Last reviewed · How we verify
Phase 1, Open-Label, Dose Escalation Study of I-131-CLR1404 in Patients With Relapsed or Refractory Multiple Myeloma
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 sponsor | Cellectar Biosciences, Inc. |
|---|---|
| Phase | Phase 1 |
| Status | COMPLETED |
| Enrolment | 31 |
| Start date | 2015-02 |
| Completion | 2022-08-10 |
Conditions
- Multiple Myeloma
Interventions
- I-131-CLR1404
- dexamethasone
- I-131-CLR1404
Primary outcomes
- Number of participants with dose limiting toxicities (DLT) — up to 85 days
DLT will be assessed by physical examination, vital signs, ECG, and laboratory values
Countries
United States