Multiple Myeloma Clinical Trials

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A Phase 3 Randomized Study Comparing QLS32015 Monotherapy Versus Pomalidomide, Dexamethasone (Pd) or Selinexor, Dexamethasone (Sd) in Participants With Relapsed or Refractory Multiple Myeloma

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

The purpose of this study is to compare the safety and efficacy of QLS32015 with Pd/Sd for the treatment of relapsed or refractory multiple myeloma.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥18 years old, regardless of gender.

• Subjects should be willing and able to comply with the study schedule and protocols.

• Documented initial diagnosis of multiple myeloma according to International Myeloma Working Group (IMWG) diagnostic criteria.Must have measurable disease as defined by the following: Serum M-protein greater than or equal to 1 g/dL; OR Urine M-protein greater than or equal to 200 mg/24 hours; OR Serum free light chain (FLC) assay; involved FLC level greater than or equal to 10 mg/dL provided the serum FLC ratio is abnormal.

• Received at least 3 prior lines of therapy, including a proteasome inhibitor (PI), an immunomodulatory drug, and an anti-CD38 monoclonal antibody (mAb).

Locations
Other Locations
China
National Clinical Research Center for Blood Diseases
RECRUITING
Tianjin
Contact Information
Primary
Gang An, Professor
angang@ihcams.ac.cn
008613502181109
Time Frame
Start Date: 2025-11-07
Estimated Completion Date: 2029-12
Participants
Target number of participants: 228
Treatments
Experimental: QLS32015
Participants will receive teclistamab monotherapy.
Experimental: Pomalidomide, Dexamethasone (Pd) or Selinexor and Dexamethasone (Sd)
Participants will receive either Pd or Sd based on principal investigator's choice.
Related Therapeutic Areas
Sponsors
Leads: Qilu Pharmaceutical Co., Ltd.

This content was sourced from clinicaltrials.gov

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