About this trial
To evaluate the efficacy and safety of post-marketing Regiorense injection secondary infusion in the treatment of adult patients with relapsed or refractory B-cell lymphoma.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Informed Consent Form (ICF) was obtained from the patients.
Diagnosed relapsed or refractory B-cell lymphomas
diffuse large B-cell lymphoma-not otherwise specified
diffuse large B-cell lymphoma transformed from follicular lymphoma
Disqualifiers
Patients with hypersensitivity to the active ingredient or any excipients (dimethyl sulfoxide, compound electrolyte injection, human serum albumin);
Patients had uncontrolled systemic fungal, bacterial, viral, or other infections
Trial design
Single group
Treatments tested in this trial
Relmacabtagene Autoleucel Injection
DrugFor patients who had undergone at least one disease assessment after the first treatment of Relmacabtagene Autoleucel injection and whose disease status was not complete remission, the investigators decided to give the patients a second treatment of Relmacabtagene Autoleucel injection based on clinical practice, and the specific dosage was determined by the investigators according to the patient's condition and dose reserve.
Treatment groups
Trial outcomes
Primary outcomes
Objective Response Rate
Objective Response Rate (ORR) : The investigator-assessed best disease status of patients with relapsed or refractory B-cell lymphoma was the rate of Complete Response (CR) or Partial Response (PR) at 3 months after a second infusion of remifolenafil.
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: