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US FDA Accepts Tabelecleucel BLA Resubmission for EBV-PTLD
The US FDA has accepted Pierre Fabre’s tabelecleucel BLA resubmission for EBV-positive PTLD, with a target decision date of March 31, 2027.
Adriana Herrera | 15/10/2026 | By News Bureau
Pierre Fabre Resubmits Tabelecleucel BLA to FDA
Pierre Fabre Pharmaceuticals resubmits tabelecleucel BLA for treatment of Epstein-Barr virus positive -post-transplant lymphoproliferative disease to the FDA.
Adriana Herrera | 03/10/2026 | By News Bureau
Pierre Fabre Pharmaceuticals Reports FDA Update on Tabelecleucel BLA
Pierre Fabre Pharmaceuticals aligns with US Food and Drug Administration (FDA) on BLA resubmission path for tabelecleucel, an allogeneic T-cell therapy for Epstein-Barr virus positive post-transplant lymphoproliferative disease.
Adriana Herrera | 08/05/2026 | By News Bureau | 125
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