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Study details
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A Study to Evaluate the Safety, PK/PD of OriCAR-017 in Subjects With RR/MM - RIGEL Study

OriCell Therapeutics Co., Ltd.
NCT IDNCT06271252ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

81

Study length

about 4 years

Ages

18–75

Locations

1 site in GA

About this study

Researchers are testing a treatment called OriCAR-017 for people with relapsed or refractory multiple myeloma. The trial will evaluate how safe and effective this treatment is.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take OriCAR-017
PhasePhase 1
Primary goalDose-limiting toxicity (DLT)

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low14%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

Endpoints

Primary: Dose-limiting toxicity (DLT), Maximum tolerated dose (MTD) of OriCAR-017 US-P1

Secondary: Assessment of Disease Control Rate (DCR), Assessment of Duration of Response (DOR) of treatment in patients with RR/MM, Assessment of Overall Response Rate (ORR), Assessment of Overall Survival (OS) of treatment in patients with RR/MM, Evaluate PD parameters of OriCAR-017 in subjects with relapsed/refractory MM, Evaluate PK parameters of OriCAR-017 in subjects with relapsed/refractory MM, Progress-Free Survival (PFS) of treatment in patients with RR/MM

Body systems

Cardiology / Heart, Oncology