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Dr Reddy s Proposed Rituximab Biosimilar Application Accepted for Review by USFDA, EMA and MHRA

In January 2023, the company had announced the successful completion of the full set of clinical studies of its proposed rituximab biosimilar candidate DRL RI, with the intention to file in the United States, European Union and other regionsFollowing dossier submission in April 2023, the regulatory agencies have now.

Dr Reddys Labs (RDY) Completes Full Set of Studies for DRL_RI in US and EU

Dr Reddys Labs (RDY) Completes Full Set of Studies for DRL_RI in US and EU
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Dr Reddy s Completes Clinical Trials Of Rituximab For Rheumatoid Arthritis

Hyderabad: Dr. Reddy’s Laboratories Ltd., a global pharmaceutical company, announced that it has successfully completed the full set of clinical studies of its proposed rituximab biosimilar candidate, DRL RI, for filing in highly regulated markets such as the United States, Europe and other regions.

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