Trial to Evaluate the Effect of Inclisiran Treatment on Low Density Lipoprotein Cholesterol (LDL-C) in Subjects With Heterozygous Familial Hypercholesterolemia (HeFH)

Inclusion Criteria:

Participants may be included if they meet all of the following inclusion criteria prior to
randomization:

1. Male or female participants ≥18 years of age.

2. History of HeFH with a diagnosis of HeFH by genetic testing; and/or a documented
history of untreated LDL-C of >190 mg/dL, and a family history of familial
hypercholesterolemia, elevated cholesterol or early heart disease that may indicate
familial hypercholesterolemia.

3. Serum LDL-C ≥2.6 millimoles (mmol)/liter (L) (≥100 mg/dL) at screening.

4. Fasting triglyceride <4.52 mmol/L (<400 mg/dL) at screening.

5. Participants on statins should be receiving a maximally tolerated dose.

6. Participants not receiving statins must have documented evidence of intolerance to all
doses of at least 2 different statins.

7. Participants on lipid-lowering therapies (such as a statin and/or ezetimibe) should be
on a stable dose for ≥30 days before screening with no planned medication or dose
change during study participation.

Exclusion Criteria:

Participants will be excluded from the study if any of the following exclusion criteria
apply immediately prior to randomization:

1. New York Heart Association (NYHA) class IV heart failure.

2. Uncontrolled cardiac arrhythmia

3. Uncontrolled severe hypertension

4. Active liver disease

5. Females who are pregnant or nursing, or who are of childbearing potential and
unwilling to use at least 2 methods of highly effective contraception (failure rate
less than 1% per year) (combined oral contraceptives, barrier methods, approved
contraceptive implant, long-term injectable contraception, or intrauterine device) for
the entire duration of the study. Exemptions from this criterion:

1. Women >2 years postmenopausal (defined as 1 year or longer since last menstrual
period) AND more than 55 years of age.

2. Postmenopausal women (as defined above) and less than 55 years of age with a
negative pregnancy test within 24 hours of randomization.

3. Women who are surgically sterilized at least 3 months prior to enrollment.

6. Males who are unwilling to use an acceptable method of birth control during the entire
study period (condom with spermicide).

7. Treatment with other investigational products or devices within 30 days or 5
half-lives of the screening visit, whichever is longer.

8. Treatment (within 90 days of screening) with monoclonal antibodies directed towards
PCSK9.

The above information is not intended to contain all considerations relevant to a
participant's potential participation in a clinical trial.