The Food and Drug Administration says it will hold a joint meeting of the Pediatric Advisory Committee and Drug Safety and Risk Management Advisory Committee on September 26 and 27.
On September 26, the committees will discuss the required pediatric-focused safety review for OxyContin (oxycodone hydrochloride) extended-release tablets, as mandated by law. The committees will also discuss pediatric data considerations for opioid analgesics labeling and Pediatric Research Equity Act studies for opioids generally, using Opana (oxymorphone) immediate-release as an example.
Opioid analgesics serve an important medical purpose in the care of certain pediatric patients when a physician deems them appropriate, including in pediatric patients with cancer and sickle cell disease or, more commonly, those who have suffered traumas, burns or have surgery to correct birth defects. In 2015, the FDA approved an expanded indication for OxyContin to include the management of pain severe enough to require daily, around-the-clock, long-term opioid treatment and for which alternative treatment options are inadequate in opioid-tolerant pediatric patients 11 years of age and older who already receive and tolerate a minimum daily opioid analgesic dose of at least 20 mg oxycodone orally or its equivalent.
Although there have been no new safety issues identified for OxyContin among pediatric patients since then, in the interest of transparency, the agency will present the legislatively mandated review of the safety information to the committees in a public forum.
“Without data specific to the pediatric population, there may be insufficient knowledge of the dosing, safety and efficacy of drugs intended for use in children – putting them at risk for negative health impacts or limiting access to the treatments they need,” said Susan McCune, MD, Director of the FDA’s Office of Pediatric Therapeutics. “While these meetings generally focus on particular drugs or classes of drugs, they are also a time to talk about the unique aspects of pediatric drug approvals and the education and outreach associated with drugs approved for pediatric populations, as one way to obtain the feedback we need to make decisions about pediatric drugs.”
On the second day, the committees will hear information about safety signals associated with montelukast, a medicine that has been approved for use in the U.S. since 1998 and is prescribed to over two million pediatric patients (infants to 16 years of age) each year for asthma or allergic rhinitis. In 2009, the label for montelukast and other leukotriene modifiers (zafirlukast and zileuton) was updated to include a warning for neuropsychiatric events, including agitation, anxiety, depression, sleep abnormalities, and suicidal thinking and suicide. Two years ago, in response to public feedback, the FDA commissioned a study in children to explore the adverse effects associated with montelukast. The focus of the study was on neuropsychiatric events including serious depression, self-harm and suicide. The committees will discuss the results of that recently completed Sentinel study.
