CompletedPhase 2NCT00963053
VA111913 Dysmenorrhoea Efficacy and Safety Proof of Concept
Studying Oculocerebral hypopigmentation syndrome, Cross type
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Vantia Ltd
- Principal Investigator
- David BellBio-Kinetic Europe Limited
- Intervention
- VA111913 TS and placebo(drug)
- Enrollment
- 146 target
- Eligibility
- 18-35 years · FEMALE
- Timeline
- 2009 – 2010
Study locations (4)
- Pivotal Research Centers, Peoria, Arizona, United States
- Premier Research Group, Austin, Texas, United States
- Jean Brown Research, Salt Lake City, Utah, United States
- Bio-Kinetic Europe Limited, Belfast, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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