The purpose of this study is to evaluate the safety and tolerability of givosiran (ALN-AS1) in AIP patients as well as to characterize pharmacokinetics (PK) and pharmacodynamics (PD) of ALN-AS1 in AIP patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
40
Single or multiple doses of ALN-AS1 by subcutaneous (sc) injection
calculated volume to match active comparator
Clinical Trial Site
Birmingham, Alabama, United States
Clinical Trial Site
San Francisco, California, United States
Clinical Trial Site
New York, New York, United States
Clinical Trial Site
Galveston, Texas, United States
The safety of givosiran evaluated by the proportion of subjects experiencing adverse events (AEs), serious adverse events (SAEs), and AEs leading to study drug discontinuation
Time frame: Part A (SAD phase): through day 42; Part B (MAD) phase: through Day 70; Part C (MD) phase: through Day 168
Profile of Pharmacokinetics (PK) of givosiran
Cmax
Time frame: Part A (SAD) phase: predose - 42 days post-dose; Part B (MAD) phase: predose - 70 days post-dose; Part C (MD) phase: predose - 168 days post-dose
Profile of Pharmacokinetics (PK) of givosiran
tmax
Time frame: Part A (SAD) phase: predose - 42 days post-dose; Part B (MAD) phase: predose - 70 days post-dose; Part C (MD) phase: predose - 168 days post-dose
Profile of Pharmacokinetics (PK) of givosiran
AUC
Time frame: Part A (SAD) phase: predose - 42 days post-dose; Part B (MAD) phase: predose - 70 days post-dose; Part C (MD) phase: predose - 168 days post-dose
Profile of Pharmacokinetics (PK) of givosiran
t1/2
Time frame: Part A (SAD) phase: predose - 42 days post-dose; Part B (MAD) phase: predose - 70 days post-dose; Part C (MD) phase: predose - 168 days post-dose
The change in delta-aminolevulinic acid (ALA) from baseline
Time frame: Part A (SAD) phase: screening - 42 days post-dose; Part B (MAD) phase: screening - 70 days post-dose; Part C (MD) phase: screening - 168 days post-dose
The change in Porphobilinogen (PBG) from baseline
Time frame: Part A (SAD) phase: screening - 42 days post-dose; Part B (MAD) phase: screening - 70 days post-dose; Part C (MD) phase: screening - 168 days post-dose
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Clinical Trial Site
Stockholm, Sweden
Clinical Trial Site
London, United Kingdom