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199 Resultados da pesquisa.

Serious Adverse Events Mepolizumab HES NCT00086658 - Serious Adverse Events

- 05/06/2017 - 1 Formulário, 12 Grupos de itens, 55 Elementos de dados, 1 Idioma

Grupos de itens: Serious Adverse Events, Document section, Document section SAE, Document section Demography data, Document section, Document section Causations SAE, Document section Medical Conditions, Document section Risk factors, Document section Concomitant Medications, Document section, Document section, Document section

Study part: .A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Non-Serious Adverse Events Mepolizumab HES NCT00086658 - Non-Serious Adverse Events

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 11 Elementos de dados, 1 Idioma

Grupo de itens: Non-Serious Adverse Events

Study part: Non-Serious Adverse Events.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pharmacogenetic Research Mepolizumab HES NCT00086658 - PGx- Pharmacogenetic Research

- 05/06/2017 - 1 Formulário, 4 Grupos de itens, 11 Elementos de dados, 1 Idioma

Grupos de itens: consent Pharmacogenetic Test, BLOOD SAMPLE COLLECTION, WITHDRAWAL OF CONSENT, BLOOD SAMPLE DESTRUCTION

Study part: PGx- Pharmacogenetic Research.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Corticosteroid Medication Mepolizumab HES NCT00086658 - Corticosteroid Medication

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 8 Elementos de dados, 1 Idioma

Grupo de itens: Medication Corticosteroid

Study part: Corticosteroid Medication.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Concomitant Medication Mepolizumab HES NCT00086658 - Concomitant Medication

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 11 Elementos de dados, 1 Idioma

Grupo de itens: Concomitant Medication

Study part: Concomitant Medication.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Investigational Product Discontinuation Mepolizumab HES NCT00086658 - Investigational Product Discontinuation

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 4 Elementos de dados, 1 Idioma

Grupo de itens: Investigational Product Discontinuation

Study part: Investigational Product Discontinuation.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Status of treatment blind Mepolizumab HES NCT00086658 - Status of treatment blind

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 5 Elementos de dados, 1 Idioma

Grupo de itens: Status of treatment blind

Study part: Status of treatment blind.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Study conclusion Mepolizumab HES NCT00086658 - Study conclusion

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 5 Elementos de dados, 1 Idioma

Grupo de itens: STUDY CONCLUSION

Study part: Study conclusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pregnancy Information Study Conclusion Mepolizumab HES NCT00086658 - Pregnancy Information Study Conclusion

- 05/06/2017 - 1 Formulário, 1 Grupo de itens, 1 Elemento de dados, 1 Idioma

Grupo de itens: PREGNANCY INFORMATION

Study part: Pregnancy Information Study Conclusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Eligibility Criteria Day 1 Pre-Infusion Mepolizumab HES NCT00086658 - Eligibility Criteria Day 1 Pre-Infusion

- 04/06/2017 - 1 Formulário, 3 Grupos de itens, 21 Elementos de dados, 1 Idioma

Grupos de itens: Eligibility criteria, Inclusion Criteria, Exclusion Criteria

Study part: Eligibility Criteria Day 1 Pre-Infusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Vital Signs Screening Visit Mepolizumab HES NCT00086658 - Vital Signs Screening Visit

- 04/06/2017 - 1 Formulário, 1 Grupo de itens, 9 Elementos de dados, 1 Idioma

Grupo de itens: VITAL SIGNS

Study part: Vital Signs Screening Visit.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

12-Lead ECG Screening Visit Mepolizumab HES NCT00086658 - 12-Lead ECG Screening Visit

- 04/06/2017 - 1 Formulário, 1 Grupo de itens, 3 Elementos de dados, 1 Idioma

Grupo de itens: 12-Lead ECG

Study part: 12-Lead ECG Screening Visit.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

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