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Biosimilar
23 Articles Available
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Biosimilar
Dr. Reddy's Laboratories Announces the Launch of Versavo® (bevacizumab biosimilar) in India
PR-M08-19-NI-063
Biosimilar
Prestige BioPharma Releases Positive Results from Phase I Study of HD204, Biosimilar Candidate to Bevacizumab
PR-M07-19-NI-020
FDA Approval
Pfizer Receives U.S. FDA Approval for Its Oncology Biosimilar, ZIRABEV™ (bevacizumab-bvzr)
PR-M07-19-NI-015
Biosimilar Approval
Herceptin Biosimilar Approved in the U.S.
PAO-M06-19-NI-017
Biosimilar
Successful Results Reported for Another Rituximab Biosimilar
PAO-M05-19-NI-020
Biosimilar
Amgen And Allergan Announce Positive Top-Line Results From Phase 1/ Phase 3 Study Of ABP 798, Biosimilar Candidate To Rituximab
PR-M01-19-NI-079
Biosimilar
Amgen Submits Biologics License Application for ABP 710 (Biosimilar Infliximab) To US Food And Drug Administration
PR-M01-19-NI-002
Investment
US Tax Savings Help AbbVie
PAO-M11-18-NI-012
Biosimilars
Herceptin Biosimilar Gets Positive Opinion in Europe
PAO-M10-18-NI-024
FDA
Another Biosimilar Gets Nod from Independent FDA Panel
PAO-M10-18-NI-018
Biosimilars
Mylan and Biocon Announce Positive CHMP Opinion for Ogivri®, Biosimilar Trastuzumab
PR-M10-18-NI-071
Biosimilars
Innovent Receives IND Approval to Initiate Clinical Trials in China with Sintilimab in Combination with its Biosimilar to Bevacizumab
PR-M10-18-NI-056
Biosimilars
U.S. Department of Veterans Affairs Signs Contract with Merck for its Remicade Biosimilar
PAO-M10-18-NI-010
Biosimilar
Legislation Introduced to Require Reporting of Biosimilar Agreements
PAO-M08-18-NI-020
Biosimilars
Amgen Announces Top-Line Results From Phase 3 Study Of ABP 710, Biosimilar Candidate To Infliximab
PR-M06-18-NI-100
Biosimilars
Another mAb Biosimilar on the Horizon in Europe
PAO-M06-18-NI-006
Oncology
MSD Launches Herceptin Biosimilar in UK
PAO-M03-18-NI-015
Biosimilar
Mylan to Bring a Biosimilar of BOTOX to the Market Through a Collaboration and License agreement with Revance Therapeutics
PR-M03-18-NI-017
Biosimilars
Pfizer Announces Positive Top-Line Results For Potential Biosimilar To Rituxan®/MabThera®
PR-M01-18-NI-092
Regulatory
Sandoz regulatory submission for proposed biosimilar adalimumab accepted by FDA
PR-M01-18-NI-060
FDA Guidance
FDA Received Numerous Comments on Its Draft Guidance for Evaluating Biosimilarity
PAO-M01-18-NI-004
Drug Development
Chinese Biopharma Receives Series A Financing
PAO-M12-17-NI-031
Regulatory
FDA Approves New Pfizer Biosimilar
PR-M12-17-NI-010
