UPDATE 2-U.S. FDA panel backs Valeant psoriasis drug with risk program

Tue Jul 19, 2016 4:22pm EDT
Email This Article |
Share This Article
  • Facebook
  • LinkedIn
  • Twitter
| Print This Article | Single Page
[-] Text [+]

(Adds comments from panelists)

By Toni Clarke

July 19 (Reuters) - Valeant Pharmaceuticals International Inc's experimental drug to treat the skin disorder psoriasis should be approved as long as certain measures are put in place to mitigate the risk of suicide, an advisory committee to the U.S. Food and Drug Administration concluded on Tuesday.

The FDA is not obliged to follow the advice of its advisory committees but typically does so.

In clinical trials of the drug, brodalumab, there were six suicides across all programs: four in psoriasis studies, one in a rheumatoid arthritis study and one in a psoriatic arthritis study. Even so, the committee voted 18-0 that the drug should be approved, saying the benefit outweighed the potential risk.

Of those, 14 voted that the drug should only be prescribed alongside a strong risk management program that goes beyond simply including the information in the label. Such programs can include medication guides and communications plans for healthcare providers.

Panelists said there was a need for new drugs for psoriasis and they would like to have brodalumab available as an option. They offered various suggestions about how to mitigate the suicide risk, including a boxed warning and a patient registry to collect patient data and more clearly assess suicide risk.

Some thought the registry should be mandatory and others thought it should be voluntary. Some thought any registry would create unnecessary barriers to accessing the drug and may not reflect a true estimate of the suicide risk.

Valeant itself has a risk management proposal that includes participation in a registry and enhanced communication but no boxed warning.   Continued...