Pharmaceutical Business review

Debiopharm begins CPP disease study

The study, which will enroll 44 children from the US, Chile and Mexico, aims to decrease luteinizing hormone (LH) to prepubertal levels at month 6 (Day 169) in children with CPP using triptorelin pamoate 22.5 mg.

Debiopharm president and founder Rolland-Yves Mauvernay said Debiopharm is excited to be part of the first Debiopharm-sponsored clinical trial using triptorelin for the treatment of CPP.

"Our aim is to show that a gonadotropin-releasing hormone (GnRH) agonist therapy prevents the social and psychological difficulties associated with premature sexual development, and has a positive impact on compromised adult height," Mauvernay added.

"The 6-month-formulation would entail an improved compliance in a paediatric indication for which no other 6-month GnRH agonist formulation is currently approved, whilst reducing the frequency of injections in children."

GnRH-dependent CPP is defined by pubertal development occurring before the age of 8 years in girls and 9 years in boys.