Welcome to our dedicated page for Inmed Pharmaceuticals SEC filings (Ticker: INM), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Reading a biotech filing shouldn’t feel like deciphering a lab notebook. InMed Pharmaceuticals’ SEC reports are packed with clinical data, patent claims, and trial costs that can easily exceed two hundred pages. Whether you’re tracking cash burn before the next Phase 2 readout or watching management’s share purchases, the details matter—and they’re buried deep in the documents.
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Stop scrolling through PDFs and start understanding InMed SEC documents with AI. From InMed executive stock transactions Form 4 to fresh S-3 shelf registrations, every filing type is here, updated the moment EDGAR releases it. Complex science, clear disclosures—now summarized for quicker, smarter decisions.
InMed Pharmaceuticals Inc. (INM) 10-K highlights key operational progress, financing and risks. The company reported continued operating losses with a net loss widening to $8.69 million for the latest year and an accumulated deficit of about $117.2 million. Management states cash resources are sufficient into the fourth quarter of calendar 2026, but concluded there is substantial doubt about the company’s ability to continue as a going concern without additional financing. Commercial operations at BayMedica are producing some revenues tied to bulk rare cannabinoids, and the company received gross proceeds of approximately $5.0 million from a private placement and $6.2 million from share issuances under a SEPA during the year.
On the R&D side, INM-901 (Alzheimer’s candidate) showed preclinical anti-inflammatory and behavioral benefits across multiple preclinical studies and was presented at AAIC 2025. INM-755 advanced through Phase 1 and a Phase 2 EB study (19 of 20 enrolled) with reported safety and some efficacy signals. The company holds multiple patent families across product and manufacturing processes and continues CMC, GLP and scale-up activities. Major risks disclosed include clinical, regulatory, intellectual property, manufacturing, controlled-substance regulation, Nasdaq listing compliance and cybersecurity.
Form 8-K (Item 7.01 – Regulation FD): InMed Pharmaceuticals (Nasdaq: INM) announced it will present new pre-clinical data from its cannabinoid-based INM-901 program for Alzheimer’s disease at the Alzheimer’s Association International Conference (AAIC) 2025. The disclosure, dated 28 Jul 2025, is being furnished—not filed—so it carries no liability under Exchange Act §18 and will not be automatically incorporated into other SEC filings.
No financial results, guidance, or transactional details accompany the notice; the company simply alerts investors to an upcoming scientific presentation. Exhibit 99.1 (news release) and Exhibit 104 (XBRL cover data) are provided as furnished exhibits.
Because the information is limited to a pipeline update and occurs at the pre-clinical stage, any commercial or financial impact remains undetermined within the filing.
InMed Pharmaceuticals has announced promising new preclinical data for their drug candidate INM-901 on June 24, 2025. The research demonstrates significant reduction in inflammation in ex vivo models of neuroinflammation, strengthening the compound's potential as a therapeutic treatment for Alzheimer's disease.
Key points from the 8-K filing:
- The announcement falls under Regulation FD Disclosure (Item 7.01)
- The company is classified as an emerging growth company
- Common shares trade on Nasdaq under symbol INM
- The disclosure is being furnished rather than "filed" under SEC regulations
This development represents a significant milestone in InMed's neurodegenerative disease pipeline, though specific efficacy data and trial details were not disclosed in the filing. The news was signed off by President & CEO Eric A Adams.
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