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Immuneering to Highlight Atebimetinib’s Broad Potential for Combinations in Pancreatic and Anaplastic Thyroid Cancers at the 2026 EORTC-NCI-AACR Symposium

The research explores additional combinations while atebimetinib is being evaluated in Phase 3 for first-line pancreatic cancer.

(Moderate)

Sentiment and the balance of points

Rhea-AI Sentiment reads the wording of the document, how positive or negative its language is on a 1 to 5 scale. The balance of points shown with the takes weighs what the document actually discloses, so the two can disagree, for example when a trial that missed its main goal is described in upbeat language.

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Immuneering (Nasdaq: IMRX) will present atebimetinib combination research at the EORTC-NCI-AACR Symposium taking place November 17–19, 2026.

The company said new preclinical findings support potential combinations with targeted therapies in pancreatic cancer and with chemotherapy in anaplastic thyroid cancer. The pancreatic cancer abstract received a Poster Spotlight slot on November 19; the thyroid cancer poster is scheduled for November 18.

Previously presented Phase 2 results included 17.3 months median overall survival in first-line pancreatic cancer patients receiving atebimetinib plus mGnP chemotherapy. Atebimetinib is currently being evaluated in the Phase 3 MAPKeeper 301 trial in first-line pancreatic cancer.

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4 points · 0 major

How this balance works

Rhea-AI gives every point it takes from this document a weight. Minor counts 1, Moderate 3 and Major 9, so one Major point outweighs several Minor ones. The bar adds up the weights on each side, and when neither side holds more than 65% of the total the balance reads Mixed.

It reads the document as published, with the same rules for every company, and it does not look at what the market expected or at how the stock traded, so a point can be objectively good on a day the stock falls.

Rhea-AI Sentiment measures something else, the tone of the wording.

0 major · 0 points

How the balance works

Positive

  • Moderate pointPhase 2 results included 17.3 months median overall survival with atebimetinib plus mGnP in first-line pancreatic cancer.
  • Minor pointPhase 3 MAPKeeper 301 is currently evaluating atebimetinib in first-line pancreatic cancer.
  • Minor pointPancreatic cancer preclinical findings support potential targeted-therapy combinations, the company said.
  • Minor pointAnaplastic thyroid cancer preclinical findings support potential chemotherapy combinations, the company said.

Negative

  • None.
Argus Nov 4 session 5 alerts
+2.17% close to close 0.9x rel. volume Open Argus
Details

News Market Reaction – IMRX

$250.63M Mkt Cap at Peak Alert

On Nov 4, the day this news came out, IMRX closed 2.17% above the previous close. Our momentum scanner recorded 5 alerts for this stock that day.

Data tracked by StockTitan Argus for the Nov 4 session.

Key Figures

Median overall survival: 17.3 months
Median overall survival
17.3 months
Phase 2 first-line pancreatic cancer patients treated with atebimetinib + mGnP; presented in June

Key Terms

median overall survival, pancreatic ductal adenocarcinoma, mek, mapk pathway
4 terms
median overall survival medical
"17.3 months median overall survival in first-line pancreatic cancer patients"
Median overall survival is the middle point of how long patients live after starting treatment, meaning half live longer and half live shorter. It helps doctors understand how effective a treatment is and gives patients an idea of what to expect about their future.
pancreatic ductal adenocarcinoma medical
"in 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.
mek technical
"a deep cyclic inhibitor of MEK, combined with chemotherapy"
MEK (methyl ethyl ketone) is a common industrial solvent used to dissolve paints, coatings, adhesives and some plastics, similar to how gasoline thins oil. Investors care because MEK’s availability, price and regulatory status affect manufacturing costs, product quality and environmental or safety liabilities for companies that use or produce it; shifts in supply, regulation or handling rules can change profit margins or require costly compliance steps.
mapk pathway technical
"designed to provide Deep Cyclic Inhibition of the MAPK pathway"
A MAPK pathway is a chain of proteins inside cells that passes signals from the cell surface to the nucleus to control key behaviors like growth, division and survival; think of it as a relay race where each runner (protein) activates the next to produce a specific response. Investors care because drugs or tests that alter this pathway can change the course of diseases such as many cancers and inflammatory conditions, affecting drug trial outcomes, regulatory risk, and the commercial value of biotech assets.

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

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- Atebimetinib in combination with chemotherapy has shown excellent results in Phase 2 clinical trials, including 17.3 months median overall survival in first-line pancreatic cancer patients treated with atebimetinib + mGnP, as presented in June at ASCO - 

- Poster spotlight session will highlight broad set of additional opportunities to combine atebimetinib with agents targeting multiple oncogenic pathways in pancreatic cancer -

- New preclinical data supports atebimetinib’s use in a wide range of cancer types, including anaplastic thyroid cancer, a highly aggressive malignancy with limited treatment options -

- Atebimetinb is currently being evaluated in Phase 3 MAPKeeper 301 trial in first-line pancreatic cancer -

NEW YORK, Nov. 04, 2026 (GLOBE NEWSWIRE) -- Immuneering Corporation (Nasdaq: IMRX), a late-stage clinical oncology company focused on keeping cancer patients alive and helping them thrive, today announced that two abstracts evaluating atebimetinib (IMM-1-104), its lead investigational candidate designed to provide Deep Cyclic Inhibition of the MAPK pathway, have been accepted for presentation at the 2026 EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics, taking place November 17–19, 2026.

