Herpes Simplex Type 1 Suppression in Hepatitis C

Chronic Hepatitis C Infection Clinical Trial

— HSV1/HCV  

Official title:

HSV-1 Suppression in HCV Infected Veterans Who Are Seronegative for HSV-2

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01580995
• Other study ID #: CLIN-001C-10F
• Status: Completed
• Phase: Phase 2
• First received: April 13, 2012
• Last updated: May 12, 2015
• Start date: April 2012
• Est. completion date: March 2015

Study information

• Verified date: May 2015
• Source: VA Office of Research and Development
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to examine the effects of valacyclovir in patients who have chronic hepatitis C, antibodies to herpes simplex type 1 infection but do not have antibodies to herpes simplex type 2 infection. Herpes simplex type 1 infection commonly causes cold sores or fever blisters, also known as herpes labialis, but most persons do not have any symptoms at all. Valacyclovir is a medication which is approved by the Food and Drug administration to treat herpes labialis. Valacyclovir has not been approved to treat chronic hepatitis C infection.

The study will take 16 weeks. Participants will be assigned to take either the study drug, valacyclovir, or a sugar pill that looks exactly like valacyclovir. The researchers and patients will not know which medication they are receiving. Study visits will occur every two weeks and will take approximately 30-45 minutes. All study visits will occur at the G.V. Sonny Montgomery VA Medical Center in Jackson, Mississippi.

Description:

This is a randomized double-blind placebo-controlled clinical trial evaluating the effect of 500 mg valacyclovir twice daily on HCV viral load in HSV-1/HCV co-infected patients seronegative for HSV-2. Potential participants will be recruited from the Jackson VAMC viral hepatitis clinics. Eligible individuals will be invited to enroll in the study in a noncoercive manner. Study personnel will obtain full informed consent.

Using a computer generation randomization scheme, patients will be randomized 1:1 in blocks of 4 to receive valacyclovir 500 mg po twice daily or matching placebo. Patients will be counseled on the signs and symptoms of herpes labialis and genital herpes and complete a questionnaire to document medical/social history. Venipuncture will be performed every four weeks (i.e., at every other follow-up visit) to monitor complete blood cell count, liver function tests, serum levels of hepatitis C RNA and Herpeselect IgG HSV-2 ELISA. A de-identified baseline serum sample will be collected and stored in VA approved research space for future testing. At each visit, pill-count and tolerability of medications will be assessed. Patients will be asked about signs or symptoms of genital herpes. Data will be kept in a study chart labeled with the participant's coded study number in a locked office. Information from each study visit will be recorded into the chart by the PI or RA and entered into an encrypted database on a secure VA server. Baseline characteristics of the placebo and intervention group will be compared using appropriate parametric tests. HCV viral loads will be log10 transformed and analyzed using an intention to treat model.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: March 2015
• Est. primary completion date: December 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Chronic hepatitis C infection with a detectable HCV RNA in the serum on two occasions, 6 months apart

• Focus HSV-2 IgG negative and Focus HSV-1 IgG positive, using manufacturer's cut-offs

Exclusion Criteria:

• Antiherpes or immunomodulatory therapy during the past 30 days,

• HIV or chronic hepatitis B infection,

• Decompensated liver disease (ascites, hepatic encephalopathy, coagulopathy, jaundice/icterus),

• Creatinine clearance <50 ml/min.,

• Female subject who is pregnant or nursing,

• Gastrointestinal disorder which might result in malabsorption of valacyclovir,

• History of erythema multiforme major, thrombotic thrombocytopenia purpura or hemolytic uremic syndrome,

• Allergy to valacyclovir or related drug.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Hepatitis C Infection
• Hepatitis
• Hepatitis A
• Hepatitis C
• Hepatitis C, Chronic
• Hepatitis, Chronic

Intervention

Drug:
• Valacyclovir
Valacyclovir 500 mg po bid
• Placebo
Placebo tablet twice daily

Locations

Country	Name	City	State
United States	G.V. (Sonny) Montgomery VA Medical Center, Jackson, MS	Jackson	Mississippi

Sponsors (2)

Lead Sponsor	Collaborator
VA Office of Research and Development	GlaxoSmithKline

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in HCV RNA viral load	Measure change in HCV RNA viral load in treatment group as compared with placebo	Baseline, 12 weeks, 16 weeks	No