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NCT07412288 · ClinicalTrials.gov registry record · Phase 1

First-in-human Study of Orally Administered KT-579 in Healthy Adult Participants

A Phase 1 study of Healthy Participants, sponsored by Kymera Therapeutics.

Recruiting
Registry status
Phase 1
Development phase
96
Enrollment target
1
Study location

NCT07412288 is a Phase 1 study of Healthy Participants that is actively recruiting participants, run by Kymera Therapeutics. The registered enrollment target is 96 participants, above the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (48% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT07412288, a Phase 1 study of Healthy Participants, is actively recruiting participants, sponsored by Kymera Therapeutics.

RECRUITING
Registry status
Phase 1
Development phase
96 participants
Enrollment target
1
Study location

Study Summary

This is a first-in-human study to evaluate safety and tolerability, pharmacokinetics, and pharmacodynamics of single and multiple dose levels of KT-579 in healthy male and female adult participants.

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG KT-579

Study Locations (1)

Nebraska

  • Celerion - Lincoln

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 2026-02-23
Est. Completion 2026-12
Phase Phase 1

Sponsor

Kymera Therapeutics

10 total trials

What the Registry Record Tells You About NCT07412288

The ClinicalTrials.gov registry entry for NCT07412288 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 96 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 65-participant average among 119 other Healthy Participants trials with a reported enrollment target (48% higher). The listed sponsor is Kymera Therapeutics, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Participants appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT07412288 reports 1 study location spanning 1 distinct geographic area - top geographies include Nebraska.

Frequently Asked Questions

What is clinical trial NCT07412288 about?

NCT07412288 is a clinical study titled "First-in-human Study of Orally Administered KT-579 in Healthy Adult Participants". This is a first-in-human study to evaluate safety and tolerability, pharmacokinetics, and pharmacodynamics of single and multiple dose levels of KT-579 in healthy male and female adult participants.

What is the current status of trial NCT07412288?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 96 participants. The study started on 2026-02-23. Estimated completion is 2026-12.

What conditions does trial NCT07412288 study?

This clinical trial studies the following conditions: Healthy Participants.

What interventions are being tested in trial NCT07412288?

The interventions under investigation include: Placebo (DRUG), KT-579 (DRUG).

Who is sponsoring clinical trial NCT07412288?

This trial is sponsored by Kymera Therapeutics, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07412288 being conducted?

This trial has 1 study location across Nebraska. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.