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Clinical Trial Summary

This phase II trial investigates how well pamiparib and temozolomide work in treating patients with hereditary leiomyomatosis and renal cell (kidney) cancer. Poly adenosine diphosphate-ribose polymerase (PARPs) are proteins that help repair DNA mutations. PARP inhibitors, such as pamiparib, can keep PARP from working, so tumor cells can't repair themselves, and they may stop growing. Chemotherapy drugs, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving pamiparib and temozolomide may help treat patients with hereditary leiomyomatosis and renal cell cancer.


Clinical Trial Description

PRIMARY OBJECTIVE: I. Evaluate response rate of pamiparib plus low-dose temozolomide. SECONDARY OBJECTIVES: I. To evaluate the progression-free survival with pamiparib plus low-dose temozolomide. II. To evaluate the safety (adverse events [AE's]) with pamiparib plus low-dose temozolomide. TRANSLATIONAL OBJECTIVES: I. To determine the association between plasma and tumor 2-hydroxyglutarate (2HG), fumarate, and succinate levels and response to treatment. II. To analyze the association of the genomic mutational signature (by whole genome sequencing) of the tumor to treatment. OUTLINE: Patients receive orally (PO) twice daily (BID) on days 1-28 and temozolomide PO once daily (QD) on days 1-7. Cycles repeat every 28 days for up to 36 months in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up every 4 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04603365
Study type Interventional
Source Jonsson Comprehensive Cancer Center
Contact
Status Withdrawn
Phase Phase 2
Start date October 18, 2021
Completion date May 7, 2023

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