Comparison of Rituximab originator (MabThera) to biosimilar (Truxima) in patients with immune‐mediated thrombotic thrombocytopenic purpura

Author:

Stubbs Matthew J.1ORCID,Low Ryan1,McGuckin Siobhan1,Newton Rosalind1,Thomas Mari12,Westwood John P.1,Shah Raakhee1,Cheesman Simon1,Scully Marie A.12ORCID

Affiliation:

1. Department of Haematology UCLH NHS Foundation Trust London UK

2. Department of Haematology UCLH and Cardiometabolic Programme‐NIHR UCLH/UC BRC London London UK

Publisher

Wiley

Subject

Hematology

Reference16 articles.

1. Barriers to the Access and Use of Rituximab in Patients with Non-Hodgkin’s Lymphoma and Chronic Lymphocytic Leukemia: A Physician Survey

2. The US Approach to Biosimilars

3. Pharmacokinetics, efficacy and safety of the rituximab biosimilar CT-P10

4. Perspectives on the Current State of the Biosimilar Regulatory Pathway in the United States

5. EMA. (2012)Guideline on similar biological medicinal products containing monoclonal antibodies – non‐clinical and clinical issues. EMA/CHMP/BMWP/403543/2010. European Medicines Agency London UK.https://www.ema.europa.eu/documents/scientific-guideline/guidelinesimilar-biological-medicinal-products-containing-monoclonal-antibodies-nonclinical_en.pdf

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