Study of Lumasiran in Healthy Adults and Patients With Primary Hyperoxaluria Type 1

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

52

Participants

Timeline

Start Date

March 8, 2016

Primary Completion Date

January 23, 2019

Study Completion Date

January 23, 2019

Conditions
Primary Hyperoxaluria Type 1 (PH1)
Interventions
DRUG

Lumasiran

Lumasiran will be administered SC once in Part A. In Part B lumasiran will be administered SC qM (Days 1, 29 and 57) or q3M (Days 1 and 85).

DRUG

Placebo

Matching placebo (sterile saline: 0.9% sodium chloride \[NaCl\]) will be administered SC once in Part A. In Part B matching placebo will be administered SC qM (Days 1, 29 and 57) or q3M (Days 1 and 85).

Trial Locations (9)

Unknown

Clinical Trial Site, Bordeaux

Clinical Trial Site, Lyon

Clinical Trial Site, Paris

Clinical Trial Site, Bonn

Clinical Trial Site, Haifa

Clinical Trial Site, Jerusalem

Clinical Trial Site, Amsterdam

Clinical Trial Site, Birmingham

Clinical Trial Site, London

Sponsors
All Listed Sponsors
lead

Alnylam Pharmaceuticals

INDUSTRY