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CGEN

CompugenA
Nasdaq / Pharmaceuticals, Biotechnology & Life Sciences
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2026-06-02
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2026-05-26
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Earnings documents stored for CGEN.

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Investor releaseQuarter not tagged2026-05-26

Compugen Ltd (CGEN) Q1 2026 Earnings Call Highlights: Strategic Advances Amid Financial Challenges

GuruFocus.com

This article first appeared on GuruFocus. Cash Balance: Approximately $134.9 million as of March 31, 2026. Revenue: Approximately $2.2 million for Q1 2026, compared to $2.3 million in Q1 2025. R&D Expenses: Approximately $6.9 million for Q1 2026, up from $5.8 million in Q1 2025. G&A Expenses: Approximately $2.3 million for Q1 2026, compared to $2.4 million in Q1 2025. Net Loss: Approximately $7.7 million or $0.08 per share for Q1 2026, compared to $7.2 million or $0.08 per share in Q1 2025. Cash Runway: Expected to fund operations into 2029. Warning! GuruFocus has detected 6 Warning Signs with CGEN. Is CGEN fairly valued? Test your thesis with our free DCF calculator. Release Date: May 18, 2026 For the complete transcript of the earnings call, please refer to the full earnings call transcript. Compugen Ltd (NASDAQ:CGEN) is making significant progress with its fully owned clinical program, COM701, which has shown promising results in ovarian cancer treatment. The company has initiated the MAIA-ovarian adaptive platform trial to test COM701 as a maintenance therapy, with active patient enrollment across the United States, Israel, and France. Compugen Ltd (NASDAQ:CGEN) has a solid financial position with a cash runway expected to last into 2029, providing stability and flexibility for future developments. Partnership with AstraZeneca is progressing well, with multiple abstracts presented at the AACR Annual Meeting, reinforcing confidence in the rilvegostomig program. The Unigen discovery engine continues to be a valuable asset, having already discovered targets for COM701, COM902, and GS-0321, and is expected to identify more innovative programs. Revenues for the first quarter of 2026 were slightly lower than the comparable period in 2025, indicating potential challenges in revenue growth. Research and development expenses have increased, primarily due to higher clinical expenses related to the MAIA-ovarian trial and drug supply costs. The net loss for the first quarter of 2026 increased compared to the same period in 2025, reflecting ongoing financial challenges. The MAIA-ovarian trial is exploratory, and the full magnitude of benefit from COM701 is still uncertain, with benchmarks for control arm PFS ranging widely. There is no specific timeline or guidelines for disclosing future development candidates from the Unigen platform, which may lead to uncertainty...

Investor releaseQuarter not tagged2026-05-18

Compugen Q1 Earnings Call Highlights

MarketBeat

Compugen (NASDAQ:CGEN) said it remains on track to report interim progression-free survival data in the first quarter of 2027 from its MAIA-ovarian study, as the clinical-stage immuno-oncology company outlined first-quarter 2026 results and updates across its internal and partnered programs. On the company’s first-quarter earnings call, President and Chief Executive Officer Dr. Eran Ophir said 2026 is “shaping up to be a significant year” for Compugen as it advances COM701, its wholly owned antibody targeting PVRIG, and monitors progress on partnered assets with AstraZeneca and Gilead. → 3 Crucial Aerospace Component Makers That Analysts Love Compugen’s lead wholly owned clinical program, COM701, is being evaluated in the MAIA-ovarian adaptive platform trial as maintenance monotherapy compared with placebo in patients with relapsed platinum-sensitive ovarian cancer who responded to their most recent line of chemotherapy. Ophir said the company initiated the study based on prior data presented at ESMO, where pooled clinical data showed COM701, as monotherapy and in combinations, was well-tolerated and produced “consistent, durable responses” in heavily pretreated patients with platinum-resistant ovarian cancer. → 3 Stocks to Own If Gas Prices Keep Rising The company is now testing COM701 in an earlier ovarian cancer setting, with the rationale that patients may have lower tumor burden and a less compromised immune system, potentially improving the likelihood of benefit from COM701’s mechanism of action. Ophir said all clinical sites are open and enrolling across the United States, Israel and France. He said that gives the company confidence in its ability to complete enrollment on schedule for interim median progression-free survival data in the first quarter of 2027. → Peloton Stock Gives Back Gains After Upbeat Earnings Report Chief Medical Officer Dr. Michelle Mahler said during the question-and-answer session that Compugen is not currently commenting on specific enrollment numbers, but remains “on track” for the planned interim analysis. She said the study is stratified by second-line versus third-line treatment, not by PD-L1 status. Ophir added that prior clinical signals with COM701 have been seen in both PD-L1-positive and PD-L1-negative patients, saying PD-L1 stratification may not be the critical factor for the PVRIG-targeting approach. Mahler said t...

