RecruitingPhase 3NCT07623798

A Study in Participants With Relapsed or Refractory Multiple Myeloma for IBI3003

A Phase 3 Randomized Study Comparing IBI3003 Versus Treatment Per Investigator's Choice in Participants With Relapsed or Refractory Multiple Myeloma


Sponsor

Innovent Biologics (Suzhou) Co. Ltd.

Enrollment

255 participants

Start Date

Jun 11, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate how well IBI3003 works when compared with the investigator's choice regimen (DPd or PVd or SVd)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Bortezomib for Injection, a drug called Daratumumab Injection (Subcutaneous Injection), and others for people with relapsed or refractory multiple myeloma. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGPomalidomide Capsules

1. The DPd treatment regimen, one cycle every 28 days: Pomalidomide 4mg/d orally, on days 1-21; 2. The PVd treatment regimen, one cycle every 21 days: Pomalidomide 4 mg/d orally, on days 1-14 of each treatment cycle;

DRUGBortezomib for Injection

The PVd treatment regimen, with one cycle every 21 days: Bortezomib on days 1, 4, 8, and 11 of cycles 1-8, and on days 1 and 8 from cycle 9 onwards.

DRUGDaratumumab Injection (Subcutaneous Injection)

The DPd treatment regimen, one cycle every 28 days: on days 1, 8, 15, and 22 of cycles 1 and 2; on days 1 and 15 from cycles 3-6; and on day 1 from cycle 7 onwards.

DRUGIBI3003

According to body weight

DRUGSelinexor Tablets

The SVd treatment regimen, with one cycle every 35 days: Bortezomib on days 1, 8,15,22 and 29 ,100 mg/d orally.


Locations(1)

ZhongShan Hospital FuDan University

Shanghai, Shanghai Municipality, China

View Full Details on ClinicalTrials.gov

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NCT07623798


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