reACHin: A Phase 2, Multicenter, Double-Blind, Randomized, Placebo-controlled Trial, evaluating Safety, Tolerability, and Efficacy of Subcutaneous Doses of TransCon CNP Administered Once Weekly for 52 Weeks in Infants (0 to <2 years of age) with Achondroplasia followed by an Open Label Extension (OLE) period

Project: Clinical studiesClinical Study (Industry project)

Project Details

StatusActive
Effective start/end date30.06.202431.12.2030

Fields of science

  • 302035 Paediatrics and adolescent medicine