TGA approves palovarotene as the first FOP treatment available in Australia

We are excited to share that the Australian Therapeutic Drug Administration has approved the first ever treatment for Fibrodysplasia Ossificans Progressiva!

Palovarotene capsules (Sohonos) have been approved for use in adults and some children (females 8 years of age or older, males 10 years of age or older) who have FOP. This means that palovarotene is now approved for use, though processes for reimbursement and getting supply of the drug will still need to be developed.

If you have FOP, palovarotene may or may not be an option for you – we encourage you to discuss the potential benefits and side effects, and your individual circumstance, with your treating doctor (particularly with clinical trials of other developing drugs currently open for enrolment in Australia and New Zealand; see trial sites listed at https://fopaustralia.org/updated-clinical-trial-resources/).

This announcement is possible because of clinical trials around the world, including Australia, relying on people with FOP undergoing trial and placebo therapy. The studies showed that palovarotene can possibly have some effect on stopping extra bone formation (heterotopic ossification). We would like to acknowledge the generosity and efforts of all the people who participated in these trials, and their families and research teams, for making this milestone  possible.

Representatives from FOP Australia and Ipsen will be meeting in the coming days, and we look forward to sharing further posts about this announcement. The TGA listing is publically available at:

https://www.tga.gov.au/resources/artg/394001

*Edited 1/12/23 to emphasise that processes for supply and reimbursement of the drug within Australia are still to be developed*


Updated clinical trial resources

With multiple clinical trials now open for enrolment for people in Australia and New Zealand, it is an exciting time for the FOP community.  This is exciting progress in just a small number of years since the first ever FOP clincial trial! It represents the generosity and commitment of the FOP community, and amazing work by researchers around the world – thank you to everyone who has helped make  this possible.
To help keep track of developments, the International FOP Association have developed a global map of trial sites so that people with FOP and their health care teams can know what options are available to them. This includes sites in Australia and New Zealand. Please contact the trial sites directly with any questions about the trials. Even if you think you may not be eligible/able to enrol, if you are interested in enrolling we encourage people with FOP to discuss your individual circumstances with the trial sites, and your treating health care teams.
If you are having trouble finding site contact details, let us know via info@fopaustralia.org and we will do our best to assist.
See also: Clinical Trials page for more links.

2024 Calendars available now!

We are very excited to help launch the Jack’s Movement 2024 Wildlife Photography Calendars at https://fopaustralia.org/fundraising/calendars
These A4 wall calendars feature exclusive wildlife images taken by Jack, who is 17 years old and lives with Fibrodysplasia Ossificans Progressiva. Following the success of his 2023 fundraising calendars, Jack was the inaugural recipient of the Oliver Collins Education Grant in 2023, and used the grant to continue to build his photography skills. With thanks to Jack, and his parents Rory and Melissa, all proceeds will go to FOP Australia to support people living with FOP and their fight for a cure.
More information and the secure online order form are available here.