Investor releaseQuarter not tagged2026-05-18

Compugen surges after revenue tops forecasts despite quarterly loss miss (CGEN)

InvestorsHub

Compugen Ltd. (NASDAQ:CGEN) shares jumped more than 18% in premarket trading on Monday after the biotechnology company reported first-quarter revenue ahead of analyst expectations, despite posting a slightly wider-than-expected quarterly loss. The clinical-stage cancer immunotherapy company reported a quarterly loss of $0.08 per share for the period ended March 31, missing analyst estimates that had projected a loss of $0.07 per share. Revenue came in at $2.2 million, exceeding consensus expectations of $1.63 million. However, quarterly revenue was down 4% compared with $2.3 million reported in the first quarter of 2025. Compugen said revenue during the quarter reflected recognition of portions of both the upfront payment and the IND milestone payment tied to its licensing agreement with Gilead. Despite the earnings miss, investors appeared encouraged by stronger-than-expected revenue and continued advancement across the company’s clinical development programs. Compugen said enrollment in its COM701 MAIA-ovarian study is continuing across all participating clinical sites in the United States, Israel and France. The company remains on schedule to conduct an interim analysis during the first quarter of 2027. “Q1 2026 reflects continued execution across all of our programs in line with our strategic priorities,” said Eran Ophir, president and chief executive of Compugen. “With enrollment progressing across all COM701 MAIA-ovarian trial sites, we remain on track for having the median progression-free survival at the interim analysis by Q1 2027, a key potential inflection point for COM701 as a maintenance therapy in a patient population with significant unmet medical need and no current standard of care.” Research and development expenses increased to $6.9 million from $5.8 million a year earlier, primarily driven by higher clinical trial spending related to the MAIA-ovarian program and increased drug supply costs. General and administrative expenses edged slightly lower to $2.3 million from $2.4 million. Compugen reported total cash, cash equivalents, short-term bank deposits and marketable securities of approximately $134.9 million as of March 31, 2026. The company said its current financial resources are expected to support operations through 2029 based on existing development plans. Compugen also noted that partner AstraZeneca is continuing development of ril...

Investor releaseQuarter not tagged2026-05-18

Compugen: Q1 Earnings Snapshot

Associated Press

HOLON, Israel (AP) — HOLON, Israel (AP) — Compugen Ltd. (CGEN) on Monday reported a loss of $7.7 million in its first quarter. The Holon, Israel-based company said it had a loss of 8 cents per share. The results did not meet Wall Street expectations. The average estimate of three analysts surveyed by Zacks Investment Research was for a loss of 7 cents per share. The drug developer posted revenue of $2.2 million in the period. _____ This story was generated by Automated Insights (http://automatedinsights.com/ap) using data from Zacks Investment Research. Access a Zacks stock report on CGEN at https://www.zacks.com/ap/CGEN

Investor releaseQuarter not tagged2026-05-18

Compugen Reports First Quarter 2026 Results

PR Newswire

COM701 MAIA-ovarian trial actively enrolling patients across all clinical sites in the U.S., Israel, and France; interim analysis on track by Q1 2027 Partner AstraZeneca is advancing rilvegostomig across 11 ongoing Phase 3 trials and presented clinical and pre-clinical rilvegostomig data at AACR 2026, including late-breaking Phase 2 data in HER2-positive gastric cancer (DESTINY-Gastric03), with new data to be released at ASCO 2026 Gilead-partnered GS-0321 Phase 1 trial continues to progress as planned Solid financial position with cash runway expected to fund operations into 2029 HOLON, Israel, May 18, 2026 /PRNewswire/ -- Compugen Ltd. (NASDAQ: CGEN) (TASE: CGEN) a clinical-stage cancer immunotherapy company and a pioneer in computational target discovery powered by AI/ML, today reported financial results for the first quarter of 2026 and provided a corporate update. "Q1 2026 reflects continued execution across all of our programs in line with our strategic priorities," said Eran Ophir, Ph.D., President and CEO of Compugen. "With enrollment progressing across all COM701 MAIA-ovarian trial sites, we remain on track for having the median progression-free survival at the interim analysis by Q1 2027, a key potential inflection point for COM701 as a maintenance therapy in a patient population with significant unmet medical need and no current standard of care." Dr. Ophir continued, "Our partner AstraZeneca continues to broadly advance rilvegostomig. Data presented by AstraZeneca at AACR 2026 reinforces our confidence in its differentiated bispecific design and potential as an immuno-oncology backbone across multiple tumor types, as AstraZeneca progresses rilvegostomig across 11 Phase 3 trials. In addition, we continue to advance the Gilead-partnered GS-0321 Phase 1 trial." Dr. Ophir concluded, "Our solid financial position with cash runway expected into 2029, based on our current plans, enables us to advance our differentiated immuno-oncology pipeline and leverage our AI/ML powered computational discovery platform Unigen™, to discover novel ways to activate the immune system against cancer. I remain encouraged by the progress of our fully owned programs, strengthened by validating partnerships with AstraZeneca and Gilead, which together offer approximately $1 billion in potential milestones plus royalties." First Quarter 2026 Financial Highlights Cash: As of Mar...

