Von Hippel

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

Retrieved on: 
Wednesday, May 13, 2020

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.

Genetic Cancer Patients Report COVID-19 Crisis Impacts Medical Care

Retrieved on: 
Wednesday, April 22, 2020

VHL, or von Hippel-Lindau disease, is a genetic disorder characterized by tumors in up to ten areas of the body.

Key Points: 
  • VHL, or von Hippel-Lindau disease, is a genetic disorder characterized by tumors in up to ten areas of the body.
  • The tumors can be benign or cancerous, and appear and grow unpredictably throughout a patient's life.
  • Renal and pancreatic neuroendocrine cancers, paralysis, loss of vision and hearing, are among the dangers faced by VHL patients.
  • The VHL Alliance (VHLA) is the preeminent resource and clearinghouse for those affected by von Hippel-Lindau disease, including patients, caregivers, researchers, and the medical community.