Neumora's NMRA-215 shows significant weight loss potential, set for Phase 1 trials in 2026, targeting obesity treatment.
Quiver AI Summary
Neumora Therapeutics announced promising preclinical results for its oral NLRP3 inhibitor, NMRA-215, highlighting its potential as a leading treatment for obesity. The data shows NMRA-215 achieved significant weight loss—up to 19% as a standalone treatment and 26% when combined with semaglutide. This effectiveness is attributed to NMRA-215's strong pharmacological profile and its ability to penetrate the brain, targeting neuroinflammation linked to appetite regulation. Neumora plans to initiate Phase 1 clinical trials in early 2026 and emphasizes the potential of NMRA-215 in modern obesity treatment strategies. Further data will be presented during a virtual R&D day on October 27, 2025.
Potential Positives
- NMRA-215 demonstrated class-leading weight loss of up to 26% in combination with semaglutide, indicating a strong potential for effectiveness in obesity treatment.
- The company plans to initiate a Phase 1 clinical study for NMRA-215 in the first quarter of 2026, which marks a significant step towards advancing this treatment to human trials.
- Positive preclinical data from diet-induced obesity mouse studies validate NMRA-215's potential as a novel, brain-penetrant oral NLRP3 inhibitor, reinforcing its promise in neuroscience drug development.
Potential Negatives
- Neumora plans to initiate Phase 1 clinical study in the first quarter of 2026, indicating a significant delay in moving from preclinical to clinical stages.
- The press release includes a cautionary note about forward-looking statements, highlighting potential risks and uncertainties associated with clinical drug development, which could undermine investor confidence.
- Risks related to serious or undesirable side effects of NMRA-215 are mentioned, raising concerns about the therapeutic candidate's safety profile.
FAQ
What is NMRA-215?
NMRA-215 is a potentially best-in-class, highly brain-penetrant, oral NLRP3 inhibitor aimed at treating obesity.
How effective is NMRA-215 for weight loss?
NMRA-215 demonstrated up to 19% weight loss as a monotherapy and 26% when combined with semaglutide.
When will NMRA-215 enter clinical trials?
Neumora plans to initiate Phase 1 clinical studies for NMRA-215 in the first quarter of 2026.
What is the mechanism of action for NMRA-215?
NMRA-215 targets NLRP3 in the hypothalamus to modulate appetite control and reduce food intake.
What other diseases is Neumora targeting?
Besides obesity, Neumora is exploring NMRA-215 for the treatment of Parkinson’s disease.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$NMRA Hedge Fund Activity
We have seen 51 institutional investors add shares of $NMRA stock to their portfolio, and 70 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- BLACKROCK, INC. removed 3,472,424 shares (-54.6%) from their portfolio in Q2 2025, for an estimated $2,546,328
- UBS GROUP AG removed 2,455,852 shares (-79.1%) from their portfolio in Q2 2025, for an estimated $1,800,876
- STATE STREET CORP removed 1,370,559 shares (-79.6%) from their portfolio in Q2 2025, for an estimated $1,005,030
- GEODE CAPITAL MANAGEMENT, LLC removed 1,059,487 shares (-53.6%) from their portfolio in Q2 2025, for an estimated $776,921
- TWO SIGMA ADVISERS, LP added 1,052,900 shares (+597.6%) to their portfolio in Q2 2025, for an estimated $772,091
- BANK OF AMERICA CORP /DE/ removed 797,642 shares (-91.8%) from their portfolio in Q2 2025, for an estimated $584,910
- GSA CAPITAL PARTNERS LLP added 717,030 shares (+384.0%) to their portfolio in Q2 2025, for an estimated $525,798
To track hedge funds' stock portfolios, check out Quiver Quantitative's institutional holdings dashboard.
$NMRA Analyst Ratings
Wall Street analysts have issued reports on $NMRA in the last several months. We have seen 1 firms issue buy ratings on the stock, and 1 firms issue sell ratings.
Here are some recent analyst ratings:
- JP Morgan issued a "Underweight" rating on 09/16/2025
- Needham issued a "Buy" rating on 05/13/2025
To track analyst ratings and price targets for $NMRA, check out Quiver Quantitative's $NMRA forecast page.
$NMRA Price Targets
Multiple analysts have issued price targets for $NMRA recently. We have seen 2 analysts offer price targets for $NMRA in the last 6 months, with a median target of $5.0.
