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Alpha Tau Announces Presentation of Pancreatic Cancer Data at Upcoming ASCO Annual Meeting, Showcasing Combined Results from Three Alpha DaRT Pancreatic Cancer Studies

(Positive)
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Alpha Tau (Nasdaq: DRTS) announced that an abstract titled “Combined Safety and Efficacy Results from Three Clinical Studies Evaluating Alpha Radiotherapy for Advanced Pancreatic Cancer” was accepted to the 2026 ASCO Annual Meeting (May 29–June 2, 2026).

The pooled analysis combines safety and efficacy data from 58 patients across three prospective EUS-guided intratumoral Alpha DaRT studies at centers in Montreal and Jerusalem. The abstract will be published on the ASCO website on May 21, 2026 at 5:00 PM ET. Alpha Tau said this acceptance, alongside ASCO GI and DDW presentations, reflects growing scientific interest in its pancreatic program.

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Positive

  • Abstract accepted at ASCO Annual Meeting
  • Pooled data from 58 patients across three studies
  • Studies conducted at tertiary centers in Canada and Israel
  • Abstract publication date: May 21, 2026 at 5:00 PM ET
  • Ongoing multicenter IMPACT and ACAPELLA trials

Negative

  • Data are pooled early-phase results, not randomized phase III outcomes
  • No new regulatory approvals or definitive efficacy endpoints reported

News Market Reaction – DRTS

-2.22% 1.7x vol
10 alerts
-2.22% Session close to close
-3.7% Trough in 6 hr 17 min
$667.11M Market Cap
1.7x Rel. Volume

In the Apr 27 session, DRTS declined 2.22%, reflecting a moderate negative market reaction. Argus tracked a trough of -3.7% from its starting point during tracking. Our momentum scanner triggered 10 alerts that day, indicating notable trading interest and price volatility. Trading volume was above average at 1.7x the daily average, suggesting increased trading activity.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement highlights external validation of Alpha Tau’s pancreatic program, with pooled data...
Analysis

This announcement highlights external validation of Alpha Tau’s pancreatic program, with pooled data from 58 patients across three studies selected for the 2026 ASCO Annual Meeting. In recent months, the company expanded the IMPACT trial, initiated the European ACAPELLA trial, and secured prior conference presentations, indicating a steady build in its clinical evidence base. Investors may watch upcoming ASCO publication details, enrollment progress, and any subsequent regulatory interactions as key markers of program maturation.

Key Figures

Pooled patient count: 58 patients Number of studies: 3 studies ASCO abstract publication: May 21, 2026, 5:00 PM ET +1 more
4 metrics
Pooled patient count 58 patients Combined across three prospective pancreatic cancer Alpha DaRT studies
Number of studies 3 studies Prospective EUS-guided intratumoral Alpha DaRT pancreatic cancer trials in Canada and Israel
ASCO abstract publication May 21, 2026, 5:00 PM ET Planned posting of pooled pancreatic data on ASCO website
ASCO Annual Meeting dates May 29 – June 2, 2026 Conference hosting Alpha DaRT pancreatic pooled analysis presentation

Historical Context

5 past events · Latest: Apr 23 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Apr 23 FDA IDE supplement Positive -1.2% FDA approved IDE supplement expanding IMPACT pancreatic cancer trial from 30 to 40 patients.
Apr 23 Clinical trial update Positive -1.2% First European pancreatic cancer patient treated in ACAPELLA multicenter Alpha DaRT trial.
Mar 31 Conference presentation Positive +7.9% Acceptance of first-ever oral presentation of Alpha DaRT pancreatic data at DDW 2026.
Mar 16 Investor conference Neutral +1.4% Announcement of CFO presentation at Sidoti Virtual Small Cap investor conference.
Mar 09 Earnings results Neutral +1.9% Full-year 2025 results with $76.9M cash, Japanese approval, trials progress, and $42.6M net loss.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent clinically focused announcements have sometimes led to positive reactions, but key pancreatic and FDA-related updates in April saw modest negative moves, indicating occasional divergence between strong clinical/regulatory milestones and short-term price action.

Recent Company History

Over recent months, Alpha Tau has reported multiple milestones building its oncology profile. On Mar 9, 2026, full-year 2025 results highlighted $76.9M cash and Japanese marketing approval for head and neck cancer. Subsequent March releases covered conference presentations and first-ever oral pancreatic data at DDW, which coincided with a 7.94% gain. In April, the company expanded its U.S. IMPACT pancreatic trial via FDA IDE approval and treated the first European pancreatic patient in ACAPELLA, though both announcements were followed by modest share declines.

