drugset / Trial / NCT07667868

A Phase I, Open-label, Multicenter Study to Evaluate the Safety and Tolerability of BP2202 in Patients With Relapsed/Refractory Multiple Myeloma

NCT07667868 ↗

Phase 1 Not yet recruiting 18 enrolled BrightPath Biotherapeutics
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to find out if BP2202 is safe and can treat participants with Relapsed/Refractory Multiple Myeloma.

Timeline

Start
2026-10-01
Primary completion
2027-12-31
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BP2202 Unknown — Intravenous