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NCT05759962 · ClinicalTrials.gov registry record · Phase 1

Phase 1 Study of LQT-1213 in Healthy Adults

A Phase 1 study, sponsored by Thryv Therapeutics.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target

NCT05759962: Completed Phase 1 study, sponsored by Thryv Therapeutics.

NCT05759962 is a Phase 1 study that has completed, run by Thryv Therapeutics. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05759962, a Phase 1 study, has completed, sponsored by Thryv Therapeutics.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

This is a single-center, randomized, double-blind, placebo-controlled study to be conducted in 2 parts: single ascending dose (SAD) incorporating a food effect arm and multiple ascending dose (MAD). Potential participants for each part will undergo screening procedures within 28 days of enrollment.

Primary Outcome

Number of Participants with Adverse Events

Interventions

  • OTHER Placebo
  • DRUG LQT-1213

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2022-09-14
Est. Completion 2023-03-05
Phase Phase 1
Thryv Therapeutics

5 total trials

What the finished NCT05759962 record still lists

NCT05759962 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT05759962 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05759962 about?

NCT05759962 is a clinical study titled "Phase 1 Study of LQT-1213 in Healthy Adults". This is a single-center, randomized, double-blind, placebo-controlled study to be conducted in 2 parts: single ascending dose (SAD) incorporating a food effect arm and multiple ascending dose (MAD). Potential participants for each part will undergo screening procedures within 28 days of enrollment.

What is the current status of trial NCT05759962?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2022-09-14. Estimated completion is 2023-03-05.

What interventions are being tested in trial NCT05759962?

The interventions under investigation include: Placebo (OTHER), LQT-1213 (DRUG).

Who is sponsoring clinical trial NCT05759962?

This trial is sponsored by Thryv Therapeutics, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05759962's enrollment target sits among peer trials

50 973rd of 2000 higher than 984 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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Source: ClinicalTrials.gov NCT05759962, the US trial registry maintained by the National Library of Medicine. NCT05759962 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.