Glaxo Seeks Label Expansion Of Nucala In Pediatric Patients

 | Nov 20, 2018 03:52AM ET

GlaxoSmithKline plc (NYSE:GSK) announced the submission of a supplemental Biologics License Application (sBLA) for its asthma drug, Nucala (mepolizumab), to the FDA. The sBLA is seeking label expansion of Nucala as an add-on treatment in pediatric patients with severe eosinophilic asthma. The drug is already approved for adolescent and adult patients for the same indication

The sBLA is supported by data from a pediatric open-label study which evaluated Nucala for pharmacokinetics, pharmacodynamics and long-term safety in patients aged six to 11 years.

Notably, Nucala received approval for similar indication in Europe in August 2018. In December 2017, Nucala was also approved for eosinophilic granulomatosis with polyangiitis in the United States.

Glaxo’s shares have gained 13.7% so far this year, outperforming the industry ’s rally of 8.2%.