RECRUITING

Study of Treatment for HPV16+ ASC-US or LSIL

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Phase I clinical trial to assess safety of pNGVL4aCRTE6E7L2 DNA and TA-CIN protein vaccinations, and to seek the appropriate dose of the pNGVL4aCRTE6E7L2 DNA vaccine

Official Title

Phase I Clinical Trial Assessing the Safety and Feasibility of Intramuscular pNGVL4aCRTE6E7L2 and TA-CIN Administration for the Treatment of Patients With Persistent HPV16+ ASC-US or LSIL

Quick Facts

Study Start:2023-07-10

Study Completion:2025-02-28

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT03913117

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:19 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
1. Patients with persistent (\>6 month period) ASC-US/LSIL determined by cervical cytology at study entry (ThinPrep with imaging) 2. Patients whose cytologic samples are persistent (\>6 month period) HPV16+ by Roche Cobas 4800, Roche Linear Array HPV Genotyping test or other FDA-approved HPV genotyping test at study entry. Co-infections with HPV types other than HPV16 are permissible for study entry. 3. Age ≥ 19 years 4. Baseline Eastern Cooperative Oncology Group 5. Patients must have adequate organ function at the time of enrollment as defined by the following parameters: * White blood cell count \> 3,000 * Absolute lymphocyte number \> 500 * Absolute neutrophil count \> 1,000 * Platelets \> 90,000 * Hemoglobulin \> 9 * Total bilirubin \<3 X the institutional limit of normal * AST(SGOT)/ALT(SGPT) \<3 X the institutional limit of normal * Creatinine \< 2.5X the institutional limit of normal 6. Women of child-bearing potential must agree to use two forms of contraception (hormonal and barrier) prior to study entry and for 3 months after study completion. 7. Ability to understand and the willingness to sign a written informed consent document. 8. Subject is able to adhere to the study visit schedule and other protocol requirements.	1. Patients with ASC-US/LSIL determined by cervical cytology at study entry that are HPV16 negative. 2. Histologic evidence of CIN2+ 3. Patients with a diagnosis of immunosuppression or prolonged, active use of immunosuppressive medications such as steroids. 4. Prior vaccination with any HPV antigen (prophylactic or therapeutic). 5. Patients who are receiving any other investigational agents within 28 days prior to the first dose. 6. Patients with an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements. 7. Patients with a history of autoimmune disease such as multiple sclerosis, exclusive of a history of thyroiditis, psoriasis, Sjrogen's, or inflammatory bowel disease. 8. Patients with a history of allergic reactions attributed to compounds used in agent preparation. 9. Patients who are pregnant or breast feeding. 10. Patient with active or chronic infection of HIV, HCV, or HBV. 11. Patients who have had a prior LEEP or cervical conization procedure. 12. History of prior malignancy permitted if patient has been disease free for ≥ 5 years; however individuals with completely resected basal cell or squamous cell carcinoma of the skin within this interval may be enrolled. 13. Inability to understand or unwillingness to sign an informed consent document.

Inclusion Criteria

Exclusion Criteria

1. Patients with persistent (\>6 month period) ASC-US/LSIL determined by cervical cytology at study entry (ThinPrep with imaging)
2. Patients whose cytologic samples are persistent (\>6 month period) HPV16+ by Roche Cobas 4800, Roche Linear Array HPV Genotyping test or other FDA-approved HPV genotyping test at study entry. Co-infections with HPV types other than HPV16 are permissible for study entry.
3. Age ≥ 19 years
4. Baseline Eastern Cooperative Oncology Group
5. Patients must have adequate organ function at the time of enrollment as defined by the following parameters:
* White blood cell count \> 3,000
* Absolute lymphocyte number \> 500
* Absolute neutrophil count \> 1,000
* Platelets \> 90,000
* Hemoglobulin \> 9
* Total bilirubin \<3 X the institutional limit of normal
* AST(SGOT)/ALT(SGPT) \<3 X the institutional limit of normal
* Creatinine \< 2.5X the institutional limit of normal
6. Women of child-bearing potential must agree to use two forms of contraception (hormonal and barrier) prior to study entry and for 3 months after study completion.
7. Ability to understand and the willingness to sign a written informed consent document.
8. Subject is able to adhere to the study visit schedule and other protocol requirements.

1. Patients with ASC-US/LSIL determined by cervical cytology at study entry that are HPV16 negative.
2. Histologic evidence of CIN2+
3. Patients with a diagnosis of immunosuppression or prolonged, active use of immunosuppressive medications such as steroids.
4. Prior vaccination with any HPV antigen (prophylactic or therapeutic).
5. Patients who are receiving any other investigational agents within 28 days prior to the first dose.
6. Patients with an uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
7. Patients with a history of autoimmune disease such as multiple sclerosis, exclusive of a history of thyroiditis, psoriasis, Sjrogen's, or inflammatory bowel disease.
8. Patients with a history of allergic reactions attributed to compounds used in agent preparation.
9. Patients who are pregnant or breast feeding.
10. Patient with active or chronic infection of HIV, HCV, or HBV.
11. Patients who have had a prior LEEP or cervical conization procedure.
12. History of prior malignancy permitted if patient has been disease free for ≥ 5 years; however individuals with completely resected basal cell or squamous cell carcinoma of the skin within this interval may be enrolled.
13. Inability to understand or unwillingness to sign an informed consent document.

Contacts and Locations

Study Contact

Wendy Wu, MS

CONTACT

+886 2 8226 8451

wendy@papivax.com.tw

Yung-Nien Chang, Ph.D.

CONTACT

410-804-9662

changyn@papivax.com

Study Locations (Sites)

UAB | The University of Alabama at Birmingham

Birmingham, Alabama, 35249

United States

Johns Hopkins University

Baltimore, Maryland, 21231

United States

Collaborators and Investigators

Sponsor: University of Alabama at Birmingham

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-07-10

Study Completion Date2025-02-28

Study Record Updates

Study Start Date2023-07-10

Study Completion Date2025-02-28

Terms related to this study

Keywords Provided by Researchers

HPV16

Additional Relevant MeSH Terms

ASC-US
LSIL