A Phase II, Open-Label, Multicenter Study With a Safety Run-In to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics and Pharmacodynamics of MT027 Administrated Intracerebroventricularly in Patients With Recurrent or Progressive Glioblastoma (WHO Grade 4)
Latest Information Update: 16 Feb 2026
At a glance
- Drugs MT 027 (Primary)
- Indications Glioblastoma
- Focus Adverse reactions; Therapeutic Use
- Acronyms GLIOMAX-101
- Sponsors T-Maximum Pharmaceutical
Most Recent Events
- 04 Feb 2026 Status changed from planning to not yet recruiting.
- 12 Jan 2026 New trial record
- 21 Dec 2025 According to a T-MAXIMUM Pharmaceutical media release, MT027, has received IND Clearance from the U.S. Food and Drug Administration (FDA) to initiate a Phase II clinical trial for the treatment of recurrent glioblastoma (rGBM).