Designation of Ivacaftor (VX-770) as an Orphan Drug - Vertex Pharmaceuticals (Australia)

Administered by Department of Health, Disability and Ageing

Legislation au C2014G01597 In force Gazette

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COMMONWEALTH OF AUSTRALIA

Department of Health
Therapeutic Goods Administration

THERAPEUTIC GOODS ACT 1989

 

DESIGNATION OF Ivacaftor (VX-770) AS AN ORPHAN DRUG

 

I, Dr Anthony Gill, Delegate of the Secretary for the purposes of 16J of the Therapeutic Goods Regulations 1990 (“the Regulations”), acting under subregulation 16J(2) of the Regulations, designate Ivacaftor (VX-770) as an orphan drug on 22 September 2014 in combination with Lumacaftor (VX-809) for the treatment of cystic fibrosis (CF) in patients who are homozygous for the F508del mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.

The dose form of Ivacaftor (VX-770) for this indication is tablets.

The sponsor of Ivacaftor (VX-770) is Vertex Pharmaceuticals (Australia) Pty Ltd.

 

 

(Signed by)

 

Dr Anthony Gill

Delegate of the Secretary

22 September 2014

 

 

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Sourced from the Federal Register of Legislation at 26 August 2026. For the latest information on Australian Government law please go to https://www.legislation.gov.au.