A Phase 1 Study of LJPC-501 in Patients With Hepatorenal Syndrome

PHASE1TerminatedINTERVENTIONAL
Enrollment

6

Participants

Timeline

Start Date

March 31, 2014

Primary Completion Date

November 30, 2015

Study Completion Date

December 31, 2015

Conditions
Hepatorenal Syndrome Type I and Type II
Interventions
DRUG

LJPC-501

Patients will receive LJPC-501 at titrated doses, with a starting range from 1 to 100 ng/kg/min, by continuous infusion on Days 1 through 5. In Group 1, drug doses will be titrated to 5, 15, and 25 ng/kg/min, after which doses will be titrated in multiples of 25 ng/kg/min. In Groups 2-5, drug doses will be titrated by 25 ng/kg/min. Dose titrations will occur every 2 hours until a MAP of 110 mmHg is reached, maximum urine output is achieved, or a dose of 250 ng/kg/min is achieved. Dosing will then continue at the maximum dose achieved through Day 5.

Trial Locations (1)

75246

Annette C. & Harold C. Simmons Transplant Institute @ Baylor University Medical Center, Dallas

All Listed Sponsors
lead

La Jolla Pharmaceutical Company

INDUSTRY

NCT01906307 - A Phase 1 Study of LJPC-501 in Patients With Hepatorenal Syndrome | Biotech Hunter | Biotech Hunter