First in Human Study in Healthy Volunteers of Antimicrobial Peptide PL-18 Vaginal Suppositories

NCT ID: NCT05340790

Last Updated: 2023-12-11

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-08-01
• Study Completion Date: 2024-03-01

Brief Summary

This is a Single-center, Randomized, Double-blind, Placebo-controlled Phase I Study to Evaluate the Safety, Tolerability and PK Profiles of Single and Multiple Ascending Doses of Antimicrobial Peptide PL-18 Vaginal Suppositories.

Detailed Description

Subjects who provide written informed consent to participate voluntarily in the clinical study will be screened. Eligible subjects will be sequentially enrolled into the above five sequential cohorts and randomized to receive PL-18 (cohort 1: n=8; cohort 2/3/4/5: n=6) or matching placebo (n=2). Subjects will be observed for 3 days after a single dose and receive PL-18 or placebo, once daily, for 6 consecutive days, if no grade ≥2 drug-related adverse events (AEs) occur. During the study, PK sample collection, physical examination, vital signs, laboratory tests, electrocardiography (ECG) and tolerance evaluation will be performed based on the protocol schedule.

To ensure the safety of the subjects, two sentinel subjects will be enrolled first in each cohort; one subject will be randomized to receive PL-18, and the other subject randomized to receive placebo. The safety data of the two sentinel subjects from initiation of single dosing to the last drug administration of multiple dosing on D11 will be reviewed by the investigator and sponsor before the subsequent subjects in that dose cohort are enrolled. Subsequent subjects could be simultaneously enrolled, with one randomized to receive placebo and others randomized to receive PL-18.

Conditions

Colpomycosis; Bacterial Vaginosis; Mixede Vaginitis

Study Design

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

Study Groups

Antimicrobial Peptide PL-18 Vaginal Suppositories

Dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Group Type: EXPERIMENTAL

Dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Intervention Type: DRUG

Escalating doses of 1 mg (0.1%)、2.5mg (0.25%)、5 mg (0.5%)、10mg (1%)、15 mg (1.5%)；single dose administration；topical vaginal suppository ；multiple-dose administration after single dose administration a 3-day wash out period ; once-daily for 6 consecutive days;

Placebo dose

Placebo dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Group Type: PLACEBO_COMPARATOR

Placebo dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Intervention Type: DRUG

Dose 1、2、3、4 and 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories respective placebos；single dose administration；topical vaginal suppository ；multiple-dose administration after single dose administration a 3-day wash out period ; once-daily for 6 consecutive days;

Interventions

Dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Escalating doses of 1 mg (0.1%)、2.5mg (0.25%)、5 mg (0.5%)、10mg (1%)、15 mg (1.5%)；single dose administration；topical vaginal suppository ；multiple-dose administration after single dose administration a 3-day wash out period ; once-daily for 6 consecutive days;

Intervention Type: DRUG

Placebo dose 1 to 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories

Dose 1、2、3、4 and 5 of Antimicrobial Peptide PL-18 Vaginal Suppositories respective placebos；single dose administration；topical vaginal suppository ；multiple-dose administration after single dose administration a 3-day wash out period ; once-daily for 6 consecutive days;

Intervention Type: DRUG

Other Intervention Names

AMP PL-18; Placebo PL-18

Eligibility Criteria

Inclusion Criteria

• A subject will be eligible for inclusion in this study only if all of the following criteria are met:

1. Voluntarily signed written informed consent;

2. Ability to comprehend the purpose of the study; ability to co-operate with the investigator and comply with all study requirements;

3. Adult females aged between 18 and 55 years (inclusive);

4. Body weight between 50 and 100 kg (inclusive) and body mass index (BMI) within 18~32 kg/m2 (inclusive).

5. In good health as determined by screening tests. Good health is defined as having no clinically relevant abnormalities identified by a detailed medical history, full physical examination (including measurement of blood pressure and pulse rate), 12-lead ECG, and clinical laboratory tests:

• Vital signs (measured after resting for 5 minutes seated position) within normal range, or outside the normal range and not considered clinically significant by the Investigator;
• Standard 12-lead ECG parameters (recorded after resting for 5 minutes in supine position) in the following ranges; QTc (Fridericia algorithm recommended) ≤470 ms, and normal ECG tracing, or abnormal ECG tracing not considered clinically relevant by the Investigator;
• Laboratory parameters demonstrating no clinically significant abnormalities, as determined by the Investigator. A total bilirubin outside the normal range may be acceptable if total bilirubin does not exceed 1.5 × ULN conjugated bilirubin (with the exception of a participant with documented Gilbert syndrome).

