On Demand Antiretroviral Pre-exposure Prophylaxis for HIV Infection in Men Who Have Sex With Men

HIV Infection Clinical Trial

— IPERGAY  

Official title:

On Demand Antiretroviral Pre-exposure Prophylaxis for HIV Infection in Men Who Have Sex With Men

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01473472
• Other study ID #: 2011-002645-35
• Secondary ID: IPERGAY
• Status: Completed
• Phase: Phase 3
• First received: November 8, 2011
• Last updated: May 10, 2017
• Start date: January 2012
• Est. completion date: December 15, 2016

Study information

• Verified date: May 2017
• Source: French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase III, multi-centre, comparative, double-blind, randomized trial on 2 parallel groups is designed to evaluate a strategy for the prevention of HIV infection including "on demand" antiretroviral pre-exposure with Truvada versus placebo, associated with overall prevention (counselling, condoms, sexually transmitted diseases (STD) screening, hepatitis B virus (HBV) and hepatitis A virus (HAV) vaccinations and post-exposure treatment of HIV infection) in men who have sex with men (MSM), exposed to the risk of HIV infection. Indeed recent studies have reported a higher incidence of new HIV infection in MSM as compared to the general population, new approaches to the prevention of HIV infection are, therefore, necessary in order to consider the limits of current strategies.

Description:

The trial has been taken place in two phases in order to ensure the general feasibility of the study:

• a first enrollment phase for at least 300 participants to ensure the possibility for recruitment in France and Canada and to validate the tools put into place as part of the trial to enroll and follow participants

• a second phase of 1600 additional participants. This extension phase started on July 2014.

The recruitment has been suspended following the recommendations of Data Safety and Monitoring Board (DSMB): the placebo arm has been stopped and Truvada was available for all the participants of the trial since November 2014. The initial protocol was amended and 361 participants were enrolled in the open-label phase. Sub-studies were proposed to the participants:

• Sub-study on the outcome of participants receiving sofosbuvir/ledipasvir treatment for recent HCV infection (protocol amendment on April 2015)

• Randomized sub-study to evaluate the efficacy of doxycycline post-exposure prophylaxis on sexually transmitted infections (protocol amendment on July 2015)

• Sub-study to evaluate Truvada adherence with Medication Event Monitoring System (MEMS) (protocol amendment on December 2015)

• Sub-study on drugs use and the impact on sexual behavior and Truvada adherence (protocol amendment on December 2015).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 400
• Est. completion date: December 15, 2016
• Est. primary completion date: June 30, 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years old

• Male (or transgender) having sex with men

• Not infected with HIV-1 or HIV-2

• Elevated risk of HIV contamination : anal sexual relations with at least 2 different sexual partners within the past 6 months without the systematic use of a condom

• Satisfactory kidney function with a clearance of more than 60 mL/min (Cockcroft formula)

• Alanine aminotransferase (ALT) < 2.5 Upper Limit of Normal (ULN),

• Neutrophil granulocytes = 1 000/mm3, haemoglobin = 10 g/dL, platelets = 150 000/mm3

• Negative HBs antigen and negative hepatitis C virus (HCV) serology (or negative HCV PCR if positive serology)

• Agrees to be contacted personally, if possible by telephone, short message system (SMS) or e-mail

• Agrees to the constraints imposed by the trial (visits every 2 months)

• Subjects enrolled in or a beneficiary of a Social Security program (State Medical Aid or Aide médicale de l'Etat (AME) is not a Social Security program).

• Signature of the informed consent form.

Exclusion Criteria:

• Subject in a stable and exclusive relationship with a person

• Systematic use of a condom during sexual relations

• Expected to go abroad for more than 3 consecutive months or move expected to a city where the study is not being conducted.

• Presence of significant glycosuria or proteinuria > 1+ in the urine dipstick, in the absence of infection.

• Presence of significant haematuria or leukocyturia > 2+ in the urine dipstick, in the absence of infection.

