very excited about our AI initiatives, but they're focused on practicality today, on improving our efficiency and our effectiveness on internal operations.

David Saxon

Okay. Thanks for that, Gerry. Maybe my second one might be for Robert, just on the supply chain centers in Paris and Santa Ana, both in the second half. I guess, what's baked into guidance from those two starting to come online? When could we start seeing customer audits of those facilities? Anything from a gross margin perspective we should be aware of. Thanks so much.

Robert Stefanovich

No, absolutely. You know, these initiatives that we started in 2025, you know, are gonna be completed this year. You know, one is the Paris, France site that we already went operational with our biologistics in November of last year. That's already starting to ramp, and clients are doing their audits. We're gonna complement that with our BioServices in Q3 of this year. The second one is the Santa Ana, California site that gives us, obviously, a significant West Coast presence. It's consolidating 3 of our current existing locations into one and expanding that to about 94,000 sq ft to offer biologistics, BioServices, consulting, testing, and ultimately also have space for IntegriCell.

Robert Stefanovich

Those are significant initiatives that we have underway that are really driven by client demand. From a guidance perspective, you know, the revenue contribution is obviously smaller because they're just going online in the second half of the year. Clients certainly will conduct their audits of the facilities this year, and they'll start contributing, you know, obviously more significantly in 2027.

David Saxon

Great. Anything on gross margin from that or just generally speaking, how should we think about gross margin?

Robert Stefanovich

Yeah. I think what we mentioned in our year-end, and that still applies, albeit we did come in higher on services gross margins than I initially expected. We did expect gross margins definitely in the second half to start rebounding, have some pressure in the first half of the year, which we didn't really see in Q1. Certainly, you know, it'll start, you know, coming back more significantly in the second half of this year.

David Saxon

Great. Thanks so much.

Operator

Thank you. Your next question comes from the line of Subbu Nambi from Guggenheim. Please go ahead.

Ricki Levitus

Hi, this is Rikki on for Subbu. Thanks for taking our question. I'll keep it to one and a follow-up. The commercial cell and gene therapy revenue grew 26% year-over-year in the first quarter. Would you say that's the right growth rate that we could think about for the year, or should we expect more acceleration as newer approvals ramp? Is the growth concentrated in a few key therapies like Carvykti, or is it broad-based across your supported commercial products? Thank you.

Robert Stefanovich

No, I would, you know, on commercial revenues, if you look at in general, you know, research reports on the market, it'll range anywhere between on the low end, 20%, on the high end, 40%. I mean, you're absolutely right. We saw, you know, solid, you know, revenue growth on the commercial side. We do expect that, you know, 2026 will be a very good year for commercial revenue. You know, the guidance in terms of revenue guidance is really based on the existing commercial therapies that we're supporting. While, you know, there may be some revenue contribution from new approvals, the guidance really is we're looking at the existing platform that we have for 2026.

Thomas Heinzen

With, Sorry, it's Tom jumping in, Rikki. Bristol Myers and J&J have already reported, and they did report a strong Q1. We can't really talk about the rest of our commercial therapies we support because they haven't reported their quarters yet.

Ricki Levitus

Totally understand that. Thanks for the color there.

Thomas Heinzen

No problem.

Operator

Thank you. Your next question comes on the line of David Larsen from BTIG. Please go ahead.

David Larsen

Hey, congratulations on the great quarter. Sticking with the idea or the theme of commercial products, can you just remind me how many commercial products you're supporting now? Did I hear you say that you could have potentially 8 more launch within the next 12 months?

Thomas Heinzen

We're supporting 21 today, Dave. Yes, there are 8 potential more approvals of new therapies this year. 5 of them already have PDUFA dates. That's dates set by the FDA when they plan to make a decision.

David Larsen

Can you talk a little bit about the dynamics of a commercial product that you're supporting versus a clinical trial product? Is there a difference in margins, or is there any sort of difference in revenue per, I guess, product that you're supporting? I guess what I'm getting at is, on the commercial side, since they're in the market being used, I would think that there would be much more revenue potential per product because it's basically being used, you know, across the world for patients. It's not limited to one specific clinical trial. Any color there on the revenue potential and margin relative to clinical trials.

