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Immuneering Corp. Class A (IMRX)
NASDAQ:IMRX
US Market

Immuneering (IMRX) AI Stock Analysis

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IMRX

Immuneering

(NASDAQ:IMRX)

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Neutral 56 (OpenAI - 5.2)
Rating:56Neutral
Price Target:
$5.50
▲(8.91% Upside)
Action:ReiteratedDate:03/07/26
The score is primarily weighed down by weak financial performance (minimal revenue, sustained losses, and cash burn despite low debt), partially offset by a positive earnings-call outlook driven by encouraging Phase 2a survival data and an extended cash runway into 2029. Technicals are mixed but improving near-term, while valuation metrics are constrained by negative earnings and no dividend.
Positive Factors
Robust clinical survival data
Durable, materially improved overall survival in a first-line pancreatic cohort strengthens the probability of a successful pivotal program and regulatory support. Persistent survival gains versus SOC can underpin label differentiation, durable clinician adoption, and durable endpoint-driven trial design advantages into commercialization.
Extended cash runway
A multi-year cash runway through 2029 materially reduces near-term refinancing risk, allowing Immuneering to fund pivotal Phase 3 starts and partner studies. This financial cushion supports consistent execution on development milestones and negotiation leverage without immediate dilutive capital raises.
IP protection and strategic collaborations
Long-term patent exclusivity plus experimentally validated collaborations with large pharma provide a structural moat and optionality. Patents secure market exclusivity timing, while strategic partnerships broaden development expertise, trial execution capacity and potential co-development routes across indications.
Negative Factors
Pre-revenue with heavy cash burn
Sustained negative operating and free cash flow with no product revenue creates persistent dependence on external financing. Even with low debt, recurring losses force dilution or partnerships to fund pivotal trials, which can hinder long-term balance-sheet efficiency and shareholder returns until commercialization.
Regulatory and timeline dependency
Progress hinges on regulatory alignment and timing; any delays or additional data requests can push pivotal starts, increase costs and extend time to meaningful clinical readouts. Such timeline risk materially affects program de-risking and the company’s multi-year planning and capital deployment.
Tolerability limits for combinations
Combination tolerability constraints narrow the addressable patient pool and complicate development strategies. If optimal combos are limited to fitter patients, overall market applicability and trial enrollment speed may be constrained, raising execution risk and lowering broader clinical impact.

Immuneering (IMRX) vs. SPDR S&P 500 ETF (SPY)

Immuneering Business Overview & Revenue Model

Company DescriptionImmuneering Corporation, a biopharmaceutical company, focuses on the oncology and neuroscience product candidates. Its lead product candidates include IMM-1-104, a dual-MEK inhibitor to treat patients with cancer, including pancreatic, melanoma, colorectal, and non-small cell lung cancer caused by mutations of RAS and/or RAF; and IMM-6-415 to treat solid tumors. The company also has five oncology programs in the discovery stage that are designed to target components of the MAPK or mTOR pathway; and two discovery stage neuroscience programs. Immuneering Corporation was incorporated in 2008 and is based in Cambridge, Massachusetts. Immuneering Corporation was a former subsidiary of Teva Pharmaceutical Industries Limited.
How the Company Makes MoneyImmuneering makes money primarily through the development and commercialization of its proprietary drug candidates. The company invests in research and development to advance its pipeline of therapies, with the potential for revenue generation upon successful clinical trials and regulatory approvals. Key revenue streams include milestone payments and royalties from partnerships with larger pharmaceutical companies that may license Immuneering's technology or drug candidates. Additionally, the company may engage in collaborations or licensing agreements to leverage its computational biology platform, providing further financial opportunities.

