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A Study of Remternetug (LY3372993) in Healthy Participants

← catalyst calendar

NCT07056309

Sponsored by Eli Lilly and Company (industry) · LLY — their whole pipeline →.

Phase
Phase 1
Status
Completed
Study type
Interventional
Design
Randomized · None · Basic science
Enrollment
72actual
Sites
3
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-06-24actualWhen the study began enrolling
Primary completion2025-12-15actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-12-15actualThe whole study's end, after follow-up
First posted2025-07-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-01-23actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Healthy

Interventions

  • Drug: Remternetug (Test) — also filed as LY3372993
  • Drug: Remternetug (Reference) — also filed as LY3372993

Primary outcomes

what the primary-completion date above is the date OF
Pharmacokinetic (PK): Maximum Concentration (Cmax) of Remternetug
measured Predose up to Day 85
Pharmacokinetic (PK): Area Under the Concentration Versus Time Curve from Zero to time t [AUC(0-t)] of Remternetug
measured Predose up to Day 85
Pharmacokinetic (PK): Area Under the Concentration Versus Time Curve from Zero to Infinity [AUC(0-inf)] of Remternetug
measured Predose up to Day 85

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