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CompletedNCT03015701

S9005 Mifepristone in Meningioma

Double Blind Randomized Trial of the Anti-Progestational Agent Mifepristone In The Treatment of Unresectable Meningioma

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
193 (actual)
Sponsor
SWOG Cancer Research Network · Network
Sex
All
Age
18 Years – 120 Years
Healthy volunteers
Not accepted

Summary

To compare daily oral mifepristone vs placebo with respect to time to treatment failure in patients with unresectable meningioma.

Detailed description

To compare daily oral mifepristone vs placebo with respect to time to treatment failure in patients with unresectable meningioma and to address issues of safety in this patient population.

Conditions

Interventions

TypeNameDescription
DRUGMifepristonea 19 norsteroid with anti-progesterone and anti glucocorticoid activity which competitively inhibits binding of the hormone to its receptor
OTHERPlaceboplacebo matching mifepristone

Timeline

Start date
1992-08-01
Primary completion
2001-10-01
Completion
2012-11-01
First posted
2017-01-10
Last updated
2019-12-23

Source: ClinicalTrials.gov record NCT03015701. Inclusion in this directory is not an endorsement.

S9005 Mifepristone in Meningioma (NCT03015701) · Clinical Trials Directory