70
Participants
Start Date
November 29, 2017
Primary Completion Date
October 28, 2019
Study Completion Date
October 28, 2019
LJPC-401
LJPC-401 subcutaneous injection, up to 20 mg weekly for 16 weeks. The minimum weekly dose will be 5 mg and the maximum weekly dose of LJPC-401 will be 20 mg.
Placebo
0.9% Sodium Chloride Injection, USP, or equivalent
Investigative Site, Westmead
Investigative Site, Liverpool
Investigative Site, Melbourne
Investigative Site, Herston
Investigative Site, Brisbane
Investigative Site, Murdoch
Investigative Site, New York
Investigative Site, Manhasset
Investigative Site, East Setauket
Investigative Site, Jacksonville
Investigative Site, Pessac
Investigative Site, Rennes
Investigative Site, Jackson
Investigative Site, Orléans
Investigative Site, Indianapolis
Investigative Site, Wyoming
Investigative Site, North Little Rock
Investigative Site, Dallas
Investigative Site, Fort Worth
Investigative Site, Houston
Investigative Site, San Antonio
Investigative Site, Los Angeles
Investigational Site, San Diego
Investigative Site, Rialto
Investigative Site, Bondy
Investigative Site, San Francisco
Investigative Site, Palo Alto
Investigative Site, Seattle
Investigative Site, Bradford
Investigative Site, Newcastle upon Tyne
Investigative Site, Portsmouth
Lead Sponsor
Collaborators (1)
PRA Health Sciences
INDUSTRY
La Jolla Pharmaceutical Company
INDUSTRY