Patient Guide: A Study to Evaluate the Efficacy, Safety, Participant Choice and Preference of an Oral Once-daily Regimen or a Long-acting Injectable Regimen Every Two Months for Treatment of Human Immunodeficiency Virus (HIV-1) in Adults Who Have Not Previously Taken Antiretroviral Therapy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 47 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05917509
Status: ACTIVE_NOT_RECRUITING
Condition: HIV Infections
Phase: PHASE3

Where You Can Participate

This study is available at 47 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Bakersfield, California
  • • Fort Lauderdale, Florida
  • • And 44 more locations

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A Study to Evaluate the Efficacy, Safety, Participant Choice and Preference of an Oral Once-daily Regimen or a Long-acting Injectable Regimen Every Two Months for Treatment of Human Immunodeficiency Virus (HIV-1) in Adults Who Have Not Previously Taken Antiretroviral Therapy - Join Clinical Trial NCTNCT05917509

How to Join This Clinical Trial - NCTNCT05917509

Learn how to participate in this PHASE3 trial studying an investigational therapy for HIV Infections. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
HIV Infections
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05917509 - 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 47 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35205 - United States

Status: Contact for availability

Clinical Research Site

Bakersfield, California 93301 - United States

Status: Contact for availability

Clinical Research Site

Fort Lauderdale, Florida 33308 - United States

Status: Contact for availability

Clinical Research Site

Fort Pierce, Florida 34982 - United States

Status: Contact for availability

Clinical Research Site

Orlando, Florida 32804 - United States

Status: Contact for availability

Clinical Research Site

Pensacola, Florida 32504 - United States

Status: Contact for availability

Clinical Research Site

Berkley, Michigan 48072 - United States

Status: Contact for availability

Clinical Research Site

Kansas City, Missouri 64111 - United States

Status: Contact for availability

Clinical Research Site

Omaha, Nebraska 68198 - United States

Status: Contact for availability

Clinical Research Site

Henderson, Nevada 89106 - United States

Status: Contact for availability

And 37 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for HIV Infections:

  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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