Key Terms

american society of clinical oncology, asco, endoscopic ultrasound, eus-guided, +4 more
8 terms
american society of clinical oncology medical
"Abstract accepted at the American Society of Clinical Oncology (ASCO) Annual Meeting"
A professional organization of cancer doctors, researchers and care teams that publishes clinical guidelines and hosts major conferences where new treatment trial results are presented. Investors watch its announcements because its guidelines and conference findings often shape which drugs and technologies are accepted by doctors and hospitals—similar to a respected referee whose rulings can change the commercial prospects and perceived value of healthcare companies.
asco medical
"Abstract accepted at the American Society of Clinical Oncology (ASCO) Annual Meeting"
ASCO is the American Society of Clinical Oncology, a leading professional group whose annual meetings and publications are where cancer treatment trial results and clinical data are first shared with doctors and researchers. Investors watch ASCO closely because new clinical results announced there can change a drug’s perceived effectiveness and approval prospects, much like a product review that suddenly boosts or harms a company’s future sales outlook.
endoscopic ultrasound medical
"evaluating endoscopic ultrasound (EUS)-guided intratumoral Alpha DaRT treatment"
A procedure that uses a thin, flexible tube with a built‑in ultrasound probe to take detailed pictures and samples of organs near the digestive tract, like the pancreas or lymph nodes; think of it as a camera that can also “see” beneath the surface. It matters to investors because its use and adoption affect demand for specialized medical devices, clinical diagnostics, treatment planning and hospital revenue, and can influence regulatory approvals and reimbursement decisions that impact companies’ sales and growth.
eus-guided medical
"The EUS-guided intratumoral approach has proven to be technically feasible"
A medical technique in which an ultrasound probe mounted on an endoscope is used to visualize internal organs from inside the digestive tract and guide needles or instruments to a precise spot for diagnosis or treatment. Think of it like using a camera with built‑in sonar to aim a needle without open surgery. For investors, the term indicates demand for specialized devices, procedural adoption, regulatory clearance and reimbursement decisions that can affect revenue and clinical uptake.
intratumoral medical
"EUS-guided intratumoral Alpha DaRT treatment in patients with locally advanced"
"Intratumoral" describes something that occurs or exists within a tumor, which is an abnormal growth of tissue. For investors, understanding intratumoral is important because it relates to medical treatments or research aimed at targeting the tumor directly, potentially leading to more effective therapies. Think of it as focusing treatment straight into the problem area, much like fixing a leak by working directly on the pipe itself.
pancreatic ductal adenocarcinoma medical
"patients with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC)"
A fast-growing cancer that starts in the cells lining the pancreas’ small ducts; it is the most common and aggressive form of pancreatic cancer. It matters to investors because its severity and limited treatment options drive high unmet medical need, large potential markets for effective drugs or diagnostics, and strong sensitivity of company valuations to clinical trial results, regulatory approvals, or changes in treatment guidelines—similar to how fixing a main leak can prevent major damage in a building.
pdac medical
"patients with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC)"
PDAC stands for pancreatic ductal adenocarcinoma, the most common and aggressive form of pancreatic cancer that starts in the pancreas’s duct cells. It matters to investors because PDAC represents a large unmet medical need with high patient mortality, driving intense drug development, clinical trial activity and potential regulatory milestones—like a critical, hard-to-fix engine part whose failure creates urgent demand for effective solutions, affecting a company’s valuation and risk profile.
capecitabine medical
"ACAPELLA trial - a multicenter study in France evaluating Alpha DaRT alongside capecitabine"
An oral chemotherapy prodrug that converts in the body into an active cancer-fighting agent similar to 5-fluorouracil; think of it as a timed-release package that becomes active after swallowing. It matters to investors because its use, safety profile, patent status and competition from generics or alternative treatments directly affect sales, clinical-program value and regulatory risk for companies involved in oncology medicines.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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- Abstract accepted at the American Society of Clinical Oncology (ASCO) Annual Meeting - the world’s largest and most prestigious medical oncology conference -

- Pooled analysis combines safety and efficacy data from 58 patients across three prospective clinical studies conducted at centers in Canada and Israel -

- Acceptance of abstract comes in the same year as presentations at the ASCO Gastrointestinal Cancers Symposium and at Digestive Disease Week (DDW), reflecting growing interest within the expert scientific community in Alpha DaRT pancreatic cancer clinical data -

