Activity of Valomaciclovir in Infectious Mononucleosis Due to Primary Epstein-Barr Virus Infection

Phase 1

Completed

Conditions: Infectious Mononucleosis

Interventions: Drug: Valomaciclovir
Drug: placebo

Registration Number: NCT00575185

Lead Sponsor: University of Minnesota

Brief Summary: This will be a randomized, placebo-controlled, double-blind single-center proof of concept study to evaluate the anti-EBV activity of 4 grams of valomaciclovir (2 grams BID) for 21 days in subjects with infectious mononucleosis documented to be caused by primary EBV infection. Otherwise healthy subjects (≥15 years old) referred to us with a clinical diagnosis of primary infectious mononucleosis will be screened and those with laboratory-confirmed primary EBV infection will be enrolled.

Detailed Description: Subjects will be seen 2 times a week for 3 weeks and then weekly for 3 weeks. Clinical findings, clinical lab tests, EBV viral loads, and EBV antibody titers will be obtained at each clinic visit.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 23

Inclusion Criteria

Age 15 years or older
Within 14 days of initial symptoms of present illness diagnosed by a health care provider as infectious mononucleosis and confirmed to be due to primary EBV by antibody profile. The criteria for antibody confirmation of primary EBV at the screening visit are: 1)Positive for anti-EBV VCA IgM antibody and negative for anti-EBV EBNA1 IgG antibody; 2)EBV antibody testing will be done in the Clinical Virology Research Laboratory using commercial ELISA kits (Diamedix Corporation, Miami, FL).
Willingness to sign the Informed Consent Form (ICF)
Willingness to contribute samples of blood and oral washings at regular intervals
Males and females must use effective contraception during treatment and for at least 90 days following treatment
Negative pregnancy test result at the Screening Visit for females of childbearing potential (including females who have had a bilateral tubal ligation). Female patients of childbearing potential must be willing to use an approved method of double-barrier contraception (hormonal plus barrier or barrier plus barrier, eg, diaphragm plus condom) from the time of first dose administration until 90 days after completion of dosing and male patients with female partners of childbearing potential must be willing to use a condom. Patients who are sterile or infertile (defined as those who are postmenopausal or have undergone a complete hysterectomy) are eligible.
Estimated creatinine clearance (Cockcroft and Gault method) ≥ 60 ml/min
Absolute neutrophil count ≥ 1000 cells/microliter
Platelets ≥ 100,000/microliter
Hemoglobin ≥ 9.5 g/dL

Exclusion Criteria

Previous history of infectious mononucleosis-like illness
Immunosuppressed due to medical disease and/or immunosuppressive or immunomodulating medications (e.g., corticosteroids prior to enrollment, cytotoxic drugs, interferons)
Another intercurrent viral infection (including HIV), based on history or referring physician medical evaluation
More than 7 days elapsed since onset of illness (including screening time)
The following concomitant medications are prohibited: probenecid, trimethoprim, myelosuppressive therapies, and medications known to be nephrotoxic
Breast feeding during the study
Corticosteroids are not permitted. If they are prescribed by the subject's primary physician for treatment of this acute disease after the subject has enrolled, the subject will be replaced.

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Valomaciclovir	Valomaciclovir	Valomaciclovir 2 grams orally twice daily for 21 days
placebo	placebo	placebo 2 tablets twice daily for 21 days

Primary Outcome Measures

Name	Time	Method
Number of Participants With Improvement in Clinical Symptoms and Reductions in Viral Burden From Baseline	21 days	All subjects had confirmed cases of EB and will be assessed for Improvement of clinical symptoms (ie: tiredness, nausea etc)and reduction in viral burden from baseline

Secondary Outcome Measures

Name	Time	Method
Number of Participants Who Experienced Adverse Events During the Study Safety and Tolerability	15 days	Assessing adverse events in participants to see if this drug causes more or less side effects