TranscriptFY2026 Q12026-05-18

FY2026 Q1 earnings call transcript

Earnings source - 46 paragraphs
Operator

Ladies and gentlemen, thank you for joining us today. Welcome to Compugen's first quarter 2026 results conference call. At this time, all participants are in listen-only mode. An audio webcast of this call is available in the Investors section of Compugen's website at www.cgen.com. As a reminder, today's call is being recorded. I will now hand the call over to Lindsey Trickett, Head of Investor Relations and Corporate Communications to begin. Lindsey, please go ahead.

Lindsey Trickett

Thank you, operator. Good morning and good afternoon, everyone, welcome to Compugen's first quarter 2026 financial results conference call. With us today are Dr. Eran Ophir, President and Chief Executive Officer, and David Silberman, Chief Financial Officer. Dr. Michelle Mahler, Chief Medical Officer, will join us for the Q&A portion of the call.

Lindsey Trickett

Before we begin, I'd like to remind you that during this call, the company may make projections or forward-looking statements regarding future events, business outlook, development efforts and their potential outcome, the company's discovery platform, anticipated progress and plans, results and timelines for our programs, including disclosure of clinical data, financial and accounting related matters, as well as statements regarding our cash position and cash runway.

Lindsey Trickett

We wish to caution you that such statements reflect only the company's current beliefs, expectations, and assumptions, and that actual results, performance, or achievements of the company may differ materially. These statements are subject to known and unknown risks and uncertainties, and we refer you to our SEC filings for more details on these risks, including the company's most recent annual report on Form 20-F. The company undertakes no obligation to update projections and forward-looking statements in the future. With that, I'll now turn the call over to Dr. Eran Ophir, President and CEO.

Eran Ophir

Thank you, Lindsey, and good morning and good afternoon, everyone. Before I turn to our business update, I want to take a moment to formally welcome Lindsey, our new Head of Investor Relations and Corporate Communications, to Compugen. Lindsey joined us with strong experience in investor relations, and we are thrilled to have her leading our communication with the investor community. Welcome, Lindsey, and we are glad to have you on board.

Eran Ophir

Now, let's start with our business update. 2026 is shaping up to be a significant year for Compugen, and I'm pleased to share our progress in the first quarter of 2026 as we continue executing on our strategic priorities. Starting with our fully owned clinical program, COM701, a potential first-in-class antibody targeting PVRIG, which is an immune checkpoint with unique biology, much differentiated from other [PIC] checkpoints, including PD-1 and TIGIT.

Eran Ophir

We believe this unique biology underlies the clinical activity demonstrated for COM701 in less inflamed indications such as ovarian cancer. As a reminder, at ESMO last year represented the pooled analysis of clinical data showing that COM701 in monotherapy and combinations was well-tolerated and showed consistent, durable responses in patients with heavily pretreated platinum-resistant ovarian cancer.

Eran Ophir

Based on these results, we decided to progress the development of COM701 and test it in earlier settings of ovarian cancer as a maintenance therapy in patients with relapsed platinum-sensitive ovarian cancer that responded to their most recent line of chemotherapy. The rationale is to allow COM701 to induce its antitumor activity in early line patients with lower tumor burden, less compromised immune system, and by that increase the likelihood of these patients to benefit from COM701 unique mode of action.

Eran Ophir

For this purpose, we initiated the MAIA-ovarian adaptive platform trial. In sub-study I of this trial, COM701 is randomized as maintenance monotherapy versus placebo in patients with relapsed platinum-sensitive ovarian cancer. We are actively enrolling patients in clinical sites across the U.S., Israel, and France. Having all sites open and enrolling, spanning leading academic centers in the U.S. and Israel, as well as sites from the French cooperative group, gives us confidence in our ability to complete enrollment on schedule for having the MAIA-ovarian median PFS data at interim analysis by Q1 2027.

