UPCC 39418: A Phase II Single Arm Multicenter Open Label Trial to Determine the Efficacy and Safety of Tisagenlecleucel (CTL019) In Adult Patients with Refractory or Relapsed Follicular Lymphoma
Enrolling By Invitation
99 years or below
All
Phase
2
10 participants needed
1 Location
Brief description of study
To evaluate the efficacy of tisagenlecleucel therapy among adult patients with refractory or relapsed follicular lymphoma as measured by complete response rate determined by Independent Review Committee in the full analysis set based on Lugano 2014 classification response criteria.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: lymphoma
-
Age: 99 years or below
-
Gender: All
Updated on
19 Feb 2024.
Study ID: 831805
If you need help finding a study or have any questions, please contact us at psom-ocr@pobox.upenn.edu
