Comparison · NCT03110770-5dff3b50
Part B, Group 4: VRC-ZKADNA090-00-VP (4 mg), 2 Injections vs Part B, Group 5: Placebo (VRC-PBSPLA043-00-VP), 2 Injections: Number of Participants With Virologically Confirmed Cases of ZIKV (Part B Only)
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Part B, Group 4: VRC-ZKADNA090-00-VP (4 mg), 2 Injections vs Part B, Group 5: Placebo (VRC-PBSPLA043-00-VP), 2 Injections: Number of Participants With Virologically Confirmed Cases of ZIKV (Part B Only). Trial comparisons, record NCT03110770-5dff3b50. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03110770-5dff3b50
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.000855 | 0.000151 | 0.00483 | wilson | |
| Risk in group 2 | 0.00171 | 0.00047 | 0.00622 | wilson | |
| Risk difference, group 1 minus group 2 | -0.000858 | -0.00542 | 0.0033 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.499 | 0.0453 | 5.5 | log | |
| Odds ratio, group 1 over group 2 | 0.499 | 0.0452 | 5.51 | log | |
| Number needed to treat, for one fewer participant with the outcome on Part B, Group 4: VRC-ZKADNA090-00-VP (4 mg), 2 Injections than on Part B, Group 5: Placebo (VRC-PBSPLA043-00-VP), 2 Injections | 1,170 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: placebo.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Part B, Group 4: VRC-ZKADNA090-00-VP (4 mg), 2 Injections | ZIKVwt DNA vaccine (VRC-ZKADNA090-00-VP), in 2 limbs (both arms) on Day 0, Day 28 (+/-7 days), and Day 56 (-7/+14 days); 4 mg of vaccine administered IM by a needle-free injection device~VRC-ZKADNA090-00-VP: VRC-ZKADNA090-00-VP is composed of a single closed-circular DNA plasmid (VRC 5283) that encodes with wild type (wt) precursor transmembrane M (prM) and envelope (E) proteins from the H/PF/2013 strain of ZIKV | 1 | 1,170 | OG000 |
| Group 2 | Part B, Group 5: Placebo (VRC-PBSPLA043-00-VP), 2 Injections | Sterile phosphate-buffered saline (PBS) (VRC-PBSPLA043-00-VP), the placebo, in 2 limbs (both arms) on Day 0, Day 28 (+/-7 days), and Day 56 (-7/+14 days); 1 mL of placebo administered IM by a needle-free injection device~VRC-PBSPLA043-00-VP: A sterile phosphate-buffered saline (PBS) prepared for human administration as a placebo | 2 | 1,168 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- PRIMARY
- Title
- Number of Participants With Virologically Confirmed Cases of ZIKV (Part B Only)
- Description
Virologically confirmed Zika infection, irrespective of symptoms, by polymerase chain reaction (PCR) in blood or in urine were recorded from receipt of first study product administration through the last expected study visit.
- Time frame
- Day 0 through Day 672
- Population
All randomized participants in the study, analyzed according to the randomized study product. One placebo participant, who had a virologically confirmed case of ZIKV from a sample collected prior to first product administration, is not counted as a virologically confirmed case.
Source ClinicalTrials.gov
Trial
- Title
- VRC 705: A Zika Virus DNA Vaccine in Healthy Adults and Adolescents
- NCT number
- NCT03110770
- Phases
- PHASE2
- Conditions
- Zika Virus, Zika Virus Infection, Virus Diseases, Flavivirus Infections, Flaviviral Diseases, Flaviviridae Infections, RNA Virus Infections
- Interventions
- VRC-ZKADNA090-00-VP, VRC-PBSPLA043-00-VP
- Lead sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Results first posted
- 2020-12-04
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT03110770?tab=results
Source ClinicalTrials.gov
Source
- Release
- trial-comparisons-2026-03-23-0.1.0
- Release manifest SHA-256
- f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
- AACT copy
- 2026-03-23
- Tables read
- outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet
Source ClinicalTrials.gov
Sources 2
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
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
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.
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