Tenofovir/Emtricitabine With Doxycycline for Combination HIV and Syphilis Pre-exposure Prophylaxis in HIV-negative MSM

HIV Clinical Trial

— DuDHS  

Official title:

Use of Tenofovir/Emtricitabine With Immediate or Deferred Doxycycline 100mg PO Daily for Combination HIV and Syphilis Pre-exposure Prophylaxis in HIV-negative Men Who Have Sex With Men: a Pilot Study of Dual Daily HIV and Syphilis PrEP. (The DuDHS Trial).

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02844634
• Other study ID #: BritishCCDC
• Status: Active, not recruiting
• Phase: Phase 4
• Start date: May 15, 2018
• Est. completion date: June 30, 2020

Study information

• Verified date: July 2019
• Source: British Columbia Centre for Disease Control
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Men who have sex with men remain at high risk for HIV infection. Targeting prevention interventions to MSM at highest risk of seroconversion is an important goal of combination prevention interventions. Antecedent diagnosis of another sexually transmitted infection (STI), particularly syphilis, may serve as an entry point for biomedical prevention as these individuals are at highest risk for incident HIV. The use of the antiretroviral combination of tenofovir/emtricitabine has been shown to be associated with an overall 44% reduction in HIV acquisition in high-risk MSM when taken daily as PrEP. In those individuals with detectable drug levels, the benefit was as high as 90% risk reduction. In real-world evaluations of PrEP, high-risk sexual behaviour may continue as evidenced by high rates of intercurrent sexually transmitted infections. As such, biomedical interventions that may offer additional reduction in acquisition of common sexually transmitted infections should also be evaluated.

Recently a small pilot study has demonstrated potential benefit from a similar strategy for syphilis prevention. In this study 30 MSM were randomized to receive either 100mg doxycycline once daily or contingency management strategies linked to remaining free of sexually transmitted diseases at progressive study visits. Overall, those receiving doxycycline were significantly less likely to be diagnosed with any STI during followup than those in the comparator arm.

The investigators therefore propose to undertake a pilot study to evaluate the feasibility of using both tenofovir/emtricitabine and doxycycline (immediate or deferred use) for pre-exposure prophylaxis amongst HIV-negative MSM with recent history of syphilis infection in Vancouver, Canada.

Description:

1. Rationale:

1.1 Men who have sex with men with antecedent diagnosis of another sexually transmitted infection, particularly syphilis, are at high risk for HIV infection.

Men who have sex with men (MSM) continue to experience high rates of HIV incident infections in Canada and a disproportionately high burden of disease relative to the general population. In 2011, approximately 48% of new diagnoses occurred in MSM across Canada, a figure that has been relatively stable for the last decade. Within British Columbia (BC), although HIV new diagnosis rates overall have been declining over the last decade (dropping from a rate of 10.6 cases/100,000 in 2004 to 5.9 cases/100,000 in 2013), MSM made up an increasing majority of new diagnoses (59%) within BC in 2013. Within Vancouver Coastal Health Authority (VCH), approximately 70% of all new HIV diagnoses annually from 2012-15 were amongst MSM.

Targeting prevention interventions to MSM at highest risk is important when determining potential publicly funded biomedical interventions, particularly the use of HIV pre-exposure prophylaxis (PrEP). Antecedent diagnosis of another sexually transmitted infection (STI) may serve as an entry point for biomedical prevention as these individuals are at highest risk for incident HIV. In an evaluation of HIV incidence following diagnosis of syphilis infection in New York City, the annual HIV incidence was 3.6% (95% Confidence Interval [CI]: 3.27% - 3.97%), with overall HIV incidence amongst MSM of 5.56% (1). In those males with syphilis and a subsequent additional STI the HIV incidence was even greater at 7.89% (95% CI: 6.62% - 9.24%). A similar analysis of clients attending STI clinics in BC has revealed that antecedent STI is predictive of an elevated risk for subsequent HIV seroconversion with clients who ever had a diagnosis of syphilis having an HIV incidence of 3.6% person-years (95%CI: 2.5-4.9), gonorrhea (2.0%; 95%CI: 1.6-2.5), rectal gonorrhea (4.5% person-years; 95%CI: 3.4-5.8), while individuals with rectal gonorrhea and syphilis had an incidence rate of 12.6 % person-years (95%CI: 8.4-21.8).

