Clinical Study of HPV Therapeutic DNA Vaccine (NWRD08) in Patients With Cervical HPV16 and/or HPV18 Positive

Newish Technology

Status: Enrolling

Conditions: HSIL of Cervix

Treatments: Biological: NWRD08

Study type: Interventional

Funder types: Industry

Identifiers

NCT05905354

NEWISH-HPV-001

Details and patient eligibility

About

This is an open-label exploratory clinical study. The main objective is to explore the immunogenicity of HPV therapeutic DNA vaccine NWRD08.

Full description

The main objective is to explore the immunogenicity of HPV therapeutic DNA vaccine NWRD08.The secondary objective was to observe the safety of NWRD08 in cervical patients who were positive for HPV16 and/or HPV18, and to initially explore the efficacy of NWRD08.

Enrollment: 12 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Age ≥18 years old;
2. women who have sex;
3. HPV16 and/or 18 DNA and E6E7 mRNA were positive;
4. Patients with highly squamous intraepithelial lesions of the cervix confirmed by histology and cytology, or persistent cervical PV16 and/or 18 infection for more than 12 months;
5. Cervical tissue specimens/sections should be provided 4 weeks before the first treatment of HISL;
6. Electrocardiogram (ECG) is normal;
7. Women of reproductive age must have a negative serum pregnancy test within 1 week prior to the first dose and have agreed to use effective contraception during the study drug use period and within 6 months after the last dose of the study drug. For males, it should be surgical sterilization or consent to effective contraception during the study drug use period and within 6 months after the last study drug administration;
8. Have fully understood the study and voluntarily signed the ICF, be able to communicate well with the investigator and complete all treatments, examinations and visits required by the study protocol.

Exclusion criteria

1. any histopathologically confirmed adenocarcinoma in situ (AIS), high-grade vulvar, vaginal or anal intraepithelial tumors, or invasive cancers;
2. Patients with unsatisfactory colposcope;
3. Patients who were satisfied with colposcopy but not satisfied with ECC (patients who were positive for HPV18 or had abnormal adenocytes on cervical cytology but satisfied with colposcopy should undergo ECC examination);
4. Positive HPV type 31 or 33 or 45 or 52 or 58;
5. Have received cervical physical therapy;
6. pregnant, breastfeeding, or considering becoming pregnant during the study period;
7. previous history of therapeutic or preventive HPV vaccination;
8. Received any non-investigational inactivated vaccine injection within 2 weeks;
9. Received any non-investigational live vaccine within 4 weeks;
10. Acute or chronic bleeding or coagulopathy;
11. Less than two sites can be used for intramuscular injection;
12. Received chemotherapy, molecular targeted therapy, biological immunotherapy, or Chinese patent drugs for cervical lesions within 30 days before or during screening;
13. participated in other clinical trials within 30 days prior to screening, or was in the observation period of other clinical trials;
14. Continuous (more than 1 week) glucocorticoid therapy (dose equivalent to prednisone > 10 mg/ day), except hormone replacement therapy and endotracheal administration;
15. History of immune deficiency or autoimmune disease (such as rheumatoid joint disease, systemic lupus erythematosus, multiple sclerosis, etc.);
16. with uncontrolled severe infection;
17. Patients with a history of hepatitis B virus (HBV), hepatitis C virus (HCV) infection or human immunodeficiency virus (HIV) infection or syphilis carriers;
18. Patients with severe other organ dysfunction or cardiopulmonary disease, including myocardial infarction, stroke, congestive heart failure, severe lung disease, metabolic diseases, wound healing abnormalities, ulcers or fractures;
19. Epilepsy accompanied by medication (such as steroids or antiepileptic drugs);
20. Previous or present malignant neoplasms;
21. A history of severe allergies, or a history of allergic diseases, or an allergic constitution, or a severe iodine contrast allergy, meeting any of these criteria;
22. serious mental disorders;
23. A history of drug or alcohol abuse;
24. A pregnant or lactating woman, or a woman of childbearing age who has a positive blood pregnancy test, or a patient of childbearing age and her spouse who is unwilling to take effective contraceptive measures during the clinical study period and within 6 months after the end of treatment;
25. Patients deemed unsuitable for this clinical trial by the investigator.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Sequential Assignment

Masking: None (Open label)

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12 participants in 1 patient group

lose dose,high dose

Experimental group

Description:

Four dose groups were set up: dose group 1, a single dose of 2mg, administered at week 0, 4 and 12, three times in total; Dose group 2, a single dose of 6mg, respectively at the 0, 4, 12 weeks, a total of 3 times; Dose group 3, a single dose of 2mg, was given at the 0, 2, 4, 12 weeks, a total of 4 times; Dose group 4, with a single dose of 6mg, was given 4 times at week 0, 2, 4 and 12, respectively. There were 3 subjects in each group. Climb from the low dose group to the high dose group.

Treatment:

Biological: NWRD08