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A study to evaluate the pharmacokinetics of Retapamulin Ointment, 1%, in pediatric subjects (2-24 months) with secondarily-infected traumatic lesions, secondarily-infected dermatoses, or impetigo (bullous and non-bullous).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm 1 | Experimental | Single Arm Retapamulin 1% Ointment |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Retapamulin Ointment, 1% | Drug | 1% Ointment |
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| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Measurable Plasma Concentrations, by Age Group | Pharmacokinetic (PK) samples were collected randomly in the window of 4 to 8 hours post-dose (except one at 3 hours and one at 11 hours post-dose) after the first daily dose of treatment on Day 3 or Day 4. The lower limit of quantification (LLQ) for retapamulin was 0.5 ng/mL. | Days 3 to 4; 4 to 8 hours post-dose of the first dose of the day |
| Measure | Description | Time Frame |
|---|---|---|
| Number of Participants With Clinical Success at Follow-up, by Type of Skin Infection and by Age | SID = Secondarily Infected Dermatoses; SITL = Secondarily Infected Traumatic Lesions. Clinical Success is the number of participants with resolution of signs/symptoms of infection or improvement such that no additional antibiotic therapy was needed. | Follow-up, Days 12 to 16 |
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Inclusion criteria:
The subject has a small laceration, sutured wound or abrasion, which has a secondary bacterial infection. The infected portion of the laceration or sutured wound should not exceed 10cm in length with surrounding erythema not extending more than 2cm from the edge of the wound. Abrasions should not exceed 2% of the total body surface area with surrounding erythema not extending more than 2cm from the edge of the abrasion.
The subject has a diagnosis of inflammatory skin disease (i.e., dermatosis), such as atopic dermatitis or contact dermatitis, which has a secondary bacterial infection. The infected portion of the lesion(s) should not exceed 2% of the total body surface area.
Impetigo: The subject has a lesion or group of £10 discrete localized lesions on otherwise healthy skin, characterized by red spots or blisters without crusts which later progress to lesions which ooze and form yellow or honey-colored crusts surrounded by an erythematous margin.
Exclusion criteria:
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| Name | Affiliation | Role |
|---|---|---|
| GSK Clinical Trials | GlaxoSmithKline | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| GSK Investigational Site | Tuscaloosa | Alabama | 35401 | United States | ||
| GSK Investigational Site |
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| Label | URL |
|---|---|
| Researchers can use this site to request access to anonymised patient level data and/or supporting documents from clinical studies to conduct further research. | View source |
| ID | Type | URL | Comment |
|---|---|---|---|
| TOC106489 | Annotated Case Report Form | View IPD |
Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.
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| ID | Title | Description |
|---|---|---|
| FG000 | Retapamulin Ointment, 1% | Retapamulin ointment, 1%, administered twice daily for 5 consecutive days |
| Title | Milestones | Reasons Not Completed | |||||
|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| Bacteriological Success Rate at Follow-up, by Baseline Pathogen | Bacteriological success is defined as: (1) Bacteriological Eradication, elimination of the baseline pathogen via culture results; (2) Presumed Bacteriological Eradication, clinical success plus no culturable material from the wound; or (3) Colonization, new pathogen identified at Follow-up in a non-symptomatic participant who does not require additional antibiotic therapy. The number of pathogens eradicated out of the number isolated (shown as "n" in the category title) for each respective category is shown. | Follow-up, Days 12 to 16 |
| Number of Participants by Age With Therapeutic Response of Success | Therapeutic response is a measure of the overall efficacy response; a response of "therapeutic success" was based on both clinical success and bacteriological success in a given participant. | Follow-up, Days 12 to 16 |
| Bentonville |
| Arkansas |
| 72712 |
| United States |
| GSK Investigational Site | Orange | California | 92868 | United States |
| GSK Investigational Site | Woburn | Massachusetts | 01801 | United States |
| GSK Investigational Site | Cleveland | Ohio | 44106 | United States |
| GSK Investigational Site | Houston | Texas | 77090 | United States |
| GSK Investigational Site | Ciudad Autonoma de Buenos Aires | Buenos Aires | C1425BEA | Argentina |
