A Study of LY3473329 in Healthy Participants

NCT04472676 | Completed Phase 1

• 3 other identifiers: 17611J2O-MC-EKBA2020-002522-91
• Study Type: interventional
• Target: 86
• Locations: 1 country
• Sites: 1

Brief Summary

The main purpose of this study in healthy participants is to learn more about the safety of LY3473329 and any side effects that might be associated with it. Blood tests will be performed to check how much LY3473329 gets into the bloodstream and how long the body takes to eliminate it. This is a two-part study. Participants may only enroll in one part. For each participant:

• Part A will last up to about 19 weeks and may include 9 visits.
• Part B will last up to about 28 weeks and may include 11 visits.

Conditions

Healthy

Outcome Measures

Primary Outcomes (1)

• Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration

  A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module

  Baseline up to Day 137

Secondary Outcomes (2)

• Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY3473329

  Baseline up to Day 137

• PK: Maximum Observed Drug Concentration (Cmax) of LY3473329

  Baseline up to Day 137

Study Arms (4)

LY3473329 (Part A)

EXPERIMENTAL

LY3473329 administered orally.

Drug: LY3473329

Placebo (Part A)

PLACEBO COMPARATOR

Placebo administered orally.

Drug: Placebo

LY3473329 (Part B)

EXPERIMENTAL

LY3473329 administered orally.

Drug: LY3473329

Placebo (Part B)

EXPERIMENTAL

Placebo administered orally.

Drug: Placebo

Interventions

LY3473329 DRUG

Administered orally.

LY3473329 (Part A); LY3473329 (Part B)

Placebo DRUG

Administered orally.

Placebo (Part A); Placebo (Part B)

Eligibility Criteria

• Age: 18 Years - 54 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Males and females must adhere to contraception restrictions
• Have clinical laboratory test results within normal reference range or with acceptable deviations
• Body mass index (BMI) less than or equal to (≤)30 kilograms per square meter (kg/m²)
• For Part B:
• Lipoprotein (a) (Lp\[a\]) greater than or equal to (≥)75 nanomoles per Liter (nmol/L) or 30 milligrams per deciliter (mg/dL) at screening
• Plasminogen is within the normal range at screening

You may not qualify if:

• Are currently enrolled in, or discontinued within the past 30 days from, a clinical trial involving an investigational drug that has not received regulatory approval for any indication, except for any trial involving antisense Lp(a), for which 6 months must have passed from the participant's last study drug dose
• Have previously completed or withdrawn from this study or any other study investigating LY3473329
• Are pregnant or breast feeding
• Glomerular filtration rate (GFR) is lower than estimated GFR 60 milliliters per minute per 1.73 square meters (mL/min/1.73 m2) using the Modification of Diet in Renal Disease Study equation
• Have a history or presence of medical illness including, but not limited to, any cardiovascular, thromboembolism or bleeding disorder, hepatic, respiratory, hematological, endocrine, immune, psychiatric or neurological disease, convulsions, or any clinically significant laboratory abnormality that, in the judgment of the investigator, indicate a medical problem that would preclude study participation
• Have an abnormality in the 12-lead electrocardiogram (ECG) that, in the opinion of the investigator, increases the risks associated with participating in the study. In addition, participants with the following findings will be excluded: Confirmed Fridericia's corrected QT interval greater than (\>)450 milliseconds (msec) for men and \>470 msec for women. One additional ECG may be performed if required
• Have an elevated high-sensitivity C-reactive protein (\>3 milligrams per Liter \[mg/L\]) or have a prothrombin time/international normalized ratio (PT/INR) or activated partial thromboplastin time (aPTT) \>1.25 times (x) upper limit of normal (ULN)
• Are an investigator or site personnel directly affiliated or immediate families. Immediate family is defined as a spouse, parent, child or sibling, whether biological or legally adopted
• Are Lilly employees or contractors or an immediate family member of such
• Show evidence of human immunodeficiency virus (HIV) and/or positive human HIV antibodies, hepatitis C and/or positive hepatitis C antibody, or hepatitis B and/or positive hepatitis B surface antigen
• Have donated more than 500 milliliters (mL) of blood within the past month
• Are unwilling to stop alcohol consumption while resident in the clinical research unit (CRU)
• Have an average weekly alcohol intake that exceeds 21 units per week (1 unit = 12 ounces \[oz\] or 360 mL of beer; 5 oz or 150 mL of wine; 1.5 oz or 45 mL of distilled spirits)
• Have an abnormal blood pressure (supine) defined as diastolic blood pressure \>95 or less than (\<)45 millimeters of Mercury (mmHg) and/or systolic blood pressure \>160 or \<90 mmHg. Re-testing may occur once during screening within 2 hours of the initial abnormal blood pressure measurement at the discretion of the investigator at screening
• Have positive findings for known drugs of abuse on urinary drug screening

Sponsors & Collaborators

• Eli Lilly and Company: lead

Study Sites (1)

PRA Health Sciences

Groningen, 9728, Netherlands

Location

Related Publications (2)

• Karp A, Jacobs M, Barris B, Labkowsky A, Frishman WH. Lipoprotein(a): A Review of Risk Factors, Measurements, and Novel Treatment Modalities. Cardiol Rev. 2025 Jul-Aug 01;33(4):352-358. doi: 10.1097/CRD.0000000000000667. Epub 2024 Feb 28.

  PMID: 38415744 DERIVED

• Nicholls SJ, Nissen SE, Fleming C, Urva S, Suico J, Berg PH, Linnebjerg H, Ruotolo G, Turner PK, Michael LF. Muvalaplin, an Oral Small Molecule Inhibitor of Lipoprotein(a) Formation: A Randomized Clinical Trial. JAMA. 2023 Sep 19;330(11):1042-1053. doi: 10.1001/jama.2023.16503.

  PMID: 37638695 DERIVED

Study Officials

• Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST)

  Eli Lilly and Company

  STUDY DIRECTOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, INVESTIGATOR
• Purpose: BASIC SCIENCE
• Intervention Model: SEQUENTIAL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: July 14, 2020
• First Posted: July 15, 2020
• Study Start: August 18, 2020
• Primary Completion: November 9, 2021
• Study Completion: November 9, 2021
• Last Updated: December 14, 2021

Record last verified: 2021-12

Data Sharing

• IPD Sharing: Will not share

Locations

NL (1)