Lisocabtagene maraleucel in follicular lymphoma: mysterious study discontinuation

15 July 2025 - The BMS has not provided any study data suitable for early benefit assessment. It initiated a randomised ...

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Verastem Oncology granted fast track designation for VS-7375 for the treatment of KRAS G12D mutated locally advanced or metastatic pancreatic cancer

24 July 2025 - Enrollment is on-going in US Phase 1/2a trial for VS-7375, an oral KRAS G12D (ON/OFF) inhibitor, ...

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Revolution Medicines announces FDA breakthrough therapy designation for elironrasib

23 July 2025 - Designation based on encouraging clinical data observed with elironrasib in patients with advanced KRAS G12C non-small ...

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GSK announces extension of US FDA an review period for Blenrep (belantamab mafodotin-blmf) in relapsed/refractory multiple myeloma

23 July 2025 - New PDUFA date scheduled for 23 October 2025. ...

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European Commission approves Imbruvica (ibrutinib) as the first targeted therapy for patients with previously untreated mantle cell lymphoma who would be eligible for autologous stem cell transplant

23 July 2025 - Data from the Phase 3 TRIANGLE study defines the fixed-duration ibrutinib-based regimen as a new standard of ...

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DualityBio's next generation HER3 ADC DB-1310 granted FDA fast track designation

21 July 2025 - DualityBio announced that the US FDA has granted fast track designation to its next-generation HER3 targeting antibody ...

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Bayer’s Nubeqa (darolutamide) receives EU approval in third indication for patients with advanced prostate cancer

21 July 2025 - Approval is based on positive results from the pivotal Phase 3 ARANOTE trial and reinforces darolutamide’s established ...

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Amivantamab in combination with lazertinib for the first-line treatment of patients with advanced EGFR mutation positive non-small cell lung cancer

4 July 2025 - The Department of Health and Social Care has NICE to produce guidance on the use of ...

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Genentech provides update on supplemental biologics license application for Columvi combination for people with relapsed or refractory diffuse large B-cell lymphoma

18 July 2025 - Genentech announced today that the US FDA issued a complete response letter for Genentech’s supplemental biologics ...

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Johnson & Johnson receives US FDA priority review for TAR-200 NDA in high-risk non-muscle invasive bladder cancer

17 July 2025 - New drug application supported by results from the Phase 2b SunRISe-1 study. ...

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Enhertu plus pertuzumab granted breakthrough therapy designation in the US as first-line therapy for patients with HER2 positive metastatic breast cancer

17 July 2025 - Ninth breakthrough therapy designation for Daiichi Sankyo and AstraZeneca’s Enhertu with the latest based on DESTINY-Breast09 ...

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Thousands more breast cancer patients to benefit from new NHS treatment

17 July 2025 - NICE approves ribociclib combination therapy to help prevent cancer returning in early stage disease. ...

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BeOne bets Tevimbra will beat rivals to PD-1 reimbursement in Korea

15 July 2025 - BeOne Medicines (formerly BeiGene) is doubling down on Korea’s immunotherapy market with an early access push ...

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FDA grants Zenith’s ZEN-3694 fast track status

14 July 2025 - Zenith Epigenetics is pleased to announce the designation of ZEN-3694 as a fast track product by the ...

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Astellas Korea renews bid to reimburse targeted gastric cancer drug Vyloy

11 July 2025 - Astellas Korea will reapply for health insurance coverage for its new drug Vyloy (zolbetuximab), a targeted ...

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