Robert Stefanovich

I think there's 2 things related to the commercial therapies. 1, obviously, you know, just the pathway from us supporting the clinical trials, you know, we then work with their commercial team in preparing for the launch of the commercial therapies, whether it's, you know, in 1 country or globally. We're part of the launch team in a way, and we provide program management that's built separately as well. When you see the increase in commercial revenue, it's really driven by the patient population, right? As more and more commercial therapies come to market, as more and more commercial therapies move from the teaching hospitals to regional settings or to the outpatient settings, you know, so does, you know, really the acceleration of patients being treated, you know, occur.

Robert Stefanovich

This obviously drives more revenue. The other part is obviously we're continuously expanding our services platform. Initially biologistics, adding BioServices, ultimately adding IntegriCell preservation services. That further expands the revenue on a per patient basis as we provide our services along the supply chain of the cell and gene therapy market.

David Larsen

Okay. That's very helpful. Just one more quick follow-up. Obviously your revenue growth this quarter versus, call it 2 years ago, huge positive this quarter, obviously. Just what do you attribute the resurgence in growth to? Is it simply a matter of the cell and gene therapy market coming back after everybody's worked through the IRA? Just what do you attribute this impressive growth to? Thanks very much.

Robert Stefanovich

I think it's a number of things. You know, one, obviously, as I mentioned, that we've broadened our revenue stream. You saw BioServices, which is a newer offering, increase really over the last couple of quarters, you know, 20% plus year-over-year, and we expect that to continue. On the product side, you know, we do see, and we saw that in the second half of 2025, you know, demand normalizing and coming back. If you look at all of our different revenue streams, we're seeing, you know, stronger demand picking back, and that's been driving revenue in the last, you know, 2, 3 quarters of 2025, and also, driven a very, very strong performance for Q1 of this year, which led us to, you know, increase the guidance for the full year.

David Larsen

Thanks very much. Congrats on a great quarter.

Robert Stefanovich

Thank you.

Operator

Thank you. Your next question comes on the line of Richard Baldry from ROTH Capital. Please go ahead.

Richard Baldry

Thanks. Just sort of curious on the commercial acceleration, if it's been concentrated around the CAR T area with the regulatory burden sort of easing or if you think that's still a catalyst that's ahead that hasn't really had an impact yet.

Thomas Heinzen

The cell therapies are the majority of our commercial customers, Rich. The gene therapies have had, I think it's kind of public out there, an even start. The cell therapies are pulling the wagon. That's, you know, Bristol Myers, Gilead, J&J.

Robert Stefanovich

You look at our clinical trial portfolio, you know, close to 90% of the clinical trials we're supporting are autologous immunogenetic cell therapies.

Richard Baldry

Got it. Thanks.

Robert Stefanovich

Thank you.

Operator

Thank you. Your next question comes on line of Matthew Hewitt from Craig-Hallum Capital Group. Please go ahead.

Matthew Hewitt

Good afternoon and nice start to the year. Maybe first up, regarding the Fusion 800 Series, could you talk a little bit about the pipeline? You mentioned a little bit about the positive response and obviously a couple patient adoptions already, but I'm just curious what that pipeline looks like.

Jerry Shelton

It's kind of early to comment on the pipeline. We sell through distributors. The first thing we do is get our distributors excited about the Fusion 800, and they are. We're moving out very nicely, but it's early to comment on the pipeline.

Matthew Hewitt

Got it. Maybe switching gears a little bit, obviously we're approaching 1 year since the REMS was removed. Obviously there was a lot of buildup, as, you know, they were moving the patients out of the hospital to some of these ambulatory and other centers. I'm curious if that momentum that you initially saw, has that continued? Are you seeing that opportunity continue to expand beyond the core hospital setting? If so, what can that mean for growth later this year and into next year? Thank you.

