FDA approves Pfizer’s Ngenla, a long-acting once weekly treatment for paediatric growth hormone deficiency

28 June 2023 - New, longer-acting treatment offers option to reduce the frequency of injections for children with growth hormone ...

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FDA approves Bayer’s Ultravist (iopromide) injection for contrast-enhanced mammography

23 June 2023 - Ultravist-300, -370 is now the only contrast agent in the US indicated to visualise known or suspected ...

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UCB announces US FDA approval of Rystiggo (rozanolixizumab-noli) for the treatment of adults with generalised myasthenia gravis

27 June 2023 - US FDA approval is based on the pivotal Phase 3 MycarinG study in gMG2, a large phase ...

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FDA approves Pfizer’s Litfulo (ritlecitinib) for adults and adolescents with severe alopecia areata

23 June 2023 - Litfulo is the first and only treatment for severe alopecia areata approved for patients as young ...

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Intercept receives complete response letter from FDA for obeticholic acid as a treatment for pre-cirrhotic fibrosis due to NASH

22 June 2023 - Company to discontinue all NASH-related investment and restructure the Company’s operations to strengthen its focus on rare ...

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FDA approves first gene therapy for treatment of certain patients with Duchenne muscular dystrophy

22 June 2023 - Today, the US FDA approved Elevidys, the first gene therapy for the treatment of pediatric patients 4 ...

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Aldeyra Therapeutics provides regulatory update on ADX-2191

21 June 2023 - Based on US FDA determination of lack of adequate and well controlled investigations in the scientific literature, ...

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FDA grants full approval for Blincyto (blinatumomab) to treat minimal residual disease positive B-cell precursor acute lymphoblastic leukaemia

21 June 2023 - Conversion from accelerated to full approval. ...

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argenx announces US FDA approval of Vyvgart Hytrulo (efgartigimod alfa and hyaluronidase-qvfc) injection for subcutaneous use in generalised myasthenia gravis

20 June 2023 - Efficacy of Vyvgart Hytrulo was established by demonstrating a comparable pharmacodynamic effect to Vyvgart in Phase 3 ...

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FDA approves talazoparib with enzalutamide for HRR gene mutated metastatic castration-resistant prostate cancer

20 June 2023 - Today, the FDA approved talazoparib (Talzenna, Pfizer) with enzalutamide for homologous recombination repair (HRR) gene mutated ...

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FDA approves new class of medicines to treat paediatric type 2 diabetes

20 June 2023 - Today, the US FDA approved Jardiance (empagliflozin) and Synjardy (empagliflozin and metformin hydrochloride) as additions to diet ...

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US FDA approves first anti-inflammatory drug for cardiovascular disease

20 June 2023 - Lodoco can reduce the risk of cardiac events in patients with established cardiovascular diseases by 31% on ...

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F2G receives complete response letter from FDA for new drug application for Olorofim for the treatment of invasive fungal infections; plans resubmission with additional data and analyses

19 June 2023 - Complete response letter is related to the request for additional data and analyses. ...

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U.S. Food and Drug Administration approves addition of positive data from Phase 3 VALOR-HCM study to Camzyos (mavacamten) label

15 June 2023 - VALOR-HCM is the second Phase 3 trial in which Camzyos demonstrated significant improvement in symptoms of ...

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FDA approves Genentech’s Columvi, the first and only bispecific antibody with a fixed duration treatment for people with relapsed or refractory diffuse large B-cell lymphoma

15 June 2023 - Pivotal study showed durable responses, with a 56% overall response rate, a 43% complete response (remission) rate, ...

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