6. Self-report regular menstrual cycle (21-35 days), and planned to avoid menstruation from the first administration until 7 days after the last administration;

7. Negative human papilloma virus (HPV) test result (at screening or negative HPV test result performed in study site within 2 months prior to screening;

8. History of sexual life, including vaginal intercourse;

9. Be willing to use vaginal suppositories;

10. Currently in a mutually monogamous sexual relationship or no sexual activity;

11. Sexual abstinence from 72 hours prior to the first drug administration until 7 days after the last administration;

12. Agreement to avoid the use of any other intravaginal products (i.e., contraceptive creams, gels, foams, sponges, lubricants, irrigation solutions, etc.) from screening until 7 days after the last administration;

13. Subjects in a intercourse relationship must agree to use highly effective methods of contraception (as specified in Section 4.6.3) from informed consent obtained until 3 months after the last administration, and pregnancy test results must be negative at screening.

Exclusion Criteria

1. Significant deep epithelial disruption by colposcopy at screening;

2. Anatomical anomalies of the genito-urinary tract and vaginal prolapse;

3. Genitourinary infections at screening or within 21 days prior to screening, including but not limited to bacterial urinary tract infection, bacterial vaginosis, trichomoniasis and vulvovaginal candidiasis;

4. Known, active sexually transmitted infection (STI) in partner, as per anamnesis;

5. Two or more confirmed trichomoniasis, gonococcal, chlamydia trachomatis or syphilis spirochete infections within 180 days prior to screening;

6. History of recurrent genital herpes or active herpes simplex virus (HSV) at screening;

7. Hepatitis B virus, hepatitis C virus, human immunodeficiency virus (HIV), syphilis infection, or positive hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb), hepatitis C virus antibody (HCVAb), HIV antibody (HIVAb), treponema pallidum antibody (TP-Ab) at screening;

8. History of clinically severe relevant cardiovascular, hepatic, renal, pulmonary, gastrointestinal, endocrine, or neurological diseases that, in the investigator's opinion, may interfere with the aim of the study or affect the subject's safety;

9. Uncontrolled or acute illness that may complicate the study evaluation in the investigator's opinion;

10. History of hysterectomy;

11. Pelvic surgery within 90 days prior to screening;

12. Cervical cryotherapy or cervical laser treatment within 90 days prior to screening;

13. Intrauterine device insertion or removal within 90 days prior to screening;

14. Any antibiotic or antifungal therapy (intravaginal or systemic) within 30 days prior to screening;

15. Immunosuppressive therapy within 60 days prior to screening;

16. Ascertained or presumptive hypersensitivity (including allergies) to any ingredient of the investigational medicinal product (IMP); history of other significant anaphylaxis to drugs or allergic reactions in general;

17. Pregnant or lactating women, or women within 60 days of the last pregnancy;

18. Subjects who consume or are unable to abstain from products containing caffeine/xanthine within 24 hours before a visit or admission;

19. History of drug or alcohol abuse within 1year prior to screening, or a positive result of drug abuse or alcohol breath test at screening or check-in;

20. Previously dosed with an investigational drug within 3 months prior to Day 1 or still participating in another trial at the time of screening;

21. Any vaccination from the 28 days prior to administration of the first dose until 28 days after the last dose;

22. Those considered by the investigator as inappropriate to participate in the study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Protelight Pharmaceuticals Australia PTY LTD

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John McNeil, Professor

Role: STUDY_CHAIR

90768825

Locations

Q-Pharm Pty. Ltd

Brisbane, Queensland, Australia

Site Status: RECRUITING

Countries

Australia

Central Contacts

Kristi McLendon, Dr

Role: CONTACT

Phone: 37072720

Email: k.mclendon@nucleusnetwork.com.au

Facility Contacts

Kristi McLendon, Dr

Role: primary

Other Identifiers

JSPL-PL-18-101

Identifier Type: -

Identifier Source: org_study_id