Lexicon Pharmaceuticals announces update on submission of additional data to US FDA supporting the benefit-risk profile of Zynquista in type 1 diabetes

23 September 2025 - Data obtained from ongoing third-party funded, investigator-sponsored trials have been submitted in effort to address the December ...

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Idebenone accepted by FDA for priority review for Leber hereditary optic neuropathy

22 September 2025 - Chiesi Global Rare Diseases today announced the US FDA is evaluating the regulatory submission of idebenone to ...

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Update on the US regulatory review of tolebrutinib in non-relapsing, secondary progressive multiple sclerosis

22 September 2025 - The US FDA has extended by three months the target action date of its review of the ...

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Tremfya (guselkumab) achieves US approval for subcutaneous induction in adults with ulcerative colitis, now the first and only IL-23 inhibitor with a fully subcutaneous regimen

19 September 2025 - Johnson & Johnson is initiating a head to head study seeking to demonstrate the superiority of Tremfya ...

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Otsuka and Lundbeck receive complete response letter from US FDA for sNDA of Rexulti (brexpiprazole) in combination with sertraline for the treatment of adults with post-traumatic stress disorder

20 September 2025 - Otsuka and Lundbeck) announce that Otsuka has received a Complete Response Letter from the US FDA regarding ...

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FDA grants accelerated approval to first treatment for Barth syndrome

19 September 2025 - New treatment for Barth syndrome showcases FDA’s commitment to bringing effective and safe medications to patients in ...

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Incyte announces additional FDA approval of Opzelura (ruxolitinib) cream in children ages 2-11 with atopic dermatitis

18 September 2025 - Opzelura is the first topical Janus kinase inhibitor approved in the US for paediatric atopic dermatitis. ...

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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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Biocon Biologics receives US FDA approval for Bosaya and Aukelso, denosumab biosimilars

17 September 2025 - Biocon Biologics today announced that the US FDA has approved Bosaya (denosumab-kyqq) 60 mg/mL injection for subcutaneous ...

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Corstasis Therapeutics announces FDA approval of Enbumyst (bumetanide nasal spray) for the treatment of oedema associated with congestive heart failure, liver disease and kidney disease

15 September 2025 - Enbumyst is the first and only intranasal loop diuretic approved in the US offering a self-administered alternative ...

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Intercept announces voluntary withdrawal of Ocaliva for primary biliary cholangitis from the US market

11 September 2025 -  Intercept Pharmaceuticals today announced its decision to voluntarily withdraw Ocaliva (obeticholic acid) from the US market ...

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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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FDA accepts biologics license application for Sobi's NASP for patients with uncontrolled gout

10 September 2025 - Sobi today announced that the US FDA has accepted the biologics license application seeking approval for Nanoecapsulated ...

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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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