Phase II Study to Evaluate the Efficacy and Safety of Two Dosing Regimens of MN-001 in Patients With Interstitial Cystitis



Status:Archived
Conditions:Other Indications, Urology
Therapuetic Areas:Nephrology / Urology, Other
Healthy:No
Age Range:Any
Updated:7/1/2011

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Trial Summary
Trial Overview
Inclusion Criteria

A Phase II, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy and Safety of Two Dosing Regimens of MN-001 in Patients With Interstitial Cystitis


To evaluate the safety and efficacy of 8 weeks of treatment with MN-001 at 500 mg bid, 500
mg once daily vs. placebo in patients with Interstitial Cystitis.



We found this trial at
18
sites
MediciNova Investigational Site
Aventura, Florida 33180
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Aventura, FL
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New York Oncology Hematology PC-Albany
Albany, New York 12206
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Albany, NY
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MediciNova Investigational Site
Albany, New York 12206
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Albany, NY
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MediciNova Investigational Site
Atlanta, Georgia 30309
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Atlanta, GA
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MediciNova Investigational Site
Birmingham, Alabama 35294
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Birmingham, AL
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MediciNova Investigational Site
Boulder, Colorado 80304
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Boulder, CO
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MediciNova Investigational Site
Centralia, Illinois 62801
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Centralia, IL
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MediciNova Investigational Site
Cincinnati, Ohio 45212
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Cincinnati, OH
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MediciNova Investigational Site
Corsicana, Texas 75110
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Corsicana, TX
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MediciNova Investigational Site
Greer, South Carolina 29650
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Greer, SC
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MediciNova Investigational Site
Las Vegas, Nevada 89109
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Las Vegas, NV
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MediciNova Investigational Site
Marlton, New Jersey 08053
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Marlton, NJ
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MediciNova Investigational Site
Mountlake Terrace, Washington 98043
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Mountlake Terrace, WA
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MediciNova Investigational Site
Ogden, Utah 84403
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Ogden, UT
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MediciNova Investigational Site
Royal Oak, Michigan 48073
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Royal Oak, MI
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MediciNova Investigational Site
Shreveport, Louisiana 71106
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Shreveport, LA
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MediciNova Investigational Site
Tualatin, Oregon 97062
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Tualatin, OR
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MediciNova Investigational Site
Winston Salem, North Carolina 27103
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from
Winston Salem, NC
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