RecruitingPhase 2NCT07532265

A Phase 2 Clinical Study to Evaluate the Efficacy and Safety of Frevecitinib (KN-002) in Patients With Severe Asthma

A Phase 2 Randomized Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Three Doses of Frevecitinib (KN-002) in Patients With Severe Asthma


Sponsor

Kinaset Therapeutics Inc

Enrollment

512 participants

Start Date

Jul 16, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

A Phase 2 Dose Ranging Study to Evaluate the Efficacy and Safety of Frevecitinib (KN-002) Over a 12-Week Treatment Period in Patients With Severe Asthma Not Controlled With Medium to High Dose ICS/LABA


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Frevecitinib and a drug called Placebo for people with severe asthma. The study is currently recruiting participants at 14 locations. People eligible for this study include aged 18 Years to 75 Years.

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

DRUGFrevecitinib

Frevecitinib (KN-002) delivered via a dry powder inhaler (DPI)

DRUGPlacebo

Matching placebo to frevecitinib


Locations(14)

Research site

Lancaster, California, United States

Research site

San Jose, California, United States

Research site

Brandon, Florida, United States

Research site

Miami, Florida, United States

Research site

Tampa, Florida, United States

Research site

Chicago, Illinois, United States

Research site

Kansas City, Missouri, United States

Research site

Charlotte, North Carolina, United States

Research site

Pittsburgh, Pennsylvania, United States

Research site

Rock Hill, South Carolina, United States

Research site

Dallas, Texas, United States

Research site

Houston, Texas, United States

Research site

San Antonio, Texas, United States

Research site

Williamsburg, Virginia, United States

View Full Details on ClinicalTrials.gov

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NCT07532265


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