Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

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 is a Phase 1 study that has completed, run by Thryv Therapeutics. The registered enrollment target is 50 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

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.

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

Sponsor

Thryv Therapeutics

5 total trials

What the Registry Record Tells You About NCT05759962

The ClinicalTrials.gov registry entry for NCT05759962 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Thryv Therapeutics, which has 5 total studies on file at ClinicalTrials.gov.

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

NCT05759962 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.