Trial · NCT00332930
ITV Extension Study
NCT00332930, Phase 1, Phase 2, Completed, Kirby Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. ITV Extension Study. Trials, record NCT00332930. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00332930
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- ITV Extension Study
- NCT number
- NCT00332930
- Status
- Completed
- Phases
- Phase 1, Phase 2
- Enrollment
- 35 participants
- Lead sponsor
- Kirby Institute
- Conditions
- HIV
- Interventions
- recombinant fowlpoxvirus (rFPV) expressing HIV gag-pol antigens, HIV gag-pol antigens and interferon-gamma (IFN-y)
- First posted
- 2006-06-02
- Last updated
- 2007-02-27
Source ClinicalTrials.gov
Registered outcomes8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Time weighted area under the curve change from plasma HIV-RNA VL at baseline (day 0) until reintroduction of antiretroviral therapy | ||
| Secondary | Log plasma HIV-RNA load after cessation of combination ART (post-vaccination viral load (VL) set-point) | ||
| Secondary | Kinetics and rate of VL recrudescence and median time to re-initiation of ART | ||
| Secondary | CD8+ T-cell responses to HIV antigens assessed through: | ||
| Secondary | Enzyme linked immunospot (ELISPOT) assay of IFN-y secreting cells | ||
| Secondary | Intracellular Cytokine Cytometry (ICC) for IFN-y and CD69 | ||
| Secondary | Human Leucocyte Antigen (HLA) class I/ I matched tetramer analyses for HIV epitope specific CD8+/CD4+ T -cells | ||
| Secondary | CD4+/CD8+ T-cell count changes |
Source ClinicalTrials.gov
Outcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00332930
GET https://conductscience.org/api/trials/v1/NCT00332930/registered