Effects of Long-Term Treatment With Valaciclovir (Valtrex) on Epstein-Barr Virus - Full Text View

Sponsored by:	National Institute of Allergy and Infectious Diseases (NIAID)
Information provided by:	National Institutes of Health Clinical Center (CC)
ClinicalTrials.gov Identifier:	NCT00005924

Purpose

This study will examine the effects of long-term antiviral therapy with valaciclovir (Valtrex) on Epstein-Barr virus infection. This virus infects more than 95 percent of people in the United States. Most are infected in childhood, have no symptoms, and are unaware of their infection. People infected as adolescents or adults may develop infectious mononucleosis, which usually resolves completely. Once infected, most people shed the virus from their throat occasionally, and all carry the virus in their white blood cells for life. This study will determine whether the amount of virus in the blood declines or disappears with long-term valaciclovir treatment.

Normal volunteers who are not taking any antiviral medicines and patients enrolled in NIH's protocol no. 97-I-0168 (Evaluation of Valaciclovir for Prevention of Herpes Simplex Virus Transmission) or Glaxo-Wellcome protocol HS2AB 3009 at collaborating centers may be eligible for this study. Patients in the multi-center study must be about to start valaciclovir therapy for at least 1 year. All candidates must be 18 years of age or older.

Study participants will be seen in clinic for about 1 hour every 3 months for a year. During these visits, they will provide information about the medicines they are taking, gargle twice with salt water and spit the fluid into a tube, and have blood drawn (no more than 8 teaspoons each visit). The blood and gargled fluid will be tested for the amount of Epstein-Barr virus and antibodies to the virus. (Blood samples will also be tested for HLA type in order to do immunologic studies in the laboratory. HLA is a marker of the immune system that is similar to blood-typing testing.)

The results in people taking valaciclovir will be compared with those in people not taking the drug. People whose results show the virus has disappeared from the body will continue to be followed twice a year for 5 years with the blood and gargling tests to continue to look for evidence of virus. Also, people who develop symptoms resembling mononucleosis (e.g., enlarged lymph nodes with fever and sore throat) will be asked to have their blood tested for the virus.

Condition
Epstein Barr Virus Infection Healthy

U.S. FDA Resources

Study Type:	Observational
Official Title:	Persistence of Epstein-Barr Virus in Vivo

Further study details as provided by National Institutes of Health Clinical Center (CC):

Estimated Enrollment:	125
Study Start Date:	June 2000

Detailed Description:

Epstein-Barr virus (EBV) is the cause of heterophile-positive infectious mononucleosis. After primary EBV infection, the virus persists in resting memory B lymphocytes and can be detected in oropharyngeal secretions. Short term (1 month) treatment with oral acyclovir, which inhibits EBV replication, results in loss of virus shedding from the oropharynx, but the virus persists in B cells. The goal of this study is to determine if EBV will no longer persist in B cells in patients treated with long term (20 month) oral valaciclovir (which is metabolized to acyclovir). Blood samples and throat washings will be obtained every three months from individuals who are receiving valaciclovir for treatment of genital herpes simplex virus infection. These samples will be analyzed for EBV DNA to determine if the level of EBV DNA declines or becomes negative with long term antiviral therapy. If the level of EBV DNA becomes undetectable in EBV-seropositive persons during the study, we will ask the patients to return twice a year for five years or if they develop symptoms of mononucleosis, so that EBV DNA in their blood and throat washings can be studied. Knowledge gained from this study should provide important insights into the mechanism of persistence of EBV infection.

Eligibility

Ages Eligible for Study:	18 Years and older
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

INCLUSION CRITERIA:
1. 18 years of age or older and deemed healthy by current medical status and laboratory tests.
2. Willing to be seen every three months for one year.
3. Have symptomatic recurrent genital herpes disease confirmed by their private medical doctor.
4. Eligible for suppressive antiviral therapy for genital herpes disease: history of genital herpes AND either a positive culture for HSV from the genital area or a positive serology for HSV-2 from the patient's private physician. If the subject does not have a positive HSV genital culture or HSV-2 serology, we will confirm the diagnosis by an HSV-2 Western Blot.
5. Recurrence rate between 3 and 9 recurrences a year.
6. Have never taken or have been off HSV suppressive therapy for three months prior to entering study.
7. In opinion of investigator, subjects must be able to comply with protocol requirements.

EXCLUSION CRITERIA:

Subjects who are known or suspected to be immunocompromised. This includes subjects receiving immunosuppressive therapy, subjects with malignancy or subjects who acknowledge being seropositive for HIV.
Subjects with a history of 10 or more HSV recurrences per year.
Impaired real function as defined by serum creatine greater than 1.5 mg/dl (133uM).
Impaired hepatic function as defined by an alanine transaminase (ALT) level greater than 3 times the normal upper limit.
Known hypersensitivity to acyclovir, valaciclovir, famciclovir, or ganciclovir.
Malabsorption syndrome or other gastro-intestinal dysfunction that might impair drug dynamics.
Women contemplating pregnancy within the year's duration of receiving valaciclovir from us.
Women of child bearing potential not using an effective method of contraception. Effective contraception is use of birth control pills or use of a barrier method (e.g. condom) with a spermicide.
Positive pregnancy test (or pregnant females or nursing mothers).
Swallowing disorders which would make gargling difficult.

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00005924

Locations

United States, Maryland
National Institutes of Health Clinical Center, 9000 Rockville Pike
Bethesda, Maryland, United States, 20892

Sponsors and Collaborators

National Institute of Allergy and Infectious Diseases (NIAID)

More Information

Additional Information:

NIH Clinical Center Detailed Web Page This link exits the ClinicalTrials.gov site

Publications:

Khan G, Miyashita EM, Yang B, Babcock GJ, Thorley-Lawson DA. Is EBV persistence in vivo a model for B cell homeostasis? Immunity. 1996 Aug;5(2):173-9.

Miyashita EM, Yang B, Lam KM, Crawford DH, Thorley-Lawson DA. A novel form of Epstein-Barr virus latency in normal B cells in vivo. Cell. 1995 Feb 24;80(4):593-601.

Babcock GJ, Decker LL, Volk M, Thorley-Lawson DA. EBV persistence in memory B cells in vivo. Immunity. 1998 Sep;9(3):395-404.

Study ID Numbers:	000163, 00-I-0163
Study First Received:	June 24, 2000
Last Updated:	September 19, 2008
ClinicalTrials.gov Identifier:	NCT00005924 History of Changes
Health Authority:	United States: Federal Government

Keywords provided by National Institutes of Health Clinical Center (CC):

B Cell
Epstein-Barr Virus

Study placed in the following topic categories:

Valacyclovir
Virus Diseases
DNA Virus Infections

Epstein-Barr Virus Infections
Healthy
Herpesviridae Infections

Additional relevant MeSH terms:

Virus Diseases
Neoplasms
Tumor Virus Infections
DNA Virus Infections

Epstein-Barr Virus Infections
Infection
Neoplasms, Experimental
Herpesviridae Infections

ClinicalTrials.gov processed this record on May 07, 2009