The primary objective of this study is to assess the overall response rate (ORR) of von
Hippel-Lindau (VHL) disease-associated clear cell renal cell carcinoma (ccRCC) tumors in
VHL participants treated with MK-3795.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT03108066.
This open-label Phase 2 study will evaluate the efficacy, safety, PK, and PD of MK-3795
in participants with VHL disease who have at least 1 measurable VHL disease-associated
ccRCC tumor (as defined by RECIST 1.1). MK-3795 will be administered orally and treatment
will be continuous. Changes in VHL disease-associated non-ccRCC tumors will also be
evaluated.
Lead OrganizationPeloton Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)