Eran Ophir

This patient population, comprised of those progressing post PARP inhibitors and/or Bev, or who are not candidates for such treatments, represent a significant unmet medical need with no current standard of care. We believe that clear prolongation of PFS in these patients could inform a registration path for COM701 and make it a potential backbone for drug combinations in this population, while also enabling a potential broader clinical development plan across earlier and later lines of ovarian cancer treatments, as well as in other indications where clinical signals previously seen for COM701.

Eran Ophir

We're happy to see our partner AstraZeneca's progress on their broad rilvegostomig program. We remain confident in rilve's potential based on its differentiated bispecific antibody format in addition to its clinical and combination strategies. Last month, AstraZeneca presented multiple abstracts featuring rilve at the AACR annual meeting in San Diego, reinforcing our confidence in its differentiated design and growing potential.

Eran Ophir

This includes preclinical data demonstrating potential opportunities for rilve as an IO backbone for combinations, late-breaking data from the DESTINY-Gastric03 phase II trial evaluating rilve in combination with the blockbuster ADC ENHERTU and chemotherapy as first-line treatment for HER2-positive gastric cancers. This data showed promising antitumor activity and also demonstrated combinability of rilve from safety perspective.

Eran Ophir

These AACR publications continue to reinforce our confidence in rilve as AZ continues to advance it along 11 phase III trials across multiple indications, including the recently opened trial in gastric in combination with the claudin 18.2 ADC. We are looking forward to the release of additional clinical data on rilve along the year, including at the next ASCO meeting at the end of the month.

Eran Ophir

As a reminder, AstraZeneca has previously estimated a non-risk-adjusted peak annual revenue potential of more than $5 billion for rilve. We are eligible for additional $995 million in future regulatory and commercial milestone payments, plus mid-single-digit tiered royalties on sales. Moving to GS-0321, formerly known as COM503, our potential first-in-class anti-IL-18 binding protein antibody licensed to Gilead. GS-0321 represents a novel antibody approach to harness cytokine biology for the treatment of cancer, potentially overcoming the limitations of direct cytokine administration.

Eran Ophir

The ongoing phase I dose-escalation trial continues to progress as we planned. As a reminder, we received to date $90 million from Gilead of this asset and are eligible to receive up to $758 million in additional milestone payments, plus up to double-digit tiered royalties. Now to the early-stage pipeline and Unigen discovery engine. Beyond our clinical assets, we continue to invest in our early-stage immune oncology pipeline. Unigen, our AI-powered computational target discovery platform, has already discovered the targets of COM701, COM902, and GS-0321.

Eran Ophir

We remain committed to identifying and advancing the next wave of innovative programs grounded in novel mechanism of action designed to activate the immune system against cancer. Importantly, we have a solid financial position with a cash runway expected into 2029 following the December 2025 transaction with AZ, through which we received $65 million in non-diluted capital by monetizing only a small portion of our future rilve royalties.

Eran Ophir

Our financial stability allows us to fully focus on advancing our pipeline and reaching key value-creating milestones with both our internal and partnered programs. Throughout all of this, we continue to benefit from a deeply talented and highly committed team here at Compugen. I am proud of what we have built and energized by the opportunities ahead. With that, let me hand over to David for the financial update before we open the floor for Q&A.

David Silberman

Thank you, Eran, and I would like to add my own warm welcome to Lindsey as well. It is a pleasure to have you join the Compugen team, Lindsey, and we look forward to working together. I am pleased to say that we continue to advance into 2026 with a solid balance sheet and financial flexibility. Cash runway, assuming no further cash inflows, is expected to fund our operating plans into 2029. We anticipate using this runway to continue advancing our COM701 platinum-sensitive ovarian cancer trial, MAIA-ovarian, and to support the progression of GS-0321 in the clinic, together with continued investment in our early-stage pipeline.

David Silberman

Now going into the details, I will start with our cash balance. As of March 31st, 2026, we had approximately $134.9 million in cash equivalents, short-term bank deposits, and investment in marketable securities. Revenues for Q1 2026 were approximately $2.2 million compared to approximately $2.3 million of revenue for the comparable period in 2025. The revenues in Q1 2026 and 2025 reflect the recognition of fulfillment of both the upfront payment and the R&D milestone payment from the license agreement with Gilead. Expenses for Q1 2026 were in line with our plans. R&D expenses for Q1 2026 were approximately $6.9 million compared to approximately $5.8 million in Q1 2025.

