Status and phase
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About
To determine the safety of extended treatment with Proellex® in women who have successfully completed either study ZPV-201 [NCT02323646] or ZPU-203 [NCT02301897] and meet eligibility criteria.
Full description
This study will be for participants who had completed either ZPV-201 or ZPU-203.
Enrollment
Sex
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Volunteers
Inclusion criteria
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Primary purpose
Allocation
Interventional model
Masking
20 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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