drugset / Trial / NCT06495723

Polyspecific Antibodies in Lymphoproliferative T-cell Disorders

NCT06495723 ↗

Phase 1/2 Recruiting 54 enrolled Xenothera SAS
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

Drugs

EvaluationDrugModalityDoseRoute
Subject LIS1 Protein / enzyme biologic 2 mg/kg Intravenous
Subject LIS1 Protein / enzyme biologic 4 mg/kg Intravenous
Subject LIS1 Protein / enzyme biologic 6 mg/kg Intravenous