HLX15-SC

A Randomized, Double-blind, Parallel-controlled Phase I Study to Compare the Pharmacokinetic Characteristics, Safety, Tolerability, and Immunogenicity of HLX15-SC With DARZALEX FASPRO® in Combination With Lenalidomide and Dexamethasone (Rd) in Transplant-ineligible Patients With Newly Diagnosed Multiple Myeloma

What's the purpose of the trial?

The purpose of this study is to compare the pharmacokinetic (PK) similarity, safety, tolerability, immunogenicity, and efficacy of HLX15-SC versus US-DARZALEX FASPRO® following single and multiple subcutaneous (SC) injections in newly diagnosed MM patients ineligible for transplant. 

Trial status

Accepting patients

Phase
Phase 1
Enrollment
258
Last Updated

Participating Centers

There are 9 centers participating in this trial. Enter a location below to find the closest center.

Experimental Treatments

Learn more about the experimental treatments being evaluated in this clinical trial.

  • Lenalidomide
  • Daratumumab
  • Dexamethasone
  • HLX15-SC

Arms / Cohorts

Explore eligibility, treatments and learn more about potential cohorts.

Accepting patients

DARZALEX FASPRO®-Rd

Accepting patients

HLX15-SC-Rd

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