FDA staff flags possible dosing risk with Collegium painkiller

Reuters Health Information: FDA staff flags possible dosing risk with Collegium painkiller

FDA staff flags possible dosing risk with Collegium painkiller

Last Updated: 2015-09-09

By Samantha Kareen Nair and Natalie Grover

(Reuters) - The U.S. Food and Drug Administration's staff expressed concerns over the risk of incorrectly administering Collegium Pharmaceuticals Inc's long-acting opioid painkiller.

The experimental pill, to be called Xtampza, is designed to be taken after eating as data has shown the absorption of the opioid increases in the presence of food. (http://1.usa.gov/1MaT3GL)

Inadequate pain control caused by lack of food could lead to overdosing, reviewers said. Prescription opioid abuse has the potential to produce euphoric highs and disrupt the parts of the brain that control breathing.

Collegium has proposed to make clear on the label that Xtampza, an oral formulation of oxycodone, should only be taken after eating.

But reviewers argued that the packaging design would be "inadequate" in eliminating the risk of an administration error, noting that most oral opioid products can be given without respect to food intake.

The sole exception is Endo International Plc's Opana ER (oxymorphone), which is taken on an empty stomach.

Reviewers said if the FDA eventually determines that Xtampza's benefits outweigh its risks, the company should assess the effectiveness of its packaging in preventing incorrect use.

The review was published on the FDA's website on Wednesday ahead of a meeting on Friday of a panel of outside advisers who will recommend whether the drug should be approved.

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

© Copyright 2013-2020 GI Health Foundation. All rights reserved.
This site is maintained as an educational resource for US healthcare providers only. Use of this website is governed by the GIHF terms of use and privacy statement.