BENITIONSClinical Trial Intelligence

Tipifarnib for the Treatment of Advanced Solid Tumors, Lymphoma, or Histiocytic Disorders With HRAS Gene Alterations, a Pediatric MATCH Treatment Trial

2期 进行中(已停止招募) NCT04284774

适应症Malignant Solid Neoplasm, Recurrent Adrenal Gland Pheochromocytoma, Recurrent Ectomesenchymoma, Recurrent Ependymoma
分期2期
申办方National Cancer Institute (NCI)
状态进行中(已停止招募)
受试者人数5 人
干预(药物)Tipifarnib
开始日期2020年10月13日
完成日期2024年3月31日
结果公布日2025年6月3日

摘要

This phase II pediatric MATCH trial studies how well tipifarnib works in treating patients with solid tumors that have recurred or spread to other places in the body (advanced), lymphoma, or histiocytic disorders, that have a genetic alteration in the gene HRAS. Tipifarnib may block the growth of cancer cells that have specific genetic changes in a gene called HRAS and may reduce tumor size.

Objective Response Rate (Complete Response + Partial Response) in Pediatric Patients Treated With Tipifarnib

Up to 2 years from study entry · percentage of patients

Treatment (Tipifarnib)0 percentage of patients

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。