ID
42578
Description
Study ID: 105874 Clinical Study ID: 105874 Study Title: Bridging Safety & Immunogenicity Study of GSK Biologicals' Candidate Malaria Vaccine RTS,S/AS01E (0.5 mL Dose) to RTS,S/AS02D (0.5 mL Dose) Administered IM According to a 0, 1, 2-Month Schedule in Gabonese Children Aged 18 Months to 4 Years Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00307021 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK Biologicals' candidate Plasmodium falciparum malaria vaccine 257049 Trade Name: N/A Study Indication: Malaria ODM derived from https://clinicaltrials.gov/ct2/show/NCT00307021. A Phase II randomized, double-blind bridging study of the safety and immunogenicity of GlaxoSmithKline Plasmodium falciparum malaria vaccine RTS,S/AS01E (0.5 mL dose) to RTS,S/AS02D (0.5 mL dose) administered IM according to a 0, 1, 2- month vaccination schedule in children aged 18 months to 4 years living in Gabon. Clinical Visits: This study has a total of 7 visits. Visit 1 = Screening, Visits 2-6 are during the double-blind phase (Month 0-3) and Visit 7 is during the single-blind phase (Month 4-14). Vaccine administration takes place during visits 2, 4, and 5 (Visit 2 = Dose 1; Visit 4 = Dose 2; Visit 5 = Dose 3). Field-worker Visits: During the double-blind phase, clinical visits are accompanied by daily field-worker visits subsequent to each vaccine administration visit. Additional field-worker visits also take place during months 4 to 13 of the single-blind phase. The full laboratory tests form should be completed at visits 2, 6, and 7, whilst a partial version should be completed at visits 3 and 5. All questions for visit 2 relate to blood samples taken at visit 1 (screening visit). For visit 3, only the sections for clinical chemistry and haematology need to be considered. For visit 5, only the sections for serology and CMI need to be considered. Please note that informed consent has to be obtained prior to any study procedure.
Lien
https://clinicaltrials.gov/ct2/show/NCT00307021
Mots-clés
Versions (2)
- 24/08/2021 24/08/2021 -
- 04/09/2021 04/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
4 septembre 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 4.0
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Safety & Immunogenicity of two GSK Biologicals' Candidate Malaria Vaccines in young children, NCT00307021
Laboratory Tests
- StudyEvent: ODM
Description
Biochemistry
Alias
- UMLS CUI-1
- C0008000
Description
(For visit 2 only: Has a blood sample for biochemistry been taken at screening visit 1?) If yes, please complete the items below. This item group does not need to be filled in for visit 5.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0008000
Description
Please complete only if date of collection of blood specimen is different from visit date. (For visit 2 only: Please complete only if date of collection of blood specimen is different from date of screening visit 1.)
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0008000
- UMLS CUI [1,3]
- C0011008
Description
Please fill in results for ALT measurement or indicate if not done in the following item.
Type de données
integer
Unités de mesure
- IU/L
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if ALT has not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
Alanine aminotransferase measurement abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0201836
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Please fill in results for creatinine measurement or indicate if not done in the following item.
Type de données
integer
Unités de mesure
- µmol/L
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if creatinine has not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
Creatinine measurement abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0201975
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Please fill in results for bilirubin measurement or indicate if not done in the following item.
Type de données
float
Unités de mesure
- µmol/L
Alias
- UMLS CUI [1,1]
- C0344395
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if bilirubin has not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0344395
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0344395
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
Bilirubin measurement abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0344395
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Haematology
Alias
- UMLS CUI-1
- C0018941
Description
(For visit 2 only: Has a blood sample for haematology been taken at screening visit 1?) If yes, please complete the items below. This item group does not need to be filled in for visit 5.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0018941
Description
Please complete only if date of collection of blood specimen is different from visit date. (For visit 2 only: Please complete only if date of collection of blood specimen is different from date of screening visit 1.)
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0018941
- UMLS CUI [1,3]
- C0011008
Description
Please fill in results for haemoglobin measurement or indicate if not done in the following item.
Type de données
integer
Unités de mesure
- g/dL
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if haemoglobin has not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
Haemoglobin measurement abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0518015
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Please fill in results for WBC measurement or indicate if not done in the following item.
