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Type(s) of Cancer
CNS
Study Phase
Phase 3
Study Completion Date
October 2001
NCT03015701Uploaded 07-26-2017
Access via NCI by Request
PDS UID: nci-data-364
Double Blind Randomized Trial of the Anti-Progestational Agent Mifepristone In The Treatment of Unresectable Meningioma
Provider Information
Provider Data DescriptionNCT03015701-D3-Dataset.csv provides adverse event data from both the blinded and open label treatment epochs.
SponsorSouthwest Oncology Group
Data ProviderNational Cancer Institute
Clinical Trials.gov Information
Brief SummaryTo compare daily oral mifepristone vs placebo with respect to time to treatment failure in patients with unresectable meningioma.
ConditionsMeningioma
Intervention TypeDrug: Mifepristone
Other: Placebo
Drug(s)Drug: Mifepristone
Total Enrolled193
RandomizationRandomized
Blinding MethodQuadruple
Arms InterventionArm 1 - Experimental
Arm 2 - Placebo Comparator
Secondary IDU10CA032102
PubMed (PMID)N/A
Collaborator(s)National Cancer Institute (NCI)
Region(s)N/A
Age Range18 Years to 120 Years (Adult, Older Adult)
Files: NCT03015701-D3
Data DictionaryNCT03015701-D3-Data-Dictionary.pdf
DATANCT03015701-D3-Dataset.csv
OTHERREADME.pdf
Files: NCT03015701-D2
Data DictionaryNCT03015701-D2-Data-Dictionary.pdf
DATANCT03015701-D2-Dataset.csv
OTHERREADME.pdf
Files: NCT03015701-D1
Data DictionaryNCT03015701-D1-Data-Dictionary.pdf
DATANCT03015701-D1-Dataset.csv
OTHERREADME.pdf
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