Neumora Therapeutics Updates Pipeline and Anticipates 2026 Milestones
Neumora Therapeutics announced key pipeline updates and anticipated 2026 milestones that support the Company's mission to redefine neuroscience drug development with the next generation of novel therapies that offer improved treatment outcomes and quality of life for patients living with brain diseases. Navacaprant: Planned joint readout of KOASTAL-2 and -3 in second quarter of 2026: Neumora announced that it plans to increase enrollment in each of the KOASTAL studies, targeting up to 25 percent enrollment beyond the original target of 332, as the study protocols permit. The Company expects a joint topline data readout for both KOASTAL-2 and KOASTAL-3 in the second quarter of 2026 and believes this approach optimizes assessment of navacaprant efficacy in major depressive disorder in the KOASTAL program. NMRA-215: Plans to initiate Phase 1 clinical program following class-leading preclinical data: Neumora expects to initiate a clinical program evaluating NMRA-215 monotherapy and combination therapy for the treatment of obesity in the first half of 2026. The Company expects to report weight loss data following treatment with NMRA-215 around the end of 2026. M4 Positive Allosteric Modulator Franchise: Progressing Phase 1 clinical studies for NMRA-898 and NMRA-861: Neumora expects to provide a comprehensive M4 franchise update in mid-2026, including potentially advancing development of one or both programs. NMRA-511: Reported positive results from Phase 1b study in Alzheimer's disease agitation: In January 2026, NMRA-511, an oral, highly potent, brain-penetrant and selective antagonist of the vasopressin 1a receptor met the goal of the Phase 1b study, demonstrating a clinically meaningful effect size in people with AD agitation. In the study, NMRA-511 demonstrated a favorable tolerability and safety profile with no reports of somnolence or sedation. The Company is in a strong financial position and expects its cash, cash equivalents and marketable securities to support operations into the third quarter of 2027.
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- Significant Clinical Effect: In the Phase 1b study targeting Alzheimer’s patients, NMRA-511 showed a placebo-adjusted change of -2.6 and -2.1 in CMAI total scores at Weeks 6 and 8, respectively, indicating its clinically meaningful impact on reducing agitation behaviors.
- Favorable Safety Profile: NMRA-511 demonstrated good tolerability and safety, with treatment-emergent adverse events (TEAEs) typically mild to moderate, and a low discontinuation rate of only 2.5% due to TEAEs, establishing a solid foundation for future clinical applications.
- Clear Next Steps: Neumora plans to launch a multiple ascending dose extension study at higher doses in 2026, develop an extended-release formulation for once-daily dosing, and initiate a Phase 2/3 dose-ranging study, reflecting strong confidence in NMRA-511's long-term development.
- KOASTAL Study Expansion: Neumora also announced plans to increase enrollment in the KOASTAL studies by targeting an additional 25% beyond the original target of 332 participants, with a joint topline data readout for KOASTAL-2 and KOASTAL-3 expected in Q2 2026, further enhancing its research footprint in the depression space.

- Clinical Trial Success: Neumora Therapeutics announced that NMRA-511 demonstrated a significant treatment effect in its Phase 1b study for agitation associated with Alzheimer's, achieving a 15.7-point reduction in the mean Cohen-Mansfield Agitation Inventory score, indicating clinical significance across a broad patient population.
- Favorable Safety Profile: The drug exhibited an unmatched effect size in a pre-specified subgroup of patients with elevated anxiety, while also showing a favorable safety and tolerability profile, laying a solid foundation for further development.
- Future Research Plans: Following these positive results, Neumora plans to initiate a multiple ascending-dose extension study of NMRA-511 in 2026 and advance the drug into a Phase 2/3 dose-ranging study, aiming to further validate its clinical application potential.
- Positive Market Reaction: Following the announcement, Neumora's shares rose over 10% in premarket trading, reflecting investor optimism about the drug's prospects, despite closing at $1.66 on Friday, down 7.3% from previous levels.
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- Stock Price Rebound: Following the announcement, ZIM's shares rose 7.6% in pre-market trading to $21.38, reflecting market optimism about the company's future prospects and potentially attracting more investor interest.
- Enhanced Strategic Value: By actively assessing acquisition proposals, ZIM not only strengthens its market position but also may achieve operational efficiencies through resource integration, thereby delivering higher returns to shareholders.
- Positive Market Reaction: The stock price increase indicates investor confidence in ZIM's potential acquisitions, which could further boost the company's competitiveness and market share in the shipping industry.
- FDA Approval Milestone: Novo Nordisk's once-daily Wegovy obesity pill received FDA approval, leading to a 9.48% increase in after-hours trading to $52.66, marking a significant advancement in obesity treatment that is expected to drive sales growth and enhance market competitiveness.
- Cardiovascular Risk Reduction: Wegovy is not only indicated for weight loss but also approved to reduce the risk of major cardiovascular events in obese patients, which will likely attract more patients with related conditions, thereby expanding the potential market.
- Rising Investor Interest: Despite no new updates, Neumora Therapeutics and BioRestorative Therapies saw increases of 16.02% and 6.90% respectively, indicating broad investor interest and optimism in the biotech sector, which may fuel a wave of investment across the industry.
- Clinical Trial Progress: IDEAYA Biosciences announced full enrollment of 435 patients in its Phase 2/3 trial, with progression-free survival data expected in Q1 2026, potentially paving the way for accelerated approval in the U.S. and further solidifying the company's position in cancer treatment.








