Fasenra approved for treatment of children aged 6 to 11 with severe asthma

11 April 2024 - AstraZeneca’s Fasenra (benralizumab) is now approved by the US FDA for add-on maintenance treatment for patients ...

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ViiV Healthcare announces US FDA approval of Dovato (dolutegravir/lamivudine) for adolescents living with HIV

8 April 2024 - Dovato is now the first and only oral, two drug, single-tablet regimen available for people aged 12 ...

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Solid Biosciences receives rare paediatric disease designation from the FDA for Duchenne muscular dystrophy gene therapy candidate SGT-003

1 April 2024 - Site initiations scheduled for April; patient dosing expected to begin in Q2 ,2024. ...

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FDA Approves Medexus's supplemental biologics license application for Ixinity to treat haemophilia B in paediatric patients

26 March 2024 - Expanded indication includes patients under 12 years of age, based on Phase 3/4 data demonstrating safety and ...

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Paladin Labs announces approval of Wakix (pitolisant hydrochloride tablets) for use in paediatric patients in Canada

28 March 2024 - Indication includes children ages 6 years and older and weighing at least 30 kg. ...

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Tonix Pharmaceuticals receives rare paediatric disease designation from the FDA for TNX-2900 for the treatment of Prader-Willi syndrome

25 March 2024 - TNX-2900 is a proprietary magnesium-potentiated formulation of intranasal oxytocin, a naturally occurring hormone that reduces appetite and ...

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FDA grants Argenica rare paediatric disease designation for ARG-007 in the treatment of HIE

25 March 2024 - Argenica Therapeutics is pleased to announce the US FDA has granted its neuroprotective drug ARG-007 rare ...

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Lisata Therapeutics announces US FDA rare paediatric disease designation granted to LSTA1 for the treatment of osteosarcoma

21 March 2024 - Lisata Therapeutics today announced that the US FDA has granted rare paediatric disease designation to LSTA1, the ...

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A lifesaving therapy for children with a rare disease is now the world’s most expensive drug, raising questions about access

20 March 2024 - A new gene therapy for the fatal genetic disorder metachromatic leukodystrophy, or MLD, will carry a ...

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FDA approves first gene therapy for children with metachromatic leukodystrophy

18 March 2024 - Today, the US FDA approved Lenmeldy (atidarsagene autotemcel), the first FDA approved gene therapy indicated for the ...

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PepGen receives US FDA orphan drug and rare paediatric disease designations for PGN-EDO51 for the treatment of Duchenne muscular dystrophy

13 March 2024 - PepGen today announced that the US FDA granted both orphan drug and rare paediatric disease designations for ...

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European Commission approves Pfizer’s Prevenar 20 to help protect infants and children against pneumococcal disease

13 March 2024 - Prevenar 20 (20 valent pneumococcal conjugate vaccine) offers the broadest serotype coverage of any paediatric pneumococcal ...

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Praluent (alirocumab) injection receives FDA approval to treat children with genetic form of high cholesterol

11 March 2024 - Approval extends treatment of Praluent to children aged 8 and older with heterozygous familial hypercholesterolaemia. ...

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FDA approves inotuzumab ozogamicin for paediatric patients with acute lymphoblastic leukaemia

6 March 2024 - Today, the FDA approved inotuzumab ozogamicin (Besponsa, Pfizer) for paediatric patients 1 year and older with ...

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Vertex receives CHMP positive opinion for Kalydeco for the treatment of infants with cystic fibrosis ages 1 month and older

23 February 2024 - If approved, Kalydeco will be the first and only medicine approved in Europe to treat the underlying ...

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