Jerry Shelton

Tom, you may want to comment on that.

Thomas Heinzen

Yeah. It's definitely, you can look in the companies that already reported J&J and Bristol and their outpatient growth and their community hospital growth is really helping to drive their revenue, which in turn helps to drive ours.

Matthew Hewitt

Got it. Thank you.

Thomas Heinzen

Thank you.

Operator

Thank you. Your next question comes from the line of Jacob Johnson from Stephens. Please go ahead.

Mac Etoch

Hey, good afternoon, and thank you for taking my questions. Maybe just to follow up on the margin aspects that y'all have highlighted in the previous questions. MVE product margins were, you know, relatively light compared to our expectations. I'd just like to get a sense of what you're seeing in terms of the storage industry in general and how energy prices are factoring in to performance in the quarter and how that's expected to factor into the remainder of the year.

Robert Stefanovich

Yeah, no. On the margin side, energy prices have not factored into the quarter for our products business. It's really purely a result of specific product mix. If you look at, you know, year-over-year margins, they're pretty close to each other. Sequentially, it's down, but it's really related to product mix that we typically see, especially in the first quarter of the year. There's no pricing erosion or competitive element. It's product mix related.

Mac Etoch

I appreciate that. It's been, you know, call it six months since funding really started to tick back up. As you look at how 2Q is shaping up quarter to date, you know, what can you tell us about the level of activity and sentiment that you're seeing within your customer base today?

Robert Stefanovich

I think overall it's obviously very good for the industry and especially for companies that are in need to raise funds to drive their clinical trial portfolio. You know, look at a lot of the clients that we serve are very well-established, very well-funded. Especially if you look at, you know, the huge number of phase II and phase III we have. They're really getting close to the finish line, pre-commercial. I don't think that we see a huge risk there on the funding side. It's really mostly on smaller companies in need of funding. It's certainly good for the industry to see funding coming back, you know, with strong funding, especially in the month of April of this year.

Thomas Heinzen

Maybe to just peek under the hood a minute with our clinical trial count, it increased by 6 net sequentially. There were 29 new trial adds in the quarter and 23 removed. There's the net 6. Of those 23 removed, 16 of the trials were completed. That's a great thing. That shows the maturation of our pipeline. That means 1s are gonna go to 2 and 2s are gonna go to 3.

Mac Etoch

I appreciate y'all taking the questions.

Thomas Heinzen

Thanks, Matt.

Robert Stefanovich

Thank you.

Operator

Thank you. Your next question comes from the line of Matthew Stanton from Jefferies. Please go ahead.

Matt Stanton

Hey, thanks. Robert, maybe just one to close the loop on margins. Just given some of the inflationary pressures we've seen over the last few months on commodities and logistics side, could you just help remind us your pricing structure? I believe you're able to pass along that object as part of the contracts you have in place, but can you just kinda remind us the mechanics on the pricing side as it relates to some of the inflationary pressures coming back into the P&L type and the macro for the rest of the year? Thanks.

Robert Stefanovich

No, that's a very valid, you know, question. Look, in transportation and logistics, that component of our solution, fuel surcharges are the norm. It may go up or down, fuel surcharges are passed on, yeah, to our client base. That's common business practice. It does not impact our growth margins as a, as a company. From a product side, we really haven't seen an impact, you know, from the increased prices, oil prices, at this point. We're certainly keeping an eye out on it like everyone else.

Matt Stanton

Okay, thanks. Maybe just on the product side, I think, Jerry, you said that market could grow high singles. I think prior you guys thought products could maybe be mid-singles for the year, maybe high singles if things kinda came back better, you know, after a strong 1Q. Do you feel like products is more like a high single digit business in 2026 than mid-singles for you? I just wanted to get clarify that in terms of what you're penciling in for product growth in 2026. Thanks.

Jerry Shelton

No, I do feel like it's high single growth. high single digit growth, Matt. It seems like it's solidifying in every aspect across the globe. I have no reason to think any differently.

