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

Last updated:
2026-09-12
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View trial details

Overview

Official protocol title:

A PHASE 2A MULTICENTER, RANDOMIZED, DOUBLE-BLINDED, PLACEBO-CONTROLLED STUDY EVALUATING SAFETY, TOLERABILITY AND EFFICACY OF LIRIS® 400 MG IN WOMEN WITH INTERSTITIAL CYSTITIS FOLLOWED BY AN OPEN LABEL EXTENSION

Intervention/treatment:
LIRIS
Medical condition:
INTERSTITIAL CYSTITIS/BLADDER PAIN SYNDROME
Protocol code:
TAR-100-202
Control number:
163224
Status:
Closed
Approved:
April 10, 2013
Date Completed:
Trial phase:
Phase 2
For more information:
ClinicalTrials.gov - NCT01824303
This is an external link. The information is not authorized by the Government of Canada.

Eligibility

Sex: FEMALE
Age
18 Years and older
Accepts healthy volunteers: No

Contacts and locations

Contact
Name
Therapeutic Area Head,
Organization
Allergan, Inc
Phone:
714-246-4500
Sponsor
TARIS BIOMEDICAL INC

Locations

British Columbia

Exdeo Clinical Research Inc.
Abbotsford British Columbia, British Columbia, V2S 3N6

Ontario

Centre for Applied Urological Research
Kingston, Ontario, K7L 3J7

Results

See the results from the trial NCT01824303. This is an external link. The information is not authorized by the Government of Canada.

Date posted:
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