A Phase II, Placebo-controlled Trial Evaluating the Efficacy of Antroquinonol in Patients With Atopic Dermatitis

NCT ID: NCT04110873

Last Updated: 2019-10-01

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-07-27
• Study Completion Date: 2019-06-25

Brief Summary

Primary Objective:

To evaluate the activity of Antroquinonol in patients with atopic dermatitis.

Secondary Objective:

To assess the mechanism and cytokines change of Antroquinonol in patients with atopic dermatitis.

Exploratory Objective:

To explore potential relationships between Antroquinonol exposure and safety and efficacy endpoints.

Detailed Description

This is a Phase II, three-arms, double-blind, dosing-ranging, placebo-controlled trial evaluating the efficacy of Antroquinonol in patients with atopic dermatitis. The study is conducted in compliance with the guidelines for Good Clinical Practice and the Declaration of Helsinki. Approval is obtained from the local ethics committee or institutional review board at each study center. All the patients provided written informed consent.

60 patients totally (20 patients per arm) with atopic dermatitis will receive Antroquinonol or placebo. A patient will have received at one dose of Antroquinonol or placebo with tropical urea ointment and have three baseline scores assessment (see Statistical Methods). Enrollment will continue until the target number of evaluable patients has been enrolled.

Written informed consent must be obtained from all patients before initiating Screening. The Screening period will be up to 14 days in duration (Days -14 to -1). Following completion of all Screening assessments and confirmation of eligibility criteria, patients will receive Antroquinonol 50mg, 100mg or placebo per day (QD) on Day 0 for 12 weeks or until documented evidence of unacceptable toxicity, non-compliance or withdrawal of consent by the patient, or the investigator decides to discontinue treatment, whichever comes first. The time of study drug administration should be recorded in the patient diary.

Patients will attend study visits on Days 0, 28, 56 and 84. The following procedures will be performed according to the schedule of assessments: physical examination, vital signs, performance status, clinical laboratory tests, adverse events (AEs), concomitant medication and patient compliance.

Scores assessments will be performed at Screening, Day 28, Day 56 and Day 84 including EASI score, SCORAD, sIGA score, BSA affected by atopic dermatitis and pruritus verbal rating scale.

The primary endpoint is the percentage improvement between baseline and week 12 in Eczema Area and Severity Index (EASI).

Conditions

Atopic Dermatitis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Antroquinonol capsule 50mg

patients will receive Antroquinonol 50mg per day (QD) on Day 1 for 12 weeks

Group Type: EXPERIMENTAL

Antroquinonol Capsule 50mg

Intervention Type: DRUG

patients will receive Antroquinonol 50mg per day (QD) on Day 1 for 12 weeks

Antroquinonol capsule 100mg

patients will receive Antroquinonol 100mg per day (QD) on Day 1 for 12 weeks

Group Type: EXPERIMENTAL

Antroquinonol Capsule 100mg

Intervention Type: DRUG

patients will receive Antroquinonol 100mg per day (QD) on Day 1 for 12 weeks

Placebo oral capsule

patients will receive placebo per day (QD) on Day 1 for 12 weeks

Group Type: PLACEBO_COMPARATOR

Placebo oral capsule

Intervention Type: DRUG

patients will receive placebo per day (QD) on Day 1 for 12 weeks

Interventions

Antroquinonol Capsule 50mg

patients will receive Antroquinonol 50mg per day (QD) on Day 1 for 12 weeks

Intervention Type: DRUG

Antroquinonol Capsule 100mg

patients will receive Antroquinonol 100mg per day (QD) on Day 1 for 12 weeks

Intervention Type: DRUG

Placebo oral capsule

patients will receive placebo per day (QD) on Day 1 for 12 weeks

Intervention Type: DRUG

Other Intervention Names

Antroquinonol 50mg; Antroquinonol 100mg; Placebo

Eligibility Criteria

Inclusion Criteria

1. Patients between the ages of 20 and 65 years who had moderate-to-severe atopic dermatitis (using the Hanifin and Rajka Diagnostic Criteria)

2. Patients with body weight ≥ 25 kg and ≤ 120 kg, signing informed consent

3. To be eligible to participate, patients were required to have

1. a score of at least 5 on the Eczema Area and Severity Index (EASI), which ranges from 0 to 72, with higher scores indicating worse disease severity;

2. a score for pruritus of at least 30 mm on a visual-analogue scale, which ranges from 0 (no itch) to 100 mm (worst itch imaginable);

3. a score of at least 2 on the static Investigator's Global Assessment (sIGA), which ranges from 0 (clear) to 4 ( severe disease).

4. BSA affected or PSAI ≥ 5%

Exclusion Criteria

Patients meeting any of the following criteria must not be enrolled in the study:

1. Patients with active dermatologic diseases concomitant with atopic dermatitis.

2. Patients with severe medical condition(s) that in the view of the investigator prohibits participation in the study

3. Subjects with defective epidermal barrier(e.g Netherton's syndrome)

4. Any subject who is immunocompromised or has a history of malignant disease. This information will be gathered verbally from the patient while taking a medical history from the patient, and will not involve further testing such as an HIV test.

5. Subjects with a history of psychiatric disease or history of alcohol or drug abuse that would interfere with the ability to comply with the study protocol

6. Any noticeable breaks or cracks in the skin on either arm, including severely excoriated skin or skin with open or weeping wounds suggestive of an active infection or increased susceptibility to infection.

7. Ongoing participation in another investigational trial

8. Use of any oral or topical antibiotic for up to four weeks prior to the Treatment visit or active infection that in the opinion of the investigator would compromise the patient's ability to tolerate therapy

9. Use of any systemic immunosuppressive therapy (e.g. CsA, MTX, etc.) within four weeks of the Treatment visit.

10. Participant who has a condition or is in a situation that, in the investigator's opinion, may put the patient at significant risk, or may significantly interfere with the patient's participation in the study.

11. Subjects with prosthetic heart valves, pacemakers, intravascular catheters, or other foreign or prosthetic devices.

12. History of food or drug-related severe anaphylactoid or anaphylactic reaction(s)

13. Pregnancy or breastfeeding

14. History or presence of epilepsy, significant neurological disorders, cerebrovascular attack or ischemia

15. History or presence of myocardial infarction or cardiac arrhythmia under drug therapy

16. Patients who are unable to complete questionnaires on paper.

17. Clinically significant laboratory abnormalities.

18. History of malignancy of any organ system, treated or untreated.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Golden Biotechnology Corporation

INDUSTRY

Sponsor Role: collaborator

Chung Shan Medical University

OTHER

Sponsor Role: lead

Responsible Party

Cheng-Chung Wei

Chung Shan Medical University Hospital

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Wei C- C, M.D.

Role: PRINCIPAL_INVESTIGATOR

Chung Shan Medical University

Locations

Chung Shan Medical University Hospital

Taichung, , Taiwan

Countries

Taiwan

Other Identifiers

CS17155

Identifier Type: -

Identifier Source: org_study_id