Matt Stanton

Okay, thanks. Maybe Mark, just one for you to go back to IntegriCell. Now that you've seen the customers in those 2 sites, you know, start to actually move product, any finer point you can talk to in just in terms of the volume or the size of product you expect there? I know it takes a while to kinda get things validated and started, but now that they're started, I guess, you know, how meaningful, even though it's 2 customers, could that kinda be as IntegriCell ramps up? I think prior you'd, you know, been pretty bullish in terms of the revenue opportunity given the number of kinda products and services you're pushing through as part of IntegriCell. Thank you.

Jerry Shelton

Yeah. You know, Matt, we are bullish. We're bullish about everything that we do. Ever since we formed the company, we've set standards in the industry. IntegriCell is another example of our industry leading a movement forward based on what the markets need, based on conversations with clients and what they need. IntegriCell is off to a good start, I would say. And I, you know, we always would like to have a more robust start no matter what it is, but it's off to a very good start right now. And it's gaining a lot of attention. It does take time for these things to take hold for other clients to come in and for our integrated services approach to take effect. Stay tuned.

Jerry Shelton

As Mark said, it will be unquestionably a very important contributor to Cryoport in the future.

Matt Stanton

Super. Thank you.

Operator

Thank you. There are no further questions at this time. I will now hand the call back to Mr. Jerrell Shelton for any closing remarks.

Jerry Shelton

Thank you, operator. Ladies and gentlemen, thank you for your questions and our discussions. They've been very good. I appreciate them very much. In closing, I'd just like to remind you that we continue to be the market leader. We have had a great start to 2026, marked by a 16% revenue growth year-over-year and strong double-digit growth across both our reporting segments. Our Life Sciences Services segment grew 18% year-over-year, driven by 21% growth in BioStorage/BioServices revenue, a 26% increase in revenue from commercial cell and gene therapy support, and clinical trial-related revenue growth of 18%. At this time, at the same time rather, our Life Sciences Products segment grew by 15%, driven by global demand for MVE's cryogenic systems. Remember, MVE is the world leader in cryogenic systems.

Jerry Shelton

Our top-line growth was accompanied by solid gross margins, contained operating, and continued operational discipline, which resulted in a $2.2 million year-over-year improvement in adjusted EBITDA from continuing operations, pushing us further down our pathway to profitability. Based on these results and the progress we have made with our strategic initiatives, we're more positive on our outlook for the year than when we last spoke to you in our year-end earnings call. That's led us to raise our full-year revenue guidance as we continue to see opportunities ahead of us. We look forward to keeping you up to date on our progress. We thank you for joining us this evening. We appreciate your continued interest and support, and we're looking forward to speaking with you again when we report our second quarter financial results.

Jerry Shelton

We wish all of you a good evening.

Operator

This concludes today's call. Thank you for participating. You may all disconnect.

