drugset / Trial / NCT04879043

Study to Assess Safety of HDP-101 in Patients With Relapsed Refractory Multiple Myeloma

NCT04879043 ↗

Phase 1/2 Recruiting 78 enrolled Heidelberg Pharma AG
NaSingle-groupOpen-labelTreatment

Summary

This study will assess the safety, tolerability, pharmacokinetics (PK) and the therapeutic potential of HDP-101 in patients with plasma cell disorders including multiple myeloma.

Timeline

Start
2022-02-07
Primary completion
2028-03
Completion
2028-09

Publications

  • Background Strassz A, Raab MS, Orlowski RZ, Kulke M, Schiedner G, Pahl A. A First in Human Study Planned to Evaluate HDP-101, an Anti-BCMA Amanitin Antibody-Drug Conjugate with a New Payload and a New Mode of Action, in Multiple Myeloma. Blood 2020; 136 (Supplement 1): 34. doi: https://doi.org/10.1182/blood-2020-142285

Drugs

EvaluationDrugModalityDoseRoute
Subject HDP-101 Unknown — Intravenous

Indications