A Study of Maribavir in Chinese Adults With Cytomegalovirus (CMV) Infections

Cytomegalovirus (CMV) Clinical Trial

Official title:

An Open-label, Single-arm Study to Evaluate the Safety, Tolerability, Efficacy and Pharmacokinetics of Maribavir in Chinese Transplant Recipients With Cytomegalovirus (CMV) Infections That Are Refractory or Resistant to Treatment With Ganciclovir, Valganciclovir, Cidofovir or Foscarnet

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06439342
• Other study ID #: TAK-620-3002
• Status: Not yet recruiting
• Phase: Phase 3
• Start date: March 14, 2025
• Est. completion date: February 5, 2027

Study information

• Verified date: June 2024
• Source: Takeda
• Contact: Takeda Contact
• Phone: +1-877-825-3327
• Email: medinfoUS[@]takeda.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The main aim of this study is to learn how safe maribavir is in Chinese adults who have undergone hematopoietic stem cell or organ transplantation and have a cytomegalovirus (CMV) infection and how well they tolerate treatment with maribavir. Other aims are to see how effective maribavir is in treating CMV infection and getting rid of the symptoms, the recurrence rate of CMV infection after treatment with maribavir and if the treatment is required again. Researchers will also check for changes (mutations) occurring in the virus which may cause treatment with maribavir to no longer work well or to not work at all (resistance to maribavir). The participants will be treated with maribavir for 8 weeks. During the study, participants will visit their study clinic 18 times.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: February 5, 2027
• Est. primary completion date: February 5, 2027
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria

• The participant or the participant's legally acceptable representative is willing and able to understand and fully comply with study procedures and requirements, in the opinion of the investigator.
• The participant/participant's legally representative has provided informed consent (that is, in writing, documented via a signed and dated informed consent form [ICF]) and any required privacy authorization prior to the initiation of any study procedures.
• The participant is aged 18 years or older (ie, greater than or equal to [>=] 18 years) at the time of signing the ICF.
• The participant must be of Chinese descent, defined as born in China and having Chinese parents and Chinese maternal and paternal grandparents.
• The participant must be a recipient of hematopoietic stem cell or solid organ transplant.
• The participant must have a documented CMV infection in whole blood or plasma, with a screening value of >=1,365 International unit per milliliter IU/mL in whole blood or >=455 IU/mL in plasma in 2 consecutive assessments, separated by at least 1 day, as determined by local laboratory quantitative polymerase chain reaction (qPCR) or comparable quantitative CMV DNA results. Both samples should be taken within 14 days prior to receiving the investigational product with second sample obtained within 5 days prior to receiving the investigational product. The same laboratory and same sample type (whole blood or plasma) must be used for these assessments.
• The participant must have a current CMV infection that is refractory to the most recently administered of the 4 anti-CMV treatment agent(s) eg, intravenous (IV) ganciclovir/oral valganciclovir, IV foscarnet, or IV cidofovir. Refractory is defined as documented failure to achieve greater than (>) 1 log10 (common logarithm to base 10) decrease in CMV DNA level in whole blood or plasma after a 14 day or longer treatment period with the above 4 agents.
• Participants who have documentation of 1 or more CMV genetic mutations associated with resistance to ganciclovir/valganciclovir, cidofovir, or foscarnet must also meet the definition of refractory CMV infection.
• Have all the following results as part of screening laboratory assessments:
• Absolute neutrophil count >=1000 per cubic millimeter (/mm^3) (1*10^9 per liter [/L]).
• Platelet count >= 25,000/mm^3 (25*10^9/L)
• Hemoglobin >= 8 grams per deciliter (g/dL)
• Estimated glomerular filtration rate >= 30 milliliter per minute per 1.73 square meter (mL/min/1.73 m^2) as assessed by Modification of Diet in Renal Disease (MDRD) formula.
• The participant must have life expectancy of at least 8 weeks.
• The participant has a body weight of at least 35 kilogram (kg).
• The female participant either be of nonchildbearing potential, or if of childbearing potential then have a negative serum human chorionic gonadotropin (hCG) or beta-hCG (ß-hCG) pregnancy test at screening. Males, or nonpregnant, nonlactating female participants who are sexually active must agree to comply with the applicable contraceptive requirements of this protocol during the investigational product administration period and for 90 days after the last dose of investigational product.
• The participant must be able to swallow tablets, or receive tablets crushed and/or dispersed in water via a nasogastric or orogastric tube.

