Merck’s Novel HIF-2α Inhibitor Showed an Objective Response Rate of Nearly 30% in Patients with von Hippel-Lindau (VHL) Disease-Associated Clear Cell Renal Cell Carcinoma
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Wednesday, May 13, 2020
Oncology, Health, Clinical trials, Research, Science, Pharmaceutical, Biotechnology, Health, Clinical medicine, Medicine, Rare diseases, Autosomal dominant disorders, Genodermatoses, Syndromes, Von Hippel–Lindau disease, Von Hippel–Lindau tumor suppressor, Renal cell carcinoma, Merck & Co., Von Hippel, MK-6482, Merck
Von Hippel-Lindau disease is a rare hereditary condition affecting multiple organs, which puts patients at risk for several cancers, including renal cell carcinoma.
Key Points:
- Von Hippel-Lindau disease is a rare hereditary condition affecting multiple organs, which puts patients at risk for several cancers, including renal cell carcinoma.
- Follow Merck on Twitter via @Merck and keep up to date with ASCO news and updates by using the hashtag #ASCO20.
- This study is a Phase 2, open-label, single-arm trial evaluating MK-6482 for the treatment of VHL-associated ccRCC (ClinicalTrials.gov, NCT03401788 ).
- Patients received MK-6482 120 mg orally once daily until disease progression, unacceptable toxicity, or investigators or patients decision to withdraw.