Last updated on September 2020

Evaluation of S-600918 in Adults With Refractory Chronic Cough


Brief description of study

The primary objective of this study is to determine the optimal dose of S-600918 in patients with refractory chronic cough by evaluating the change from baseline in 24-hour cough frequency (coughs per hour) with S-600918 compared with placebo.

Clinical Study Identifier: NCT04110054

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Pulmonary Associates

Phoenix, AZ United States
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American Health Research Inc

Charlotte, NC United States
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Southeastern Research Center

Winston-Salem, NC United States
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Clinical Research of Rock Hill

Rock Hill, SC United States
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Tohno Chuo Clinic

Mizunami-shi, Japan
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Lee's Clinic

Osaka-shi, Japan
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Lenus Research & Medical Group

Sweetwater, FL United States
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Minnesota Lung Center

Woodbury, MN United States
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New Horizons Clinical Research

Cincinnati, OH United States
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ADAC Research, PA

Greenville, SC United States
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Diagnostics Research Group

San Antonio, TX United States
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Nishi Fukuoka Hospital

Fukuoka-shi, Fukuoka, Japan
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Lee's Clinic

Osaka-shi, Osaka, Japan
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KONO Medical Clinic

Setagaya-ku, Tokyo, Japan
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Research Solutions of Arizona

Litchfield Park, AZ United States
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Minnesota Lung Center

Edina, MN United States
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Minnesota Lung Center

Woodbury, MN United States
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New Horizons Clinical Research

Cincinnati, OH United States
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ADAC Research, PA

Greenville, SC United States
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Diagnostics Research Group

San Antonio, TX United States
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Tohno Chuo Clinic

Mizunami-shi, Japan
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Lee's Clinic

Osaka-shi, Japan
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MUDr. I. iern -Peterov s.r.o.

Brandýs nad Labem-Stará Boleslav, Czechia
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West Walk Surgery

Yate, United Kingdom
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The Clinical Research Center, LLC

Saint Louis, MO United States
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Atlantic Research Center, LLC

Ocean City, NJ United States
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Respiratory Clinical Trials

Cottingham, United Kingdom
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BMI Bishops Wood Hospital

Northwood, United Kingdom
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Recruitment Status: Open


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