Hereditary Cancer Syndromes
Clinical trial pipeline · Data from ClinicalTrials.gov
See which Hereditary Cancer Syndromes trials may be worth asking aboutClinical trial pipeline · Data from ClinicalTrials.gov
See which Hereditary Cancer Syndromes trials may be worth asking aboutNorth America
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The iCaRe2 is a multi-institutional resource created and maintained by the Fred \& Pamela Buffett Cancer Center to collect and manage standardized, multi-dimens…
RATIONALE: Gathering information about older patients with cancer may help the study of cancer in the future. PURPOSE: This research study is gathering informa…
As part of a post-approval commitment, the Korean health authority requests a study to characterize safety and effectiveness in patients treated with Koselugo (…
This study will collect medical records, scan results, and complete surveys to create a registry about people with a neurofibromatosis type 1-associated brain t…
.Neurofibromatosis type 2 is an inherently autosomal dominant genetic disease, but cases of mosaicism or de novo mutation are not uncommon. the prevalence is es…
This is a study to evaluate the efficacy and safety of belzutifan monotherapy in participants with advanced pheochromocytoma/paraganglioma (PPGL), pancreatic ne…
Background: Clinical Genetics Branch (CGB) researchers study individuals and populations at high genetic risk of cancer in order to improve our understanding o…
This study will monitor for potential chronic liver injury and liver fibrosis, in participants treated with cannabidiol oral solution.