drugset / Trial / NCT02278315

Dose Escalation Study of I-131-CLR1404 in Patients With Relapsed or Refractory Multiple Myeloma

NCT02278315 ↗

Phase 1 Completed 31 enrolled Cellectar Biosciences, Inc.
NaSingle-groupOpen-labelTreatment

Summary

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.

Timeline

Start
2015-02
Primary completion
2020-12-09
Completion
2022-08-10

Outcome

Met primary endpoint

release “Data from Cohort 6 showed improved efficacy and a clear dose response compared to prior cohorts, including a 50% overall response rate” cellectar.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 40 mg Oral
Subject I-131-CLR1404 Small molecule — Intravenous

Indications