Safety, Efficacy and Pharmacokinetic Characteristics of KR230109 Cream in Facial Acne Vulgaris

NCT ID: NCT07345390

Last Updated: 2026-01-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2026-01-10
• Study Completion Date: 2026-11-30

Brief Summary

This study will evaluate the safety, efficacy and pharmacokinetics of KR230109 cream compared with placebo in Patients (18-40 Years) with Acne vulgaris

Conditions

Acne Vulgaris

Study Design

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

Study Groups

KR230109 cream 0.025%

Participants applied KR230109 cream once daily for 12 consecutive weeks.

Group Type: EXPERIMENTAL

KR230109 cream 0.025%

Intervention Type: DRUG

KR230109 cream 0.025% is indicated for the topical treatment of acne vulgaris in patients

KR230109 cream 0.05%

Participants applied KR230109 cream once daily for 12 consecutive weeks.

Group Type: EXPERIMENTAL

KR230109 cream 0.05%

Intervention Type: DRUG

KR230109 cream 0.05% is indicated for the topical treatment of acne vulgaris in patients

placebo

Participants applied placebo once daily for 12 consecutive weeks.

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Vehicle cream manufactured to mimic look and feel of KR230109 Cream but without the active ingredient.

Interventions

KR230109 cream 0.025%

KR230109 cream 0.025% is indicated for the topical treatment of acne vulgaris in patients

Intervention Type: DRUG

KR230109 cream 0.05%

KR230109 cream 0.05% is indicated for the topical treatment of acne vulgaris in patients

Intervention Type: DRUG

Placebo

Vehicle cream manufactured to mimic look and feel of KR230109 Cream but without the active ingredient.

Intervention Type: DRUG

Other Intervention Names

Vehicle cream

Eligibility Criteria

Inclusion Criteria

1. Age between 18 and 40 years old (as of the time of signing the informed consent form), regardless of gender;

2. Patients clinically diagnosed with mild to moderate facial acne vulgaris (refer to the "Chinese Acne Treatment Guidelines" 2019 revised edition), and with an overall facial IGA (Investigator Global Assessment) score of 2 to 3 by the study doctor;

3. Baseline requirements: For patients with mild to moderate acne, the count of facial inflammatory lesions (papules and/or pustules) should be >=10 and <=40; the count of non-inflammatory lesions (open and/or closed comedones) should be >=20 and <=60; no facial nodules should exist;

4. Participants must be willing to use only non-acne-treating skin care products during the trial and comply with the precautions required by the protocol;

5. Fully understand the purpose and requirements of this trial, voluntarily participate in the clinical trial and sign the written informed consent form, and be able to complete the entire trial process as required;

6. From the time of signing the informed consent form to 3 months after the last administration, female participants of childbearing age or male participants whose partners are of childbearing age must agree and be able to take effective contraceptive measures, such as avoiding sexual activity or using reliable contraceptive methods like condoms or intrauterine devices.

Exclusion Criteria

1. Those known to be allergic to KR230109 or drugs with the same mechanism of action such as tazarotene, adapalene, or any of their components;

2. Those with a history of any serious clinical systemic diseases or surgeries, such as diseases of the circulatory system, nervous system, hematological system, immune system, or mental system;

3. Those with concurrent other obvious skin diseases at the affected area that may affect the clinical evaluation of the researchers or require concurrent treatment, such as solar dermatitis, psoriasis, seborrheic dermatitis, rosacea, eczema, severe acne, and extremely severe acne (such as conglobate acne, fulminant acne, etc.);

4. Those with secondary acne, such as occupational acne and acne caused by corticosteroids;

5. Those with facial skin or hair conditions that may interfere with clinical assessment (such as significant beards, sideburns, or mustaches);

6. Those who plan to use any adjunctive therapies or concomitant treatments for acne during the trial;

7. Those who have used acne-specific functional skin care products within one week before the start of treatment;

8. Those who have used topical retinoids, antibiotics, corticosteroids, or other topical acne treatments on the face within two weeks before the trial;

9. Those who have taken oral retinoids, antibiotics, corticosteroids (including intramuscular or intralesional injections, except for stable use of inhaled, intranasal, or intraocular corticosteroids for the treatment of underlying diseases and without impact on acne treatment), spironolactone, or other acne medications within four weeks before the trial;

10. Those who have undergone physical or chemical acne treatments within four weeks before the trial;

11. Those who have participated in other clinical trials and used trial drugs or medical devices within 90 days before screening or plan to participate in other clinical trials during the trial;

12. Those whose vital signs, physical examinations, laboratory tests (blood routine, urine routine, blood biochemistry), electrocardiograms, etc., are abnormal and have clinical significance as assessed by the researchers and may affect the evaluation of this trial;

13. Those who are positive for hepatitis B surface antigen, hepatitis C antibody, syphilis-specific antibody, or human immunodeficiency virus antibody;

14. Pregnant or lactating women or those with positive blood or urine pregnancy tests;

15. Those who need prolonged or excessive exposure to sunlight, such as sunbathing;

16. Those with a history of alcohol abuse or drug abuse;

17. Those who, in the opinion of the researchers, have poor compliance, or have conditions that may interfere with the study outcome, or those who, in the opinion of the researchers, have any other conditions that make them unsuitable for participation in this clinical trial.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Jiangxi Kerui Pharmaceutical Co., Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

jianzhong zhang, Master

Role: CONTACT

rmpkzc@163.com

+86 18001315877

cheng zhou, Doctor

Role: CONTACT

rmzjz@126.com

+86 18910291182

Other Identifiers

KR230109-202503

Identifier Type: -

Identifier Source: org_study_id