NCT06334497 Letermovir-based Dual Therapy for Treatment of Cytomegalovirus Infections
| NCT ID | NCT06334497 |
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Condition | Cytomegalovirus Infection |
| Study Type | INTERVENTIONAL |
| Enrollment | 80 participants |
| Start Date | 2024-08-14 |
| Primary Completion | 2027-09 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
Phase 3 trials are large pivotal studies comparing the treatment to current standard of care or placebo. Your participation directly contributes to the evidence needed for regulatory approval.
This trial targets 80 participants in total. It began in 2024-08-14 with a primary completion date of 2027-09.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The purpose of this study is to evaluate the efficacy and the tolerance of letermovir as part of dual antiviral therapy (in association with valganciclovir) in renal transplant recipients with CMV DNAemia, requiring valganciclovir treatment per investigator's judgment.
Eligibility Criteria
Inclusion Criteria: 1. Age ≥ 18 years 2. Weight ≥ 30 kg 3. Kidney transplant recipient 4. Have a documented CMV infection or disease, with (i) a screening value of CMV DNA ≥ 3000 IU/mL in whole blood or plasma in 2 consecutive assessments separated by ≥ 1 day, as determined by local laboratory quantitative polymerase chain reaction (qPCR). Both samples should be taken within 14 days prior to randomization with the second sample obtained within 5 days prior to randomization OR (ii) a screening value of CMV DNA ≥ 30000 IU/mL in whole blood or plasma, as determined by local laboratory quantitative polymerase chain reaction (qPCR), in 1 sample obtained within 5 days prior to randomization 5. Eligible for treatment with oral valganciclovir, per investigator's judgment 6. For patients of childbearing age (following menarche): negative bHCG and effective method of contraception (sexual abstinence, hormonal contraception containing ethinylestradiol and levonorgestrel, intrauterine device or hormone-releasing system, cap, diaphragm or sponge with spermicide, condom) until 30 days after the end of relevant systemic exposure (week 13). For male an effective method of contraception (sexual abstinence, condom) until 90 days after the end of relevant systemic exposure (week 13). 7. Have life expectancy of ≥ 8 weeks 8. French speaking 9. Affiliated to social security regime or an equivalent system 10. Informed consent and signed Exclusion Criteria: 1. Have a current CMV infection that is considered refractory or resistant due to inadequate adherence to antiviral treatment, to the best knowledge of the investigator. 2. Have a CMV infection that is known to be genotypically resistant to valganciclovir and/or letermovir on documented evidence. 3. Be on treatment with anti-CMV agents (ganciclovir, valganciclovir, foscarnet, cidofovir, letermovir or maribavir) for the current CMV infection for longer than 72 hours. However, patients experiencing CMV infection while receiving ganciclovir or valganciclovir prophylaxis (i.e. at prophylactic dosages) or letermovir prophylaxis can be included. 4. Have an eGFR \< 15 mL/min/1.73m² (using the CKD-EPI Creatinine Equation (2009)). 5. Have serum aspartate aminotransferase (AST) ≥ 5 times higher than the upper limit of normal (ULN), or serum alanine aminotransferase (ALT) ≥ 5 times the ULN, or total bilirubin ≥ 3 times the ULN (except for documented Gilbert's syndrome). Note: Subjects with biopsy confirmed CMV hepatitis will not be excluded from study participation despite AST or ALT ≥ 5 times ULN 6. Have a severe chronic liver disease (Child-Pugh Class C) 7. Have a known human immunodeficiency virus (HIV) infection with plasma HIV RNA ≥ 50 copies/mL within the 3 months before inclusion. 8. Require mechanical ventilation or vasopressors for hemodynamic support. 9. Be pregnant or breastfeeding. 10. Have received anti-CMV vaccine at any time. 11. Be receiving leflunomide or artesunate when study treatment is initiated. 12. Be receiving strong inhibitors or inducers of hepatic CYP enzymes including rifampicin, phenytoin, clarithromycin, ritonavir, or cobicistat or St. John's wort (Hypericum perforatum) when study treatment is initiated. 13. Be receiving efavirenz, etravirine, nevirapine, lopinavir, pimozine, ergot alkaloids, dabigatran, atorvastatine (at a daily dose \> 20mg, and / or if co-administered with cyclosporin A), pravastatin ( if co-administered with cyclosporin A), simvastatine, rosuvastatine, pitavastatine or imipenem-cilastatine when study treatment is initiated. 14. Have known hereditary intolerance to galactose, with lactose Lapp deficiency, glucose or galactose malabsorption syndrome. 15. Have known hypersensitivity to letermovir or to an excipient for a study treatment. 16. Have any clinically significant medical or surgical condition that in the investigator's opinion could interfere with the interpretation of study results, contraindicate the administration of the assigned study treatment, or compromise the safety or well-being of the subject. 17. Participation to another clinical trial on medicinal products for human use 18. Have an absolute neutrophil count less than 500 cells/µl, or platelet count less than 25,000/µl, or haemoglobin less than 8 g/dl
Contact & Investigator
Marianne LERUEZ-VILLE, MD, PhD
STUDY CHAIR
Virology laboratory- reference national Lab for CMV infection -Hôpital Necker Enfants malades, Paris
Frequently Asked Questions
Who can join the NCT06334497 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Cytomegalovirus Infection. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
What phase is the NCT06334497 trial and what does that mean for participants?
Phase 3 trials are large-scale studies comparing the new treatment to existing standards of care or a placebo. They provide the evidence needed for regulatory approval. This trial targets 80 participants.
Is NCT06334497 currently recruiting?
Yes, NCT06334497 is actively recruiting participants. Contact the research team at pierre.frange@aphp.fr for enrollment information.
Where is the NCT06334497 trial being conducted?
This trial is being conducted at Paris, France, Paris, France, Paris, France, Paris, France and 1 additional location.
Who is sponsoring the NCT06334497 clinical trial?
NCT06334497 is sponsored by Assistance Publique - Hôpitaux de Paris. The principal investigator is Marianne LERUEZ-VILLE, MD, PhD at Virology laboratory- reference national Lab for CMV infection -Hôpital Necker Enfants malades, Paris. The trial plans to enroll 80 participants.