Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Refractory Chronic Cough

PHASE2CompletedINTERVENTIONAL
Enrollment

185

Participants

Timeline

Start Date

October 3, 2017

Primary Completion Date

August 15, 2018

Study Completion Date

September 6, 2018

Conditions
Refractory Chronic Cough
Interventions
DRUG

5 mg Serlopitant Tablets

Serlopitant Tablets

DRUG

Matching Placebo Tablets

Placebo Tablets

Trial Locations (39)

14618

Study Site 125, Rochester

28054

Study Site 111, Gastonia

28117

Study Site 114, Mooresville

28207

Study Site 103, Charlotte

29420

Study Site 129, Charleston

29732

Study Site 104, Rock Hill

32789

Study Site 107, Winter Park

33778

Study Site 118, Largo

45231

Study Site 122, Cincinnati

53228

Study Site 105, Greenfield

55441

Study Site 115, Plymouth

55905

Study Site 110, Rochester

74136

Study Site 112, Tulsa

75231

Study Site 102, Dallas

Study Site 120, Dallas

76712

Study Site 109, Waco

78229

Study Site 101, San Antonio

80230

Study Site 108, Denver

80907

Study Site 106, Colorado Springs

Study Site 113, Colorado Springs

90048

Study Site 130, Los Angeles

92108

Study Site 123, San Diego

92691

Study Site 128, Mission Viejo

95117

Study Site 127, San Jose

95207

Study Site 131, Stockton

97202

Study Site 116, Portland

97401

Study Site 117, Eugene

98225

Study Site 126, Bellingham

07712

Study Site 121, Ocean Township

BT9 7AB

Study Site 133, Belfast

B9 5SS

Study Site 139, Birmingham

HU16 5JQ

Study Site 136, Cottingham

SA14 8QF

Study Site 141, Llanelli

SE5 9RS

Study Site 138, London

SW3 6HP

Study Site 137, London

M23 9LT

Study Site 132, Manchester

OX3 7LE

Study Site 135, Oxford

PR2 9HT

Study Site 134, Preston

TA2 5DA

Study Site 140, Taunton

All Listed Sponsors
lead

Vyne Therapeutics Inc.

INDUSTRY

NCT03282591 - Study of the Efficacy, Safety, and Tolerability of Serlopitant for the Treatment of Refractory Chronic Cough | Biotech Hunter | Biotech Hunter