ISB 1442

Phase 1/2 Study of ISB 1442 in Relapsed/Refractory Multiple Myeloma

What will happen during the trial?

The study will be conducted in two phases:

Phase 1: Dose escalation in R/R MM
Phase 2: Dose expansions in select R/R MM

Cohort A: R/R MM

Cohort B: R/R MM Post-T-Cell Directed Therapy Participants will be treated at escalating dose levels in Phase 1 (dose-escalation phase) of the study. Once the safety of ISB 1442 is confirmed and a Recommended Phase 2 Dose (RP2D) is established in Phase 1 for a given indication, Phase 2 will be initiated for that indication.
Participants will receive ISB 1442, until disease progression, unacceptable toxicity, or any criterion for stopping the study drug or withdrawal from the trial occurs.

More Information

Trial Status
Accepting patients
Trial Phase
Phase 1/2
Enrollment
121 patients (estimated)
Sponsors
Ichnos Sciences SA
Tags
Bispecific Antibody, CD38, CD47
Trial Type
Treatment
Last Update
2 weeks ago
SparkCures ID
1327
NCT Identifier
NCT05427812

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