Testing a new vaginal suppository for infections in healthy women

A Phase 1 Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Single and Multiple Ascending Doses of Antimicrobial Peptide PL-18 Vaginal Suppositories in Healthy Adult Subjects

This study is testing a new vaginal suppository to see if it can safely help prevent infections in healthy women aged 18 to 55.

Quick facts

• Phase: Phase 1
• Study type: Interventional
• Enrollment: 50 (estimated)
• Ages: 18 Years to 55 Years
• Sex: Female
• Sponsor: Protelight Pharmaceuticals Australia PTY LTD (Industry-sponsored)
• Locations: 1 site (Brisbane, Queensland)
• Trial ID: NCT05340790 on ClinicalTrials.gov

What this trial studies

This clinical trial is a Phase I, single-center, randomized, double-blind, placebo-controlled study aimed at evaluating the safety, tolerability, and pharmacokinetics of the antimicrobial peptide PL-18 delivered as vaginal suppositories. Healthy female volunteers aged 18 to 55 will be enrolled and randomized to receive either the active treatment or a placebo. Participants will be monitored for adverse events and undergo various assessments, including physical exams and laboratory tests, over a period of 11 days. The study will include ascending doses to determine the appropriate dosing and safety profile of PL-18.

Who should consider this trial

Good fit: Ideal candidates for this study are healthy adult females aged 18 to 55 with a body weight between 50 and 100 kg and a BMI of 18-32.

Not a fit: Patients with existing vaginal infections or those outside the specified age and health criteria may not benefit from this study.

Why it matters

Potential benefit: If successful, this treatment could provide a new option for managing vaginal infections, improving women's health outcomes.

How similar studies have performed: While this approach is novel, similar studies evaluating antimicrobial peptides have shown promise in other contexts.

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:

* A subject meeting any of the following exclusion criteria will not be allowed to participate in this study:

  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.

Where this trial is running

Brisbane, Queensland

• Q-Pharm Pty. Ltd — Brisbane, Queensland, Australia (Recruiting)

Study contacts

• Study coordinator: Kristi McLendon, Dr

Conditions Colpomycosis; Bacterial Vaginosis; Mixede Vaginitis