David Silberman

The increase is mainly due to an increase in clinical expenses related to MAIA-ovarian trial, as well as higher drug supply costs supporting our trials. Our G&A expenses for the first quarter of 2026 were approximately $2.3 million compared to approximately $2.4 million for the comparable period in 2025. For the first quarter of 2026, our net loss was approximately $7.7 million or $0.08 per basic and diluted share, compared to a net loss of approximately $7.2 million or $0.08 per basic and diluted share in the first quarter of 2025. With that, I will hand over to the operator to open the call for questions.

Operator

Thank you. Ladies and gentlemen, at this time, we will begin the question-and-answer session. If you have a question, please press star one. If you wish to decline from the polling process, please press star two. If you are using speaker equipment, kindly leave the handset before pressing the numbers. Please stand by while we poll for your questions. The first question is from Daina Graybosch of Leerink Partners. Please go ahead.

Daina Graybosch

Hi. Thank you for the question. Lindsey, welcome. Nice to see you here. Going into ASCO, I wonder if you could talk about more specifically the datasets AstraZeneca is gonna present with rilvegostomig and help set the context for, you know, what we should expect to see and, you know, are there benchmarks that we should be keeping in mind when we review the datasets?

Eran Ophir

Sure. Thanks, Daina. We're talking about two datasets, clinical data. Obviously, the actual data is not released yet, and I would be cautious on setting expectations on behalf of AstraZeneca. Overall, we talk about on the I-SPY trial in the testing rilvegostomig in adjuvant settings with ENHERTU, which is by itself a blockbuster drug, which is very exciting to see these combinations. Again, I would be cautious about setting expectations, but I think looking again, and this is a platform trial, so really trying to look across, not a randomized study, but trying to look about rilve versus other datasets.

Eran Ophir

The combinability is again going to be very important and to show again, how the Fc-reduced format of rilvegostomig is easier to combine with such ADCs. The second set is the German hepatobiliary, which is in combination with chemotherapy. Here again, will be good to see. I think it's a bit of a longer follow-up from what was reported before, so it'll be interesting to see about the long-term effect, how the PFS, how the I'm not sure if there will be an OS data, but how the long-term effects are shaping, including the long-term safety in combination with chemo, having in mind that there is, for this trial, there's an ongoing phase III study ongoing. I guess the comparison to a single control should be with caution and still probably is gonna be made.

Daina Graybosch

Great. Thank you.

Operator

The next question is from Stephen Willey of Stifel. Please go ahead.

Stephen Willey

Yeah, good morning. Thanks for taking the questions. Maybe you can just talk a little bit about how you're thinking about disclosing future development candidates that are discovered off the Unigen platform. I think the IL-18 binding protein antibody wasn't announced until it was ready for clinical development. Is that kind of how we should expect incremental assets to emerge out of the pipeline once they're ready for an IND submission? Thanks.

Eran Ophir

Thanks, Steve. I think it's really dependent. Eventually, definitely the biggest group in Compugen is the one which continue to work to bring additional innovative assets like COM503, which is called today GS-0321. Specifically for that asset, it was right for this asset and for Compugen at these times to out-license it in preclinical stage. This also influenced the stage in which we disclosed it, which was relatively early. It doesn't mean necessarily that we have any specific guidelines that we're reporting on early assets only when it's ready for IND or only on its selection. It really depends on the actual assets, on the stage of the risking in which we want to start comment and committing.

Eran Ophir

I wouldn't learn too much from the story of IL-18 binding protein other than the fact that it was another demonstration how our computational platform can bring such innovative approaches, in that case, not only first-in-class asset, but the first-in-class approach to harness cytokine biology for the treatment of cancer. We are looking into different MOAs, not necessarily similar to that, to bring, again, another innovative options that could really make difference to patients.

Stephen Willey

All right. Thanks.

Operator

The next question is from Leland Gershell of Oppenheimer. Please go ahead.

Leland Gershell

Great. Good morning. Thanks for taking our questions. Could you remind us if the MAIA-ovarian trial, is that stratifying for patients who are PD-L1 or PD-1 expression, you know, status? Also want to ask when we see the interim data in the first quarter. Given that this is an adaptive trial, would that mean that the interim data could inform some change to your design, or would you simply, you know, keep going as planned? Thank you.

Eran Ophir

Thank you, Leland.

Michelle Mahler

Hi.

Eran Ophir

I think, Michelle can take this one.

Michelle Mahler

I'm happy to take this one. Yeah. The MAIA-ovarian trial actually is not stratified according to PD-L1 subgroup. We are stratified by second versus third line of treatment. In Q1 2027 when it reads out, we have multiple options ahead of us in terms of adjustments to the trial. We would consider adding additional arms, and a lot of it's going to depend on the totality of the data and also plans towards engaging with the regulators and steps towards a pivotal trial.

Leland Gershell

Thank you.

