Mallinckrodt Gets FDA Committee Vote For Abuse-Deterrent Drug

 | Nov 15, 2018 04:09AM ET

Mallinckrodt plc (NYSE:MNK) subsidiary, SpecGx LLC, reported the outcome of an FDA joint advisory committee meeting on MNK-812, an abuse-deterrent, immediate-release reformulation of Roxicodone (oxycodone hydrochloride tablets USP).

We note that SpecGx is advancing this reformulation with properties designed to deter intravenous and intranasal abuse under the company's 505(b)2 new drug application for MNK-812.

In a joint meeting, the FDA’s Anesthetic and Analgesic Drug Products Advisory Committee and Drug Safety and Risk Management Advisory Committee voted in the ratio of 10 to 7 to approve the SpecGx’s experimental abuse-deterrent formulation of immediate-release, single-entity oxycodone tablets for the management of pain severe enough to require an opioid analgesic, and for which alternative treatments are inadequate.

Both the committees also voted in the ratio of 12 to 5 for the drug to be labeled as an abuse-deterrent product by the nasal route of abuse. The committees also voted in 10 to 7 ratio for the drug to be not labeled as an abuse deterrent product by the intravenous route of abuse.

Although the FDA takes the recommendation of the committees in consideration, it is not bound by it.

A tentative approval will boost Mallinckrodt’s diverse portfolio.

Mallinckrodt recently reported strong third-quarter results, beating on both sales and earnings estimates. The hospital franchise (Inomax and Ofirmev) has gained traction, which is positively impacting sales. The company also raised its annual guidance. However, Acthar, Mallinckrodt’s largest product, is being negatively impacted by the residual impact of the previously reported patient withdrawal issues.

Mallinckrodt’s stock has gained 37% in the year so far, against the industry ’s decline of 6.8%.