Safety and Pharmacokinetic Study of ALO-02 in Children Ages 7-17 With Pain

PHASE4TerminatedINTERVENTIONAL
Enrollment

32

Participants

Timeline

Start Date

January 21, 2016

Primary Completion Date

January 10, 2018

Study Completion Date

January 24, 2018

Conditions
Moderate-severe Pain
Interventions
DRUG

ALO-02

Oral/Capsule, twice per day dosing; Treatment duration consists of a 1 to 4 week Conversion/Titration Phase leading to a 2 to 4 week Maintenance Treatment duration.

Trial Locations (16)

27834

East Carolina University Brody School of Medicine(ECU), Greenville

Leo Jenkins Cancer Center Pharmacy, Greenville

29425

Medical University of South Carolina Children's Hospital, Charleston

Medical University of South Carolina, Investigational Drugs Services, Charleston

Medical University of South Carolina, Rutledge Tower, Pediatric Clinic, Charleston

Medical University of South Carolina, SCTR Research Nexus, Charleston

60612

University of Illinois at Chicago Clinical Research Center, Chicago

University of Illinois Hospital and Health Sciences Systems, Chicago

University of Illinois Hospital at the Medical Center, Chicago

78249

Road Runner Research, Ltd, San Antonio

90027

Children's Hopsital Los Angeles, Los Angeles

Children's Hospital Of Los Angeles - University Of Southern California School Of Medicine, Los Angeles

93534

Research Center For Clinical Studies-West, Inc., Lancaster

95817

Shriners Hospitals For Children Northern California, Sacramento

UC Davis Health Attn: Peter Trovitch, PharmD, Sacramento

University of California Davis, Sacramento

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Pfizer

INDUSTRY

NCT02680847 - Safety and Pharmacokinetic Study of ALO-02 in Children Ages 7-17 With Pain | Biotech Hunter | Biotech Hunter