InMed targets 2027 Phase 1 trial start for INM-901 and plans FDA pre-IND meeting in Q3 2026

Reuters03-09

InMed targets 2027 Phase 1 trial start for INM-901 and plans FDA pre-IND meeting in Q3 2026

InMed said it is preparing for a pre-IND meeting with the FDA in Q3 2026 for its INM-901 Alzheimer’s program and is targeting an IND submission and Phase 1 trial start in 2027. In preclinical studies, INM-901 significantly reduced inflammatory biomarkers including IFN-γ and TNF-α in a 5xFAD mouse model. In an LPS-induced neuroinflammation model, INM-901 significantly reduced inflammasome activation and pro-inflammatory markers including NLRP3 and IL-6. InMed also said it plans a pre-IND meeting with the FDA in Q4 2026 for INM-089 in dry age-related macular degeneration.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. InMed Pharmaceuticals Inc. published the original content used to generate this news brief via Newsfile (Ref. ID: 202603090730NEWSFILECNPR____20260309_287694_1) on March 09, 2026, and is solely responsible for the information contained therein.

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