HSV529 Vaccine in HSV-2 Seropositive Adults

Completed · Phase 1

Conditions studied: Herpes Simplex Virus 2

In brief

The purpose of the study is to determine the safety of HSV529 vaccine in healthy volunteers with HSV infection and to determine if administration of the HSV529 vaccine increases the immune response in genital skin.

Key facts

Study ID

NCT02571166

Run by

Fred Hutchinson Cancer Center

People needed

10

Starts

2015-11-01

Expected to finish

2018-12-01

Last updated by the study team

2019-01-14

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• HSV-2 seropositive by UW Western blot with a history of recurrent genital herpes, with lesions in an area amenable to biopsy.
• Aged 18 to 55 years on the day of enrollment.
• In good general health with absence of significant health problems as determined by medical history, physical examination, and laboratory screening performed during screening visits.
• Hemoglobin, hematocrit, white blood cell count, platelet count, serum creatinine, and liver function (ALT, AST, alkaline phosphatase, total bilirubin) screening laboratory results do not fall into the range of values that are Grade 1 or greater as per the toxicity grading scale.
• Female subjects must be of non-childbearing potential i.e. surgically sterilized (bilateral tubal ligation, hysterectomy) or, if of child-bearing potential and sexually active with a male partner, she must be willing to use a highly effective method of contraception (e.g., intrauterine device (IUD); oral contraceptives, diaphragm or condom in combination with contraceptive foam, jelly or cream; Norplant, DepoProvera, contraceptive skin patch or cervical ring) for at least 30 days prior to vaccination and until 30 days after final vaccination or be in a monogamous relationship with a male partner who has undergone a vasectomy at least 6 months prior to first dose of HSV529.
• Willingness to attend all scheduled visits and able to comply with all trial procedures (e.g., blood draws, biopsies, completion of diary cards, return for follow-up visits, accessible by phone or pager, able to self-sample for assessment of asymptomatic shedding of HSV, and not planning on moving from study area).
• HIV seronegative.
• Subject is willing not to use antiviral therapy 3 days before each injection and during swabbing periods. If recurrences occur during swabbing periods, participants will be asked NOT to take antiviral therapy.
• Subject is willing to forgo receipt of a licensed, live vaccine in the 30 days preceding each dose of vaccine or in the 30 days following each dose of vaccine. The inactivated flu vaccine can be used ≥14 days before or ≥14 days after administration of study vaccine, if this is felt to be necessary.
• Persons who have close contact with infants or immunocompromised individuals are willing to avoid such contact for 3 days after each injection.

You may not qualify if…

• Subject is pregnant or nursing OR planning to become pregnant in the timeframe that begins 30 days prior to the first vaccination and ends 30 days after the third vaccination.
• Body Mass Index greater than 35.
• Hepatitis C seropositive
• Hepatitis B surface antigen positive
• Participation in another clinical trial investigating a vaccine, drug, medical device, or medical procedure in the 4 weeks preceding the first trial vaccination or planned participation during the study period up to 6 months after the last dose of vaccine. The non-interventional follow-up for an earlier study (e.g., long-term surveillance) will be allowed.
• Severe active infection or serious HSV-2 related or unrelated medical conditions that, in the opinion of the investigator, would prevent study completion.
• Subjects with 9 or more symptomatic recurrences of genital herpes disease within the year prior to Day 0.
• A history of HSV infection of the eye (e.g., herpes simplex interstitial keratitis or uveitis).
• A history of herpes gladiatorum, herpetic whitlow or eczema herpeticum.
• A history of lesions caused by HSV on either arm.
• A history of herpes-associated erythema multiforme.
• A history of a clinically significant autoimmune disorder.
• Known or suspected congenital or acquired immunodeficiency.
• Receipt of anti-cancer chemotherapy or radiation therapy within the preceding 6 months.
• Subjects using corticosteroids (excluding topical, inhaled or nasal) or any immunomodulating drugs (see Prohibited Medications Section) within 42 days prior to the first vaccination. An immunosuppressive dose of corticosteroids is defined as ≥10 mg prednisone equivalent per day for >14 days.
• Subjects without a spleen.
• Subjects receiving immunoglobulin within the past 6 months or anticipated receipt of immunoglobulin during the 28 days following each vaccination.
• Bleeding disorder, or receipt of anticoagulants that, in the opinion of the Investigator, would interfere with the subject's participation in the trial.
• Known allergy or intolerance to vaccine components [e.g., potassium glutamate (possible cross-reaction to monosodium glutamate), sucrose] or to a vaccine containing any of the same substances.
• Known allergy or intolerance to silver nitrate or lidocaine.
• Known allergy or intolerance to acyclovir or valacyclovir.
• Chronic illness that, in the opinion of the Investigator, is at a stage where it might interfere with trial conduct or completion.
• History of keloid formation or excessive scarring.
• History of frequent cellulitis or boils (>3 episodes in past 2 years) requiring antibiotic therapy.
• Prior receipt of an HSV vaccine.

Where it is running

• University of Washington Virology Research Clinic — Seattle, Washington, United States

Full record on ClinicalTrials.gov

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