Safety, Tolerability, and Immunogenicity of GTL001 Vaccine Adjuvanted With Imiquimod Cream in HPV 16- and/or HPV 18-Infected Women Aged 25 to 65 Years, With Normal Cytology, ASCUS, or LSIL

Stopped early · Phase 1

Conditions studied: HPV 16- and/or HPV 18-Infected Women With Normal Cytology, ASCUS, or LSIL

In brief

A Phase 1, Open-Label Study to Evaluate the Safety, Tolerability, and Immunogenicity of GTL001 Vaccine Adjuvanted With Imiquimod Cream in HPV 16- and/or HPV 18-Infected Women Aged 25 to 65 Years, With Normal Cytology, ASCUS, or LSIL.

Key facts

Study ID

NCT02689726

Run by

Genticel

People needed

13

Starts

2015-08-01

Expected to finish

2016-08-01

Last updated by the study team

2016-12-02

Who can join

Age: 25 and older, up to 65. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Females between the ages of 25 and 65 years, inclusive, at the time of screening.
• Subject is in generally good health based on medical history and on clinically acceptable results, in the judgment of the investigator, on the following assessments: physical examination, vital signs, clinical chemistry, and hematology.
• Cervical HPV 16 and/or 18 infection confirmed by cobas® HPV Test (Roche Molecular Systems, Inc) real-time polymerase chain reaction (RT PCR) assay at screening.
• Cervical cytological evaluation with a normal, ASCUS, or LSIL result.
• Subjects of childbearing potential must use effective contraception at the time of GTL001 injection and for at least 12 months after the first vaccination. Effective methods of birth control include those that result in a low failure rate (ie, less than 1% per year) when used consistently and correctly, such as implants, injectable, combined oral contraceptives, desogestrel only pill, levonorgestrel-releasing intrauterine system, intrauterine devices, vasectomized partner, and true sexual abstinence. Subjects not of childbearing potential include those who are surgically sterile or postmenopausal (no menses for the previous 12 months).
• Subject is capable of understanding the written informed consent, provides signed and witnessed written informed consent, and agrees to comply with protocol requirements.
• In the opinion of the investigator, the subject is able to comply with the protocol and has a high probability of completing the study.

You may not qualify if…

• Current or history of untreated high-grade cervical lesion (either CIN2 or CIN3).
• Current or history of cervical, vulvar, or vaginal cancer.
• Prior exposure to HPV prophylactic vaccine, regardless of number of doses received, or participation in another HPV vaccination clinical trial.
• Current acute or chronic disease, other than HPV 16/18 infection, which would be expected to interfere with the protocol-defined evaluations.
• Clinically significant gynecological abnormalities that could interfere with study procedures (eg, prolapse, severe vaginal atrophy, myoma, hysterectomy) in the judgment of the investigator.
• Malignancy, or treatment for malignancy, within the previous 2 years, with the exception of basal cell or squamous cell carcinoma of the skin.
• Clinically important abnormalities in the physical examination or laboratory tests during the screening period (ie, hemoglobin level <9.5 g/dL, white blood cells <2500 cells/mm3, aspartate aminotransferase and/or alanine aminotransferase ≥1.5 × the upper limit of normal [ULN], creatinine ≥1.25 × ULN, alkaline phosphatase ≥2 × ULN, and total bilirubin >ULN).
• Administration of any live viral vaccine within 3 months or any inactivated (nonlive) vaccine within 2 weeks prior to screening.
• Primary or secondary systemic immunosuppression (defined as prolonged [≥7 days] use of corticosteroids that is ≥20 mg/day of prednisone equivalent or any other immunosuppressive drug).
• History of severe allergy requiring hospital care or history of severe asthma requiring oral or parenteral drug management in the last year.
• Known hypersensitivity to imiquimod.
• History of a severe reaction to any drug or vaccination.
• Medical condition with clinical and/or biological consequences judged by the investigator to be incompatible with ID vaccination.
• History of, or positive test results at screening for, human immunodeficiency virus, hepatitis B virus surface Ag, or hepatitis C virus.
• Current episode of symptomatic vaginal or genital infection.
• Current episode or history of genital herpes.
• Subject is pregnant or lactating/breastfeeding.
• Use of any investigational drug within 30 days before screening or current participation in another clinical trial.
• History of recent (within 1 year) alcohol/drug abuse.
• Employee or family member of the investigator or study site personnel.
• Enrollment goals have been reached in the subject's age cohort

Where it is running

• University of Louisville — Louisville, Kentucky, United States
• Wake Research Associates, LLC — Raleigh, North Carolina, United States
• Clinical Research Advantage, Inc./ Columbus Obstetricians and Gynecology, Inc. — Columbus, Ohio, United States
• Planned Parenthood Southeastern Pennsylvania — Philadelphia, Pennsylvania, United States

Full record on ClinicalTrials.gov

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