GRAND CAYMAN, Cayman Islands--(BUSINESS WIRE)--Ironshore Therapeutics Inc., a privately held pharmaceutical company focused on the commercialization of JORNAY PM® (methylphenidate HCl) extended-release capsules (CII) for patients with ADHD, today announced the appointments of Lewis Warrington as Chief Medical Officer, Nelson F. Isabel as Chief Financial Officer, Nilay Patel as Chief Legal Officer and Tim Branz as Chief Information Officer. Additionally, Ironshore welcomes Micheal Westphall as Chief People Officer and Aron Chuc as Vice President, Market Access Strategy.
RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)--Ironshore Pharmaceuticals Inc. (“Ironshore”), a wholly owned subsidiary of Highland Therapeutics Inc. and a leader in the commercialization of novel treatments for Attention-Deficit/Hyperactivity Disorder (“ADHD”), today announced the publication of an original paper in the Journal of Child and Adolescent Psychopharmacology (“JCAP”) that describes new data showing the effect of JORNAY PM® (methylphenidate HCl) extended-release capsules CII on caregiver strain as measured by the Caregiver Strain Questionnaire (“CGSQ”). The data are derived from a Phase 3 clinical trial in child and adolescent patients with ADHD. The journal article provides the first validation of the CGSQ to measure caregiver strain over a preceding three-week period. JORNAY PM was approved in August 2018 by the U.S. Food and Drug Administration (FDA) for the treatment of ADHD in patients 6 years and older.
RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)--Ironshore Pharmaceuticals Inc. (“Ironshore”), a wholly owned subsidiary of Highland Therapeutics Inc. and a leader in the commercialization of novel treatments for Attention-Deficit/Hyperactivity Disorder (“ADHD”), today announced the publication of an original paper in the Journal of Child and Adolescent Psychopharmacology (“JCAP”) that describes new data showing the effect of JORNAY PM® (methylphenidate HCl) extended-release capsules CII on caregiver strain as measured by the Caregiver Strain Questionnaire (“CGSQ”). The data are derived from a Phase 3 clinical trial in child and adolescent patients with ADHD. The journal article provides the first validation of the CGSQ to measure caregiver strain over a preceding three-week period. JORNAY PM was approved in August 2018 by the U.S. Food and Drug Administration (FDA) for the treatment of ADHD in patients 6 years and older.