FDA Panel Shoots Down Intellipharma Opioid

Independent advisers said there wasn't enough evidence to approve Intellipharma's opioid painkiller as there wasn't adequate data on the abuse potential of the drug.

A U.S. FDA panel of independent advisers said there was not enough evidence to support the approval of Toronto-based Intellipharmaceutics International's long-acting opioid painkiller, according to a Reuters article.

The painkiller was developed as an abuse-deterrent version of Purdue Pharma's OxyContin, which already has tamper-resistant properties. The drug has a blue dye that is emitted if the tablet is manipulated, which could help identify abusers, and a nasal irritant to discourage misuse, the story said.

Read the full article

Sign up for our eNewsletters
Get the latest news and updates