Eran Ophir

If I may add additional comment, Leland, about the, about the PD-L1 stratification. I would like to remind you that PVRIG, probably because of its unique biology, we saw in other indication, and specifically in ovarian cancer, we saw responses across PD-L1 positive and PD-L1 negative patients. For now, we didn't see that necessarily, like for other checkpoints, that the PD-L1 subset is the one responding to COM701. Again, I think this is because that unique biology very much differentiated from PVRIG to PD-1. Again, not necessarily PD-L1 stratification is the critical stratification here.

Leland Gershell

Thanks so much, Eran. Thank you.

Operator

The next question is from R.K. of H.C. Wainwright. Please go ahead.

R.K. Swayampakula

Thank you. Thank you, Eran, for taking my questions. A couple more questions on the ovarian cancer trial. Now that, you know, you have all the sites active, what is, you know, any commentary on the enrollment status itself and also because this is an event-driven trial, any commentary on the required events that needs to happen for the interim analysis? The third question is, what are you assuming, you know, for the control on PFS and what sort of an hazard ratio do you need to see to consider that as a win?

Eran Ophir

Thanks, R.K. Michelle, do you want to take it?

Michelle Mahler

Yeah, sure. Firstly, with respect to our enrollment, we're not commenting at this point in time, but I will say to you that we are on track for our interim analysis as planned in Q1 2027. Our participating investigators have a high level of engagement and are working really well with us. Regarding the events and the benchmarking, the trial is an exploratory trial, at this point in time, we don't know the full magnitude of benefit.

Michelle Mahler

The benchmark for the control arm from prior clinical trials in the second line and third line of maintenance, in those trials where patients did not get treatment, the same patient population had a benchmark of approximately 5.5 months, although there was a range. In some studies, it was as low as 3.8 months and others as high as 5.8 months. We're hoping to be able to show that there is meaningful single agent clinical activity of COM701, and we've hypothesized that we would like to see a three month or greater improvement of the benchmark PFS.

R.K. Swayampakula

Perfect. Thank you. Thanks for taking my questions.

Michelle Mahler

Sure.

Investor releaseQuarter not tagged2026-05-14

Adherex Technologies Inc. (FENC) Beats Q1 Earnings and Revenue Estimates

Zacks

Adherex Technologies Inc. (FENC) came out with quarterly earnings of $0.01 per share, beating the Zacks Consensus Estimate of a loss of $0.02 per share. This compares to a loss of $0.04 per share a year ago. These figures are adjusted for non-recurring items. This quarterly report represents an earnings surprise of +157.14%. A quarter ago, it was expected that this company would post earnings of $0.03 per share when it actually produced a loss of $0.11, delivering a surprise of -466.67%. Over the last four quarters, the company has surpassed consensus EPS estimates two times. Adherex Technologies, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $15.11 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 8.36%. This compares to year-ago revenues of $8.75 million. The company has topped consensus revenue estimates three times over the last four quarters. The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call. Adherex Technologies shares have lost about 12.1% since the beginning of the year versus the S&P 500's gain of 8.8%. While Adherex Technologies has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock? There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately. Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions. Ahead of this earnings release, the estimate revisions trend for Adherex Technologies was unfavorable. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #5 (Strong Sell) for the stock. So, the shares are expected to underperform the market in the near f...

Investor releaseQuarter not tagged2026-05-05

BioMarin Pharmaceutical (BMRN) Q1 Earnings Lag Estimates

Zacks

BioMarin Pharmaceutical (BMRN) came out with quarterly earnings of $0.76 per share, missing the Zacks Consensus Estimate of $0.94 per share. This compares to earnings of $1.13 per share a year ago. These figures are adjusted for non-recurring items. This quarterly report represents an earnings surprise of -18.96%. A quarter ago, it was expected that this rare disease biopharmaceutical would post earnings of $0.25 per share when it actually produced earnings of $0.46, delivering a surprise of +84%. Over the last four quarters, the company has surpassed consensus EPS estimates three times. BioMarin, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $766.21 million for the quarter ended March 2026, surpassing the Zacks Consensus Estimate by 0.50%. This compares to year-ago revenues of $745.15 million. The company has topped consensus revenue estimates three times over the last four quarters. The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call. BioMarin shares have lost about 9% since the beginning of the year versus the S&P 500's gain of 5.6%. While BioMarin has underperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock? There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately. Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions. Ahead of this earnings release, the estimate revisions trend for BioMarin was mixed. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #3 (Hold) for the stock. So, the shares are expected to perform in line with the market in the near future. You can see the complete list of t...