Evaluating the use of PrEP in MSM with antecedent STI is an important component to inform HIV prevention programs in BC and nationally. The STI clinics operated by the BC Centre for Disease Control are well-positioned for this evaluation as about 15 and 25% of all HIV diagnoses in BC and VCH, respectively are diagnosed at these clinics.

1.2. STI prevention strategies may also benefit from biomedical prevention interventions

Novel biomedical strategies have been shown to be effective in preventing acquisition of STI such as HIV, and are now considered to be standard of care for at-risk MSM in the United States. The use of the antiretroviral combination of tenofovir/emtricitabine has been shown to be associated with an overall 44% reduction in HIV acquisition in high-risk MSM when taken daily as PrEP. In those individuals with detectable drug levels, the benefit was as high as 90% risk reduction. In real-world evaluations of PrEP, high-risk sexual behaviour may continue as evidenced by high rates of intercurrent STI (50% of PrEP users after 12 months in a study of 657 PrEP initiators in San Francisco). As such, biomedical interventions that may offer additional reduction in acquisition of common sexually transmitted infections should be evaluated.

Recently a small pilot study has demonstrated potential benefit from a similar strategy for syphilis prevention (2). In this study 30 MSM were randomized to receive either 100mg doxycycline once daily or contingency management strategies linked to remaining free of sexually transmitted diseases at progressive study visits. Doxycycline 100mg daily was chosen based on prior studies indicating that doses as low as once weekly doxycycyline could serve as prophylaxis for leptospirosis, another spirochete infection.

Overall, those receiving doxycycline were significantly less likely to be diagnosed with any STI during follow-up than those in the comparator arm (odds ratio [OR] 0.27; 95% CI 0.09 - 0.83). Specific protection against syphilis infection was not seen during the on-treatment phase (OR 0.27; 95% CI 0.04 - 1.73), possibly reflecting the small sample size. During the study period, no change in sexual behaviours between arms was noted, supporting the potential role of doxycycline prophylaxis. A larger pilot evaluation of this strategy, in combination with HIV PrEP, would be a novel syndemic approach to addressing both the HIV and syphilis burden amongst the highest risk MSM.

The investigators therefore propose to undertake a randomized trial of immediate vs. deferred doxycycline in conjunction with daily tenofovir/emtricitabine to determine the feasibility of combined HIV and syphilis pre-exposure prophylaxis amongst HIV-negative MSM with recent history of syphilis infection in Vancouver, Canada.

2. Objectives:

We propose to undertake a pilot trial of immediate vs. deferred doxycycline in conjunction with daily tenofovir/emtricitabine to determine the feasibility of combined HIV and syphilis pre-exposure prophylaxis amongst HIV-negative MSM with recent history of syphilis infection in Vancouver, Canada. We will meet this aim through the following objectives:

1. To assess feasibility of using dual daily HIV and syphilis PrEP, as defined by:

a. Evaluation of feasibility of recruitment for a larger study i. Proportion of participants approached for study who are eligible and agree to participate.

b. Adherence to 6 or 12 months of tenofovir/emtricitabine and doxycycline i. Determine proportion of individuals with >95% adherence to dual therapy over 6 and 12 months ii. Proportion of individuals with detectable doxycycline plasma level at each study visit.

Additional measures of feasibility will include the assessment of:

c. Tolerability of dual PrEP i. Comparison of grade 3 or 4 adverse events in those receiving immediate vs. deferred PrEP

2. To evaluate antimicrobial resistance over time.

a. Change in proportion of participants with evidence of tetracycline class resistance in common flora, namely Staphylococcus aureus, Streptococcus pyogenes and Streptococcus pneumoniae from baseline to 6 and 12 months.

