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Sellas Life Sciences Group Inc reported a $26.9M net loss for fiscal 2025. See the full SLS financial statements: income statement, balance sheet, cash flow and ratios, each column linked to its SEC filing.

SELLAS Life Sciences to Present Preclinical Data on SLS009 in Pancreatic Ductal Adenocarcinoma at the 2026 AACR Conference on Pancreatic Cancer

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SELLAS Life Sciences (SLS) will present three preclinical poster abstracts on its CDK9 inhibitor SLS009 (tambiciclib) in pancreatic ductal adenocarcinoma (PDAC) at the AACR Conference on Pancreatic Cancer: New Frontiers in Biology and Therapeutic Development, held September 25–28, 2026, in San Diego, CA.

The studies, conducted with the University of Wisconsin School of Medicine and Public Health, use patient-derived KRAS mutant organoid models to investigate mechanistic and translational rationale for CDK9 inhibition in PDAC. Presentations will cover MYC allelic imbalance and therapeutic response, synthetic lethality via combined BET and CDK9 inhibition in MYC-amplified PDAC, and dual CDK9 and KRASG12D-selective inhibition as a novel combination strategy.

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Negative

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Market Context

Prior reactions included -8.46% on March 19 and 25.1% on May 12. That dispersion places this preclin...
Analysis

Prior reactions included -8.46% on March 19 and 25.1% on May 12. That dispersion places this preclinical announcement in a mixed historical context; the active S-3ASR and high short positioning remain risks to monitor.

Key Figures

Poster presentations: 3 posters Abstracts: 3 abstracts Conference dates: September 25–28, 2026 +1 more
4 metrics
Poster presentations 3 posters 2026 AACR Conference on Pancreatic Cancer
Abstracts 3 abstracts SLS009 preclinical PDAC studies
Conference dates September 25–28, 2026 AACR Conference on Pancreatic Cancer
Poster numbers A036, B127, B043 Three SLS009 presentations

Historical Context

5 past events · Latest: Aug 11 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Aug 11 Second-quarter earnings Neutral +6.7% Quarterly results, AML progress, and pancreatic cancer preclinical update
May 14 Investor conferences Neutral +13.6% Participation in three oncology and healthcare investor conferences
May 12 First-quarter earnings Positive +25.1% REGAL milestone progress and initiation of SLS009 newly diagnosed AML dosing
Mar 19 Full-year earnings Positive -8.5% Positive SLS009 response data and progress toward REGAL final analysis
Mar 17 AML preclinical data Positive -1.8% SLS009 activity and reduced IC50 in AML laboratory models

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

Pattern Detected

Historical reactions were mixed, with positive clinical or preclinical updates followed by both gains and declines.

Key Terms

patient-derived organoid models, cdk9 inhibitor, synthetic lethal interactions, myc-associated vulnerabilities, +1 more
5 terms
patient-derived organoid models medical
"preclinical models of pancreatic ductal adenocarcinoma (PDAC)"
Three-dimensional lab-grown cell structures created from a specific patient’s tissue that mimic the architecture and biology of that patient’s organ or tumor. Like a miniaturized, living model of a person’s disease, these organoids let researchers test how drugs or treatments affect tissue that closely resembles the real thing. For investors, they matter because they can improve drug development predictability, help stratify patients, and potentially shorten or de-risk clinical programs.
cdk9 inhibitor medical
"a potent, selective CDK9 inhibitor, in preclinical models"
A CDK9 inhibitor is a drug that blocks the action of the cellular enzyme CDK9, which acts like a control switch for making certain short‑lived proteins that cells need to survive and multiply. For investors, it matters because these drugs are being developed to shut down critical survival pathways in cancers and some viral infections—think of cutting power to a factory assembly line to halt production—which can drive trial results, regulatory decisions, and company value.
synthetic lethal interactions medical
"create synthetic lethal interactions through rational combinations"
A synthetic lethal interaction is a biological relationship where a defect or inhibition of either of two genes alone is survivable for a cell, but disrupting both at the same time causes the cell to die. For investors, this concept matters because drugs that exploit synthetic lethality can target diseased cells (for example, cancer cells with a specific mutation) while sparing normal cells, making those drugs a focused strategy in precision medicine.
myc-associated vulnerabilities medical
"its potential to exploit MYC-associated vulnerabilities"
Genes in the MYC family drive cell growth and division, and cancers that rely on too much MYC activity often develop specific weaknesses—called MYC-associated vulnerabilities—that make them more sensitive to certain drugs or genetic disruptions. These vulnerabilities matter to investors because they point to drug targets, biomarkers, or diagnostic approaches that could enable therapies selective for MYC-driven tumors; think of them as pressure points on a machine that, if found, let a targeted tool stop the whole device.
kras-directed approaches medical
"combinations with BET- and KRAS-directed approaches"
Therapies and related diagnostics designed to recognize and block the activity of the KRAS protein or its mutant forms that drive cancer growth; these can include small-molecule inhibitors, antibody or RNA-based drugs, and tests that identify patients whose tumours carry KRAS mutations. They matter to investors because success or failure in this area can change the commercial and regulatory prospects for drug developers in cancers where KRAS mutations are common, much like fixing a specific broken part in an engine can stop a car from malfunctioning.

