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AIDS vaccine (Combined use of DNA vaccine and Recombinant Vaccine Tiantan)

Phase IIa study of AIDS vaccine (Combined use of DNA vaccine and Recombinant Vaccine Tiantan)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-PRC-12002493
Enrollment
Unknown
Registered
2012-08-23
Start date
2012-07-31
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AIDS

Interventions

1:receive three shots of the DNA vaccine at week 0, 4 and 8, rTV will boost at week 16
2:receive three shots of the DNA vaccine at week 0, 4 and 8, rTV will boost at week 24
3:receive three shots of the DNA vaccine at week 0, 4 and 8, rTV will boost at week 32
4:receive three DNA injections with the addition of electroporation at week 0, 4 and 8, rTV will boost at week 24

Sponsors

National Center for AIDS/STD Control and Prevention, Chinese Center for Disease Control and Prevention
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Both male and female; 2. 18 years to 55 years; 3. Willing to be followed for the planned duration of the study, and receive intravenous blood collection and sample storage in the 16~20 months after first vaccination; 4. Understand and agree with the content of informed consent; 5. Volunteers at low risk of HIV infection, or high-risk men who have sex with men (MSM), who had have oral sex or anal sex with another man in the past 6 months; 6. Willing to be tested for HIV and syphilis; 7. Before 2 weeks of the first vaccination and after 12 months of the last vaccination, willing to use an effective method of contraception with sexual partner. Female subjects are willing to undergo urine pregnancy test before each vaccination and at the follow-up visit.

Exclusion criteria

Exclusion criteria: 1. Have close contact with people who are pregnant or lactating in the one month after vaccination of rTV vaccine; 2. Have listed diseases or medical history: 1) Have innate or acquired immune deficiency disease or have close contact with patients suffering from the above-mentioned diseases within 1 month of rTV vaccination; 2) Need treatment affecting immunization, e.g. use corticosteroids for more than 2 weeks or use immunosuppressives, e.g. alkylating, anti-metabolite or radiotherapy, etc.; or have close contact with patients suffering from the above-mentioned diseases within 1 month of rTV vaccination; 3) Suffering from immunosuppressive diseases such as cancer, organ or stem cell transplants, non-agammaglobulinemia, etc.; or have close contact with patients suffering from the above-mentioned diseases within 1 month of rTV vaccination; 4) Past or current suffering from eczema or atopic dermatitis; currently suffering from diseases that cause skin damage such as: burns, scald, chicken pox, impetigo, shingles, psoriasis, etc.; or have close contact with patients suffering from the above-mentioned diseases within 1 month of rTV vaccination; 5) Past or current high blood pressure, heart disease, diabetes, thyroid disease, asthma, angioedema, asplenia syndrome, mental illness, epilepsy, severe anemia, leukopenia and thrombocytopenia, etc.; 6) History of syncope after vaccination or allergies; 7) Currently suffering from acute infectious diseases and febrile diseases; 3. The following circumstances are: 1) Live attenuated vaccine received within 2 months or other vaccine within 2 weeks prior to enrollment; 2) Immunoglobin or blood products received within 4 months prior to enrollment; 3) Participation in another trial of a medicinal product, completed less than 30 days prior to enrollment; 4) Drug abuse, alcoholism, heavy smokers; 4. The following laboratory test abnormalities, except for the results that are assessed by researchers as being no clinical significance: 1) HIV diagnostic assay positive or suspicious, HIV RNA diagnostic assay positive; 2) Anti-DNA antibody or anti-nuclear antibody positive; 3) Other laboratory test abnormalities; 5. Not complying with study protocol or not obtaining informed consent because of medical, spiritual, social, occupational, and/or other reasons.

Design outcomes

Primary

MeasureTime frame
Hematology;Liver and kidney function tests;urinalysis;DNA/ANA antibody;CK & CK-MB;HIV diagnostic assay;HIV RNA diagnostic assay;ELISPOT;HIV antigen-specific antibody;

Secondary

MeasureTime frame
ICS;HIV neutralizing antibody;vaccinia virus antibody;

Countries

China

Contacts

Public ContactTong Zhang
drtong.zhang@gmail.com+86 010 63053963

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026