Investor releaseQuarter not tagged2026-05-04

Compugen to Release First Quarter 2026 Results on Monday, May 18, 2026

PR Newswire

HOLON, Israel, May 4, 2026 /PRNewswire/ -- Compugen Ltd. (NASDAQ: CGEN) (TASE: CGEN), a clinical-stage cancer immunotherapy company and a pioneer in computational drug target discovery powered by AI/ML, today announced that the Company will release its first quarter 2026 financial results on Monday, May 18, 2026, before the U.S. financial markets open. Management will host a conference call and webcast to review the results and provide a corporate update at 8:30 AM ET. To access the live conference call by telephone, please dial 1-866-744-5399 from the U.S., or +972-3-918-0644 internationally. The call will be available via live webcast through Compugen's website, which is located at the following link. Following the live webcast, a replay will be available on the Company's website. About Compugen Compugen is a clinical-stage therapeutic discovery and development company utilizing Unigen™, its AI/ML powered computational discovery platform, to identify novel drug targets and to develop therapeutics in the field of cancer immunotherapies. Compugen's innovative immuno-oncology pipeline consists of four clinical-stage programs: COM701, COM902, rilvegostomig and GS-0321 (previously COM503). COM701, a potential first-in-class anti-PVRIG antibody, and COM902, a potential best-in-class therapeutic anti-TIGIT antibody, have been evaluated for the treatment of solid tumors as monotherapy and in combinations of dual (PVRIG/PD-1, PVRIG/TIGIT) and triple (PVRIG/PD-1/TIGIT) blockade. Currently, the only clinical trial we sponsor and are conducting is a blinded randomized ovarian cancer platform trial evaluating COM701 as a single agent in maintenance therapy in relapsed platinum sensitive ovarian cancer (named MAIA-ovarian trial). Rilvegostomig, a PD-1/TIGIT bispecific antibody with a TIGIT component that is derived from COM902 program, is being developed by AstraZeneca pursuant to an exclusive license agreement between us and AstraZeneca and is being evaluated in multiple Phase 3, Phase 2 and Phase 1 clinical trials. GS-0321 (previously COM503), Compugen's potential first-in-class high affinity antibody, which blocks the interaction between IL-18 binding protein and IL-18, is licensed to Gilead and is being evaluated in a Phase 1 clinical trial that we sponsor and are conducting. In addition, Compugen's has an early-stage immuno-oncology pipeline consists of research pr...

Investor releaseQuarter not tagged2026-03-04

Compugen Ltd (CGEN) Q4 2025 Earnings Call Highlights: Strong Revenue Growth and Strategic ...

GuruFocus.com

This article first appeared on GuruFocus. Cash Balance: $145.6 million as of December 31, 2025. Revenue (Q4 2025): $67.3 million. Revenue (Full Year 2025): $72.8 million. R&D Expenses (Q4 2025): $5.5 million. R&D Expenses (Full Year 2025): $22.8 million. G&A Expenses (Q4 2025): $2.1 million. G&A Expenses (Full Year 2025): $8.9 million. Net Profit (Q4 2025): $56.8 million or $0.60 per share. Net Profit (Full Year 2025): $35.3 million or $0.38 per share. Cash Runway: Expected to fund operations into 2029. Warning! GuruFocus has detected 5 Warning Signs with UUUU. Is CGEN fairly valued? Test your thesis with our free DCF calculator. Release Date: March 02, 2026 For the complete transcript of the earnings call, please refer to the full earnings call transcript. Compugen Ltd (NASDAQ:CGEN) extended its cash runway into 2029 through a non-dilutive transaction with AstraZeneca, securing $65 million in upfront capital. The company initiated new clinical trials for its potential first-in-class anti-PVRIG COM701 and anti-IL-18 binding protein antibody GS-0321. Compugen Ltd (NASDAQ:CGEN) presented promising clinical updates at ESMO and SITC conferences for COM701 and GS-0321, respectively. The company has a strong financial outlook with a cash balance of approximately $145.6 million as of December 31, 2025. Compugen Ltd (NASDAQ:CGEN) reported a significant increase in revenues for 2025, totaling approximately $72.8 million, compared to $27.9 million in 2024. The interim analysis for the MAIA-ovarian trial has been delayed to Q1 2027, indicating potential challenges in trial progression. R&D expenses decreased slightly in 2025, which may suggest reduced investment in certain areas of research. The company's net profit for 2025 was largely influenced by the upfront payment from AstraZeneca, raising concerns about sustainable revenue sources. There is uncertainty regarding the timeline and requirements for the path to registration for COM701, as it depends on the totality of the data. The company is reliant on partnerships with AstraZeneca and Gilead for milestone payments, which introduces dependency on external entities for financial milestones. Q: Can you help us level set on what to expect in the 1Q '27 update with COM701 in terms of what we expect to see in that update? And then the follow-up to that is, can you help us understand the timeline and what is required for...