The presentations will highlight new preclinical findings supporting the potential of atebimetinib in combination with multiple targeted therapies in pancreatic ductal adenocarcinoma (PDAC), as well as chemotherapy combinations in anaplastic thyroid cancer (ATC). The pancreatic cancer abstract has been selected for a Poster Spotlight presentation.

Presentation Details:

Pancreatic Ductal Adenocarcinoma – Poster Spotlight Presentation
Title: Patient-aligned 3D tumor models identify biomarker-enriched atebimetinib (IMM-1-104) combination strategies in pancreatic ductal adenocarcinoma
Abstract Number: 22
Poster Number: PB-003
Presenter: Anna Travesa, Immuneering Corporation
Date: November 19, 2026
Time: 14:00–14:30 CET
Session: Poster Spotlight Session

Anaplastic Thyroid Cancer – Preclinical Poster Presentation
Title: Atebimetinib, a deep cyclic inhibitor of MEK, combined with chemotherapy: preclinical rationale for treatment of anaplastic thyroid cancer (ATC)
Abstract Number: 144
Poster Number: PB-144
Presenter: Praveen Nair, Immuneering Corporation
Date: November 18, 2026
Session: Translational Studies

Following presentation, the poster will be available on the publications section of Immuneering’s website at https://immuneering.com/publications.

About Immuneering Corporation

Immuneering is a late-stage clinical oncology company dedicated to keeping cancer patients alive and helping them thrive, with an initial focus on patients with RAS, RAF, and other MAPK-driven cancers. The Company is developing an entirely new category of cancer medicines, Deep Cyclic Inhibitors, designed to improve overall survival by three mechanisms: shrinking tumors durably with less resistance, preserving body mass by countering cachexia, and minimizing side effects to maximize performance status and combinability. Immuneering’s lead product candidate, atebimetinib, is an oral, once-daily Deep Cyclic Inhibitor of MEK, designed to improve survival across many cancer indications. The Company is conducting a global randomized pivotal trial, MAPKeeper 301, evaluating atebimetinib in combination with chemotherapy in first-line pancreatic cancer patients. The Company’s development pipeline also includes additional combination opportunities and preclinical stage programs. For more information, please visit www.immuneering.com.

Forward-Looking Statements

This press release contains forward-looking statements, including within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including, without limitation, statements regarding: the treatment potential of atebimetinib, alone or in combination with other agents to treat cancer, including chemotherapy in pancreatic cancer and anaplastic thyroid cancer, and its potential to deliver overall survival with both durability and tolerability; the tolerability profile enabling a broad range of potential combinations, expansion of the enrollment target enabling the Company to maintain or potentially accelerate the timing of the Phase 3 topline readout of the MAPKeeper 301 trial in mid-2028; the timing of a data update in the Phase 2a atebimetinib + mGnP trial in first-line pancreatic cancer; the timing of dosing and preliminary readout of the planned Phase 2 lung cancer trial; the timing of beginning IND-enabling studies in a second DCI program; our operating plans and anticipated cash runway, and the potential ability of the three design mechanisms of atebimetinib to shrink tumors durably, improve overall survival and overcome the limitations of conventional MAPK inhibition and provide a more sustained clinical benefit for patients.

These forward-looking statements are based on management’s current expectations. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: we are a late-stage clinical oncology company with a limited operating history and have not completed any registrational clinical trials; we have incurred significant losses, are not currently profitable and may never become profitable; limitations on our cash runway and potential increases in expenditures; our need for additional funding; our unproven approach to therapeutic intervention; our ability to address regulatory questions and changing regulatory standards, and the uncertainties relating to regulatory filings, reviews and approvals; the lengthy, expensive, and uncertain process of clinical drug development, including the uncertainty of whether positive preclinical or early clinical efficacy and safety results are confirmed in later-stage trials, potential delays in activation of trial sites or enrollment of trial participants, or failure to obtain regulatory approvals; our reliance on third parties and collaborators to conduct our clinical trials, manufacture our product candidates, and develop and commercialize our product candidates, if approved; failure to compete successfully against other drug companies; protection of our proprietary technology and the confidentiality of our trade secrets; potential lawsuits for, or claims of, infringement of third-party intellectual property or challenges to the ownership of our intellectual property; our patents being found invalid or unenforceable; costs and resources of operating as a public company; and unfavorable or no analyst research or reports.

These and other important factors discussed under the caption “Risk Factors” in our Quarterly Report on Form 10-Q for the period ended September 30, 2026, and our other reports filed with the U.S. Securities and Exchange Commission, 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 we may elect to update such forward-looking statements at some point in the future, except as required by law, we disclaim any obligation to do so, even if subsequent events cause our views to change. These forward-looking statements should not be relied upon as representing our views as of any date subsequent to the date of this press release.

Investor Contact:
Laurence Watts
New Street Investor Relations
laurence@newstreetir.com

Media Contact:
David Caouette
dcaouette@immuneering.com


FAQ

AI-generated questions and answers. How Rhea-AI works. Not financial advice.

What research will Immuneering present on atebimetinib at the 2026 EORTC-NCI-AACR Symposium?

Immuneering will present preclinical combination research in pancreatic ductal adenocarcinoma and anaplastic thyroid cancer. The pancreatic cancer work explores combinations with targeted therapies, while the thyroid cancer work examines combinations with chemotherapy.

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