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Phase 1 Completed N=36 Randomized Double-blind Basic Science

A Study of Donanemab (LY3002813) in Healthy Chinese Participants

Healthy
Source: ClinicalTrials.gov NCT05533411 ↗
Enrolled (actual)
36
Serious AEs
0.0%
Results posted
Oct 2024
Primary outcomePrimary: Number of Participants With One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration — 1; 2; 0; 0 participants

Summary

The main purpose of this study is to evaluate the safety and tolerability of donanemab (LY3002813) when administered as single dose in healthy Chinese participants. The study will also assess how fast donanemab gets into the blood stream and how long it takes the body to remove it. The study is open to healthy participants. The study will last up to approximately 85 days.

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
1; 2; 0; 0; 0; 0
SECONDARY
Pharmacokinetics (PK): Maximum Observed Concentration (Cmax) of Donanemab
119; 236; 539
SECONDARY
PK: Area Under the Concentration Versus Time Curve From Zero to Infinity (AUC[0-∞]) of Donanemab
9050; 22600; 53100

Eligibility Criteria

Inclusion Criteria

  • Participants who are overtly healthy as determined by medical evaluation
  • Participants are native Chinese participants. To qualify as a native Chinese, the participant, the participant's biological parents, and all four of the participant's biological grandparents must be of Chinese origin.
  • Have a body mass index (BMI) of 18.0 and 28.0, kilograms per meter squared (kg/m²), inclusive.

Exclusion Criteria

  • Are lactating.
  • Are women of childbearing potential.
  • Have known allergies to donanemab, related compounds or any components of the formulation or history of significant atopy.
  • Have received treatment with biologic agents (such as monoclonal antibodies, including marketed drugs) within three months or five half-lives (whichever is longer) prior to dosing.
  • Have participated, within the last 30 days, in a clinical study involving an investigational product; at least five half-lives or 30 days (whichever is longer) should have passed.
  • Have history of intracranial hemorrhage, cerebrovascular aneurysm or arteriovenous malformation, or carotid artery occlusion, stroke or epilepsy.
  • Participants who show evidence of positive HIV antibodies, or positive hepatitis C antibody, or positive hepatitis B surface antigen
  • Have had leukemia, lymphoma, or any malignancy within the past five years except for basal cell or squamous epithelial carcinomas of the skin that have been resected with no evidence of metastatic disease for three years. Have had breast cancer within the past 10 years.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05533411). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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