CompletedPhase 3NCT03976102
Compare Efficacy, Safety, and Immunogenicity of Proposed Rituximab Biosimilar (DRL_RI) With MabThera® in LTB Follicular Lymphoma
Studying Follicular lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Dr. Reddy's Laboratories Limited
- Principal Investigator
- Eliso Sopia, MDParexel
- Intervention
- DRL_RI (Proposed rituximab biosimilar)(biological)
- Enrollment
- 317 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2023
Study locations (4)
- The Oncology Institute of Hope and Innovation, Whittier, California, United States
- American Oncology Partners of Maryland, Bethesda, Maryland, United States
- University of Tennessee Medical Center - Cancer Institute, Knoxville, Tennessee, United States
- Gulf coast Oncology Associates, PA, Houston, Texas, United States
Collaborators
Parexel
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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