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An Open-Label, Dose-Escalation, Phase I/II Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of the MEK Inhibitor Trametinib in Children and Adolescents Subjects With Cancer or Plexiform Neurofibromas and Trametinib in Combination With Dabrafenib in Children and Adolescents With Cancers Harboring V600 Mutations
Conditions
Interventions
Trametinib
Dabrafenib
Locations
16
United States
Novartis Investigative Site
Phoenix, Arizona, United States
Novartis Investigative Site
San Francisco, California, United States
Novartis Investigative Site
Washington D.C., District of Columbia, United States
Novartis Investigative Site
Baltimore, Maryland, United States
Novartis Investigative Site
Boston, Massachusetts, United States
Novartis Investigative Site
Minneapolis, Minnesota, United States
Start Date
January 15, 2015
Primary Completion Date
December 29, 2020
Completion Date
December 29, 2020
Last Updated
July 14, 2021
NCT05053971
NCT05691465
NCT05039801
NCT03375307
NCT05673200
NCT05692635
Lead Sponsor
Novartis Pharmaceuticals
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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