- Abstract to be published on ASCO conference website on May 21, 2026, at 5:00 PM ET -

JERUSALEM, April 27, 2026 (GLOBE NEWSWIRE) -- Alpha Tau Medical Ltd. (Nasdaq: DRTS, DRTSW) (“Alpha Tau”), the developer of the innovative alpha-radiation cancer therapy Alpha DaRT®, today announced that an abstract entitled “Combined Safety and Efficacy Results from Three Clinical Studies Evaluating Alpha Radiotherapy for Advanced Pancreatic Cancer” has been accepted at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting, taking place May 29 - June 2, 2026. The abstract is expected to be published on May 21, 2026, at 5:00 PM ET on the ASCO conference website at https://www.asco.org/annual-meeting.

The ASCO Annual Meeting is widely regarded as the largest and most prestigious medical oncology conference in the world, attracting tens of thousands of leading oncologists, researchers, and healthcare professionals from across the globe. Abstract acceptance at ASCO is determined through a rigorous, peer-review process and represents recognition of the scientific merit and clinical relevance of the submitted research.

The abstract presents a pooled analysis of safety and efficacy data from three prospective clinical studies evaluating endoscopic ultrasound (EUS)-guided intratumoral Alpha DaRT treatment in patients with locally advanced or metastatic pancreatic ductal adenocarcinoma (PDAC). The studies were conducted at the Jewish General Hospital and Centre Hospitalier de l'Université de Montréal (CHUM) in Montreal, Canada, and at the Hadassah Medical Center in Jerusalem, Israel, enrolling a combined total of 58 patients. Acceptance of the abstract at the ASCO Annual Meeting, together with abstract presentation at ASCO GI and Digestive Disease Week (DDW) this year, underscores the growing scientific interest and momentum behind the Alpha DaRT pancreatic cancer program.

Uzi Sofer, CEO of Alpha Tau, stated, “The acceptance of an abstract at the ASCO Annual Meeting is a wonderful milestone for Alpha Tau and a powerful endorsement of our pancreatic cancer strategy by some of the most prestigious leaders in the field. The continued recognition of our clinical program reflects the growing maturity and strength of our evidence base, and validates the strategic vision behind our multi-study approach to pancreatic cancer: to build one of the most comprehensive intratumoral radiotherapeutic clinical programs in pancreatic cancer worldwide.”

Corey Miller, MD, MSc, Director of Therapeutic Endoscopy of the Division of Gastroenterology at the Jewish General Hospital, Assistant Professor of Medicine at McGill University, and the first and presenting author of the abstract, commented, “As the first physician to deliver Alpha DaRT into the pancreas using an endoscopic ultrasound-guided approach, it is deeply meaningful to see how far this program has come. What began as a first-in-human feasibility procedure has evolved into a robust clinical data set, made possible by the close collaboration between gastroenterology, medical oncology and radiation oncology teams. It is this combined effort that enabled the accrual of this cohort and the generation of comprehensive results now accepted at the world’s foremost oncology conference. The EUS-guided intratumoral approach has proven to be technically feasible and well-integrated into clinical workflows, and we look forward to sharing these findings with the global medical community when the abstract is published by ASCO and in the Journal of Clinical Oncology.”

Robert B. Den, MD, Chief Medical Officer of Alpha Tau stated, “This ASCO acceptance is a significant validation of our growing pancreatic cancer clinical program at a critical time. The pooled analysis provides a strong foundation of clinical evidence, and we are actively building on this momentum. Our flagship multicenter IMPACT trial in the United States continues to advance, evaluating Alpha DaRT in combination with chemotherapy in patients with newly diagnosed unresectable pancreatic cancer. In addition, we recently treated the first patient in April in the ACAPELLA trial - a multicenter study in France evaluating Alpha DaRT alongside capecitabine in patients with locally advanced pancreatic cancer. Together, these studies represent an expanding and increasingly global clinical pipeline dedicated to addressing one of the most significant unmet needs in oncology.”

About Alpha DaRT®

Alpha DaRT (Diffusing Alpha-emitters Radiation Therapy) is designed to enable highly potent and conformal intratumoral treatment of solid tumors. Alpha DaRT sources are inserted directly into the tumor, where they release short-lived therapeutic particles that disperse locally with the goal of destroying the tumor. Since the therapeutic effect is confined to a short distance, Alpha DaRT aims to mainly affect the tumor and to spare the healthy tissue around it.

About Alpha Tau Medical Ltd.

