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

Status
Active
Cancer Type
Multiple Myeloma
Trial Phase
Phase I
Eligibility
18 - 75 Years, Male and Female
Study Type
Treatment
NCT ID
NCT06271252
Protocol IDs
OriCAR-017 US-P1 (primary)
NCI-2024-05382
Study Sponsor
OriCell Therapeutics Co., Ltd.

Summary

The is a first clinical study for Oricell Therapeutics Inc. in the United States to
evaluate the safety, PK, PD and preliminary efficacy of our anti-GPRC5D cell product
(OriCAR-017) in subjects with relapsed/refractory multiple myeloma.

RIGEL Study

Objectives

This is a Phase I/II, open-label multicenter study to evaluate the safety,
pharmacokinetics, pharmacodynamics, and preliminary efficacy of anti-GPRC5D CAR-T cell
product (OriCAR-017) in subjects with relapsed/refractory multiple myeloma". The study
will consist of a Phase I dose escalation stage involving three doses as a single IV
infusion) with up to 18 evaluable subjects and a dose expansion stage with 10-15
evaluable subjects, followed by a Phase II stage with up to 48 evaluable subjects.

Eligibility

  1. Inclusion Criteria: Capable of giving signed informed consent Subjects aged 18 to 75 years (inclusive) at Screening (signing the ICF). Expected survival period is >12 weeks. Diagnosis of MM according to the IMWG criteria (2016 version). One of the following criteria must be met: If immunoglobulin (Ig)G type MM, then serum M protein >10 g/L; if IgA, IgD, IgE or IgM type MM, then serum M protein >5 g/L Urine M protein level >200 mg/24 hour If light chain type MM, then serum free light chain (sFLC) >100 mg/L and K/? FLC ratio is abnormal. Extramedullary lesions (>1 cm for diameter of the short axis). For Phase I (dose-escalation) - Subjects who had received at least 3 prior lines of therapy, had previous exposure to BCMA-Ag+ therapies, and were refractory to the last line of therapy. For Phase I (dose-expansion) and Phase II: Subjects with previous exposure to BCMA directed therapies including BCMA bispecific antibody (e.g., teclistamab), BCMA antibody directed conjugate (such as BLENREP), and BCMA-CAR-T (such as CARVYKT1TM) Subjects with adequate hematologic, renal, hepatic, pulmonary and cardiac function. Subject and partners willing to take and or use effective contraceptive measures until 2 years post IMP infusion. Exclusion Criteria: Pregnant or breastfeeding. Seropositive for history of human immunodeficiency virus Active Hepatitis B infection and or Hepatitis C infection Known active or prior history of CNS involvement History of autoimmune diseases (such as Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus) caused damage to terminal organs or required systemic application of immunosuppressive or other drugs in the past 2 years Presence of uncontrolled active infection Subjects who received autologous hematopoietic stem cell transplantation (ASCT) within 8 weeks of Screening Visit or who plan to undergo ASCT during the study. Subjects who received allogeneic stem cell therapy. Any condition that in the opinion of the Investigator, would interfere with evaluation of the IMP. Received Bendamustine treatment 1 year prior to Screening Visit.

Treatment Sites in Georgia

Northside Hospital Cancer Institute - Bone Marrow Transplant (BMT)


1000 Johnson Ferry Road NE
Atlanta, GA 30342
404-851-8523


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