FDA ticks Orkambi

July 7, 2015

Orkambi (lumacaftor 200 mg with ivacaftor 125 mg), for cystic fibrosis has now been approved for marketing by the US Food and Drug Administration. The combination product is directed at treating the cause of the disease in people who have two copies of a specific mutation, and received orphan status in Australia from the Therapeutic Goods Administration on 22 Sep last year.

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Pharmacy DailyPharmacy Daily | FDA ticks Orkambi

FDA ticks Orkambi

Other recent headlines

Prescribing endorsement consultation opens

Call for embedded rural pharmacist pilot

MTick: Behind the menopause ‘one-stop shop’

SEARCH PHARMACY DAILY

Featured video

Recent issues

INDUSTRY JOB VACANCIES