“A Phase 1/2 Study of the Oral RET Inhibitor LOXO-292 in Pediatric Patients with Advanced RET-Altered Solid or Primary Central Nervous System Tumors Safety and Tolerability, Efficacy and Pharmacokinetics in Paediatric Patients with Solid Tumours (LOXO-RET-18036)”
In this clinical trial children, adolescents and young adults between 12 and 21 years will be treated with Selpercatinib (Loxo-292).
Selpercatinib specifically inhibits the Receptor-Tyrosine Kinase (RET), meaning it blocks a type of enzyme (kinase) and helps prevent the cancer cells from growing. Before beginning treatment, the identification of a RET gene alteration must be determined using laboratory testing.
Therefore, in this clinical trial adnvanced tumours with RET-alterations are treated after standard therapy. Selpercatinib i staken orally over a 28-day cycle as gelatine capsules or as a liquid suspension.
Inclusion of patients in Heidelberg has been possible since 16 July 2020.
For more information, see the Study Registry: The study is registered with the U.S. National Institutes of Health (ClinicalTrials.gov).
See NCT03899792
EudraCT-Number: 2019-000212-28