Patient Guide: A Study of ABI-2280 Vaginal Insert (Previously Referred to as ABI-2280 Vaginal Tablet) in Participants With Cervical Intraepithelial Neoplasia

We'll Help You Connect with This Trial

Quri.ai is a free clinical trial matching service. We help patients like you connect directly with research sites conducting this study.

✓ Get matched to the right study location for you
✓ Connect directly with study coordinators at 7 participating sites
✓ Understand eligibility with our simplified screening tool
✓ Free service - we're here to help you access clinical research

Trial ID: NCTNCT05502367

Status: 🟢 Enrolling Now

Condition: Cervical Intraepithelial Neoplasia

Phase: PHASE1, PHASE2

Find a Study Location Near You

This study is available at 7 research sites. We'll help you connect with the location that's right for you.

Participating sites include:

• Darlinghurst, New South Wales
• Cusco,
• Lima,
• And 4 more locations - let us help you find the closest one

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A Study of ABI-2280 Vaginal Insert (Previously Referred to as ABI-2280 Vaginal Tablet) in Participants With Cervical Intraepithelial Neoplasia - Join Clinical Trial NCTNCT05502367

How to Join This Clinical Trial - NCTNCT05502367

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Cervical Intraepithelial Neoplasia. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Cervical Intraepithelial Neoplasia. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied: Cervical Intraepithelial Neoplasia
Treatment Being Tested: Investigational treatment
Study Phase: PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status: Currently enrolling participants
Study Identifier: NCTNCT05502367 - 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 7 locations. Find a study site near you:

Clinical Research Site

Darlinghurst, New South Wales 2010 - Australia

Status: RECRUITING

Clinical Research Site

Cusco, - Peru

Status: RECRUITING

Clinical Research Site

Lima, - Peru

Status: RECRUITING

Clinical Research Site

Bloemfontein, Free State 9301 - South Africa

Status: RECRUITING

Clinical Research Site

Sunnyside, Gauteng 0002 - South Africa

Status: RECRUITING

Clinical Research Site

Waltloo, Gauteng 0184 - South Africa

Status: RECRUITING

Clinical Research Site

Ga-Mothapo, Limpopo - South Africa

Status: RECRUITING

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Cervical Intraepithelial Neoplasia:

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

Why Choose Quri.ai as Your Clinical Trial Matching Service

Quri.ai is a free clinical trial matching service that helps patients connect with research sites. We make it easier to:

Find clinical trials that match your condition
Get matched to the right study location near you
Connect directly with study coordinators
Understand if you qualify with simplified eligibility screening
Navigate the enrollment process with personalized support
Access new treatments through clinical research participation