Founded in 2016, Alpha Tau is an Israeli oncology therapeutics company that focuses on research, development, and potential commercialization of the Alpha DaRT for the treatment of solid tumors. The technology was initially developed by Prof. Itzhak Kelson and Prof. Yona Keisari from Tel Aviv University.

Forward-Looking Statements

This press release includes “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. When used herein, words including “anticipate,” “will,” “plan,” “may,” “continue,” and similar expressions are intended to identify forward-looking statements. In addition, any statements or information that refer to the Alpha DaRT treatment in pancreatic patients, including the potential benefits and associated risks, future applications and uses, the IMPACT study, the ACAPELLA study, timing of the abstract publication, and potential indication approvals, are forward-looking. All forward-looking statements are based upon Alpha Tau’s current expectations and various assumptions. Alpha Tau believes there is a reasonable basis for its expectations and beliefs, but they are inherently uncertain. Alpha Tau may not realize its expectations, and its beliefs may not prove correct. Actual results could differ materially from those described or implied by such forward-looking statements as a result of various important factors, including, without limitation: (i) Alpha Tau’s ability to receive regulatory approval for its Alpha DaRT technology or any future products or product candidates; (ii) Alpha Tau’s limited operating history; (iii) Alpha Tau’s incurrence of significant losses to date; (iv) Alpha Tau’s need for additional funding and ability to raise capital when needed; (v) Alpha Tau’s limited experience in medical device discovery and development; (vi) Alpha Tau’s dependence on the success and commercialization of the Alpha DaRT technology; (vii) the failure of preliminary data from Alpha Tau’s clinical studies to predict final study results; (viii) failure of Alpha Tau’s early clinical studies or preclinical studies to predict future clinical studies; (ix) Alpha Tau’s ability to enroll patients in its clinical trials; (x) undesirable side effects caused by Alpha Tau’s Alpha DaRT technology or any future products or product candidates; (xi) Alpha Tau’s exposure to patent infringement lawsuits; (xii) Alpha Tau’s ability to comply with the extensive regulations applicable to it; (xiii) the ability to meet Nasdaq’s listing standards; (xiv) costs related to being a public company; (xv) changes in applicable laws or regulations; and the other important factors discussed under the caption “Risk Factors” in Alpha Tau’s annual report filed on form 20-F with the SEC on March 9, 2026, and other filings that Alpha Tau may make with the United States Securities and Exchange Commission. These and other important factors could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management’s estimates as of the date of this press release. While Alpha Tau may elect to update such forward-looking statements at some point in the future, except as required by law, it disclaims any obligation to do so, even if subsequent events cause its views to change. These forward-looking statements should not be relied upon as representing Alpha Tau’s views as of any date subsequent to the date of this press release.

Investor Relations Contact:

IR@alphatau.com


FAQ

What did Alpha Tau (DRTS) announce about ASCO 2026 pancreatic cancer data?

Alpha Tau announced acceptance of an ASCO 2026 abstract presenting pooled Alpha DaRT results from three studies. According to Alpha Tau, the analysis combines safety and efficacy data from 58 patients treated with EUS-guided intratumoral Alpha DaRT at centers in Canada and Israel.

When will the Alpha Tau ASCO abstract for DRTS be published online?

The abstract will be published on May 21, 2026 at 5:00 PM ET on the ASCO conference website. According to Alpha Tau, the ASCO Annual Meeting presentation runs May 29–June 2, 2026, where the abstract findings will be presented to clinicians.

How many patients are included in the Alpha DaRT pooled pancreatic analysis (DRTS)?

The pooled analysis includes 58 patients across three prospective clinical studies. According to Alpha Tau, these were EUS-guided intratumoral treatments performed at the Jewish General Hospital, CHUM in Montreal, and Hadassah Medical Center in Jerusalem.

What is the clinical significance of the ASCO acceptance for Alpha Tau (DRTS)?

ASCO acceptance signals peer-reviewed recognition and scientific interest in the program. According to Alpha Tau, acceptance alongside ASCO GI and DDW presentations reflects growing momentum for its pancreatic clinical evidence base and program visibility among oncologists.

What additional Alpha Tau (DRTS) pancreatic trials are ongoing following the ASCO abstract?

Alpha Tau is advancing a U.S. multicenter IMPACT trial and launched the ACAPELLA trial in France in April. According to Alpha Tau, IMPACT tests Alpha DaRT plus chemotherapy and ACAPELLA evaluates Alpha DaRT with capecitabine in locally advanced patients.