drugset / Trial / NCT06495723
Polyspecific Antibodies in Lymphoproliferative T-cell Disorders
Non-randomizedSequentialOpen-labelTreatment
Summary
This is a 2-part study consisting of a Part 1, dose escalation and dose-finding component to establish the Maximal Tolerated Dose (MTD), or Recommended Part 2 Dose (RP2D) of LIS1 as a single agent; followed by a Part 2, to investigate anti-tumors efficacy of LIS1 in selected subtypes of Peripheral TCell Lymphoma (PTCL) and to further evaluate its safety and tolerability at RP2D.
Timeline
- Start
- 2024-07-09
- Primary completion
- 2026-07-31
- Completion
- 2027-07-31