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Study identifier: NCT06082323 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Single and Multiple Ascending Dose Trial of LT-002-158 Tablets in Healthy Adult Volunteers

Condition: Healthy Volunteer · Hidradenitis Suppurativa · Atopic Dermatitis  ·  Sponsor: Leadingtac Pharmaceutical (Shaoxing) Co., Ltd.

PhasePhase 1
Planned participants127
Who can joinAll sexes, 18 Years to 55 Years
Healthy volunteersYes

About this study

LT-002-158 is an oral IRAK4 protein degrader being developed for the treatment of autoimmune disease and inflammation including Hidradenitis Suppurativa and Atopic Dermatitis. This first-in-human (FIH) study will characterize the safety, tolerability and the pharmacokinetics/pharmacodynamics (PK/PD) of a single ascending dose and multiple ascending doses of LT-002-158 in healthy volunteers. The effects of food on the pharmacokinetics of LT-002-158 will also be assessed in healthy volunteers.

This description comes directly from the study's public registry record.

Talk to the study team

Qian Chen, MD  ·  +86-012-54036058  ·  qchen@shxh-centerlab.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai Xuhui Distric Central HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06082323