RGB 03 (rituximab biosimilar)
/ Stada, Gedeon Richter
- LARVOL DELTA
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May 13, 2021
[VIRTUAL] REAL WORLD CLINICAL EFFECTIVENESS AND SAFETY OF CT-P10 IN PATIENTS WITH DIFFUSE LARGE B-CELL LYMPHOMA: RESULTS FROM A EUROPEAN NON-INTERVENTIONAL POST AUTHORIZATION SAFETY STUDY
(EHA 2021)
- "Over three quarters of patients initiated on CT-P10 achieved complete or partial response by 30 months, with CT-P10 appearing to be generally well tolerated by patients. The response and survival rates and overall safety profile for CT-P10 appear consistent with those reported for reference rituximab, supporting CT-P10 use in combination with chemotherapy as a therapeutic option for DLBCL."
Clinical • Real-world evidence • Diffuse Large B Cell Lymphoma • Follicular Lymphoma • Hematological Disorders • Hematological Malignancies • Immunology • Inflammatory Arthritis • Lymphoma • Neutropenia • Non-Hodgkin’s Lymphoma • Oncology • Rheumatology
October 08, 2016
Stada: Capital Markets Day 2016
(Stada)
- Anticipated launch in hematological malignancies and autoimmune disorders in 2019
Anticipated biosimilar launch • Biosimilar
March 27, 2015
Stada: Annual Report 2015
(Stada)
- Anticipated approval in 2018
Anticipated regulatory • Biosimilar
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