CompletedPhase 1NCT01559961
Safety Study of Single Intravesical Doses of TTI-1612 in Women With Interstitial Cystitis/Bladder Pain Syndrome
Studying Interstitial cystitis
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
- Trillium Therapeutics Inc.
- Principal Investigator
- Penka Petrova, PhD, CPSTrillium Therapeutics Inc.
- Intervention
- TTI-1612(drug)
- Enrollment
- 28 target
- Eligibility
- 18-65 years · FEMALE
- Timeline
- 2012 – 2013
Study locations (4)
- Bramalea Medical Centre, Brampton, Ontario, Canada
- Urology Associates/Urologic Medical Research, Kitchener, Ontario, Canada
- The Fe/Male Health Centres, Oakville, Ontario, Canada
- Urology & Male Fertility Clinic, Toronto, Ontario, Canada
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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