Investor releaseQuarter not tagged2026-04-21

Cryoport to Report First Quarter 2026 Financial Results on May 4, 2026

PR Newswire

NASHVILLE, Tenn., April 20, 2026 /PRNewswire/ -- Cryoport, Inc. (Nasdaq: CYRX) ("Cryoport" or the "Company"), a leading global provider of integrated temperature-controlled supply chain solutions for the life sciences, today announced that the Company will report financial results for the first quarter ended March 31, 2026 on Monday, May 4, 2026 after U.S. markets close. In addition to the earnings release, a document titled "Cryoport First Quarter 2026 in Review", providing a review of Cryoport's financial and operational performance and a general business update, will be issued at 4:05 p.m. ET on Monday, May 4, 2026. The document is designed to be read in advance of the questions and answers conference call and will be accessible at https://ir.cryoportinc.com/news-events/ir-calendar. Cryoport management will host a conference call the same day at 5:00 p.m. ET. The conference call will be in the format of a questions and answers session and will address questions members of the investment community have regarding the Company's reported results. A slide deck will accompany the call. Please allow 10 minutes prior to the call to visit this site to download and install any necessary audio software. The questions and answers call will be recorded and available approximately three hours after completion of the live event in the Investor Relations section of the Company's website at www.cryoportinc.com for a limited time. To access the replay of the questions and answers click here. A dial-in replay of the call will also be available to those interested, until May 11, 2026. To access the replay, dial 1-844-512-2921 (United States) or 1-412-317-6671 (International) and enter replay entry code: 1191652#. About Cryoport, Inc Cryoport, Inc. (Nasdaq: CYRX), is a leading global provider of integrated, temperature-controlled supply chain solutions for the life sciences, with an emphasis on regenerative medicine. We support biopharmaceutical companies, contract manufacturers (CDMOs), contract research organizations (CROs), developers, and researchers with a comprehensive suite of services and products designed to minimize risk and maximize reliability across the temperature-controlled supply chain for the life sciences. Our integrated supply chain platform includes the Cryoportal® Logistics Management Platform, advanced temperature-controlled packaging, informatics, speci...

Investor releaseQuarter not tagged2026-03-04

CryoPort Inc (CYRX) Q4 2025 Earnings Call Highlights: Record Growth in Cell and Gene Therapy Revenue

GuruFocus.com

This article first appeared on GuruFocus. Full-Year Revenue from Continuing Operations: $176.2 million, exceeding prior guidance. Fourth Quarter Commercial Cell and Gene Therapy Revenue: Increased 29% year over year to $33.4 million. Clinical Trial Revenue: Grew 14% year over year to $47.1 million. Gross Margin: 47% for 2025. Adjusted EBITDA Improvement: $12 million year-over-year improvement. Life Sciences Services Revenue Growth: Increased 18% year over year, with BioStorage and BioServices revenue growing 22%. Life Sciences Product Segment Revenue Growth: 7% year over year in 2025. Full-Year 2026 Revenue Guidance: $190 million to $194 million. Warning! GuruFocus has detected 6 Warning Signs with CYRX. Is CYRX fairly valued? Test your thesis with our free DCF calculator. Release Date: March 03, 2026 For the complete transcript of the earnings call, please refer to the full earnings call transcript. CryoPort Inc (NASDAQ:CYRX) reported full-year revenue from continuing operations of $176.2 million, exceeding the high end of their prior guidance. The company achieved double-digit growth in the fourth quarter, driven by expanding commercial cell and gene therapy activity. Revenue from commercial cell and gene therapy increased 29% year over year to a record $33.4 million. CryoPort Inc (NASDAQ:CYRX) supported a record 760 clinical trials and 20 commercial therapies worldwide in 2025. The company anticipates achieving positive adjusted EBITDA in the second half of 2026. The financials of CRYOPDP, previously part of CryoPort's Life Sciences Services segment, are now presented as discontinued operations due to its sale to DHL. The macroeconomic environment remains volatile, posing potential risks to CryoPort Inc (NASDAQ:CYRX)'s growth projections. MVE Biological Solutions, a segment of CryoPort Inc (NASDAQ:CYRX), reported only 7% revenue growth year over year, indicating slower growth compared to other segments. The integration and full benefits of the strategic partnership with DHL are expected to take time to materialize. CryoPort Inc (NASDAQ:CYRX) faces uncertainties in the timing of new product launches and their market adoption, which could impact future revenue projections. Q: Could you elaborate on the growth expectations for Cryoport's segments, particularly in commercial therapies, BioLogistics, BioStorage, and MVE? A: Jerrell Shelton, CEO, explained that...

