Invitation to comment on a clinical trial of a genetically modified adenovirus for treatment of rectal cancer (DIR 222)

Administered by Department of Health, Disability and Ageing

Legislation au C2026G00032 In force Gazette

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22 January 2026

Invitation to comment on a clinical trial of a genetically modified adenovirus for treatment of rectal cancer (DIR 222)

The Gene Technology Regulator is assessing an application from Novotech (Australia) Pty Limited to conduct a clinical trial, under limited and controlled conditions, of a genetically modified adenovirus for treatment of locally advanced rectal cancer. The trial is proposed to take place at clinical trial sites and hospitals in Australia. Up to 40 trial participants would be treated over a 4 year period.

The Regulator has prepared a Risk Assessment and Risk Management Plan (RARMP) for this application and welcomes written submissions relating to the protection of human health and safety and the environment prior to making a decision on whether to issue the licence. The consultation RARMP and related information can be obtained via the consultation hub at https://consultations.health.gov.au/ogtr/dir-222-consultation, or from the contacts below. Submissions should reference DIR 222 and be received by 5 March 2026.

Office of the Gene Technology Regulator
MDP 54 GPO Box 9848 CANBERRA ACT 2601

Telephone: 1800 181 030   Website: www.ogtr.gov.au

E-mail: ogtr@health.gov.au

 

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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.