Investor releaseQuarter not tagged2026-03-03

Compugen Ltd. Q4 2025 Earnings Call Summary

Moby

Extended cash runway into 2029 through a $65,000,000 non-dilutive royalty monetization deal with AstraZeneca, securing long-term operational stability without equity dilution. Maintained significant long-term upside in rilvegostomig by retaining the majority of royalty interests and increasing total potential milestones to $195,000,000. Attributed confidence in the TIGIT-based asset rilvegostomig to its differentiated bispecific format with reduced Fc functionality, which aims to avoid immune cell depletion seen in competing programs. Transitioned leadership to a structure combining operational focus under a new CEO with strategic continuity provided by the former CEO moving to Executive Chair. Focused clinical strategy for COM701 on earlier-line maintenance therapy in platinum-sensitive ovarian cancer, targeting a setting with no current standard of care. Leveraged the proprietary Unicigen AI/ML discovery engine to maintain a steady pipeline of novel targets, including the partnered GS-0321 program with Gilead. Validated the therapeutic approach for COM701 through pooled Phase I data showing durable responses in patients without liver metastasis, suggesting higher efficacy in lower disease burden environments. On track for a critical interim analysis of the MAIA ovarian adaptive trial in Q1 2027, which could establish a monotherapy path-to-registration. Anticipate continued expansion of AstraZeneca's Phase III program for rilvegostomig, which now includes 10 active trials and a potential 11th trial in gastric cancer. Plan to advance the Phase I dose-escalation and expansion trial for GS-0321 in collaboration with Gilead, focusing on its unique IL-18 binding protein mechanism. Expect to utilize the 2029 cash runway to reach multiple internal and partnered clinical catalysts while investing in the early-stage computational discovery pipeline. Assume BLA acceptance for rilvegostomig as the next major financial trigger, which would result in a $25,000,000 milestone payment. Reported a significant shift to net profit of $35,300,000 for 2025, primarily driven by the $65,000,000 upfront payment from the AstraZeneca transaction. Reduced R&D expenses to $22,800,000 in 2025 as the company wound down older trials to pivot resources toward the MAIA ovarian study. Confirmed all 28 clinical sites for the MAIA trial are now open across the U.S., Israel, and France after p...

Investor releaseQuarter not tagged2026-03-02

Compugen (CGEN) Beats Q4 Earnings and Revenue Estimates

Zacks

Compugen (CGEN) came out with quarterly earnings of $0.6 per share, beating the Zacks Consensus Estimate of $0.05 per share. This compares to a loss of $0.07 per share a year ago. These figures are adjusted for non-recurring items. This quarterly report represents an earnings surprise of +1,053.85%. A quarter ago, it was expected that this drug developer would post a loss of $0.09 per share when it actually produced a loss of $0.07, delivering a surprise of +22.22%. Over the last four quarters, the company has surpassed consensus EPS estimates two times. Compugen, which belongs to the Zacks Medical - Biomedical and Genetics industry, posted revenues of $67.33 million for the quarter ended December 2025, surpassing the Zacks Consensus Estimate by 276.79%. This compares to year-ago revenues of $1.47 million. The company has topped consensus revenue estimates just once over the last four quarters. The sustainability of the stock's immediate price movement based on the recently-released numbers and future earnings expectations will mostly depend on management's commentary on the earnings call. Compugen shares have added about 18.3% since the beginning of the year versus the S&P 500's gain of 0.5%. While Compugen has outperformed the market so far this year, the question that comes to investors' minds is: what's next for the stock? There are no easy answers to this key question, but one reliable measure that can help investors address this is the company's earnings outlook. Not only does this include current consensus earnings expectations for the coming quarter(s), but also how these expectations have changed lately. Empirical research shows a strong correlation between near-term stock movements and trends in earnings estimate revisions. Investors can track such revisions by themselves or rely on a tried-and-tested rating tool like the Zacks Rank, which has an impressive track record of harnessing the power of earnings estimate revisions. Ahead of this earnings release, the estimate revisions trend for Compugen was mixed. While the magnitude and direction of estimate revisions could change following the company's just-released earnings report, the current status translates into a Zacks Rank #3 (Hold) for the stock. So, the shares are expected to perform in line with the market in the near future. You can see the complete list of today's Zacks #1 Rank (Strong Buy...

As of 2026-05-30 • Updated weeklySource: Earnings sourceIngestion runbook