Letermovir in ART-treated HIV-infected Persons — Letermovir  

People Living With HIV Clinical Trial

Official title: Influence of a 3-month Letermovir Treatment on Gut Inflammation in ART-treated HIV-infected Persons in an Open Labelled Controlled Randomized Study

Status Recruiting

Clinical Trial Summary

This is a multi-centre, open-label, randomized, controlled clinical trial to assess the influence of letermovir on gut translocation marker LPS in blood in ART-treated cytomegalovirus (CMV)-seropositive adult people living with HIV (PLWH). The study will explore the influence of letermovir treatment on gut damage, with no intention for label change. Participants (n=60) should have a cluster of differentiation 4 cells (CD4) count greater than 400 cells/µl and a negative viral load. Forty (40) participants will be randomized to receive letermovir (PREVYMIS® 480 mg or 2x240mg orally) in addition to their usual ART, and 20 participants will receive standard of care alone (ART only) for 14 weeks. Study visits will include screening, 2 baselines, followed by follow-up visits at 2 and 4 weeks and at 14 weeks after starting treatment and 12 weeks after end of letermovir treatment to assess a carry-over effect. In an optional sub-study, colonoscopies and colon biopsies will be performed before and after letermovir treatment or standard of care alone to assess gut mucosa inflammation.

