Marker Therapeutics Announces Financial Results for Q3 2025 and Shares Business Developments
Clinical Study Results: The APOLLO study reported a 66% objective response rate and a 50% complete response rate for MT-601 in relapsed Non-Hodgkin lymphoma patients, demonstrating a favorable safety profile with no dose-limiting toxicities observed.
New Treatment Initiatives: Marker Therapeutics treated the first patient in the RAPID study, exploring Off-the-Shelf MAR-T cells for Acute Myeloid Leukemia and Myelodysplastic Syndrome, while also launching a clinical program for MT-601 in metastatic pancreatic cancer.
Manufacturing Collaboration: The company established a cGMP manufacturing partnership with Cellipont Bioservices to enhance production capabilities for MT-601, supporting clinical supply and future pivotal trials.
Financial Position: Marker Therapeutics raised approximately $10 million, extending its cash runway into 2026, with a reported net loss of $2 million for the third quarter of 2025, reflecting a decrease in research and development expenses compared to the previous year.
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Biotech Surge Post-Market: Inspira, MediciNova, and DiaMedica Therapeutics Among Top Performers
Biotech Stocks Performance: Several small-cap biotech and healthcare companies saw notable gains in after-hours trading, driven by recent corporate updates and clinical milestones.
Inspira Technologies Update: Inspira Technologies Oxy B.H.N. Ltd. rose 5.88% following a recent agreement for a registered direct offering and a Standby Equity Purchase Agreement, despite no new news on the day.
MediciNova's Clinical Trial Success: MediciNova, Inc. advanced 4.83% after successfully completing patient enrollment in its Phase 2 OXTOX study, which evaluates MN-166 for preventing chemotherapy-induced peripheral neuropathy.
DiaMedica's FDA Meeting: DiaMedica Therapeutics Inc. gained 2.89% after a productive pre-IND meeting with the FDA regarding its study of DM199 in preeclampsia, with an additional non-clinical study requested.
Merakris Presents MTX-001 Biologic Drug at Innovations in Wound Healing Symposium
- Scientific Exchange Platform: Merakris' Chief Scientific Officer, Dr. Roger Ilagan, has been invited to present at the Innovations in Wound Healing Symposium from December 11-14, 2025, sharing updates on MTX-001 to advance scientific dialogue in biologic drug development.
- Clinical Trial Progress: MTX-001, a first-in-class injectable biologic derived from cell-free amniotic fluid, is currently undergoing a multicenter Phase 2 trial (NCT04647240), with Part 1 completed and published in the International Wound Journal in March 2025, demonstrating promising safety and tolerability.
- Expanded Access Program: The therapy is available through an Expanded Access Program (EAP) for patients with cutaneous wounds, such as diabetic foot ulcers and pressure sores, reflecting Merakris' responsiveness to patient needs and market adaptability.
- Industry Leadership: Merakris is focused on developing biologically derived products to improve wound healing, showcasing its innovative leadership in regenerative medicine through advanced biologic manufacturing capabilities and a robust research pipeline.
