reVision Therapeutics announces US FDA grant of rare paediatric disease and orphan drug designation for REV-0100 for the treatment of Stargardt disease

28 October 2020 - reVision Therapeutics today announced that the US FDA has granted the Company's request to designate REV-0100 as ...

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Prevail Therapeutics receives U.S. FDA fast track designation for PR001 for the treatment of neuronopathic Gaucher disease

27 October 2020 - Prevail Therapeutics today announced that the U.S. FDA has granted fast track designation for the Company’s ...

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FDA granted paediatric disease designation for OXi-4503

16 September 2020 - Treatment of acute myeloid leukaemia due to genetic mutations that disproportionately affect paediatric patients. ...

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Orphazyme announces U.S. FDA acceptance and priority review of new drug application for arimoclomol for Niemann-Pick disease Type C

16 September 2020 - If approved, arimoclomol would become the first approved therapy in the U.S. for people with Niemann-Pick disease ...

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Rare disease drove two women on a mission to change FDA drug review process

19 July 2020 - Melissa Goetz and Lindsey Sutton are campaigning to improve the US drug review process for rare diseases. ...

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Dicerna receives rare paediatric disease designation from U.S. FDA for nedosiran for the treatment of primary hyperoxaluria

18 June 2020 - Dicerna Pharmaceuticals today announced that the U.S. FDA has granted rare paediatric disease designation for nedosiran, ...

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Rare disease therapy development and access remain top FDA priorities during COVID-19

11 June 2020 - The FDA’s work on behalf of people with rare diseases is more important than ever as these ...

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Clarity Pharmaceuticals announces that the US FDA grants rare paediatric disease designation to Copper Cu 67 sartate for the treatment of neuroblastoma

3 June 2020 - Clarity Pharmaceuticals is pleased to announce that the U.S. FDA has granted rare paediatric disease designation to ...

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Gilead declines 'rare disease' status for experimental coronavirus drug

25 March 2020 - In a surprising turnabout, drugmaker Gilead Sciences asked the FDA on Wednesday to rescind orphan status ...

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Orphan Technologies receives rare paediatric disease designation from FDA for OT-58 to treat cystathionine B-synthase deficiency homocystinuria

26 March 2020 - Orphan Technologies today announced that OT-58 for the treatment of cystathionine beta synthase deficiency homocystinuria has ...

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Rare Disease Day 2020: FDA continues important work on treatments for rare diseases

21 February 2020 - As leaders of the FDA, every day we see the unwavering commitment of our agency in working ...

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After a new version of a decades-old drug gets orphan status, the price suddenly skyrockets

12 February 2020 - For years, hospitals and clinics have used an injectable medicine called dehydrated alcohol to treat such ...

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ProQR receives rare paediatric disease designation from FDA for QR-421a

30 January 2020 - Designation is for the treatment of patients with retinitis pigmentosa caused by mutations in exon 13 ...

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FDA harnesses technology and collaboration to support rare disease product development

17 January 2020 - Announcing an orphan drug technology modernisation effort and the 2020 FDA Rare Disease Day meeting. ...

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Our drug policy often prioritises eliminating rare disease. One researcher asks: Is that the right goal?

26 November 2019 - Dr. Peter Bach wants to turn the entire philosophical underpinnings of America’s health care system upside ...

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