RecruitingPhase 2NCT07323654

A Study of KT-621 Administered Orally to Adult Participants With Moderate to Severe Eosinophilic Asthma

A Phase 2b, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter, Dose-ranging Study Investigating the Efficacy and Safety Profile of KT-621 Administered Orally to Adult Participants With Uncontrolled Moderate to Severe Eosinophilic Asthma


Sponsor

Kymera Therapeutics, Inc.

Enrollment

264 participants

Start Date

Jan 28, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

This Phase 2b study is designed to evaluate the safety and efficacy of KT-621 in participants with uncontrolled moderate to severe eosinophilic asthma. The main goals of this study are to investigate how effective KT-621 is at treating uncontrolled moderate to severe eosinophilic asthma, the safety and tolerability of KT-621, and how KT-621 behaves in the body.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new oral pill called KT-621 in adults with moderate to severe eosinophilic asthma — a type of asthma driven by an overactive immune response involving high levels of a white blood cell called eosinophils. Despite being on maximum inhaler therapy, these patients still experience frequent asthma attacks. **You may be eligible if...** - You are 18–75 years old - You have had a doctor's diagnosis of asthma for at least 1 year - You are already on medium to high dose inhaled corticosteroids plus a long-acting bronchodilator (LABA) for at least 12 weeks - Your eosinophil count in blood tests is elevated - Your lung function test shows airflow limitation, but still responds to a rescue inhaler - You had at least one asthma attack in the past year requiring steroids or a hospital visit - Your asthma control questionnaire score indicates poor control **You may NOT be eligible if...** - You have a serious infection, immune condition, or other uncontrolled medical problem - You are pregnant, planning to become pregnant, or not using contraception Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGKT-621

Oral drug

OTHERPlacebo

Oral placebo matched to KT-621


Locations(17)

Kymera Investigative Site

Redding, California, United States

Kymera Investigative Site

Upland, California, United States

Kymera Investigative Site

Miami, Florida, United States

Kymera Investigative Site

Miami, Florida, United States

Kymera Investigative Site

Tampa, Florida, United States

Kymera Investigative Site

East Point, Georgia, United States

Kymera Investigative Site

Edmond, Oklahoma, United States

Kymera Investigative Site

Clackamas, Oregon, United States

Kymera Investigative Site

Pittsburgh, Pennsylvania, United States

Kymera Investigative Site

North Charleston, South Carolina, United States

Kymera Investigative Site

Rock Hill, South Carolina, United States

Kymera Investigative Site

Chattanooga, Tennessee, United States

Kymera Investigative Site

McKinney, Texas, United States

Kymera Investigative Site

Belgrade, Serbia

Kymera Investigative Site

Kamenitz, Serbia

Kymera Investigative Site

Užice, Serbia

Kymera Investigative Site

Bedford, United Kingdom

View Full Details on ClinicalTrials.gov

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NCT07323654


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