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Clinical Trial Summary

The purpose of this research study is to test the safety and effectiveness of Seleno-L Methionine (SLM) when combined with the standard dose and schedule of Axitinib and Pembrolizumab in patients who have locally advanced or metastatic clear cell renal cell carcinoma (ccRCC).


Clinical Trial Description

The proposed study is a single arm, open-label Phase I/II trial of Seleno-L Methionine (SLM) in sequential combination with the standard dose and schedule of Axitinib and Pembrolizumab in previously untreated patients with advanced ccRCC. The hypothesis is that adding SLM to the Pembrolizumab and Axitinib combination will improve efficacy without added toxicity. This is a two-part study: - Escalation Part 1: The study will begin with a dose-escalation study to find the maximum tolerated dose (MTD) of study drug, SLM. - Expansion Part 2: Once the appropriate dose of SLM is determined, the second part of the study will begin. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05363631
Study type Interventional
Source University of Iowa
Contact Yousef Zakharia, MD
Phone (319) 384-8076
Email yousef-zakharia@uiowa.edu
Status Recruiting
Phase Phase 1/Phase 2
Start date September 19, 2022
Completion date December 31, 2026

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