| GSK Investigational Site | Ciudad Autonoma de Buenos Aires | Buenos Aires | Argentina |
| GSK Investigational Site | Santiago | Región Metro de Santiago | 7580206 | Chile |
| GSK Investigational Site | San José | Costa Rica |
| GSK Investigational Site | Nördlingen | Bavaria | 86720 | Germany |
| GSK Investigational Site | Bochum | North Rhine-Westphalia | 44791 | Germany |
| GSK Investigational Site | Erkrath | North Rhine-Westphalia | 40699 | Germany |
| GSK Investigational Site | Goch | North Rhine-Westphalia | 47574 | Germany |
| GSK Investigational Site | Kleve-Materborn | North Rhine-Westphalia | 47533 | Germany |
| GSK Investigational Site | México | 6720 | Mexico |
| GSK Investigational Site | Alphen aan den Rijn | 2403 JK | Netherlands |
| GSK Investigational Site | Losser | 7581 BV | Netherlands |
| GSK Investigational Site | Roelofarendsveen | 2371 RB | Netherlands |
| GSK Investigational Site | Rotterdam | 3011 TD | Netherlands |
| GSK Investigational Site | Soerendonk | 6027 RN | Netherlands |
| GSK Investigational Site | Woerden | 3443 GG | Netherlands |
| GSK Investigational Site | Benoni | 1501 | South Africa |
| GSK Investigational Site | Newtown | 2113 | South Africa |
| GSK Investigational Site | Taipei | 112 | Taiwan |
For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Individual Participant Data Set | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Statistical Analysis Plan | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Study Protocol | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Clinical Study Report | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Informed Consent Form | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| TOC106489 | Dataset Specification | View IPD | For additional information about this study please refer to the GSK Clinical Study Register |
| COMPLETED |
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| NOT COMPLETED |
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| ID | Title | Description |
|---|---|---|
| BG000 | Retapamulin Ointment, 1% | Retapamulin ointment, 1%, administered twice daily for 5 consecutive days |
| Units | Counts |
|---|---|
| Participants |
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| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | One participant was enrolled, but was withdrawn prior to assessments and did not receive study medication; therefore, this participant was not included in the study population. | Mean | Standard Deviation | months |
| |||||||||||||||||||||
| Gender | One participant was enrolled, but was withdrawn prior to assessments and did not receive study medication; therefore, this participant was not included in the study population. | Count of Participants | Participants |
| ||||||||||||||||||||||
| Race/Ethnicity, Customized | One participant was enrolled, but was withdrawn prior to assessments and did not receive study medication; therefore, this participant was not included in the study population. | Number | participants |
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| 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 | Number of Participants With Measurable Plasma Concentrations, by Age Group | Pharmacokinetic (PK) samples were collected randomly in the window of 4 to 8 hours post-dose (except one at 3 hours and one at 11 hours post-dose) after the first daily dose of treatment on Day 3 or Day 4. The lower limit of quantification (LLQ) for retapamulin was 0.5 ng/mL. | Pharmacokinetic (PK) Population: all participants who received at least one dose of study medication and who had PK samples taken. Seven participants did not have PK samples collected. | Posted | Number | participants | Days 3 to 4; 4 to 8 hours post-dose of the first dose of the day |
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| Secondary | Number of Participants With Clinical Success at Follow-up, by Type of Skin Infection and by Age | SID = Secondarily Infected Dermatoses; SITL = Secondarily Infected Traumatic Lesions. Clinical Success is the number of participants with resolution of signs/symptoms of infection or improvement such that no additional antibiotic therapy was needed. | Intent-to-Treat Clinical (ITTC) Population: all participants who received at least one dose of study medication; the number of participants who were clinical successes out of the total number in each respective category is shown | Posted | Number | participants | Follow-up, Days 12 to 16 |
