Enhertu plus pertuzumab granted priority review in the US as first-line treatment for patients with HER2 positive metastatic breast cancer

24 September 2025 - Based on DESTINY-Breast09 Phase 3 trial results, which showed Enhertu plus pertuzumab reduced the risk of ...

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New subcutaneous formulation of Opdivo receives positive INESSS recommendation for multiple tumour types

23 September 2025 - Milestone decision recognises the value of SC formulation of Opdivo to help support delivery flexibility ...

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European Commission approves Servier's Voranigo (vorasidenib) as the first targeted therapy for grade 2 IDH mutant glioma in the EU

22 September 2025 - Voranigo demonstrated significant improvement in progression-free survival with a favourable safety profile in a pivotal Phase ...

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FDA approves pembrolizumab and berahyaluronidase alfa-pmph for subcutaneous injection

19 September 2025 - Today, the FDA approved pembrolizumab and berahyaluronidase alfa-pmph (Keytruda Qlex, Merck) for subcutaneous injection for adult ...

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Minovia Therapeutics receives FDA fast track designation for MNV-201 in myelodysplastic syndrome

18 September 2025 - Minovia Therapeutics announces that the US FDA has granted fast track designation to the Company’s lead investigational ...

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FDA grants fast track designation to Corbus Pharmaceuticals’ nectin-4 targeting ADC CRB-701 in head and neck squamous cell carcinoma

16 September 2025 - Corbus Pharmaceuticals announced today that the US FDA has granted fast track designation to CRB-701 for the ...

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Hundreds of people set to benefit after life-extending lung cancer treatment given green light

16 September 2025 - Targeted immunotherapy found to significantly increase overall survival rates for people with an aggressive form of lung ...

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Raludotatug deruxtecan granted breakthrough therapy designation by US FDA for patients with CDH6 expressing platinum-resistant ovarian, primary peritoneal or fallopian tube cancers previously treated with bevacizumab

15 September 2025 - Raludotatug deruxtecan has been granted breakthrough therapy designation by the US FDA for the treatment of ...

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Enhertu type II variation application validated in the EU for previously treated patients with HER2 positive metastatic solid tumours

11 September 2025 - Submission based on three Phase 2 trials where Daiichi Sankyo and AstraZeneca’s Enhertu showed clinically meaningful ...

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FDA files Corcept’s new drug application for relacorilant as a treatment for patients with platinum-resistant ovarian cancer

10 September 2025 - Corcept Therapeutics today announced that the US FDA has accepted Corcept’s new drug application for relacorilant as ...

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FDA approves selumetinib for pediatric patients 1 year of age and older with neurofibromatosis type 1 with symptomatic, inoperable plexiform neurofibromas

10 September 2025 - Today, the FDA approved selumetinib (Koselugo, AstraZeneca Pharmaceuticals) granules and capsules for paediatric patients 1 year ...

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US FDA approval of Inlexzo (gemcitabine intravesical system) set to transform how certain bladder cancers are treated

9 September 2025 - First and only drug releasing system to provide extended local delivery of a cancer medication into the ...

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FDA approves gemcitabine intravesical system for non-muscle invasive bladder cancer

9 September 2025 - Today, the FDA approved gemcitabine intravesical system (Inlexzo, Janssen) for adults with Bacillus Calmette-Guérin unresponsive non-muscle ...

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Reimbursement delay leaves Korean patients waiting for Padcev-Keytruda first-line therapy

8 September 2025 - The first-line combination therapy of Padcev and Keytruda for metastatic urothelial carcinoma was not even submitted ...

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CERo Therapeutics receives FDA fast track designation for CER-1236 in acute myeloid leukaemia

5 September 2025 - CERo Therapeutics announces that the US FDA has granted fast track designation to the Company’s lead investigational ...

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