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RSS FeedPosted by Michael Wonder on 31 Aug 2025
FDA approval of Leqembi subcutaneous formulation charts path to combination therapies for Alzheimer's disease
29 August 2025 - Subcutaneous delivery increases accessibility and introduces potential for at home administration, following model of diabetes and ...
Posted by Michael Wonder on 28 Feb 2026
Opus Genetics announces FDA acceptance of supplemental new drug application for phentolamine ophthalmic solution 0.75% for the treatment of presbyopia
25 February 2026 - Opus Genetics today announced that the US FDA has accepted for review the supplemental new drug ...
Posted by Michael Wonder on 27 Feb 2026
Lilly's Olumiant (baricitinib) recommended by CHMP for approval of expanded use in the European Union for adolescents with severe alopecia areata
27 February 2026 - Eli Lilly and Incyte announced today that the EMA's CHMP has issued a positive opinion for Olumiant ...
Posted by Michael Wonder on 27 Feb 2026
Dupixent (dupilumab) recommended for EU approval to treat chronic spontaneous urticaria in young children with ongoing symptoms despite treatment
27 February 2026 - Regeneron Pharmaceuticals and Sanofi today announced that the EMA’s CHMP adopted a positive opinion recommending the approval ...
Posted by Michael Wonder on 27 Feb 2026
Novartis receives positive CHMP opinion for remibrutinib in chronic spontaneous urticaria
27 February 2026 - Novartis announced today that the CHMP of the EMA has adopted a positive opinion recommending marketing authorisation ...
Posted by Michael Wonder on 27 Feb 2026
Enhertu supplemental new drug application submitted in Japan as adjuvant therapy for patients with HER2 positive early breast cancer
27 February 2026 - Submission based on DESTINY-Breast05 phase 3 trial results, which showed Enhertu reduced the risk of invasive ...
Posted by Michael Wonder on 27 Feb 2026
Xspray Pharma resubmits its FDA application for Dasynoc
26 February 2026 - Xspray Pharma has resubmitted its application for market approval for Dasynoc to the US FDA. ...
Posted by Michael Wonder on 27 Feb 2026
Neurogene announces FDA breakthrough therapy designation for NGN-401 gene therapy for Rett syndrome
26 February 2026 - Breakthrough therapy designation granted based on interim NGN-401 Phase 1/2 data demonstrating clinically meaningful, durable and multi-domain ...
Posted by Michael Wonder on 26 Feb 2026
Olezarsen sNDA accepted by the FDA for priority review for the treatment of severe hypertriglyceridaemia
26 February 2026 - Ionis Pharmaceuticals today announced that the US FDA has accepted for priority review the supplemental new ...
Posted by Michael Wonder on 26 Feb 2026
FDA grants accelerated approval to zongertinib for unresectable or metastatic non-squamous non-small cell lung cancer
26 February 2026 - Today, the FDA granted accelerated approval to zongertinib (Hernexeos, Boehringer Ingelheim Pharmaceuticals), a kinase inhibitor, for ...
Posted by Michael Wonder on 26 Feb 2026
Clinical equivalence and non-inferiority within health technology assessment
23 February 2026 - Non-inferiority and clinical equivalence clinical trials can be used to determine whether a health technology is no ...
Posted by Michael Wonder on 26 Feb 2026
Vanda Pharmaceuticals announces FDA acceptance of biologics license application filing for imsidolimab for the treatment of generalised pustular psoriasis
25 February 2026 - Vanda Pharmaceuticals today announced that the US FDA has accepted the filing of its biologics license application ...
Posted by Michael Wonder on 26 Feb 2026
FDA approves drug for adult and paediatric patients aged 6 and older with allergic fungal rhinosinusitis
25 February 2026 - The US FDA has approved Dupixent (dupilumab) for the treatment of adult and paediatric patients aged 6 ...
Posted by Michael Wonder on 25 Feb 2026
MHRA approves imlunestrant tosylate (Inluryo) - a new treatment for breast cancer
24 February 2026 - The MHRA has today approved imlunestrant tosylate (Inluriyo), a new treatment for adult patients with a ...
Posted by Michael Wonder on 25 Feb 2026
Siren Biotechnology receives FDA fast track designation for SRN-101 for the treatment of recurrent high grade glioma
24 February 2026 - Siren Biotechnology today announced that the US FDA has granted fast track designation to SRN-101, the ...
Posted by Michael Wonder on 25 Feb 2026
Aktis Oncology receives US FDA fast track designation for AKY-1189, a nectin-4 miniprotein radioconjugate
24 February 2026 - Aktis Oncology today announced that the US FDA has granted fast track designation to AKY-1189 for the ...