UnknownPhase 2NCT00490789
Trial of Efficacy and Safety of Sirolimus in Tuberous Sclerosis and LAM
Studying Lymphangioleiomyomatosis
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
- Cardiff University
- Principal Investigator
- Julian R Sampson, DMCardiff Univeristy
- Intervention
- sirolimus(drug)
- Enrollment
- 14 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2005 – 2009
Study locations (3)
- University Hospital of Wales, Cardiff, Wales, United Kingdom
- Royal Sussex County Hospital, Brighton, United Kingdom
- City Hospital, Nottingham, United Kingdom
Collaborators
University of Nottingham · St Georges Hospital Medical School · Royal Sussex County Hospital · The Tuberous Sclerosis Association · Wyeth is now a wholly owned subsidiary of Pfizer
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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