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Prophylactic smallpox vaccination for personnel actively working with or in the vicinity of replicating vaccinia virus
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| IMVAMUNE® | Experimental | Two subcutaneous vaccinations with 0.5 mL IMVAMUNE® vaccine administered at a 4 week intervals |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| IMVAMUNE® | Biological | IMVAMUNE® liquid -frozen, containing 1 x 10E8 TCID50 MVA-BN® per 0.5 mL dose |
|
| Measure | Description | Time Frame |
|---|---|---|
| ELISA Seropositivity Rate | Seropositivity rate based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Seropositivity is defined as antibody titers ≥ detection limit (50). Percentages based on number of subjects with data available. | up to Week 7 |
| Measure | Description | Time Frame |
|---|---|---|
| ELISA Seroconversion Rate | Seroconversion rate based on Enzyme-linked Immunosorbent Assay (ELISA). Seroconversion is defined as the appearance of antibody titers ≥ detection limit (50) for initially seronegative subjects, or a doubling or more of the antibody titer compared to the Screening titer for initially seropositive subjects. Percentages based on number of subjects with data available. | Week 7 |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Gary Fujimoto, MD | Palo Alto Medical Foundation | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Palo Alto Medical Foundation | Palo Alto | California | 94301 | United States |
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| ID | Title | Description |
|---|---|---|
| FG000 | MVA-BN | Two s.c. vaccinations with 0.5 ml MVA-BN® vaccine containing 1 x 10E8 TCID50 / dose |
| Title | Milestones | Reasons Not Completed | ||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
|
Full Analysis Set
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| ID | Title | Description |
|---|---|---|
| BG000 | MVA-BN | Two s.c. vaccinations with 0.5 ml MVA-BN® vaccine containing 1 x 10E8 TCID50 / dose |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | ELISA Seropositivity Rate | Seropositivity rate based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Seropositivity is defined as antibody titers ≥ detection limit (50). Percentages based on number of subjects with data available. | Full Analysis Set | Posted | Number | 95% Confidence Interval | percentage of subjects | up to Week 7 |
|
|
up to 32 weeks
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | MVA-BN | Two s.c. vaccinations with 0.5 ml MVA-BN® vaccine containing 1 x 10E8 TCID50 / dose |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Fatigue | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Program Lead, Clinical Operations | Bavarian Nordic A/S | +45 3326 | 8383 | info@bavarian-nordic.com |
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| ID | Term |
|---|---|
| C527606 | smallpox and monkeypox vaccine modified vaccinia ankara-bavarian nordic |
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| ELISA GMT | Geometric Mean Titers (GMT) based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Titers below the detection limit are included with a value of '1'. | up to Week 7 |
| Serious Adverse Events | Incidence, relationship and intensity of any Serious Adverse Event (SAE). | up to 32 weeks |
| Related Grade >=3 Adverse Events | Incidence of any Grade >=3 Adverse Events possibly, probably or definitely related to the trial vaccine | within 29 days after any vaccination |
| Non-serious AEs | Incidence of non-serious AEs | within 29 days after any vaccination |
| years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Race (NIH/OMB) | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
|
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| Secondary | ELISA Seroconversion Rate | Seroconversion rate based on Enzyme-linked Immunosorbent Assay (ELISA). Seroconversion is defined as the appearance of antibody titers ≥ detection limit (50) for initially seronegative subjects, or a doubling or more of the antibody titer compared to the Screening titer for initially seropositive subjects. Percentages based on number of subjects with data available. | Full Analysis Set | Posted | Number | 95% Confidence Interval | percentage of subjects | Week 7 |
|
|
|
| Secondary | ELISA GMT | Geometric Mean Titers (GMT) based on vaccinia-specific Enzyme-linked Immunosorbent Assay (ELISA). Titers below the detection limit are included with a value of '1'. | Full Analysis Set | Posted | Geometric Mean | 95% Confidence Interval | Titer | up to Week 7 |
|
|
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| Secondary | Serious Adverse Events | Incidence, relationship and intensity of any Serious Adverse Event (SAE). | Full Analysis Set | Posted | Count of Participants | Participants | up to 32 weeks |
|
|
|
| Secondary | Related Grade >=3 Adverse Events | Incidence of any Grade >=3 Adverse Events possibly, probably or definitely related to the trial vaccine | Full Analysis Set | Posted | Count of Participants | Participants | within 29 days after any vaccination |
|
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| Secondary | Non-serious AEs | Incidence of non-serious AEs | Full Analysis Set | Posted | Count of Participants | Participants | within 29 days after any vaccination |
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|
|
| 0 |
| 22 |
| 0 |
| 22 |
| 19 |
| 22 |
| Injection site erythema | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Injection site induration | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Injection site pain | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Injection site pruritis | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Injection site swelling | General disorders | MedDRA 18.1 | Systematic Assessment |
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| Myalgia | Musculoskeletal and connective tissue disorders | MedDRA 18.1 | Systematic Assessment |
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| Headache | Nervous system disorders | MedDRA 18.1 | Systematic Assessment |
|
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