Shanghai Ming Ju Biotechnology Co., Ltd.
To evaluate the efficacy and safety of Relmacabtagene Autoleucel in the treatment of adult patients with hematologic malignancies in real-world
Lymphoma, B-Cell
Large B-cell Lymphoma
Follicular Lymphoma
Relmacabtagene Autoleucel
The purpose of this study is to observationally evaluate the efficacy and safety data of Relmacabtagene Autoleucel for the treatment of patients with hematologic malignancies for up to 15 years after infusion. The treating physician will determine the most appropriate diagnostic and therapeutic regimen for the patient based on clinical practice. No therapeutic intervention will be administered to patients in this study.
Study Type : | OBSERVATIONAL |
Estimated Enrollment : | 150 participants |
Official Title : | A Real-world Study for the Treatment of Hematologic Malignancies With Relmacabtagene Autoleucel |
Actual Study Start Date : | 2023-12-28 |
Estimated Primary Completion Date : | 2038-12-31 |
Estimated Study Completion Date : | 2038-12-31 |
Information not available for Arms and Intervention/treatment
Ages Eligible for Study: | 18 Years |
Sexes Eligible for Study: | ALL |
Accepts Healthy Volunteers: |
Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.
Not yet recruiting
Beijing Cancer Hospital
Beijing, Beijing, China, 100010
Not yet recruiting
Peking University International Hospital
Beijing, Beijing, China, 100010