A Phase 1/2a Open-label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of Modakafusp Alfa in Combination With Daratumumab Subcutaneous in Patients With Relapsed or Refractory Multiple Myeloma
Latest Information Update: 20 Aug 2025
At a glance
- Drugs Daratumumab (Primary) ; Modakafusp alfa (Primary)
- Indications Multiple myeloma
- Focus Adverse reactions; Therapeutic Use
- Acronyms iinnovate-3
- Sponsors Takeda; Takeda Development Center Americas
Most Recent Events
- 06 Aug 2025 Protocol has been amended, to include new arms (Phase 1 (Dose Escalation) Modakafusp Alfa 120 mg + Daratumumab and Experimental: Phase 1 (Dose Escalation) Modakafusp Alfa 240 mg + Daratumumab) , changed from 3 to 5.
- 06 Aug 2025 Status changed to discontinued.
- 22 Feb 2024 This trial has been discontinued in Spain, according to European Clinical Trials Database record.