Here are some recent targets:
- Graig Suvannavejh from Mizuho set a target price of $5.0 on 07/16/2025
- Ami Fadia from Needham set a target price of $5.0 on 05/13/2025
Full Release
NMRA-215 demonstrated class-leading weight loss of up to 19% as a monotherapy with semaglutide-like induction
NMRA-215 demonstrated best-in-class weight loss of up to 26% in combination with semaglutide
Class-leading weight loss driven by best-in-class pharmacology and brain penetration of NMRA-215
Neumora plans to initiate Phase 1 clinical study in the first quarter of 2026
WATERTOWN, Mass., Oct. 27, 2025 (GLOBE NEWSWIRE) -- Neumora Therapeutics, Inc. (Nasdaq: NMRA), a clinical-stage biopharmaceutical company redefining neuroscience drug development, today announced positive preclinical data for NMRA-215, a potentially best-in-class, highly brain-penetrant, oral NLRP3 inhibitor from three diet-induced obesity (DIO) mouse studies. NMRA-215 demonstrated class-leading weight loss of up to 19% as a monotherapy with semaglutide-like induction and 26% in combination with semaglutide.
“We are very encouraged by the results of the DIO studies with NMRA-215, which validate its potential as a class-leading, novel, brain-penetrant, oral NLRP3 inhibitor for obesity,” said Paul Berns, co-founder, chief executive officer and chairman, Neumora. “These data demonstrate NMRA-215 drives meaningful weight loss as a monotherapy in mice, including incretin-like induction, additive weight loss in the combination setting with semaglutide, as well as the potential to enable incretin-sparing dosing regimens. These data reinforce our conviction that NMRA-215 may be an effective, next-generation, oral treatment for obesity, both as a monotherapy as well as in combination with a GLP-1 agonist. We are looking forward to moving this program into the clinic in the first quarter of 2026.”
Neumora will present additional data during its virtual R&D day on October 27, 2025 at 8:00am ET.
Webcast Information
Neumora will host a virtual R&D day at 8:00 a.m. ET on Monday, October 27, 2025. Participants can register for the live webcast
here
. In addition, the live webcast of the event will be available on the events and presentations section of the Company’s website at
www.neumoratx.com
. A replay of the webcast will be available following the completion of the event and will be archived for up to 30 days.
About NMRA-215
NMRA-215 is a potentially best-in-class, highly brain-penetrant, oral NLRP3 inhibitor in development for the treatment of obesity. The NLRP3 inflammasome is a critical part of the innate immune system that responds to pathogens and cellular damage and is implicated in both CNS and peripheral system disorders. NLRP3-mediated neuroinflammation in the hypothalamus is lined to obesity, and targeting NLRP3 in the hypothalamus is hypothesized to modulate dysfunctional neuronal circuitry related to appetite, leading to decreased food intake. Neumora is also exploring the potential of a NMRA-215 inhibitor program for the treatment of Parkinson’s disease.
About Neumora
Neumora Therapeutics, Inc. is a clinical-stage biopharmaceutical company founded to confront the greatest medical challenges of our generation by taking a fundamentally different approach to the way treatments for brain diseases are developed. Our therapeutic pipeline currently consists of seven programs that target novel mechanisms of action for a broad range of underserved, prevalent diseases. Neumora’s mission is to redefine neuroscience drug development by bringing forward the next generation of novel therapies that offer improved treatment outcomes and quality of life for patients.
Cautionary Note Regarding Forward-Looking Statements
This press release contains forward-looking statements about Neumora Therapeutics, Inc. (the “Company,” “we,” “us,” or “our”) within the meaning of the federal securities laws, including statements related to: Neumora’s intention to redefine neuroscience drug development by bringing forward the next generation of novel therapies that offer improved treatment outcomes and quality of life for patients suffering from brain diseases; the timing, progress and plans for its therapeutic development programs, including the NMRA-215 studies, best-in-class pharmacology and the potential of NLRP3 inhibitors in obesity; the potential for Neumora to continue to advance NMRA-215; the potential benefits of NMRA-215; intellectual property protection and other statements identified by words such as “could,” “expects,” “intends,” “may,” “plans,” “potential,” “should,” “will,” “would,” or similar expressions and the negatives of those terms. Other than statements of historical facts, all statements contained in this press release are forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995. These statements are subject to risks and uncertainties that could cause the actual results to be materially different from the information expressed or implied by these forward-looking statements, including, among others: the risks related to the inherent uncertainty of clinical drug development and unpredictability and lengthy process for obtaining regulatory approvals; risks related to the timely initiation and enrollment in our clinical trials; risks related to our reliance on third parties, including contract research organizations; risks related to serious or undesirable side effects of our therapeutic candidates; risks related to our ability to utilize and protect our intellectual property rights; and other matters that could affect sufficiency of capital resources to fund operations. For a detailed discussion of the risks and uncertainties that could cause actual results to differ from those expressed in these forward-looking statements, as well as risks relating to Neumora’s business in general, please refer to the risk factors identified in the Company’s filings with the Securities and Exchange Commission (SEC), including but not limited to its Quarterly Report on Form 10-Q for the quarter ended June 30, 2025 which was filed with the SEC on August 6, 2025. Forward-looking statements speak only as of the date hereof, and, except as required by law, Neumora undertakes no obligation to update or revise these forward-looking statements.
Neumora Contact:
Helen Rubinstein
617-402-5700
[email protected]