Clinical Trial Description

INTRODUCTION, BACKGROUND, AND STUDY RATIONALE Cytomegalovirus (CMV) seropositivity is frequent in the general population and even more so in persons living with HIV (PLWH). In the general population, high anti-CMV immunoglobulins G (IgG)-titer has been associated with earlier mortality, cluster of differentiation 8 (CD8) T-cell expansion, low CD4/CD8 ratio and increased cluster of differentiation cells (CD57) senescence marker expression on T cells. Such elevated IgG titer may be linked to transient CMV replication. The investigators have shown that gut permeability is correlated with anti-CMV IgG titers in PLWH on antiretroviral therapy (ART). Increased gut permeability is associated with microbial translocation and systemic inflammation, and correlates with frequency of non-infectious/non-AIDS comorbidities such as cardiovascular diseases, neurocognitive disorders and cancer. Moreover, gut permeability has been linked with reduced response to commercialized vaccines . The investigators recently demonstrated that, in HIV elite controllers, a rare subgroup of PLWH who can control HIV replication in absence of ART, CMV coinfection and anti-CMV IgG levels were associated with CD4 count decay. As HIV replication is well controlled with ART, our findings suggest that CMV co-infection is a driving factor behind increased gut permeability and inflammation in PLWH, contributing to immune exhaustion and senescence. Hunt et al. have shown that administration of valganciclovir, an anti-CMV medication, in ART-treated PLWH for 4 weeks was associated with a decrease in immune activation markers compared to the control group. However, long-term use of valganciclovir is not convenient due to its toxicity and its activity is not specific to CMV. Furthermore, its influence on gut permeability has not been assessed. A novel anti-CMV agent with an excellent safety profile, letermovir, was approved in 2017 for anti-CMV prophylaxis in allogeneic hematopoietic cell transplant recipients. In these patients, a drastic reduction of both low-grade replication and CMV infections, combined with an improved immune reconstitution after the graft was reported. In vitro, in intestinal tissues reconstituted from primary cells, letermovir anti-CMV treatment could prevent CMV-induced epithelial disruption. Potential Risks and Benefits to Human Participants Potential Risks Associated with letermovir For this study, participants will be receiving two tablets of 240mg or one tablet of 480mg of PREVYMIS® daily, for 14 weeks in total. This corresponds to the dose recommended for anti-CMV prophylaxis in hematopoietic cell transplant recipients. In this latter population, which is the only one for which PREVYMIS® has been approved in Canada, most frequent side effects are nausea/vomiting and peripheral edema. Cardiac events constitute 13% of all adverse effects, including atrial fibrillation in 3.5, as such an ECG will be performed during the screening visit and participants with any type of known arrythmia will be excluded. In case of cardiac symptoms during follow-up, another ECG will be performed and participants with arrythmia will be withdrawn from the study and referred to a cardiologist. In practice, those side effects are unfrequent, as illustrated in the pivotal clinical trial of letermovir in which frequency and severity of adverse events were not statistically increased in the letermovir group compared to placebo group. Finally, based on the Canadian PREVYMIS® monograph, drug-on-drug interactions are possible and the concomitant administration of following medications will constitute exclusion criteria: pimozide, ergotamine, lovastatin, rosuvastatin, simvastatin or bosentan when co-administered with cyclosporine. For patients not using cyclosporine, dose of statins will be reduced by 50% for the duration of the letermovir or placebo treatment. Due to the long-term effect of statins, such a short-period of dose reduction is not expected to increase cardiovascular risk to participants. Regarding HIV medication, exclusionary agents include darunavir, efavirenz, etravirine and nevirapine. Those drugs constitute parts of ART regimens and participants who receive them will need to be excluded. However, this should not significantly impact recruitment as these drugs are only rarely prescribed in HIV clinics in Quebec. Exclusionary agents have been discussed and accepted by the Merck Investigator Studies Program Safety Committee of Merck. Potential risks to blood draws The risks of drawing blood from a vein include: discomfort at the blood draw site (often momentary); possible bruising, redness, swelling, and/or bleeding at the site (will be managed by putting pressure on site of draw); feeling of lightheadedness when blood is drawn (will be managed by ensuring participants remains seated until dizziness abates); and rarely an infection at the site where the blood was drawn (cleaning of the site prior to blood draw should prevent this from happening, and treatment in case of infection will be provided). Potential risks and/or discomforts to colon mucosal biopsies Participants from McGill University Health Centre (MUHC) will be invited to participate in an optional sub-study to collect colon mucosal biopsy. They will be asked to sign a separate consent form if they wish to take part in the sub-study. The day before this procedure, the consenting participant will be required to take measures to clear his/her bowels for the examination by drinking a picosulfate based solution and magnesium citrate as enunciated in the colonoscopy information preparation sheet (Appendix 5). The Information sheet addendum will be given to each participant referring side effects, risks, contraindications and the medication interactions for the two magnesium-based products used to clean their bowels. During the colon mucosal biopsy procedure, the participant may feel pressure in the rectum similar to the sensation felt with the urge to have a bowel movement. The participant may also feel a small amount of abdominal cramping. The most serious risk of the procedure is perforation, i.e. poking a hole in the lining of the intestine; this risk is extremely uncommon, occurring once out of every 10,000 procedures. Some bleeding will likely occur at the place where the biopsies are done. Light to moderate sedation using midazolam and fentanyl could be used during the procedure, in the absence of any contraindication. This sedation procedure is very safe, rare side effects include temporary memory loss, blood pressure drop or vomiting. If the participant experiences severe discomfort despite sedation during the colon mucosal biopsies, the procedure will be stopped immediately; he/she will be seen by a physician and the research nurse will monitor him/her until he/she is ready to go home. 1.3.4 Benefits to Participating in This Study The effects of CMV latent infection has been widely reported and include persisting inflammation, gut leakage, decreased response to vaccines and to pathogens. As such, a potential beneficial effect of letermovir on those parameters is expected, which is particularly meaningful in the light of the current COVID-19 pandemic. Altogether, findings from this study may clarify the influence of CMV on health, and help to improve treatments for PLWH. The study's results will be published and all participants will be given access to the study findings. Study Rationale Latent CMV infection and occasional replication has been linked with poorer outcome in PLWH. Our hypothesis is that inhibiting CMV replication with a safe anti-CMV agent as letermovir will prevent gut damage and favor gut epithelium repair, decreasing microbial translocation and lower non-AIDS comorbidity risks in ART-treated PLWH. Based on our experience, and recent trials such at the single arm Clinical Trials Network (CTN) PT27 Lilac study, the investigators propose a randomized controlled trial with a control arm receiving standard of care (ART only) to ensure the specificity of any changes the investigators could observe with letermovir (long term ART treatment could influence inflammation markers). Such a design is optimal for the development of future larger studies, in the case where results would show a clinical interest. STUDY OBJECTIVES AND DESIGN Overall Study Design This is a multi-centre, open-label, randomized, controlled clinical trial to assess the influence of letermovir on gut translocation marker LPS in blood in ART-treated CMV-seropositive adult PLWH. The study will explore the influence of letermovir treatment on gut damage, with no intention for label change. Participants (n=60) should have a CD4 count greater than 400 cells/µl and a negative viral load. Forty (40) participants will be randomized to receive letermovir (PREVYMIS® 480 mg or 2x240mg orally) in addition to their usual ART, and 20 participants will receive standard of care alone (ART only) for 14 weeks. Study visits will include screening, 2 baselines, followed by follow-up visits at 2 and 4 weeks and at 14 weeks after starting treatment and 12 weeks after end of letermovir treatment to assess a carry-over effect. In an optional sub-study, colonoscopies and colon biopsies will be performed before and after letermovir treatment or standard of care alone to assess gut mucosa inflammation. Primary Objective(s) To assess the influence of CMV replication inhibition with letermovir on gut translocation markers (LPS) in blood of PLWH. Secondary Objective(s) To assess the influence of CMV replication inhibition with letermovir on: Gut permeability markers in blood of PLWH (REG3α and I-FABP). Inflammation markers (IL-6, sCD14, hsCRP, d-dimers) in blood of PLWH. Anti-CMV immune response (anti-CMV IgG titers and specific T-cell response) and CMV DNA detection in plasma and Peripheral Blood Mononuclear Cells (PBMC). In a sub-study, inflammation in colon biopsies obtained by coloscopy and in CMV DNA detection in gut mucosa Exploratory Objectives(s) To assess the influence of CMV replication inhibition with letermovir on: HIV reservoir size in blood and mucosal samples. Microbiota composition. Sub-studies In an optional sub-study, colonoscopies and colon biopsies will be performed before and after letermovir treatment or standard of care alone to assess gut mucosa inflammation. ;

Related Conditions & MeSH terms

• People Living With HIV

• NCT number: NCT05362916
• Study type: Interventional
• Source: McGill University Health Centre/Research Institute of the McGill University Health Centre
• Contact: Jean-Pierre Routy
• Phone: 5143981934
• Email: jean-pierre.routy@mcgill.ca
• Status: Recruiting
• Phase: N/A
• Start date: September 26, 2022
• Completion date: December 31, 2025