Jaktinib Hydrochloride Cream For Atopic Dermatitis
- Conditions
- Atopic Dermatitis
- Interventions
- Drug: Placebo
- Registration Number
- NCT04435392
- Lead Sponsor
- Suzhou Zelgen Biopharmaceuticals Co.,Ltd
- Brief Summary
This study includes a dose escalation part and a dose extension part.
- Detailed Description
In the dose-increasing part, a multicenter, dose-increasing, randomized, double-blind, placebo-parallel control design was adopted. Subjects were enrolled into different dose groups in sequence according to the inclusion sequence, and each group was scheduled to give the drug for 8 weeks.Subjects in each group were observed for 4 weeks after administration. When the number of ≥2 grade drug-related adverse events (cases) was less than 50%, subjects in the next group could be enrolled.Otherwise, IDMC will decide whether to continue the next set of tests.Subjects in each group were randomly assigned to receive either Jaktinib cream (6 cases) or placebo (2 cases) in a ratio of 3 to 1.A total of 32 subjects are expected to be enrolled in 6 centers.
The dose expansion was a multicenter, randomized, double-blind, placebo-parallel control design in which subjects were randomly assigned to 3 groups (1 placebo group and 2 experimental drugs group).It is estimated that a total of 60 subjects will be enrolled in about 15 centers. This part is divided into two stages.Stage 2 test (9 \~ 16 weeks) : Extension test.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 107
- 18~ 65 years old (including boundary value), gender is not limited;
- Have a clinical diagnosis of atopic dermatitis;
- Have a PGA(Physician's Global Assessment) score of 2 (mild) or 3 (moderate) at baseline;
- The total area of atopic dermatitis is about 10%~20% of the total area of the body surface at baseline.
- Evidence of certain skin conditions/infections at baseline;
- Have certain laboratory abnormalities at baseline;
- Females who are pregnant, breastfeeding, or are of childbearing potential not using highly effective contraception;
- Other conditions that the investigators considered inappropriate to participate in the trial.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Dose extension: low-dose group, X% Jaktinib Hydrochloride Cream X% based on results of part 1. The Jaktinib Hydrochloride X% Cream will be applied topically twice daily Dose extension: high-dose group, Y% Jaktinib Hydrochloride Cream Y% based on results of part 1. The Jaktinib Hydrochloride Y% Cream will be applied topically twice daily Part 1: Cohort 2,1.5% Jaktinib Bid Jaktinib Hydrochloride Cream Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 1.5% Cream will be applied topically twice daily. Part 1: Cohort 3, 2.5% Jaktinib Qd Jaktinib Hydrochloride Cream Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 2.5% Cream will be applied topically Once daily. Part 1: Cohort 3, 2.5% Jaktinib Qd Placebo Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 2.5% Cream will be applied topically Once daily. Part 1: Cohort 4, 2.5% Jaktinib Bid Placebo Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 2.5% Cream will be applied topically twice daily. Part 1: Cohort 4, 2.5% Jaktinib Bid Jaktinib Hydrochloride Cream Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 2.5% Cream will be applied topically twice daily. Dose extension: Vehicle Control Placebo the Vehicle Control cream will be applied topically twice daily Part 1: Cohort 1, 0.5% Jaktinib Bid Placebo Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 0.5% Cream will be applied topically twice daily. Part 1: Cohort 2,1.5% Jaktinib Bid Placebo Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 1.5% Cream will be applied topically twice daily. Part 1: Cohort 1, 0.5% Jaktinib Bid Jaktinib Hydrochloride Cream Subjects were randomly assigned to receive either Jaktinib cream or a placebo in a ratio of 3 to 1.The Jaktinib hydrochloride 0.5% Cream will be applied topically twice daily.
- Primary Outcome Measures
Name Time Method Proportion of Participants Achieving Physician's Global Assessment (PGA) Response of Clear or Almost Clear 7 days after the last dose A total PGA score of 0 or 1 or a decrease of ≥2 from baseline
- Secondary Outcome Measures
Name Time Method Proportion of Participants With Response of Clear or Almost Clear From Baseline Treatment at 8,16 weeks PGA score of 0 or 1
Trial Locations
- Locations (1)
The Second Xiangya Hospital of Central South University
🇨🇳Changsha, Hunan, China