Immuneering Earnings Call Summary

Earnings Call Date:Nov 12, 2025
(Q3-2025)
|
% Change Since: |
Next Earnings Date:May 12, 2026
Earnings Call Sentiment Positive
The earnings call presented strong positive updates, with remarkable clinical trial results and significant financial and strategic developments. While there are some challenges with specific treatments and regulatory timelines, the overall sentiment is positive due to the company's promising progress and future potential.
Q3-2025 Updates
Positive Updates
Extraordinary Overall Survival in Pancreatic Cancer
In September, Immuneering Corporation announced 86% overall survival at nine months in 34 first-line pancreatic cancer patients treated with atebimetinib plus modified gemcitabine nab-paclitaxel, compared to approximately 47% with the standard of care.
Successful Financing and Extended Cash Runway
The company strengthened its balance sheet with $225 million in cumulative financing, including a $25 million strategic investment from Sanofi, extending the cash runway into 2029.
Positive Case Studies in Pancreatic Cancer Treatment
Noteworthy case studies demonstrated impressive responses, including complete response and conversion to surgical candidates, highlighting atebimetinib's potential in combination with FOLFIRINOX.
Patent Protection and New Collaborations
Immuneering was granted a U.S. Composition of Matter patent for atebimetinib, providing exclusivity into 2042, and announced collaborations with Eli Lilly and Regeneron for lung cancer trials.
Negative Updates
Challenges with FOLFIRINOX Combination
While demonstrating potential, the FOLFIRINOX combination is not currently prioritized due to harsher side effects, limiting its use to younger, higher fitness patients.
Regulatory and Development Timelines
The company is awaiting regulatory feedback for its pivotal Phase III trial and plans to start dosing patients in 2026, indicating potential delays in reaching the market.
Company Guidance
During the Immuneering Corporation's third-quarter 2025 conference call, CEO Benjamin Zeskind highlighted notable guidance for the company's development plans, focusing on their Phase IIa trial of atebimetinib. Immuneering plans to prioritize atebimetinib in combination with gemcitabine nab-paclitaxel due to its impressive 86% overall survival rate at nine months in first-line pancreatic cancer patients, compared to the standard 47%. The company aims to present updated results at a major medical meeting in 2026. Financially, Immuneering strengthened its position with $225 million in cumulative financing, extending its cash runway into 2029, which supports the planned pivotal Phase III trials and other developments. Additionally, the company is preparing to dose the first patient in a pivotal trial in mid-2026 and has planned studies with Regeneron and Eli Lilly, indicating broad potential for atebimetinib across various cancer types.

Immuneering Financial Statement Overview

Summary
Financials reflect a pre-revenue biotech with persistent large net losses (~$53M–$61M in 2022–2024 and ~-$56M in 2025) and material historical cash burn (free cash flow roughly -$31M to -$55M annually in 2020–2024). The balance sheet is a relative strength with low leverage (debt-to-equity ~0.02 in 2025), but ongoing losses and reliance on external funding keep the overall financial score below average.
Income Statement
18
Very Negative
The income statement reflects a pre-revenue biotechnology profile: revenue is effectively zero from 2023–2025 (and modest in 2020–2022), while losses remain large and persistent (net loss roughly $53M–$61M in 2022–2024, with another ~$56M loss in 2025). Profitability is consistently negative, and the lack of a visible revenue ramp increases reliance on funding rather than operations to support the business.
Balance Sheet
54
Neutral
Leverage is low, with total debt small relative to equity in recent annual periods (debt-to-equity ~0.02 in 2025 and ~0.10 in 2024), which is a key strength for a cash-burning biotech. However, returns on equity are deeply negative due to ongoing losses, and equity levels have been volatile over time (including negative equity in 2020), highlighting dilution/funding risk and limited balance-sheet efficiency until profitability improves.
Cash Flow
16
Very Negative
Cash generation is weak: operating and free cash flow are materially negative in 2020–2024 (free cash flow around -$31M to -$55M annually), consistent with heavy R&D and operating spend. 2025 shows operating and free cash flow reported as 0 with a -100% free-cash-flow growth figure, which is not supportive of improving underlying cash dynamics; overall, cash burn remains a central risk and implies continued external financing needs.
BreakdownDec 2025Dec 2024Dec 2023Dec 2022Dec 2021
Income Statement
Total Revenue0.000.000.00316.95K2.08M
Gross Profit-698.89K0.000.00158.83K926.89K
EBITDA-58.68M-63.69M-58.06M-51.47M-33.73M
Net Income-56.02M-61.04M-53.47M-50.51M-33.54M
Balance Sheet
Total Assets231.99M52.71M102.58M122.37M166.70M
Cash, Cash Equivalents and Short-Term Investments172.83M36.14M85.67M105.52M149.20M
Total Debt3.82M4.16M4.46M4.84M5.36M
Total Liabilities13.50M11.33M12.01M12.52M10.72M
Stockholders Equity218.48M41.39M90.58M109.85M155.98M
Cash Flow
Free Cash Flow-45.49M-55.08M-49.31M-44.84M-30.91M
Operating Cash Flow-45.34M-55.00M-48.97M-44.10M-30.85M
Investing Cash Flow-88.74M26.43M7.30M41.83M-75.62M
Financing Cash Flow226.58M5.30M28.44M19.00K144.26M

Immuneering Technical Analysis

Technical Analysis Sentiment
Negative
Last Price5.05
Price Trends
50DMA
5.18
Negative
100DMA
5.84
Negative
200DMA
5.24
Negative
Market Momentum
MACD
0.07
Negative
RSI
46.51
Neutral
STOCH
55.89
Neutral
Evaluating momentum and price trends is crucial in stock analysis to make informed investment decisions. For IMRX, the sentiment is Negative. The current price of 5.05 is below the 20-day moving average (MA) of 5.17, below the 50-day MA of 5.18, and below the 200-day MA of 5.24, indicating a bearish trend. The MACD of 0.07 indicates Negative momentum. The RSI at 46.51 is Neutral, neither overbought nor oversold. The STOCH value of 55.89 is Neutral, not indicating any strong overbought or oversold conditions. Overall, these indicators collectively point to a Negative sentiment for IMRX.

