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The role of Home packs of HIV PEPSE in High Risk Individuals

The role of Home packs of HIV Post-Exposure Prophylaxis for sexual exposure (PEPSE) to improve the speed and appropriate uptake of PEPSE in high risk individuals - HOME PEPSE

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2013-004809-24-GB
Enrollment
140
Registered
2015-04-08
Start date
2015-06-05
Completion date
Unknown
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV MedDRA version: 20.1 Level: PT Classification code 10020161 Term: HIV infection System Organ Class: 10021881 - Infections and infestations MedDRA version: 20.0 Level: PT Classification code 10020187 Term: HIV test negative System Organ Class: 10022891 - Investigations

Interventions

Trade Name: Celsentri (Trial Arm A) Pharmaceutical Form: Film-coated tablet INN or Proposed INN: MARAVIROC CAS Number: 376348-65-1 Concentration unit: mg milligram(s) Concentration type: equal Concent

Sponsors

Guy's & St. Thomas' NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Male gender at birth, age =18 years 2. HIV negative by a routinely used assay within 4 weeks prior to or on the day of randomization 3. Willing and able to provide written informed consent 4. And any one of: a. condomless anal sex with a male on >1 occasion within the 90 days prior to randomization b. bacterial sexually transmitted infection (STI) within the 90 days prior to randomization c. use of PEPSE in the 12 months prior to randomization following possible exposure to HIV through unprotected anal intercourse (UAI) with a male. Are the trial subjects under 18? no Number of subjects for this age range: 0 F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 140 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 140

Exclusion criteria

Exclusion criteria: 1. An acute viral illness that could be due to HIV seroconversion 2. Hypersensitivity to active substance 3. allergic to soy or peanuts 4. concomitant use of antihypertensive agents 5. history of postural hypotension 6. known hepBsAg positive 7. current participation in a HIV PrEP or PEPSE study 8. Any other active clinically significant condition, or findings during screening medical history or examination, or abnormality on screening laboratory blood tests that would, in the opinion of the investigator, compromise the patient’s safety or outcome in the trial.

Design outcomes

Primary

MeasureTime frame
Main Objective: To reduce the time to first dose of PEPSE in those accessing PEPSE following potential sexual exposure to HIV;Secondary Objective: To determine: a. the number of appropriate (sexual risk met the criteria for PEPSE) and inappropriate uptakes (risk did not meet the criteria for PEPSE); b. the number of missed opportunities for PEPSE initiation; c. the safety of HOME PEPSE provision with Truvada?/Maraviroc 600mg OD (Safety Objective) taken for =5 days; d. the safety of HOME PEPSE provision with Truvada?/Maraviroc 600mg OD (Safety Objective) given for a 28 day course; e. the impact of HOME PEPSE availability upon sexual health (incident bacterial STI) HIV and risk-taking behaviour. ;Primary end point(s): In those accessing PEPSE, the number of hours from HIV sexual risk exposure to initiating PEPSE over 48 weeks.;Timepoint(s) of evaluation of this end point: Arm A = 48 weeks Arm B = 72 weeks

Secondary

MeasureTime frame
Secondary end point(s): - the number of appropriate (met BASSH guidelines for sexual risk) times HOME PEPSE is accessed; - the number of inappropriate (did not meet BASSH guidelines for sexual risk) times HOME PEPSE was accessed - the number of missed opportunities for PEPSE i.e. should have taken PEPSE but did not - the number of condomless anal sex acts with individuals of unknown or HIV -positive status in the 3 months preceding week 24 and week 48 visits - HIV incidence and incidence of bacterial STI - Adherence to HOME PEPSE from initiation to first contact with sexual health team; - safety of HOME PEPSE as measured by number, type and severity of adverse events from initiation to first contact with sexual health team - safety of HOME PEPSE taken for 28 days as measured by number, type and severity of adverse events during each HOME PEPSE cycle ;Timepoint(s) of evaluation of this end point: Arm A = 48 weeks Arm B = 72 weeks

Countries

United Kingdom

Contacts

Public ContactJulie Fox

Guy's & St. Thomas' NHS Foundation Trust

Julie.fox@kcl.ac.uk+4402071882643

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026