Exclusion Criteria:

• The participant has CMV disease with central nervous system (CNS involvement) (eg, CMV encephalitis) or ophthalmic involvement (eg, CMV retinitis) as assessed by the investigator at the time of screening.
• That participant has uncontrolled other type of infection as assessed by the investigator on the date of treatment assignment.
• The participant has a history of clinically relevant alcohol or drug abuse that may interfere with treatment compliance or assessments with the protocol as determined by the investigator.
• The participant has a known hypersensitivity to maribavir or to any excipients.
• The participant has severe vomiting, diarrhea, or other severe gastrointestinal (GI) illness within 24 hours prior to the first dose of investigational product or a GI absorption abnormality that would preclude administration of oral medication.
• The participant has any clinically significant medical or surgical condition that, in the investigator's opinion, could interfere with interpretation of study results, contraindicate the administration of the investigational product, or compromise the safety or well-being of the participant.
• The participant is receiving valganciclovir, ganciclovir, cidofovir, foscarnet, letermovir, leflunomide, or artesunate when investigational product is initiated, or anticipated to require one of these agents during the 8-week treatment period.
• The participant requires mechanical ventilation or vasopressors for hemodynamic support at the time of baseline.
• The participant has previously received maribavir.
• The participant has previously completed, discontinued, or have been withdrawn from this study.
• The participant has received any investigational agent with known anti-CMV activity within 30 days before initiation of investigational product or CMV vaccine at any time.
• The participant has received any investigational agent or device within 30 days before initiation of investigational product.
• The participant has serum aspartate aminotransferase (AST) >5 times upper limit of normal (ULN) at screening, or serum alanine aminotransferase (ALT) >5 times ULN at screening, or total bilirubin >=3.0 × ULN at screening (except for documented Gilbert's syndrome), by a local laboratory. Note: Participants with biopsy confirmed CMV hepatitis will not be excluded from study participation despite AST or ALT >5 times ULN at screening.
• The participant has known (previously documented) positive results for human immunodeficiency virus (HIV). Participant must have a confirmed negative HIV test result within 3 months of study entry or, if unavailable, be tested by a local laboratory during the screening period.
• The participant has active malignancy with the exception of nonmelanoma skin cancer, as determined by the investigator. Participants who experience relapse or progression of their underlying malignancy (for which hematopoietic stem-cell transplantation (HSCT) or solid organ transplant (SOT) was performed), as determined by the investigator, are not to be enrolled.
• The participant is undergoing treatment for acute or chronic hepatitis C and hepatitis B.
• The participant is pregnant or expecting to conceive or nursing/breastfeeding.

Related Conditions & MeSH terms

• Cytomegalovirus (CMV)
• Cytomegalovirus Infections

Intervention

Drug:
• Maribavir
Maribavir tablets

Locations

Country	Name	City	State
China	Peking University People's Hospital	Beijing	North China

Sponsors (1)

