A Study of a Therapeutic DNA Vaccine for Chronic Hepatitis C Virus (HCV) Infection

Overview

  • Study type

    Interventional
  • Study phase

    I
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • During the early phases (phases 1 and 2), researchers assess safety, side effects, optimal dosages and risks/benefits. In the later phase (phase 3), researchers study whether the treatment works better than the current standard therapy. They also compare the safety of the new treatment with that of current treatments. Phase 3 trials include large numbers of people to make sure that the result is valid. There are also less common very early (phase 0) and later (phase 4) phases. Phase 0 trials are small trials that help researchers decide if a new agent should be tested in a phase 1 trial. Phase 4 trials look at long-term safety and effectiveness, after a new treatment has been approved and is on the market.

  • Site IRB
    • Jacksonville, Florida: 13-008106
    • Rochester, Minnesota: 13-008106
    NCT ID: NCT02772003
    Sponsor Protocol Number: MAY2013-02-01

About this study

The purpose of this study is to determine whether INO-8000 alone or in combination with INO-9012 (IL-12) is safe and induces a Hepatitis C virus-specific immune response.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Pre-Registration Inclusion Criteria:

  • Presence of active, chronic HCV infection confirmed by positive HCV RNA.
  • Age ≥ 18 years old.
    • Note: Because no dosing or adverse event data are currently available on the use of INO-9012 in participants <18 years of age, children are excluded from this study but will be eligible for future pediatric trials, if applicable.
  • Willingness to use adequate contraception to avoid pregnancy or impregnation for the duration of study participation.
  • Notes: 
    • The effects of INO-8000 with or without INO-9012 on the developing human fetus at the recommended therapeutic dose are unknown. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation.
    • For men and women who are not postmenopausal [i.e., ≥12 months of non-therapy-induced amenorrhea, confirmed by follicle stimulating hormone (FSH), if not on hormone replacement] or surgically sterile (vasectomy in males or absence of ovaries and/or uterus in females), agreement to remain abstinent or use highly effective or combined contraceptive methods that result in a failure rate of < 1% per year during the treatment period and at least through week 12 after last dose.
    • Abstinence is only acceptable if it is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, or post-ovulation methods) and withdrawal are not acceptable methods of contraception;
    • Examples of contraceptive methods with an expected failure rate of < 1% per year include male sterilization and hormonal implants. Alternatively, proper use of combined oral or injected hormonal contraceptives and certain intrauterine devices or two methods (e.g., two barrier methods such as a condom and a cervical cap) may be combined to achieve a failure rate of < 1% per year (barrier methods must always be supplemented with the use of a spermicide);
    • Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her study physician immediately.
    • Should a female partner of a male study participant become pregnant while the male participant is on study, the male participant should inform his study physician immediately.
  • Willingness to avoid excessive use of alcohol during the study.
    • Note: Excessive use is defined as drinking ≥8 alcoholic drinks per week on average.
  • Willingness to provide blood samples for research tests specified in the protocol.
  • Ability to understand and willingness to sign a written informed consent document.

Pre-Registration Exclusion Criteria:

  • Failure of previous HCV therapies.
  • HIV infection.
  • Any previous treatment for HCV ≤ 6 months prior to registration.
  • Other uncontrolled immune-compromising illness
  • Autoimmune disorders, transplant recipients, other immunosuppression including any concurrent condition requiring the use of immunosuppressive/ immunomodulating agents.
    • Exception: eye drop-containing and infrequent inhaled corticosteroids are permissible. Topical corticosteroids are permissible at locations other than the administration site (upper arm).
    • Note: All systemic corticosteroids must be discontinued at least 4 weeks prior to randomization. Inhaled corticosteroids must be discontinued ≥ 48 hours prior to randomization and courses of more than 2 weeks are not permissible within 4 weeks of randomization.
  • Ongoing HBV infection.
  • Documented evidence of fibrosis or cirrhosis (Metavir 2, 3,and 4) and subjects with significant extrahepatic manifestations of hepatitis C (such as cryoglobulinemia with symptoms or evidence of end-organ manifestations, renal disease, type 2 diabetes, or porphyria cutanea tarda.
  • Other known causes of significant liver disease including chronic or acute hepatitis B, acute hepatitis A, hemochromatosis, or homozygote alpha-1 antitrypsin deficiency.
  • Active malignancy.
    • Exception: non-melanoma skin cancer(s) for which diagnosis and treatment was completed ≥ 3 years prior to pre-registration.
  • History of major organ transplantation with an existing functional graft.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or psychiatric illness/social situations that would limit compliance with study requirements.
  • History of cardiac arrhythmia, controlled or uncontrolled, including ventricular and supraventricular arrhythmia.
  • Pregnant or nursing women. Note: Pregnant women are excluded from this study because INO-8000 has an unknown potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with this DNA vaccine, breastfeeding should be discontinued if the mother is treated with INO-8000.
  • Current diagnosis or history of cardiac pre-excitation syndromes (e.g., Wolff-Parkinson-White).
  • Metal implants on same limb as intended administration site.
  • Tattoos, scars, active lesions, or rashes ≤ 2 cm of the intended site of study treatment.
  • Documentation of history of seizure within previous 5 years.
  • Pacemaker or other implanted device.
  • Any condition that, in the clinical judgement of the investigator, would place a participant at unreasonably increased risk.

Registration Inclusion Criteria:

  • Serum or plasma HCV RNA level ≥ 10,000 IU/mL.
  • Screening HCV genotype, demonstrating genotype 1.
  • Alpha feto protein (AFP) levels within normal institutional limits or judged to be not clinically significant by the investigator.
    • Exception: If deemed clinically significant, then liver imaging must be available within previous 6 months (e.g., ultrasound, CT scan, MRI) showing no evidence of hepatocellular carcinoma.
  • ECOG performance status (PS) 0 or 1 (See Appendix A).
  • Screening laboratory values (serum chemistry, hematology, PT(INR)/aPTT, and CPK) obtained up to 45 days prior to administration of first vaccine injection on Day 0 within institutional normal range or judged to be not clinically significant by PI and medical monitor.
  • 12-lead ECG showing normal heart rhythm.
    • Note: If there are abnormalities, then the abnormalities must be judged to be not clinically significant by the investigator.

Registration Exclusion Criteria:

  • Receiving any other investigational agents ≤ 6 months prior to Registration.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to INO-8000 and INO-9012.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Lewis Roberts, M.B., Ch.B., Ph.D.

Open for enrollment

Contact information:

Cancer Center Clinical Trials Referral Office

855-776-0015

Rochester, Minn.

Mayo Clinic principal investigator

Lewis Roberts, M.B., Ch.B., Ph.D.

Open for enrollment

Contact information:

Cancer Center Clinical Trials Referral Office

855-776-0015