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

Notify the Multiple Myeloma Research Foundation you are interested in this trial
NCT06271252
Age 18 - 75
Sex Both
Phase Phase 1
Third Opinion Trial Synopsis
In this clinical study, researchers are exploring a new treatment approach for patients with a specific type of blood cancer. The study focuses on using a combination of therapies to improve patient outcomes. Here are some key details about the study:
  • The treatment involves a unique combination of existing therapies, which may enhance effectiveness compared to standard treatments.
  • Patients will receive personalized care based on their individual health needs and responses to the treatment.
  • The study aims to evaluate how well this combination works in managing the disease and improving quality of life.
  • Researchers are also looking at the safety of the treatment, monitoring any side effects that may occur.
  • This study includes a diverse group of participants, which helps ensure that the findings are applicable to a wide range of patients.
  • By focusing on a tailored approach, the study hopes to provide insights into more effective treatment strategies for managing the disease.
Overall, this study is significant because it seeks to improve treatment options and outcomes for patients, potentially leading to better management of their condition.
Third Opinion AI Generated Synopsis

Trial 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
from ClinicalTrials.gov

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