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| Secondary | Bacteriological Success Rate at Follow-up, by Baseline Pathogen | Bacteriological success is defined as: (1) Bacteriological Eradication, elimination of the baseline pathogen via culture results; (2) Presumed Bacteriological Eradication, clinical success plus no culturable material from the wound; or (3) Colonization, new pathogen identified at Follow-up in a non-symptomatic participant who does not require additional antibiotic therapy. The number of pathogens eradicated out of the number isolated (shown as "n" in the category title) for each respective category is shown. | ITTB (Intent-to-Treat Bacteriological) Population: participants who had at least one dose of study medication and a clinical diagnosis of infection plus a pathogen isolated at Baseline. Participants with more than one pathogen may be represented in the table more than once. | Posted | Number | number of pathogens eradicated | Follow-up, Days 12 to 16 |
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| Secondary | Number of Participants by Age With Therapeutic Response of Success | Therapeutic response is a measure of the overall efficacy response; a response of "therapeutic success" was based on both clinical success and bacteriological success in a given participant. | ITTB and ITTC Populations. The number analyzed is the number of participants who were clinical successes both in the ITTC Population and the ITTB Population; the number of participants who were therapeutic successes out of the total number in each respective category is shown. | Posted | Number | participants | Follow-up, Days 12 to 16 |
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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 | Retapamulin Ointment, 1% | Retapamulin ointment, 1%, administered twice daily for 5 consecutive days | 1 | 11 |
| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Cough | Respiratory, thoracic and mediastinal disorders | MedDRA | Systematic Assessment |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| Diarrhea | Gastrointestinal disorders | MedDRA | Systematic Assessment |
| |
| Atopic dermatitis | Skin and subcutaneous tissue disorders | MedDRA | Systematic Assessment |
| |
| Influenza | Infections and infestations | MedDRA | Systematic Assessment |
| |
| Abdominal pain | Gastrointestinal disorders | MedDRA | Systematic Assessment |
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| Vomiting | Gastrointestinal disorders | MedDRA | Systematic Assessment |
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| Dermatitis | Skin and subcutaneous tissue disorders | MedDRA | Systematic Assessment |
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| Impetigo | Infections and infestations | MedDRA | Systematic Assessment |
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| Skin fissure | Skin and subcutaneous tissue disorders | MedDRA | Systematic Assessment |
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| Hypersensitivity | Immune system disorders | MedDRA | Systematic Assessment |
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| Pharyngitis | Infections and infestations | MedDRA | Systematic Assessment |
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| Hypochromic anemia | Blood and lymphatic system disorders | MedDRA | Systematic Assessment |
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GSK agreements may vary with individual investigators, but will not prohibit any investigator from publishing. GSK supports the publication of results from all centers of a multi-center trial but requests that reports based on single-site data not precede the primary publication of the entire clinical trial.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| GSK Response Center | GlaxoSmithKline | 866-435-7343 |
| ID | Term |
|---|---|
| D002481 | Cellulitis |
| D013398 | Sudden Infant Death |
| D007169 | Impetigo |
| D012868 | Skin Abnormalities |
| D012871 | Skin Diseases |
| D007239 | Infections |
| ID | Term |
|---|---|
| D012874 | Skin Diseases, Infectious |
| D013492 | Suppuration |
| D003240 | Connective Tissue Diseases |
| D017437 | Skin and Connective Tissue Diseases |
| D007249 | Inflammation |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D003645 | Death, Sudden |
| D003643 | Death |
| D066088 | Infant Death |
| D013207 | Staphylococcal Skin Infections |
| D013203 | Staphylococcal Infections |
| D016908 | Gram-Positive Bacterial Infections |
| D001424 | Bacterial Infections |
| D001423 | Bacterial Infections and Mycoses |
| D013290 | Streptococcal Infections |
| D017192 | Skin Diseases, Bacterial |
| D000013 | Congenital Abnormalities |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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| American Indian or Alaska Native |
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| Central/South Asian |
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| East Asian |
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| Missing |
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| Title | Measurements |
|---|---|
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| >12 months to ≤24 months |
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