Multicenter, Open-label, Dose-escalation Phase I/II Study to Evaluate the Tolerability, Safety, Efficacy and Pharmacokinetics of Repeated Continuous Intravenous PPMX-T003 in Patients With Aggressive NK Cell Leukaemia (ANKL) (Physician-initiated Clinical Trial)
Latest Information Update: 08 May 2025
At a glance
- Drugs PPMX-T003 (Primary)
- Indications Large granular lymphocytic leukaemia
- Focus Adverse reactions
Most Recent Events
- 30 Apr 2025 Planned number of patients changed from 6 to 7.
- 22 Jan 2025 Planned End Date changed from 31 Mar 2025 to 31 Mar 2026.
- 22 Jan 2025 Planned primary completion date changed from 31 Mar 2025 to 31 Mar 2026.