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FDA Accepts BLA for Subcutaneous Nivolumab in Advanced or Metastatic Solid Tumors
The FDA has accepted a biologics license application for subcutaneous nivolumab for adult patients eligible for approved solid tumor nivolumab indications.
United states
Gina fusaro
Drug administration
Bristol myers squibb
European union
Prescription drug user fee act
Blinded independent central
Bristol myers
Subcutaneous nivolumab
Subcutaneous nivolumab in advanced or metastatic solid tumors
Fda bla
Checkmate 67t study nct04810078
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