9-ING-41 in Pediatric Patients With Refractory Malignancies

Complete Title: Phase 1 study of 9-ING-41, a Glycogen Synthase Kinase-3 Beta (GSK-3β) inhibitor, as a single agent or with Irinotecan in pediatric patients with refractory malignancies
Trial Phase: I
Investigator: Catherine Albert

9-ING-41 is a first-in-class, intravenously administered, maleimide-based, small molecule, potent selective GSK-3ß inhibitor with significant pre-clinical and clinical anticancer activity. In the ongoing Actuate 1801 study in a cohort of over 90 patients with advanced refractory malignancies, 9-ING-41 has exhibited no significant toxicity, including no myelosuppression, and significant anti-tumor activity. 9-ING-41 also has significant pre-clinical ability to reverse pathologic fibrosis in multiple models of pulmonary and pleural fibrosis. 9-ING-41 is very highly active against neuroblastoma in diverse pre-clinical models. This Phase 1 study is designed to evaluate the safety and efficacy of 9-ING-41, as a single agent or in combination with irinitecan, in paediatric patients with advanced malignancies and thus to establish the recommended Phase 2 dose (RP2D) for further paediatric patient studies.

Keywords:
  • Brain Cancer
  • Pediatric Cancers, Miscellaneous
  • Neuroblastoma
  • Sarcoma
  • Pontine Glioma
  • Human Papillomavirus (HPV) 16+ Relapsed/Refractory Cancer
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Adult
Pediatric
I
Catherine Albert
RG1007975
NCT04239092
Phase 1 study of 9-ING-41, a Glycogen Synthase Kinase-3 Beta (GSK-3β) inhibitor, as a single agent or with Irinotecan in pediatric patients with refractory malignancies
Brain Cancer
Pediatric Cancers, Miscellaneous
Neuroblastoma
Sarcoma
Pontine Glioma
Human Papillomavirus (HPV) 16+ Relapsed/Refractory Cancer