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

Recruiting now · Phase 1

Conditions studied: Neoplasms, Plasma Cell, Neoplasms by Histologic Type, Neoplasms, Hemostatic Disorders, Vascular Diseases, Cardiovascular Diseases, Paraproteinemias, Blood Protein Disorders, Hematologic Diseases, Hemorrhagic Disorders, Lymphoproliferative Disorders, Immunoproliferative Disorders, Immune System Diseases, Multiple Myeloma

In brief

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

Key facts

Study ID

NCT06271252

Run by

OriCell Therapeutics Co., Ltd.

People needed

81

Starts

2024-04-03

Expected to finish

2028-04-12

Last updated by the study team

2024-08-02

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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/λ 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.

You may not qualify if…

• 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.

Where it is running

• Northside Hospital — Atlanta, Georgia, United States (enrolling)

Full record on ClinicalTrials.gov

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