Investor releaseQuarter not tagged2026-03-04

Cryoport Reports Fourth Quarter and Full-Year 2025 Financial Results

PR Newswire

FY 2025 revenue increased to $176.2 million, exceeding the high end of previous guidance Life Sciences Services revenue grew 18% year-over-year in FY 2025, including a 22% rise in BioStorage/BioServices revenue Commercial cell and gene therapy revenue increased 29% year-over-year to $33.4 million in FY 2025 Supported a record 760 global clinical trials and 20 commercially approved therapies as of December 31, 2025 Full-year 2026 revenue guidance of $190 million to $194 million (8%-10% growth y-o-y) NASHVILLE, Tenn., March 3, 2026 /PRNewswire/ -- Cryoport, Inc. (NASDAQ: CYRX) ("Cryoport" or the "Company"), a leading global provider of integrated temperature-controlled supply chain solutions for the life sciences, today announced financial results for its fourth quarter (Q4) and year ended (FY) December 31, 2025. Jerrell Shelton, CEO of Cryoport, commented, "2025 was a year of strong progress for Cryoport. We delivered full-year revenue of $176.2 million, exceeding the high end of our previous guidance and reflecting continued momentum across our core markets. We achieved double-digit revenue growth driven by expanding cell and gene therapy ("CGT") activity, with revenue from the support of commercial CGTs increasing 29% year-over-year to a record $33.4 million for FY 2025. Revenue from the support of clinical trials also remained solid, growing 14% to $47.1 million for FY 2025. At year-end, we supported a record 760 global clinical trials, representing approximately 70% of CGT trials. We believe our leadership position across both clinical and commercial programs, and the breadth of the development pipeline we support, provide a substantial foundation for sustained long-term growth. "We continued to execute on our strategy of expanding our revenue streams and capturing more revenue per client as our Life Sciences Services revenue increased 18% year-over-year for FY 2025, including 22% growth in BioStorage/BioServices revenue. This performance reflects the expanding scale of the clinical and commercial programs we support and the increasing value customers place on our differentiated high-end supply chain solutions. While our primary focus remains on accelerating revenue growth and strengthening our market position, we continue to enhance operational discipline across the organization as we advance on our pathway to profitability. In 2025, our cost reduction i...

Investor releaseQuarter not tagged2026-03-04

Cryoport, Inc. Q4 2025 Earnings Call Summary

Moby

Revenue growth was primarily driven by a 29% year-over-year increase in commercial cell and gene therapy support, which now represents 20% of total revenue. The company maintains a dominant market position, supporting approximately 70% of all cell and gene therapy industry clinical trials. Management describes the clinical pipeline as 'spring-loaded' for future commercial revenue, with 86 trials in Phase III and 361 in Phase II. Operational discipline and cost reduction initiatives resulted in a $12 million year-over-year improvement in adjusted EBITDA and a 47% gross margin. The strategic sale of CRYOPDP to DHL provided a substantial capital infusion and established a partnership to leverage DHL's global scale in APAC and EMEA regions. Strategic collaborations with Cardinal Health and Parexel aim to standardize supply chain solutions and embed Cryoport deeper into the life sciences ecosystem. Internal investments focused on expanding global infrastructure, including new supply chain centers in Paris and California to support commercial client scaling. Full year 2026 revenue guidance is set at $190 million to $194 million, characterized by management as an appropriate starting point given macro volatility. Management anticipates achieving positive adjusted EBITDA in the second half of 2026 as recent infrastructure investments begin to scale. The outlook assumes significant regulatory activity, including 13 BLA or MAA filings and 9 new therapy approvals expected within the year. Growth in the Life Sciences Products segment is projected at mid-to-high single digits, supported by the launch of the Fusion 800 Series self-sustaining cryogenic freezer. The transition of therapies to outpatient community care settings is expected to serve as a significant long-term volume driver for commercial services. CRYOPDP financials are now presented as discontinued operations following the strategic partnership and sale to DHL Group. The timeline for positive adjusted EBITDA was shifted to late 2026 to accommodate accelerated investments in specific client-requested infrastructure, such as the Belgium facility. Management noted that while biopharma funding saw a strong recovery in late 2025, there is typically a half-year lag before this impacts order volume. Geopolitical tensions have had minimal impact on operations to date, with no expected flight cancellations or major d...

As of 2026-05-18 • Updated weeklySource: Earnings sourceIngestion runbook