SOLENSIA Solution for Injection for Cats containing frunevetmab

This consultation closed on 11 January 2022

Consultation period

30 November 2021 to 11 January 2022

The APVMA is considering an application for approval of the new active constituent frunevetmab and registration of the product SOLENSIA Solution for Injection for Cats, containing 7 mg/mL frunevetmab. The product is used for the alleviation of pain associated with osteoarthritis in cats.

We invite comments from 30 November 2021 to 11 January 2022 on whether approval of the active constituent and registration of the product should be granted.

The APVMA is able to consider comments relating to the legislative grounds, including:

  • chemistry and manufacture
  • occupational health and safety
  • public health
  • environmental safety
  • efficacy and target animal safety.

For more information see page 40, APVMA Gazette No. 24, 30 November 2021.

Please note: Submissions will be published on the APVMA’s website, unless you have asked for the submission to remain confidential (see public submission coversheet). 

Please lodge your submission with a public submission coversheet, which provides options for how your submission will be published.

Note that all APVMA documents are subject to the access provisions of the Freedom of Information Act 1982 and may be required to be released under that Act should a request for access be made.

Please send your written submission and coversheet by email or post to:

Case Management and Administration Unit
Australian Pesticides and Veterinary Medicines Authority
GPO Box 3262
Sydney NSW 2001
Phone: +61 2 6770 2300


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