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PTEN Gene Mutation clinical trials

View clinical trials related to PTEN Gene Mutation.

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NCT ID: NCT03680924 Completed - PTEN Gene Mutation Clinical Trials

Access to Resources for Patients With PTEN Hamartoma Tumor Syndrome

Start date: May 11, 2018
Phase:
Study type: Observational

The purpose of this study is to gain a better understanding of access to clinical and research resources for families of children affected with a phosphatase and tensin homology (PTEN) mutation. Ultimately, the researchers hope to be able to use this information to develop a standard of care for affected individuals and their family members. Family members/legal guardians of an individual with a PTEN mutation enrolled in the Rare Diseases Clinical Research Network (RDCRN) Contact Registry will be invited via email to participate in this study.

NCT ID: NCT02991807 Completed - Clinical trials for PTEN Hamartoma Tumor Syndrome

RAD001 and Neurocognition in PTEN Hamartoma Tumor Syndrome

Start date: June 12, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

Phosphatase and TENsin homolog (PTEN) gene germline mutations are associated with a spectrum of clinical manifestations characterized by neurocognitive deficits, intellectual disability, autism symptomatology, skin lesions, macrocephaly, hamartomatous overgrowth of tissues, and an increased risk of cancers. Investigators are conducting research to evaluate the potential safety and efficacy of RAD001 (everolimus) in this patient population, and the potential neurocognitive benefits from treatment with RAD001 or placebo for a six month period. The investigators hope this trial will lead to a better understanding of PTEN and to new forms of treatment that may benefit children and adults with PTEN in the future.