Immuneering Risk Analysis

Immuneering disclosed 90 risk factors in its most recent earnings report. Immuneering reported the most risks in the "Tech & Innovation" category.
Finance & Corporate - Financial and accounting risks. Risks related to the execution of corporate activity and strategy
Latest Risks Added 0 New Risks

Immuneering Peers Comparison

Overall Rating
UnderperformOutperform
Sector (51)
Financial Indicators
Name
Overall Rating
Market Cap
P/E Ratio
ROE
Dividend Yield
Revenue Growth
EPS Growth
56
Neutral
$326.08M-5.17-43.33%9.32%
55
Neutral
$491.71M-8.10-48.65%332.71%75.73%
51
Neutral
$7.86B-0.30-43.30%2.27%22.53%-2.21%
49
Neutral
$513.53M-2.29-65.76%18.39%
45
Neutral
$485.19M-1.33-91.83%-67.41%
42
Neutral
$377.21M-3.90-69.67%-11.41%
* Healthcare Sector Average
Performance Comparison
Ticker
Company Name
Price
Change
% Change
IMRX
Immuneering
5.05
3.37
200.60%
LRMR
Larimar Therapeutics
4.60
2.05
80.20%
RCKT
Rocket Pharmaceuticals
4.73
-4.10
-46.43%
IVVD
Invivyd
1.74
0.98
128.95%
AURA
Aura Biosciences Inc
5.94
-1.60
-21.22%

Immuneering Corporate Events

Business Operations and StrategyProduct-Related Announcements
Immuneering Reports Strong Phase 2a Pancreatic Cancer Survival Data
Positive
Jan 7, 2026

On January 7, 2026, Immuneering announced updated interim results from its ongoing Phase 2a trial of atebimetinib, a once-daily oral MEK inhibitor, combined with modified Gemcitabine/nab-Paclitaxel in first-line pancreatic cancer patients, showing a 64% overall survival rate at 12 months as of the December 15, 2025 cutoff in a 34-patient intent-to-treat cohort at the 320 mg dose, compared with a reported 35% 12‑month overall survival for standard of care, with median overall survival not yet reached and median progression-free survival of 8.5 months. The regimen was generally well tolerated, with no Grade 5 treatment-emergent adverse events and no new safety signals, and Immuneering signaled a rapid development path by planning additional survival and circulating tumor DNA data readouts in 2026, as well as initiating a pivotal Phase 3 trial in first-line pancreatic cancer and a combination trial with Libtayo in non-small cell lung cancer, underscoring its bid to strengthen its position in oncology and potentially enhance treatment options for patients and clinicians.

The most recent analyst rating on (IMRX) stock is a Buy with a $12.00 price target. To see the full list of analyst forecasts on Immuneering stock, see the IMRX Stock Forecast page.

Glossary
BuyA stock rated as a "Buy" is expected to perform better than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock is likely to deliver higher returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
HoldA stock rated as a "Hold" is expected to perform in line with the overall market or a specific benchmark. This rating indicates that the stock is neither particularly compelling nor unfavorable for investment. Note: This is not investment advice; please consult a financial advisor before making investment decisions.
SellA stock rated as a "Sell" is expected to perform worse than the overall market or a specific benchmark over the near-to-medium term. This rating suggests the stock may deliver lower returns compared to other stocks in the same sector or market index. Note: This is not investment advice; please consult a financial advisor before making investment decisions.

Disclaimer

This AI Analyst Stock Report is automatically generated by our AI systems using advanced algorithms and publicly available financial, technical, and market data. While the information provided aims to be accurate and insightful, it is intended for informational purposes only and should not be considered financial advice. Any content created by an AI (Artificial Intelligence) system may contain inaccuracies and/or contain errors. Investing in stocks carries inherent risks, and past performance is not indicative of future results. This report does not account for your personal financial circumstances, objectives, or risk tolerance. Always conduct your own research or consult with a qualified financial advisor before making investment decisions. The analysis and recommendations provided are based on historical and current data and may not fully reflect future market conditions or unexpected developments. Neither the creators of this report nor its affiliated entities guarantee the accuracy, completeness, or reliability of the information presented. Use this report at your own discretion and risk.Date of analysis: Mar 07, 2026