Phase 3 Study of Intranasal Carbetocin (LV-101) in Patients With Prader-Willi Syndrome

PHASE3CompletedINTERVENTIONAL
Enrollment

130

Participants

Timeline

Start Date

November 20, 2018

Primary Completion Date

May 13, 2020

Study Completion Date

July 9, 2022

Conditions
Prader-Willi Syndrome
Interventions
DRUG

3.2 mg intranasal carbetocin

three times per day with meals

DRUG

9.6 mg intranasal carbetocin

three times per day with meals

DRUG

placebo

three times per day with meals

Trial Locations (24)

4101

Queensland Children's Hospital, South Brisbane

19107

Children's Hospital of Philadelphia, Philadelphia

20010

Children's National, Washington D.C.

32608

University of Florida, Gainesville

35233

University of Alabama at Birmingham, Birmingham

37212

Vanderbilt University School of Medicine, Nashville

43205

Nationwide Children's Hospital, Columbus

55102

Children's Hospitals and Clinics of Minnesota, Saint Paul

60611

Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago

63104

Cardinal Glennon Children's Medical Center, St Louis

66160

Kansas University Medical Center, Kansas City

74135

University of Oklahoma Health Sciences Center, Tulsa

77030

Texas Children's Hospital, Houston

78207

Children's Hospital of San Antonio, San Antonio

80045

Children's Hospital Colorado, Aurora

84108

University of Utah, Salt Lake City

85006

Phoenix Children's Hospital, Phoenix

90027

Children's Hospital of Los Angeles (USC), Los Angeles

92123

Rady Children's Hospital San Diego, San Diego

02115

University of Harvard Boston Children's Hospital, Boston

T6G 2E1

University of Alberta, Edmonton

V6H 3V4

British Columbia Children's Hospital, Vancouver

M5G 1X8

Toronto Hospital for Sick Kids, Toronto

H3T 1C5

CHU Ste Justine, Montreal

Sponsors
All Listed Sponsors
lead

Levo Therapeutics, Inc.

INDUSTRY

NCT03649477 - Phase 3 Study of Intranasal Carbetocin (LV-101) in Patients With Prader-Willi Syndrome | Biotech Hunter | Biotech Hunter