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NCT06730555: ACCESS

Advancing Access to HIV/HCV Testing for People Who Inject Drugs (PWID)

Recruiting now NA Last updated 3 February 2026
What this trial tests

NA trial testing ACCESS Intervention in HIV Infections in 40 participants. Currently enrolling.

Timeline
27 June 2025
Primary endpoint
1 August 2028
1 August 2028

Quick facts

Lead sponsorUniversity of Miami
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposescreening
Enrollment40
Start date27 June 2025
Primary completion1 August 2028
Estimated completion1 August 2028
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Miami

Who can join

18 and older, any sex, with HIV Infections. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to test the effectiveness of the ACCESS strategy: an organizational-level intervention that uses funding and practice facilitation to improve the organizational capacity of syringe services programs (SSPs) to implement routine, opt-out HIV and Hepatitis C (HCV) testing and linkage to care for people who inject drugs (PWID).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. A Turning Point for Hepatitis C Care: Point-of-Care HCV RNA Authorization as a Critical First Step Towards Integrated Test-and-Treat Models in the United States.
    Furukawa NW, Kamili S, Wester C. · · 2026 · PMID 41823663 · DOI 10.1093/cid/ciag174

Verify or expand the search:

Other recruiting trials for HIV Infections

Currently open trials in the same condition.

Other University of Miami trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06730555.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing