Neumora Therapeutics (NMRA) Q3 2024 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2024 earnings summary
14 Jan, 2026Executive summary
Advanced seven clinical and preclinical neuroscience programs targeting neuropsychiatric and neurodegenerative diseases, with a focus on significant unmet needs and precision medicine approaches.
Lead asset navacaprant is in three Phase 3 trials for major depressive disorder (MDD), with additional studies in bipolar depression and Alzheimer's agitation ongoing.
No products approved or revenue from product sales; significant net losses since inception, driven by R&D and acquired in-process R&D costs.
Pipeline includes M4 muscarinic positive allosteric modulators (PAMs) and other assets for conditions such as schizophrenia, Parkinson's, and ALS.
Completed IPO in September 2023, raising $226.5 million; strong cash position of $341.3 million as of September 30, 2024, expected to fund operations into mid-2026.
Financial highlights
Total operating expenses for Q3 2024 were $76.6 million, up from $56.9 million in Q3 2023, primarily due to increased R&D activity for Phase 3 programs and business growth investments.
Net loss of $72.5 million for Q3 2024, compared to $53.0 million in Q3 2023; net loss of $185.0 million for the nine months ended September 30, 2024.
R&D expenses rose to $60.6 million in Q3 2024 from $41.6 million in Q3 2023; G&A expenses increased to $16.0 million in Q3 2024.
Cash, cash equivalents, and marketable securities totaled $341.3 million as of September 30, 2024.
Net loss per share was $0.45 (basic and diluted) for Q3 2024, with 159.6 million weighted-average shares outstanding.
Outlook and guidance
Topline results from KOASTAL-1 Phase 3 study for navacaprant in MDD expected by year-end 2024; KOASTAL-2 and -3 results in H1 2025.
Bipolar depression and Alzheimer's agitation study data expected in H2 2025.
Five clinical catalysts expected over the next 18 months, including Phase 3 and Phase 2 data for navacaprant and Phase 1b data for NMRA-511.
IND submission for next M4 PAM program planned for H1 2025.
Cash runway projected to support operations into mid-2026.
Latest events from Neumora Therapeutics
- NMRA-511 shows strong efficacy in Alzheimer's agitation; pipeline and funding support robust growth.NMRA
Guggenheim Securities Emerging Outlook: Biotech Summit 202612 Feb 2026 - Advancing brain-penetrant therapies for obesity, Alzheimer's agitation, and psychiatric disorders.NMRA
Corporate presentation11 Feb 2026 - Navacaprant’s phase III COASTAL studies for MDD are on track, targeting robust efficacy and safety.NMRA
Status Update20 Jan 2026 - Navacaprant's phase 3 trials for MDD target key endpoints, with pivotal data due by 2025.NMRA
Guggenheim Securities Inaugural Healthcare Innovation Conference14 Jan 2026 - Key phase III MDD data expected by mid-2025, supporting a robust, expanding pipeline.NMRA
Stifel 2024 Healthcare Conference13 Jan 2026 - Multiple neuroscience programs advance with strong financials and key clinical readouts ahead.NMRA
43rd Annual J.P. Morgan Healthcare Conference 202510 Jan 2026 - NMRA-511 showed strong efficacy and safety in Alzheimer's agitation, especially for anxious patients.NMRA
Study Result5 Jan 2026 - NLRP3 obesity program advances toward clinical trials, with key data and new CNS assets progressing.NMRA
H.C. Wainwright 27th Annual Global Investment Conference31 Dec 2025 - $307.6M cash and protocol enhancements support a robust pipeline as key data readouts near.NMRA
Q4 202426 Dec 2025