Secondary objectives will include:

3. To evaluate changes in sexual activity reported by study participants over the study period.

4. To compare syphilis incidence between those in the immediate vs. deferred doxycycline arms.

5. To describe frequency of other STI's diagnosed in study participants over the study period.

Exploratory objectives will include:

6. To evaluate doxycycline resistance in individuals with documented T.pallidum infection.

7. To evaluate HIV incidence and syphilis re-infection rates over a 12 month period.

8. Characterize changes in the rectal microbiome from baseline to 6 and 12 months after initiation of doxycycline

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 52
• Est. completion date: June 30, 2020
• Est. primary completion date: May 28, 2020
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 19 Years and older

Eligibility

Inclusion Criteria:

1. Age = 19 years of age.

2. Self-reported MSM status.

3. Self-report condomless anal sex with a man within the last 6 months.

4. HIV negative based on HIV nucleic acid amplification testing (NAT).

5. Prior diagnosis of syphilis within preceding 36 months (defined on the basis of a new positive serum rapid plasma reagin (RPR) test, or =2-dilution rise in titre if previous syphilis, or positive darkfield microscopy result or T. pallidum direct fluorescent antibody test or PCR from a primary lesion).

6. Able to provide informed consent.

Exclusion Criteria:

1. HIV-positive individuals.

2. Recent (within last 30 days) use of HIV post-exposure prophylaxis (PEP).

3. Impaired renal function defined as glomerular filtration rate < 60 mL/min.

4. Chronic active Hepatitis B infection.

5. History of myasthenia gravis.

6. History of tetracycline/doxycycline allergy.

Related Conditions & MeSH terms

• HIV
• Syphilis

Intervention

Drug:
• Doxycycline 100mg PO daily x 12 months
Immediate use of daily doxycycline (12 months duration, to start immediately)
• Tenofovir/emtricitabine 200/300mg PO daily
Daily use of tenofovir/emtricitabine
• Doxycycline 100mg PO daily x 6 months
Deferred use of doxycycline (6 months duration, to start 6 months post-randomization)

Locations

Country	Name	City	State
Canada	BC Centre for Disease Control	Vancouver	British Columbia

Sponsors (1)

Lead Sponsor	Collaborator
British Columbia Centre for Disease Control

Country where clinical trial is conducted

Canada, 

References & Publications (2)

Bolan RK, Beymer MR, Weiss RE, Flynn RP, Leibowitz AA, Klausner JD. Doxycycline prophylaxis to reduce incident syphilis among HIV-infected men who have sex with men who continue to engage in high-risk sex: a randomized, controlled pilot study. Sex Transm — View Citation

Pathela P, Braunstein SL, Blank S, Shepard C, Schillinger JA. The high risk of an HIV diagnosis following a diagnosis of syphilis: a population-level analysis of New York City men. Clin Infect Dis. 2015 Jul 15;61(2):281-7. doi: 10.1093/cid/civ289. Epub 20 — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	To assess the incidence of HIV in study participants	Exploratory outcome to access incidence rates for HIV infection	12 months
Other	To assess the incidence of doxycycline resistance in those with documented T. pallidum infection.	Exploratory outcome to assess incidence rates for doxycycline resistance	12 months
Other	To assess the changes in the composition of the rectal microbiome	Exploratory outcome to determine percentage changes in the bacterial genius of the rectal microbiome	6 and 12 months
Primary	The proportion of participants who are eligible and consent to participate amongst those approached.	To evaluate the feasibility of recruitment for a larger study	12 months
Primary	Proportion of participants reporting > 95% adherence to both HIV and syphilis PrEP therapies	To assess adherence of dual HIV and syphilis PrEP therapies	12 months
Primary	The proportion of individuals with detectable doxycycline at each study time point.	To assess adherence of syphilis PrEP therapy	12 months
Primary	The proportion of individuals reporting grade 3 or 4 adverse events in the immediate vs. deferred arms.	To assess the tolerability of dual HIV and syphilis PrEP therapies	12 months
Primary	The proportion of individuals with evidence of tetracycyline class resistance in common flora	To evaluate antimicrobial resistance over time	6 and 12 months
Secondary	To evaluate changes in sexual activity reported by study participants over the study period.	Evaluation of sexual activity over time	12 months
Secondary	To evaluate incidence of recurrent syphilis re-infection stratified by use immediate versus deferred doxycycline PrEP.	Evaluation of syphilis incidence rates between the two study arms	12 months
Secondary	To describe incidence of gonorrhea or chlamydia infection over the study period.	Assessment of the frequency of other STIs over time	12 months