Patient Guide: A Study to Assess the Safety, Pharmacokinetics, and Antiviral Activity of ABI-5366 in Healthy Participants and Participants Seropositive for HSV-2 With Recurrent Genital Herpes

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 17 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06385327
Status: 🟢 Enrolling Now
Condition: Recurrent Genital Herpes Simplex Type 2
Phase: PHASE1

Where You Can Participate

This study is available at 17 locations across the country.

Top locations include:
  • • Darlinghurst, New South Wales
  • • Miranda, New South Wales
  • • Surry Hills, New South Wales
  • • And 14 more locations

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A Study to Assess the Safety, Pharmacokinetics, and Antiviral Activity of ABI-5366 in Healthy Participants and Participants Seropositive for HSV-2 With Recurrent Genital Herpes - Join Clinical Trial NCTNCT06385327

How to Join This Clinical Trial - NCTNCT06385327

Learn how to participate in this PHASE1 trial studying an investigational therapy for Recurrent Genital Herpes Simplex Type 2. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Recurrent Genital Herpes Simplex Type 2. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Recurrent Genital Herpes Simplex Type 2
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1 - Early safety study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06385327 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 17 locations. Find a study site near you:

Clinical Research Site

Darlinghurst, New South Wales 2010 - Australia

Status: RECRUITING

Clinical Research Site

Miranda, New South Wales 2228 - Australia

Status: RECRUITING

Clinical Research Site

Surry Hills, New South Wales 2010 - Australia

Status: RECRUITING

Clinical Research Site

Sydney, New South Wales 2010 - Australia

Status: RECRUITING

Clinical Research Site

Sydney, New South Wales 2100 - Australia

Status: RECRUITING

Clinical Research Site

Wollongong, New South Wales 2500 - Australia

Status: RECRUITING

Clinical Research Site

Southport, Queensland 4215 - Australia

Status: WITHDRAWN

Clinical Research Site

Melbourne, Victoria 3021 - Australia

Status: RECRUITING

Clinical Research Site

Parkville, Victoria 3050 - Australia

Status: RECRUITING

Clinical Research Site

Auckland, 1010 - New Zealand

Status: RECRUITING

And 7 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1 clinical trial for Recurrent Genital Herpes Simplex Type 2:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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