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-  Three posters to highlight preclinical activity of SLS009 (tambiciclib) across patient-derived KRAS mutant organoid models of pancreatic cancer – 

-  Studies conducted in collaboration with the University of Wisconsin School of Medicine and Public Health -

NEW YORK, Sept. 02, 2026 (GLOBE NEWSWIRE) -- SELLAS Life Sciences Group, Inc. (NASDAQ: SLS) (“SELLAS’’ or the “Company”), a late-stage clinical biopharmaceutical company focused on the development of novel therapies for a broad range of cancer indications, today announced that three abstracts evaluating SLS009 (tambiciclib), a potent, selective CDK9 inhibitor, in preclinical models of pancreatic ductal adenocarcinoma (PDAC) have been accepted for poster presentation at the AACR Conference on Pancreatic Cancer: New Frontiers in Biology and Therapeutic Development. The conference will be held September 25–28, 2026, at the Hilton San Diego Bayfront in San Diego, CA.

"Pancreatic cancer remains one of the most difficult solid tumors to treat, with a significant need for new therapeutic approaches," said Angelos Stergiou, MD, ScD h.c., President and Chief Executive Officer of SELLAS. “The acceptance of three abstracts evaluating SLS009 across patient-derived organoid models reflects the breadth of our preclinical work in PDAC. We look forward to sharing these findings with the pancreatic cancer research community and discussing their potential implications for the further development of SLS009 in solid tumors."

Jeremy D. Kratz, MD, Assistant Professor of Medicine & Principal Investigator, University of Wisconsin-Madison commented: “These studies are designed to deepen our understanding of the mechanistic and translational rationale for CDK9 inhibition in pancreatic cancer. The presentations will explore the potential for SLS009 to create synthetic lethal interactions through rational combinations with BET- and KRAS-directed approaches, as well as its potential to exploit MYC-associated vulnerabilities. We look forward to sharing this work with the scientific community later this month.”

Poster presentation details:
Title: Elucidating MYC allelic imbalance and therapeutic response in pancreatic ductal adenocarcinoma via patient-derived organoids
Authors: Sawyer AG, Flannagan LE, Esguerra PN, Hossan MS, Kratz JD
Poster Number: A036

Title: Synthetic Lethality Through Combined BET and CDK9 Inhibition in MYC-Amplified Pancreatic Ductal Adenocarcinoma
Authors: Esguerra PN, Cadarso M, Livingwell S, Hossan MD, Wong O, Kratz JD
Poster Number: B127

Title: Targeting dual CDK9 and KRASG12D selective inhibition as a novel combination therapy in pancreatic ductal adenocarcinoma
Authors: Cadarso M, Esguerra P, Flannagan L, Hossan MS, Kratz JD
Poster Number: B043

About SELLAS Life Sciences Group, Inc.

