Aquestive Therapeutics announces FDA issuance of complete response letter for Anaphylm

2 February 2026 - Deficiencies limited to packaging and administration. ...

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Pharming Group receives complete response letter from US FDA for sNDA for Joenja (leniolisib) in children aged 4 to 11 years with APDS

1 February 2026 - Pharming today announced that the US FDA has issued a complete response letter to its supplemental ...

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Ultragenyx resubmits biologics license application for UX111 AAV gene therapy to treat Sanfilippo syndrome type A (MPS IIIA) to US FDA

30 January 2026 - Company expects up to six month review period per FDA guidelines. ...

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This year drug makers cut prices for several widely used drugs

29 January 2026 - Companies raise prices for most medicines but federal government policy changes drive the reductions. ...

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Elevar Therapeutics announces FDA acceptance of new drug application resubmission for rivoceranib in combination with camrelizumab as a first-line systemic treatment for unresectable hepatocellular carcinoma

30 January 2026 - Elevar Therapeutics today announced the US FDA accepted the resubmission of a new drug application for its ...

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QTX-2101 awarded FDA fast track designation for the treatment of acute promyelocytic leukaemia

29 January 2026 - Quetzal Therapeutics announced that the US FDA has granted fast track designation to QTX-2101, the company’s ...

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‘Transformative’ HIV PrEP shot slowly overcomes cost hurdles

28 January 2026 - HIV/AIDS activists heralded the approval of a new twice-yearly pre-exposure prophylaxis (PrEP) medication last year, but ...

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CMS announces selection of drugs for third cycle of Medicare drug price negotiation program, including first ever Part B drugs

27 January 2026 - The Centers for Medicare & Medicaid Services announced the selection of 15 high cost prescription drugs covered ...

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Summit Therapeutics announces US FDA acceptance of biologics license application seeking approval for ivonescimab in combination with chemotherapy in treatment of patients with EGFRm NSCLC post-TKI therapy

29 January 2026 - Summit Therapeutics today announced that the US FDA has accepted for filing Summit's biologics license application seeking ...

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Tenpoint Therapeutics announces FDA approval of Yuvezzi, the first and only combination eye drop approved to treat presbyopia

28 January 2026 - Tenpoint Therapeutics today announced that the US FDA approved Yuvezza (carbachol and brimonidine tartrate ophthalmic solution) ...

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Elevar Therapeutics submits new drug application to FDA for lirafugratinib as second-line treatment option for cholangiocarcinoma

28 January 2026 - Elevar Therapeutics today announced it submitted a new drug application to the US FDA for its investigational ...

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Immix Biopharma receives US FDA breakthrough therapy designation for NXC-201

28 January 2026 - Breakthrough therapy designation granted to NXC-201 based on positive NEXICART-2 Phase 2 interim clinical results, presented at ...

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Biogen’s litifilimab receives FDA breakthrough therapy designation for cutaneous lupus erythematosus, a disease with no targeted treatment options

28 January 2026 - Designation is based on the breadth of available litifilimab data, including the Phase 2 LILAC study result ...

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Otsuka announces FDA acceptance and priority review of new drug application for centanafadine for the treatment of ADHD in children, adolescents, and adults

27 January 2026 - The PDUFA target action date is 24 July 2026. ...

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Novel drug approvals for 2025

23 January 2026 - In 2025, the CDER approved 46 new drugs never before approved or marketed in the US, known ...

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