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Endpoints·May 28·1 min read
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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 part of its $10.1 billion buyout of ImmunoGen for an ultra-rare but aggressive form of blood cancer. On Wednesday, the ...

May 28, 2026·read at Endpoints ↗

May 28, 2026 07:20 AM EDTUpdated 02:47 PM Pharma Ab­b­Vie clinch­es FDA ap­proval for ul­tra-rare blood can­cer ADC from Im­muno­Gen pur­chase Ayisha Sharma News Reporter Ab­b­Vie said the FDA has ap­proved an an­ti­body-drug con­ju­gate it ob­tained as part of its $10.1 bil­lion buy­out of Im­muno­Gen for an … Sign up to read this article for free. Get free access to a limited number of articles, plus choose newsletters to get straight to your inbox. SIGN UP LOG IN BECOME A PREMIUM SUBSCRIBER

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Reporting by Endpoints.

read at Endpoints ↗
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companies & drugs in this story

companies
Ultragenyx Pharmaceutical Inc.3ABBVIE2
topics
Hematology3Rare Disease3Antibody-Drug Conjugate (ADC)2Approval2Oncology2Monoclonal Antibody

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