Lead Sponsor	Collaborator
Takeda

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants with Treatment-Emergent Adverse Events (TEAEs), Serious Adverse Events (SAE), and Adverse Events of Special interest (AESIs)	TEAEs will be defined as those with a start date on or after the first dose of study treatment, or with a start date before the date of first dose of study treatment but increasing in severity after the first dose of study treatment. An SAE is any untoward medical occurrence or effect that at any dose results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability / incapacity, is a congenital anomaly / birth defect or is medically important due to other reasons than the above-mentioned criteria. AESIs is defined as any adverse event of special interest.	From first dose of study drug up to Week 20
Primary	Number of Participants With Clinically Significant Changes in Vital Signs	Vital signs will include temperature, arterial blood pressure (systolic and diastolic) and pulse. Any change in vital signs assessments which will be deemed clinically significant by the investigator will be reported.	From first dose of study drug up to Week 20
Primary	Number of Participants With Clinically Significant Abnormalities in Laboratory Parameters	Clinical laboratory parameters will include chemistry, hematology, and urinalysis. Any clinical laboratory abnormalities which will be deemed clinically significant by the investigator will be recorded.	From first dose of study drug up to Week 20
Primary	Number of Participants With Clinically Significant Electrocardiogram (ECG) Findings	12-lead ECG will be evaluated. Any ECG assessments which will be deemed clinically significant by the investigator will be reported.	From first dose of study drug up to Week 20
Primary	Number of Participants Who will Discontinue From the Study Drug and Study	Participants discontinuing the study drug treatment and the study will be reported.	From first dose of study drug up to Week 20
Secondary	Percentage of Participants With Confirmed Clearance of Plasma CMV Deoxyribose Nucleic Acid (DNA) (CMV Viremia Clearance) at Week 8	Confirmed CMV viremia clearance is defined as plasma CMV DNA concentration below the lower limit of quantification (	At Week 8
Secondary	Percentage of Participants With Achievement of CMV Viremia Clearance and CMV Infection Symptom Control at Weeks 8, 12, 16, and 20	Confirmed CMV viremia clearance is defined as plasma CMV DNA concentration below the lower limit of quantification (	At Weeks 8, 12, 16 and 20
Secondary	Percentage of Participants With Achievement of CMV Viremia Clearance and CMV Infection Symptom Control at Week 8 (After Completion of 8 Weeks Therapy)	Confirmed CMV viremia clearance will be defined as plasma CMV DNA concentration	At Week 8
Secondary	Percentage of Participants With Achievement of CMV Viremia Clearance and CMV Infection Symptom Control After Completion of 8 weeks Therapy Followed by Maintenance of This Treatment Effect Through Weeks 12, 16 and 20	Confirmed CMV viremia clearance will be defined as plasma CMV DNA concentration	At Weeks 12, 16 and 20
Secondary	Percentage of Participants With Recurrence of CMV Viremia During the First 8 Weeks and Through Week 12 to Week 20	Recurrence of CMV viremia is defined as plasma CMV DNA concentrations greater than or equal to (>=) LLOQ, when assessed by central specialty laboratory, in 2 consecutive plasma samples separated by at least 5 days after achieving confirmed viremia clearance.	From first dose of study drug up to Week 8, and through Week 12 to Week 20
Secondary	Percentage of Participants With Recurrence of CMV Viremia During on Treatment and off Treatment	Recurrence of CMV viremia is defined as plasma CMV DNA concentrations >= LLOQ, when assessed by central specialty laboratory, in 2 consecutive plasma samples separated by at least 5 days after achieving confirmed viremia clearance. On treatment is the period over which participant received actual dosing (that can be before the stipulated 8 weeks of study-assigned treatment). Off treatment is the period after study treatment.	From first dose of study drug up to Week 8 (on treatment) and Week 20 (off treatment)
Secondary	Percentage of Participants With Recurrence of CMV Viremia Requiring Alternative Treatment After Achieving CMV Viremia Clearance at Study Week 8	Recurrence of CMV viremia is defined as plasma CMV DNA concentrations >=LLOQ, when assessed by central specialty laboratory, in 2 consecutive plasma samples separated by at least 5 days after achieving confirmed viremia clearance.	At Week 8
Secondary	Percentage of Participants With Mutations in the CMV Genes Conferring Resistance to Maribavir	Percentage of participants with mutations in the CMV genes conferring resistance to maribavir will be reported.	Up to Week 20
Secondary	Number of Participants With All-cause Mortality During the Study	All-cause mortality during the study will be reported.	Up to Week 20
Secondary	Maximum Observed Plasma Concentration (Cmax) at Steady State for Maribavir	Cmax at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8, and 12 hours post-dose
Secondary	Time to Reach Cmax (Tmax) at Steady State for Maribavir	Tmax at steady state of maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Minimum Observed Plasma Concentration (Cmin) for Maribavir	Cmin of maribavir will be assessed.	Pre-dose and at Weeks 1, 4, and 8
Secondary	Area Under the Plasma Concentration-Time Curve From Time 0 to Time of the Last Quantifiable Concentration Area (AUC0-t) at Steady State for Maribavir	AUC0-t at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Area Under the Plasma Concentration-Time Curve Over 1 Dosing Interval of 12 Hours (AUC0-tau) at Steady State for Maribavir	AUC0-tau at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Half -life (t1/2) at Steady State for Maribavir	t1/2 at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Terminal Elimination Rate Constant (Lambda z) at Steady State for Maribavir	Lambda z at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Apparent Volume of Distribution (Vz/F) at Steady State for Maribavir	Vz/F at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose
Secondary	Apparent Oral Clearance (CL/F) at Steady State for Maribavir	CL/F at steady state for maribavir will be assessed.	Week 1, Day 7: Pre-dose, 0.5, 1.5, 3, 4, 6, 8 and 12 hours post-dose

External Links

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