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Storia in 3 fonti

AbbVie clinches FDA approval for ultra-rare blood cancer ADC from ImmunoGen purchase

AbbVie said the FDA has approved an antibody-drug conjugate it obtained as a part of its $10.1 billion buyout of ImmunoGen for an ultra-rare but aggressive form of blood cancer.

Raccontata daendpoints.newsfiercepharma.compharmaceutical-technology.com

Confronto fonti

3 prospettive sulla stessa storia
AI · summaries
endpoints.newsStai leggendo6 h fa

AbbVie clinches FDA approval for ultra-rare blood cancer ADC from ImmunoGen purchase

AbbVie said the FDA has approved an antibody-drug conjugate it obtained as a part of its $10.1 billion buyout of ImmunoGen for an ultra-rare but aggressive form of blood cancer.

originale
pharmaceutical-technology.com2 h fa

FDA oncology roundup: AbbVie’s rare cancer approval, AstraZeneca in breast cancer limbo - Pharmaceutical…

AbbVie’s ultra-rare blood cancer ADC secured FDA clearance while AstraZeneca’s oral SERD for breast cancer remains in regulatory limbo.

Leggi questa versione → originale
fiercepharma.com5 h fa

With Elahere building steam, AbbVie nets FDA nod for another ImmunoGen cancer asset

As AbbVie continues to capitalize on its deal for ImmunoGen with the growth of commercial antibody-drug conjugate (ADC) Elahere, another of the acquired company’s clinical assets has crossed the FD | As AbbVie continues…

Leggi questa versione → originale

Timeline cronologica

  1. giovedì 28 maggio 2026·endpoints.news

    AbbVie clinches FDA approval for ultra-rare blood cancer ADC from ImmunoGen purchase

    AbbVie said the FDA has approved an antibody-drug conjugate it obtained as a part of its $10.1 billion buyout of ImmunoGen for an ultra-rare but aggressive form of blood cancer.

  2. giovedì 28 maggio 2026·fiercepharma.com

    With Elahere building steam, AbbVie nets FDA nod for another ImmunoGen cancer asset

    As AbbVie continues to capitalize on its deal for ImmunoGen with the growth of commercial antibody-drug conjugate (ADC) Elahere, another of the acquired company’s clinical assets…

  3. giovedì 28 maggio 2026·pharmaceutical-technology.com

    FDA oncology roundup: AbbVie’s rare cancer approval, AstraZeneca in breast cancer limbo - Pharmaceutical Technology

    AbbVie’s ultra-rare blood cancer ADC secured FDA clearance while AstraZeneca’s oral SERD for breast cancer remains in regulatory limbo.