drugset / Trial / NCT01080391

Study Comparing Carfilzomib, Lenalidomide, and Dexamethasone (CRd) vs Lenalidomide and Dexamethasone (Rd) in Subjects With Relapsed Multiple Myeloma

NCT01080391 ↗

Phase 3 Completed 792 enrolled Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

The primary objective was to compare progression-free survival in adults with relapsed multiple myeloma who are receiving CRd vs participants receiving Rd in a randomized multicenter setting.

Timeline

Start
2010-07-14
Primary completion
2014-06-16
Completion
2017-12-05

Outcome

Met primary endpoint

registry analysis (unspecified test); Lenalidomide and Dexamethasone (Rd) vs Carfilzomib, Lenalidomide, and Dexamethasone (CRd); p < 0.0001; Hazard Ratio (HR) 0.690 (95% CI 0.570 to 0.834); Log Rank NCT01080391 ↗

paper Progression-free survival was significantly improved with carfilzomib (median, 26.3 months, vs. 17.6 months in the control group; hazard ratio for progression or death, 0.69; PMID 25482145 ↗

release “As previously reported, the ASPIRE study met its primary endpoint by demonstrating that KRd significantly extended the time patients lived without their disease worsening” amgen.com ↗

release “Phase 3 ASPIRE trial in which Kyprolis in combination with lenalidomide and dexamethasone demonstrated a significant improvement in PFS” amgen.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Carfilzomib Other / unclassified 27 mg/m2 Intravenous
Background Dexamethasone Small molecule 40 mg Oral
Background Lenalidomide Other / unclassified 25 mg Oral

Indications