SELLAS is a late-stage clinical biopharmaceutical company focused on the development of novel therapeutics for a broad range of cancer indications. SELLAS’ lead product candidate, GPS, is licensed from Memorial Sloan Kettering Cancer Center and targets the WT1 protein, which is present in an array of tumor types. GPS has the potential as a monotherapy and combination with other therapies to address a broad spectrum of hematologic malignancies and solid tumor indications. The Company is also developing SLS009 (tambiciclib) - potentially the first and best-in-class differentiated small molecule CDK9 inhibitor with reduced toxicity and increased potency compared to other CDK9 inhibitors. Data suggests that SLS009 demonstrated a high response rate in AML patients with unfavorable prognostic factors including ASXL1 mutation, commonly associated with poor prognosis in various myeloid diseases. For more information on SELLAS, please visit www.sellaslifesciences.com.

Forward-Looking Statements

This press release contains forward-looking statements. All statements other than statements of historical facts are “forward-looking statements,” including those relating to future events. In some cases, forward-looking statements can be identified by terminology such as “plan,” “expect,” “anticipate,” “may,” “might,” “will,” “should,” “project,” “believe,” “estimate,” “predict,” “potential,” “intend,” or “continue” and other words or terms of similar meaning. These statements include, without limitation, statements related to the GPS clinical development program, including the REGAL study and the timing of future milestones related thereto. These forward-looking statements are based on current plans, objectives, estimates, expectations, and intentions, and inherently involve significant risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of these risks and uncertainties, which include, without limitation, risks and uncertainties with oncology product development and clinical success thereof, the uncertainty of regulatory approval, and other risks and uncertainties affecting SELLAS and its development programs as set forth under the caption “Risk Factors” in SELLAS’ Annual Report on Form 10-K filed on March 20, 2025 and in its other SEC filings. Other risks and uncertainties of which SELLAS is not currently aware may also affect SELLAS’ forward-looking statements and may cause actual results and the timing of events to differ materially from those anticipated. The forward-looking statements herein are made only as of the date hereof. SELLAS undertakes no obligation to update or supplement any forward-looking statements to reflect actual results, new information, future events, changes in its expectations, or other circumstances that exist after the date as of which the forward-looking statements were made.

Investor Contact

John Fraunces
Managing Director
LifeSci Advisors, LLC
jfraunces@lifesciadvisors.com


FAQ

What did SELLAS Life Sciences (SLS) announce about SLS009 at the 2026 AACR pancreatic cancer conference?

SELLAS announced that three preclinical abstracts on its CDK9 inhibitor SLS009 (tambiciclib) in pancreatic ductal adenocarcinoma have been accepted for poster presentation at the AACR Conference on Pancreatic Cancer in September 2026.

When and where will SELLAS (SLS) present SLS009 pancreatic cancer data in 2026?

SELLAS will present three SLS009 preclinical posters at the AACR Conference on Pancreatic Cancer, held September 25–28, 2026, at the Hilton San Diego Bayfront in San Diego, California.

What is SLS009 (tambiciclib) that SELLAS (SLS) is studying in pancreatic ductal adenocarcinoma?

SLS009 (tambiciclib) is described as a potent, selective CDK9 inhibitor being evaluated in preclinical models of pancreatic ductal adenocarcinoma, including patient-derived KRAS mutant organoids, to explore mechanistic and translational rationale for CDK9 inhibition.

Which research institution is collaborating with SELLAS (SLS) on the SLS009 pancreatic cancer studies?

The SLS009 pancreatic ductal adenocarcinoma preclinical studies are conducted in collaboration with the University of Wisconsin School of Medicine and Public Health, with Jeremy D. Kratz, MD, serving as a principal investigator.

What topics will the SLS009 posters from SELLAS (SLS) cover at the 2026 AACR pancreatic cancer meeting?

The three posters will address MYC allelic imbalance and therapeutic response in PDAC, synthetic lethality using combined BET and CDK9 inhibition in MYC-amplified PDAC, and a novel combination targeting dual CDK9 and KRASG12D-selective inhibition in pancreatic ductal adenocarcinoma.

What are the poster titles and numbers for SELLAS (SLS) SLS009 presentations at AACR Pancreatic Cancer 2026?

The posters are: A036 “Elucidating MYC allelic imbalance and therapeutic response in PDAC via patient-derived organoids”; B127 “Synthetic Lethality Through Combined BET and CDK9 Inhibition in MYC-Amplified PDAC”; and B043 “Targeting dual CDK9 and KRASG12D selective inhibition as a novel combination therapy in PDAC.”