Novadip receives RMAT designation for NVD003, its regenerative treatment for congenital pseudarthosis of the tibia

23 June 2025 - Novadip Biosciences is developing NVD003, an autologous therapy derived from adipose stem cells, as a potential ...

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Quoin Pharmaceuticals announces FDA grants rare paediatric disease designation for QRX003 in Netherton syndrome

24 June 2025 - Quoin Pharmaceuticals today announced that the US FDA has granted rare paediatric disease designation for the ...

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Syndax announces FDA priority review of sNDA for Revuforj (revumenib) in relapsed or refractory mNPM1 acute myeloid leukaemia

24 June 2025 - Syndax Pharmaceuticals today announced that the US FDA has granted priority review for its supplemental new drug ...

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FDA approves Benlysta (belimumab) auto-injector for children with active lupus nephritis

24 June 2025 - With this approval, paediatric patients aged five years and older with active lupus nephritis will have ...

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Revolution Medicines announces FDA breakthrough therapy designation for daraxonrasib in previously treated metastatic pancreatic cancer with KRAS G12 mutations

23 June 2025 - Breakthrough therapy designation based on promising early clinical evidence observed with daraxonrasib in patients with pancreatic ductal ...

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FDA grants accelerated approval to datopotamab deruxtecan-dlnk for EGFR-mutated non-small cell lung cancer

23 June 2025 - Today, the FDA granted accelerated approval to datopotamab deruxtecan-dlnk (Datroway, Daiichi Sankyo) for adults with locally ...

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Update on FDA review of ruxolitinib cream (Opzelura) for children ages 2-11 with atopic dermatitis

20 June 2025 - Incyte today announced that the US FDA has extended the review period for the supplemental new ...

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Cycle Pharmaceuticals’ Harliku (nitisinone) tablets receive first FDA approval as treatment for alkaptonuria

19 June 2025 - Cycle Pharmaceuticals announced that the FDA has approved Harliku (nitisinone) tablets for the reduction of urine homogentisic ...

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Dupixent (dupilumab) approved in the US as the only targeted medicine to treat patients with bullous pemphigoid

20 June 2025 - Approval based on pivotal results showing improvements in sustained disease remission and reductions in itch and oral ...

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UNAIDS urges Gilead to drop price of new HIV prevention shot

18 June 2025 - The US FDA has approved long-acting injectable lenacapavir for HIV prevention. The new medicine is administered ...

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Bayer files for approval of gadoquatrane in the US

17 June 2025 - Bayer today announced the submission of a new drug application to the US FDA for its ...

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Lilly to offer all approved doses of Zepbound (tirzepatide) single-dose vials through LillyDirect Self Pay Pharmacy Solutions

16 June 2025 - With the addition of 12.5 mg and 15 mg vials, all approved doses of Zepbound will be ...

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FDA to issue new Commissioner’s national priority vouchers to companies supporting US national interests

17 June 2025 - The US FDA today announced its Commissioner’s National Priority Voucher program to enhance the health interests of ...

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Aldeyra Therapeutics resubmits reproxalap new drug application for the treatment of dry eye disease

17 June 2025 - Aldeyra Therapeutics today announced the resubmission of a new drug application to the US FDA for ...

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FDA approves tafasitamab-cxix for relapsed or refractory follicular lymphoma

18 June 2025 - Today, the FDA approved tafasitamab-cxix (Monjuvi, Incyte) with lenalidomide and rituximab for adults with relapsed or ...

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