• History of chronic kidney disease, osteoporosis, osteopaenia

• History of pathological bone fracture not related to trauma

• Treatment with Interferon, Interleukin, or antiretrovirals

• Treatment that could inhibit or compete with the tubular secretion of antiretrovirals

• Treatment undergoing investigation

• Intravenous toxicomania

• Subject who is currently receiving or going to receive a potentially nephrotoxic treatment (long-term anti-inflammatory)

• Gastro-intestinal disease (or chronic nausea or vomiting) disrupting the absorption of treatments

• Positive HBs antigen

• Positive HCV serology with positive HCV PCR

• Life-threatening disease (lymphoma) or other serious disease (cardiovascular, renal, pulmonary, unstable diabetes) that could require treatment that could disrupt adherence to the treatment

• Subject potentially non-compliant.

Related Conditions & MeSH terms

• Acquired Immunodeficiency Syndrome
• Communicable Diseases
• HIV Infection
• HIV Infections
• Infection

Intervention

Drug:
• Truvada
2 tablets of truvada within 24 hours before first sexual relations, then 1 tablet of Truvada during the period of sexual activity including the last sexual intercourse, finally, a last dose of 1 tablet of Truvada approximately 24 hours later
• Placebo
2 tablets of placebo within 24 hours before first sexual relations, then 1 tablet of placebo every 24 hours during the period of sexual activity including the last sexual intercourse, finally, a last dose of 1 tablet of placebo approximatively 24 hours later

Locations

Country	Name	City	State
Canada	CHUM - Hôpital Hôtel Dieu	Montréal
France	Hôpital de La Croix Rousse	Lyon
France	CHU Hôtel Dieu	Nantes
France	Hôpital de l'Archet	Nice
France	Hôpital Tenon	Paris
France	Hôpital Saint-Louis	Paris Cedex 10
France	Hôpital Gustave Dron	Tourcoing

Sponsors (1)

Lead Sponsor	Collaborator
French National Institute for Health and Medical Research-French National Agency for Research on AIDS and Viral Hepatitis (Inserm-ANRS)

Countries where clinical trial is conducted

Canada,  France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Contamination with HIV-1 or -2	The primary endpoint criteria is contamination with HIV-1 or -2, defined by the first diagnostic proof of infection: positive HIV serum test (using combined latest-generation tests HIV-1 + 2) or a positive test for HIV-1-RNA Polymerase Chain Reaction (PCR) in the plasma.	From randomization to the end of the trial. The trial end date will be set by the scientific committee when the necessary number of primary endpoints has been reached without exceeding 5 years of follow-up.
Secondary	Evolution of sexual behavior and potential at-risk behavior	Self-questionnaires	Every 2 months without exceeding 5 years of follow-up.
Secondary	Incidence of clinical and biological adverse events		From randomization to the end of the trial, without exceeding 5 years of follow-up.
Secondary	Treatment adherence	Self-questionnaires, pill count. Drugs levels in plasma and hair (every 4 months).	Every 2 months without exceeding 5 years of follow-up.
Secondary	Incidence of hepatitis B		From randomization to the end of the trial, without exceeding 5 years of follow-up
Secondary	Incidence of other sexually transmitted diseases		From randomization to the end of the trial, without exceeding 5 years of follow-up
Secondary	Frequency of HIV resistance to antiretrovirals in HIV infected subjects	Genotype	At a visit as soon as the HIV infection is diagnosed
Secondary	Emtricitabine and tenofovir concentrations in plasma, saliva and rectal samples.	Ancillary study proposed between week-4 and the randomization - 12 volunteers. Blood and saliva samples at all time points and 2 sessions with rectal biopsies at two times for each volunteer (one before the drug is taken and one at one time after taking the 2 tablets)	0, 30 min, 1, 2, 4, 8 and 24 hours post-dose (2 tablets of Truvada)
Secondary	Costs evaluation	Modelling to estimate an increase of years of life expectancy and of quality adjusted life year (QALY).; Cost per avoided HIV contamination	From randomization to the end of the trial, without exceeding 5 years of follow-up.

External Links

•   sponsor of the study