Tegavivint for the Treatment of Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors

Complete Title: A Phase 1/2 Study of Tegavivint (IND#156033, NSC#826393) in Children, Adolescents, and Young Adults with Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors
Trial Phase: I/II
Investigator: Katherine Tarlock

This phase I/II trial evaluates the highest safe dose, side effects, and possible benefits of tegavivint in treating patients with solid tumors that has come back (recurrent) or does not respond to treatment (refractory). Tegavivint interferes with the binding of beta-catenin to TBL1, which may help stop the growth of tumor cells by blocking the signals passed from one molecule to another inside a cell that tell a cell to grow.

Keywords:
  • Endometrial Cancer
  • Melanoma
  • Neuroblastoma
  • Lymphoma, Non-Hodgkin (NHL)
  • Ovarian Cancer
  • Sarcoma
  • Solid Tumors
  • Wilms' Tumor
  • Neoplasms
  • Sarcoma, Ewing
  • Osteosarcoma
  • Adenocarcinoma
  • Colorectal Neoplasms
  • Carcinoma, Hepatocellular
  • Fibromatosis, Aggressive
  • Hepatoblastoma
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Adult
Pediatric
I/II
Katherine Tarlock
RG1122071
NCT04851119
A Phase 1/2 Study of Tegavivint (IND#156033, NSC#826393) in Children, Adolescents, and Young Adults with Recurrent or Refractory Solid Tumors, Including Lymphomas and Desmoid Tumors
Endometrial Cancer
Melanoma
Neuroblastoma
Lymphoma, Non-Hodgkin (NHL)
Ovarian Cancer
Sarcoma
Solid Tumors
Wilms' Tumor
Neoplasms
Sarcoma, Ewing
Osteosarcoma
Adenocarcinoma
Colorectal Neoplasms
Carcinoma, Hepatocellular
Fibromatosis, Aggressive
Hepatoblastoma