Overview

Safety, Efficacy and Pharmacokinetic Study of PRLX 93936 in Patients With Multiple Myeloma

Status:
Unknown status
Trial end date:
2014-09-01
Target enrollment:
Participant gender:
Summary
To determine the maximum tolerated dose of, and response to, PRLX 93936 as treatment for patients with relapsed or relapsed/refractory multiple myeloma.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Prolexys Pharmaceuticals