Type de données
float
Unités de mesure
- 10^3/µL
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if WBC has not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
White blood cell count procedure abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0023508
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Please fill in results for blood platelets measurement or indicate if not done in the following item.
Type de données
integer
Unités de mesure
- 10^3/µL
Alias
- UMLS CUI [1,1]
- C0005821
- UMLS CUI [1,2]
- C1274040
Description
Please indicate if blood platelets have not been tested for.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005821
- UMLS CUI [1,2]
- C1272696
Description
Please enter ONE code (e.g. 1 or 2). If [2] Preexisting/concomitant medical condition or [5] Other, please specify in the following item.
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0005821
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0600091
Description
Blood platelets abnormal reason to specify
Type de données
text
Alias
- UMLS CUI [1,1]
- C0005821
- UMLS CUI [1,2]
- C0205161
- UMLS CUI [1,3]
- C0566251
- UMLS CUI [1,4]
- C1521902
Description
Serology
Alias
- UMLS CUI-1
- C0036743
Description
(For visit 2 only: Has a blood sample for serology been taken at screening visit 1?) If yes, please complete the item below. This item group does not need to be filled in for visit 3.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0036743
- UMLS CUI [1,3]
- C0201478
- UMLS CUI [2,1]
- C0005834
- UMLS CUI [2,2]
- C0036743
- UMLS CUI [2,3]
- C3833453
- UMLS CUI [2,4]
- C0055782
Description
Please complete only if date of collection of blood specimen is different from visit date. (For visit 2 only: Please complete only if date of collection of blood specimen is different from date of screening visit 1.)
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0036743
- UMLS CUI [1,3]
- C0201478
- UMLS CUI [1,4]
- C0011008
- UMLS CUI [2,1]
- C0005834
- UMLS CUI [2,2]
- C0036743
- UMLS CUI [2,3]
- C3833453
- UMLS CUI [2,4]
- C0055782
- UMLS CUI [2,5]
- C0011008
Description
CMI | B-Cell Memory
Alias
- UMLS CUI-1
- C0020966
- UMLS CUI-3
- C0682638
Description
(For visit 2 only: Has a blood sample been taken for CMI / B-Cell Memory testing at Screening - Visit 1?) If yes, please complete the item below. This item group does not need to be filled in for visit 3.
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0020966
- UMLS CUI [2,1]
- C0005834
- UMLS CUI [2,2]
- C0682638
- UMLS CUI [2,3]
- C0032148
Description
Please complete only if date of collection of blood specimen is different from visit date. (For visit 2 only: Please complete only if date of collection of blood specimen is different from date of screening visit 1.)
Type de données
date
Alias
- UMLS CUI [1,1]
- C0005834
- UMLS CUI [1,2]
- C0020966
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [2,1]
- C0005834
- UMLS CUI [2,2]
- C0682638
- UMLS CUI [2,3]
- C0032148
- UMLS CUI [2,4]
- C0011008
Similar models
Laboratory Tests
- StudyEvent: ODM
C0008000 (UMLS CUI [1,2])
C0008000 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0018941 (UMLS CUI [1,2])
C0018941 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C1274040 (UMLS CUI [1,2])
C1272696 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
C0600091 (UMLS CUI [1,3])
C0205161 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1521902 (UMLS CUI [1,4])
C0036743 (UMLS CUI [1,2])
C0201478 (UMLS CUI [1,3])
C0005834 (UMLS CUI [2,1])
C0036743 (UMLS CUI [2,2])
C3833453 (UMLS CUI [2,3])
C0055782 (UMLS CUI [2,4])
C0036743 (UMLS CUI [1,2])
C0201478 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0005834 (UMLS CUI [2,1])
C0036743 (UMLS CUI [2,2])
C3833453 (UMLS CUI [2,3])
C0055782 (UMLS CUI [2,4])
C0011008 (UMLS CUI [2,5])
C0020966 (UMLS CUI [1,2])
C0005834 (UMLS CUI [2,1])
C0682638 (UMLS CUI [2,2])
C0032148 (UMLS CUI [2,3])
C0020966 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0005834 (UMLS CUI [2,1])
C0682638 (UMLS CUI [2,2])
C0032148 (UMLS CUI [2,3])
C0011008 (UMLS CUI [2,4])