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Resubmission

Formycon Reports BLA Resubmission Strategy for FYB201 (biosimilar- ranibizumab)

Formycon Reports BLA Resubmission Strategy for FYB201 (biosimilar- ranibizumab)

November 6, 2020

Merck & Co. Reports the Resubmission of sBLA to the US FDA for Keytruda (pembrolizumab) Six-Week Dosing Schedule

Merck & Co. Reports the Resubmission of sBLA to the US FDA for Keytruda (pembrolizumab) Six-Week Dosing Schedule

April 24, 2020

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