Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Prurigo Nodularis

PHASE3CompletedINTERVENTIONAL
Enrollment

295

Participants

Timeline

Start Date

August 29, 2018

Primary Completion Date

January 9, 2020

Study Completion Date

February 6, 2020

Conditions
PruritusPrurigo Nodularis
Interventions
DRUG

5mg Serlopitant Tablets

Serlopitant Tablets

DRUG

Placebo Tablets

Placebo Tablets

Trial Locations (40)

1130

Study Site 650, Vienna

4020

Study Site 648, Linz

8036

Study Site 649, Graz

10117

Study Site 607, Berlin

10783

Study Site 641, Berlin

14467

Study Site 640, Potsdam

15831

Study Site 620, Mahlow

21614

Study Site 642, Buxtehude

22391

Study Site 639, Hamburg

33647

Study Site 600, Bielefeld

44793

Study Site 617, Bochum

48149

Study Site 601, Münster

48455

Study Site 623, Bad Bentheim

49074

Study Site 618, Osnabrück

53127

Study Site 608, Bonn

55131

Study Site 614, Mainz

56242

Study Site 615, Selters

60590

Study Site 602, Frankfurt am Main

69115

Study Site 605, Heidelberg

70178

Study Site 643, Stuttgart

91054

Study Site 621, Erlangen

01307

Study Site 606, Dresden

04103

Study Site 611, Leipzig

85-065

Study Site 636, Bydgoszcz

38-440

Study Site 628, Iwonicz-Zdrój

30-033

Study Site 633, Krakow

31-070

Study Site 624, Krakow

31-209

Study Site 635, Krakow

90-436

Study Site 629, Lodz

10-900

Study Site 631, Olsztyn

86-031

Study Site 625, Osielsko

60-214

Study Site 645, Poznan

60-848

Study Site 644, Poznan

35-055

Study Site 634, Rzeszów

70-332

Study Site 638, Szczecin

87-100

Study Site 632, Torun

02-758

Study Site 627, Warsaw

50-566

Study Site 637, Wroclaw

53-301

Study Site 630, Wroclaw

53-658

Study Site 647, Wroclaw

All Listed Sponsors
lead

Vyne Therapeutics Inc.

INDUSTRY

NCT03677401 - Study of the Efficacy, Safety and Tolerability of Serlopitant for the Treatment of Pruritus (Itch) With Prurigo Nodularis | Biotech Hunter | Biotech Hunter