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Phase 1, Open-Label, Dose Escalation Study of I-131-CLR1404 in Patients With Relapsed or Refractory Multiple Myeloma

NCT02278315 Phase 1 COMPLETED

The primary objective of the study is to determine the safety and tolerability of I-131-CLR1404 as a single or multiple dose, with and without concurrent weekly dexamethasone, in patients with relapsed or refractory multiple myeloma who have previously been treated with, or are intolerant of, an immunomodulator and a proteasome inhibitor.

Details

Lead sponsorCellectar Biosciences, Inc.
PhasePhase 1
StatusCOMPLETED
Enrolment31
Start date2015-02
Completion2022-08-10

Conditions

Interventions

Primary outcomes

Countries

United States