TerminatedPhase 2NCT01824303

Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Interstitial Cystitis

Studying Interstitial cystitis

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Key facts

Sponsor
Allergan
Principal Investigator
Curtis Nickel, MD, MSN NP
Queen's University/Kingston General Hospital/Ontario Canada
Intervention
LiRIS 400 mg(drug)
Enrollment
31 enrolled
Eligibility
18 years · FEMALE
Timeline
20132014

Study locations (17)

Collaborators

TARIS Biomedical, Inc.

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.

Open NCT01824303 on ClinicalTrials.gov

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