Status:
RECRUITING
A Phase I Study of QLS12010 Capsules: Safety, Tolerability, PK, PD, and Food Effects in Healthy Adults and Moderate to Severe Atopic Dermatitis Patients
Lead Sponsor:
Shanghai Qilu Pharmaceutical Research and Development Center LTD
Conditions:
Atopic Dermatitis
Hidradenitis Suppurativa (HS)
Eligibility:
All Genders
18-75 years
Phase:
PHASE1
Brief Summary
The goal of this clinical trial is to evaluate the safety, tolerability, PK, and PD of single and multiple ascending doses of QLS12010 Capsules and the effect of food on their PK profiles in healthy a...
Eligibility Criteria
Inclusion
- Inclusion Criteria for Parts A-C:
- Males and females aged 18-45 (inclusive),
- Weight: ≥ 50 kg for males and ≥ 45 kg for females, body mass index (BMI): 18.0-30.0 kg/m2 (inclusive),
- Inclusion Criteria for Part D:
- Female or male participants between the ages of 18 to 75 years of age.
- Chronic AD diagnosed by the criteria of Hannifin and Rajka that has been present for at least 6 Months before the Screening Visit.
- At screening and baseline: EASI score ≥ 16, vIGA-AD™ score ≥ 3, and BSA affected by AD ≥ 10%;
- The weekly mean score of PP NRS ≥ 4 prior to the first administration (with assessment results for at least 4 days during the week before the first administration \[D-7 to D-1\]);
- As judged by the investigator, within 6 months prior to screening, the patient had an inadequate response to topical medication therapy.
- General Exclusion Criteria:
- Participants with diseases that should be excluded as judged by the investigator at screening, including but not limited to the nervous system, psychiatric system, cardiovascular system, blood and lymphatic system, immune system, respiratory system, digestive system, urinary system, metabolic and skeletal system disorders,
- The 12-lead ECG at screening shows QTcF (QT corrected using Fridericia's formula) \> 450 ms. If QTcF is \> 450 ms, the 12-lead ECG should be repeated 2 more times (at least 3 min apart), and the mean of the 3 measurements will be used to determine whether the participant meets the inclusion criteria,
- Participants who smoke more than 5 cigarettes per day on average within 6 months before screening or are currently using e-cigarettes,
- Participants who consume more than 14 units of alcohol per week (1 unit = 360 mL of beer, 45 mL of 40% spirits, or 150 mL of wine) within 6 months before screening or have a positive breath alcohol test at screening,
- Participants who have donated more than 400 mL of blood within 3 months or more than 200 mL of blood within 4 weeks before screening, or plan to donate blood during the study,
- Participants who have received any strong inhibitor or inducer of CYP3A4 within 4 weeks before screening,
- Participants who have received any prescription drugs, OTC drugs, traditional medicines, and dietary supplements within 2 weeks before the first dose or 5 half-lives (whichever is longer).
- Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Exclusion
Key Trial Info
Start Date :
March 31 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2026
Estimated Enrollment :
102 Patients enrolled
Trial Details
Trial ID
NCT06946641
Start Date
March 31 2025
End Date
April 1 2026
Last Update
July 31 2025
Active Locations (1)
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1
Peking University Third Hospital
Beijing, China