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NCT06908707 · ClinicalTrials.gov registry record · Phase 1
A Study to Investigate Safety, Tolerability and Pharmacokinetics of LAE102 in Postmenopausal Women
A Phase 1 study, sponsored by Laekna Limited.
- Completed
- Registry status
- Phase 1
- Development phase
- 32
- Enrollment target
NCT06908707: Completed Phase 1 study, sponsored by Laekna Limited.
NCT06908707 is a Phase 1 study that has completed, run by Laekna Limited. The registered enrollment target is 32 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06908707, a Phase 1 study, has completed, sponsored by Laekna Limited.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 32 participants
- Enrollment target
Study Summary
The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of LAE102 in healthy postmenopausal women
Primary Outcome
Number of participants with SAEs \- Evaluation of Safety and Tolerability of LAE102
Interventions
- DRUG Placebo IV
- DRUG Placebo SC
- DRUG LAE102 SC
- DRUG LAE102 IV
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 32 participants |
| Start Date | 2025-04-22 |
| Est. Completion | 2025-10-23 |
| Phase | Phase 1 |
What the finished NCT06908707 record still lists
NCT06908707 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (47% lower).
The record links to 0 conditions, and to 4 interventions - of which Placebo IV is the first listed.
NCT06908707 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT06908707 about?
NCT06908707 is a clinical study titled "A Study to Investigate Safety, Tolerability and Pharmacokinetics of LAE102 in Postmenopausal Women". The purpose of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of LAE102 in healthy postmenopausal women
What is the current status of trial NCT06908707?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 32 participants. The study started on 2025-04-22. Estimated completion is 2025-10-23.
What interventions are being tested in trial NCT06908707?
The interventions under investigation include: Placebo IV (DRUG), Placebo SC (DRUG), LAE102 SC (DRUG), LAE102 IV (DRUG).
Who is sponsoring clinical trial NCT06908707?
This trial is sponsored by Laekna Limited, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT06908707's enrollment target sits among peer trials
32 1296th of 2000 higher than 679 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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