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narcolepsy

FDA approve a new indication for Xywav to treat chronic sleep disorder

16 August 2021 | By Anna Begley (European Pharmaceutical Review)

The FDA have granted a first of its kind indication for Xywav for the treatment of idiopathic hypersomnia (IH) in adults.

article

Top 10 biopharma workplaces in the US

29 July 2020 | By Victoria Rees (European Pharmaceutical Review)

A Fortune report reveals the best 10 places to work in the US biopharmaceutical industry.

news

European Commission approves Sunosi^® (solriamfetol)

23 January 2020 | By Rachael Harper (European Pharmaceutical Review)

EU marketing authorisation has been given to Sunosi (solriamfetol) for excessive daytime sleepiness in adults with narcolepsy or obstructive sleep apnea.

news

EMA announces medicine approval recommendations from November meeting

18 November 2019 | By Victoria Rees (European Pharmaceutical Review)

The EMA CHMP has revealed its suggestion to grant marketing authorisation to seven medicines after its most recent meeting.

news

FDA grants Orphan Drug Designation for narcolepsy treatment

26 June 2019 | By European Pharmaceutical Review

The FDA has given the XWL-008 compound Orphan Drug Designation for the treatment of narcolepsy.

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Recommended

narcolepsy

FDA approve a new indication for Xywav to treat chronic sleep disorder

Top 10 biopharma workplaces in the US

European Commission approves Sunosi® (solriamfetol)

EMA announces medicine approval recommendations from November meeting

FDA grants Orphan Drug Designation for narcolepsy treatment

European Commission approves Sunosi^® (solriamfetol)