CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 522 enrolled
Drug / intervention
Dara SC +1 moredrug
Likely dose
Dara SC 1800 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03277105
NCT03277105Phase 3Completed

A Phase 3 Randomized, Multicenter Study of Subcutaneous vs. Intravenous Administration of Daratumumab in Subjects With Relapsed or Refractory Multiple Myeloma

Janssen Research & Development, LLC·interventional·Posted Sep 8, 2017·Updated Apr 29, 2025

In Brief

A Phase 3 clinical trial evaluating Dara SC and Dara IV for Multiple Myeloma. Completed, enrolled 522 participants across 146 sites in 18 countries.

Detailed Summary

The purpose of this study is to show that subcutaneous (SC) administration of daratumumab co-formulated with recombinant human hyaluronidase PH20 (Dara SC) is non-inferior to intravenous (IV) administration of daratumumab (Dara IV) in terms of the overall response rate (ORR) and maximum trough concentration (Ctrough).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustralia, Brazil, Canada, Czechia, France, Greece, Israel, Italy, Japan, Poland, Russia, South Korea, Spain, Sweden, Taiwan, Ukraine, United Kingdom, United States
Collaborators--

Timeline

Phase 3CompletedFinished
201820192020202120222023202420252026
First PostedSep 8, 2017
Enrollment StartOct 27, 2017
Primary CompletionJun 27, 2019
Study CompletionJan 12, 2024
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 8.8 years ago

Interventions

Dara SCdrug

Participants will receive a fixed dose of Dara SC as 1800 mg daratumumab with rHuPH20 2000 U/mL, once weekly in Cycle 1 and 2, every 2 weeks in Cycle 3 to 6, every 4 weeks in Cycle 7 and thereafter until disease progression, unacceptable toxicity or the end of study.

Dara IVdrug

Participants will receive Dara IV 16 mg/kg once weekly in Cycle 1 and 2, every 2 weeks in Cycle 3 to 6, every 4 weeks in Cycle 7 and thereafter until disease progression, unacceptable toxicity or the end of study.