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Celgene Corporation

Pathology microscopic of bone biopsy of multiple myeloma

FDA approves Abecma, the first cell-based gene therapy for adults with multiple myeloma

29 March 2021 | By Hannah Balfour (European Pharmaceutical Review)

Abecma (idecabtagene vicleucel) was approved for adults with relapsed or refractory myeloma based on its 72 percent overall response rate in a trial.

photograph of a liquid pharmaceuticals manufacturing facility

news

Chinese ABRAXANE^® supply expected to be disrupted

26 March 2020 | By Hannah Balfour (European Pharmaceutical Review)

The marketing agent for China, BeiGene, announced the China National Medical Products Administration (NMPA) suspended the importation, sales and use of ABRAXANE.

news

Bristol-Myers Squibb completes acquisition of Celgene

22 November 2019 | By European Pharmaceutical Review

After regulatory approval, Bristol-Myers Squibb has announced its successful acquisition of Celgene, completing the merger.

news

Ozanimod successful in clinical trials for multiple sclerosis

10 November 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

The findings from the two pivotal phase 3 trials pave the way for ozanimod to enter the New Drug Approval process with the FDA...

news

FDA approves new targeted treatment for acute myeloid leukemia

2 August 2017 | By Dr Zara Kassam (European Pharmaceutical Review)

The U.S. Food and Drug Administration has granted the approval of Idhifa to Celgene Corporation and RealTime IDH2 Assay to Abbott Laboratories...

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Recommended

Celgene Corporation

FDA approves Abecma, the first cell-based gene therapy for adults with multiple myeloma

Chinese ABRAXANE® supply expected to be disrupted

Bristol-Myers Squibb completes acquisition of Celgene

Ozanimod successful in clinical trials for multiple sclerosis

FDA approves new targeted treatment for acute myeloid leukemia

Chinese ABRAXANE^® supply expected to be disrupted