Marker Therapeutics Shares Positive Progress in Phase 1 APOLLO Study with Promising Response Rates in Relapsed Lymphoma
Study Results: The Phase 1 APOLLO study of MT-601 in patients with relapsed B cell lymphoma reported a 66% objective response rate, with 50% achieving complete response, demonstrating promising efficacy.
Safety Profile: The treatment exhibited a favorable safety profile, with no dose limiting toxicities or severe neurotoxicity observed, and only mild cytokine release syndrome events reported.
Next Steps: The study will proceed to a dose expansion phase to evaluate MT-601 at a maximum dose in patients with Diffuse Large B Cell Lymphoma (DLBCL) who are ineligible for CAR-T therapy.
Webcast Announcement: A live webcast is scheduled to discuss the clinical results and updates from the study, allowing attendees to engage through a Q&A feature.
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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.








