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    BMS, Macmillan and 11 NHS Trusts publish report on cancer treatment prehabilitation

    The report shows how prehabilitation can improve patient experience while alleviating capacity pressures

    - PMLiVE

    BMS acquires Orbital Therapeutics in $1.5bn deal

    The deal includes several next-gen cell therapy candidates for autoimmune diseases

    - PMLiVE

    BMS, Takeda and Astex join AI training consortium

    The initiative focuses on training AI models to aid in drug discovery and development

    - PMLiVE

    J&J’s Tremfya approved by FDA for children with plaque psoriasis and psoriatic arthritis

    The drug is the first IL-23 inhibitor approved for children from the age of six

    - PMLiVE

    Johnson & Johnson seeks first EMA approval for icotrokinra for plaque psoriasis

    Icotrokinra is a first-in-class, once-daily tablet for moderate-to-severe plaque psoriasis

    - PMLiVE

    BMS granted FDA priority review for Breyanzi in marginal zone lymphoma

    The disease accounts for approximately 7% of all non-Hodgkin lymphoma cases

    - PMLiVE

    BMS and Bain Capital launch new company to develop immunology therapies

    The newly formed company has in-licensed five investigational immunology drugs from BMS

    - PMLiVE

    FDA approves new presentation of Celltrion’s SteQeyma for paediatric psoriasis

    The Stelara biosimilar now offers all dosage forms and strengths of its reference product

    - PMLiVE

    BMS and BioNTech partner on solid tumour candidate in deal worth over $11bn

    BioNTech’s BNT327 is being evaluated in multiple clinical trials, including phase 3 studies in first-line lung cancer

    - PMLiVE

    Bristol Myers Squibb’s perioperative Opdivo regimen granted EC approval in NSCLC

    Up to 55% of patients with non-metastatic NSCLC develop recurrence despite curative resection

    - PMLiVE

    J&J/Protagonist’s icotrokinra shows promise in difficult-to-treat plaque psoriasis

    An estimated eight million people in the US are living with the immune-mediated skin disease

    - PMLiVE

    Bristol Myers Squibb’s injectable Opdivo formulation granted MHRA for solid tumours

    The new formulation reduces administration time from 30-to-60 minutes to three-to-five minutes

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