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Spots Global Cancer Trial Database for Efficacy and Safety of RAD001 in Patients Aged 18 and Over With Angiomyolipoma Associated With Either Tuberous Sclerosis Complex (TSC) or Sporadic Lymphangioleiomyomatosis (LAM)

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Trial Identification

Brief Title: Efficacy and Safety of RAD001 in Patients Aged 18 and Over With Angiomyolipoma Associated With Either Tuberous Sclerosis Complex (TSC) or Sporadic Lymphangioleiomyomatosis (LAM)

Official Title: A Randomized, Double-blind, Placebo-controlled Study of RAD0001 in the Treatment of Angiomyolipoma in Patients With Either Tuberous Sclerosis Complex (TSC) or Sporadic Lymphangioleiomyomatosis (LAM)

Study ID: NCT00790400

Study Description

Brief Summary: This study will evaluate the safety and efficacy of RAD001 in treating patients with Angiomyolipoma associated with Tuberous Sclerosis Complex or Sporadic Lymphangioleiomyomatosis.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Alabama at Birmingham, Birmingham, Alabama, United States

Barrow Tuberous Sclerosis Center, Phoenix, Arizona, United States

Massachusetts General Hospital Massachussetts General Hospita, Boston, Massachusetts, United States

Minnesota Epilepsy Group, St. Paul, Minnesota, United States

Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States

LeBonheur Childrens Medical Group SC-2, Memphis, Tennessee, United States

Novartis Investigative Site, Torono, Ontario, Canada

Novartis Investigative Site, Lyon, , France

Novartis Investigative Site, Berlin, , Germany

Novartis Investigative Site, München, , Germany

Novartis Investigative Site, Siena, SI, Italy

Novartis Investigative Site, Torino, TO, Italy

Novartis Investigative Site, Roma, , Italy

Novartis Investigative Site, Sapporo-city, Hokkaido, Japan

Novartis Investigative Site, Suita-city, Osaka, Japan

Novartis Investigative Site, Yamagata, , Japan

Novartis Investigative Site, Utrecht, , Netherlands

Novartis Investigative Site, Warszawa, , Poland

Novartis Investigative Site, Warszawa, , Poland

Novartis Investigative Site, Moscow, , Russian Federation

Novartis Investigative Site, Barcelona, Catalunya, Spain

Novartis Investigative Site, Brighton, East Sussex, United Kingdom

Novartis Investigative Site, Craigavon, Northern Ireland, United Kingdom

Novartis Investigative Site, Cardiff, Wales, United Kingdom

Novartis Investigative Site, London, , United Kingdom

Contact Details

Name: Novartis Pharmaceuticals

Affiliation: Novartis Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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