ID
42515
Beschreibung
Study ID: 106464 Clinical Study ID: 106464 Study Title: A Study of the Efficacy Against Episodes of Clinical Malaria Due to P. Falciparum Infection of GSK Biologicals Candidate Vaccine RTS, S/AS01, Administered According to a 0,1,2-months Schedule in Children Aged 5 to 17 Months Living in Tanzania & Kenya Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00380393 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: GSK malaria vaccine 257049 Vaccine, Sanofi-Pasteur's Human Diploid Cell Rabies Vaccine Trade Name: N/A Study Indication: Malaria ODM derived from https://clinicaltrials.gov/ct2/show/study/NCT00380393. This Phase IIb randomized, double-blind, controlled study of the efficacy against episodes of clinical malaria due to Plasmodium falciparum infection of GlaxoSmithKline Biologicals’ candidate vaccine RTS, S/AS01E, administered IM according to a 0, 1, 2-month vaccination schedule in children aged 5 months to 17 months living in Tanzania and Kenya. This study includes the following 7 clinical study visits (3 different visit types) during a double-blind phase (Day -60 to Month 6 1/2) and a single-blind phase including an extension for a subset of patients (month 7 to month 14). Clinical visit 1: Baseline visit, screening, and randomisation (DAY -60 to 0) Clinical visit 2: Vaccination I (MONTH 0, DAY 0 | DOSE 1 | 0 - 60 DAYS AFTER VISIT 1) Clinical visit 3: Vaccination II (MONTH 1, DAY 30 | DOSE 2 | 21 - 35 DAYS AFTER VISIT 2) Clinical visit 4: Vaccination III (MONTH 2, DAY 60 | DOSE 3 | 21 - 35 DAYS AFTER VISIT 3) Clinical visit 5: Blood Sample, ACD (MONTH 3, DAY 90 | 21 - 42 DAYS AFTER VISIT 4) Clinical visit 6: Blood Sample, ACD (MONTH 6 1/2 | CROSS-SECTIONAL VISIT FOR ACD | FINAL STUDY VISIT FOR DOUBLE-BLIND PHASE) Clinical visit 7: Blood Sample, ACD (MONTH 14 | FINAL STUDY VISIT SINGLE-BLIND PHASE) Field-worker home visits: During the vaccination period, clinical visits are accompanied by daily field-worker visits for a one-week period subsequent to each vaccine administration at clinical visits 2, 3, and 4 (visit code 21-26 following clinical visit 2; visit code 27-32 following clinical visit 3; visit code 33-38 following clinical visit 4). After completion of the vaccination period, clinical visits are then accompanied by weekly field-worker home visits (visit code 39-40 following clinical visit 4/dose 3; visit code 41-55 following clinical visit 5; visit code 56-86 following clinical visit 6). These visits serve the additional purpose of Active Case Detection (ACD). Passive Case Detection (PCD) for clinical malaria disease is performed both during the course of the double-blind (day -60 to month 6 1/2) and the single-blind phase (month 7 to month 14). Laboratory reference range for each laboratory test should be documented in this form. If the reference ranges for any test differ by age range, age units or sex, a separate form for each variation should be completed. Note that informed consent has to be obtained prior to any study procedure.
Link
https://clinicaltrials.gov/ct2/show/study/NCT00380393
Stichworte
Versionen (1)
- 11.08.21 11.08.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
11. August 2021
DOI
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Lizenz
Creative Commons BY-NC 4.0
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Efficacy of P. Falciparum Vaccine Against Malaria in Children NCT00380393
Laboratory Reference Ranges
- StudyEvent: ODM
Beschreibung
Laboratory Reference Ranges
Alias
- UMLS CUI-1
- C0883335
Beschreibung
Laboratory Reference Ranges
Alias
- UMLS CUI-1
- C0883335
Beschreibung
Enter the reference range for each test. If the reference ranges for any test differ by age range, age units or sex, complete a separate version of this repeating item group for each variation (e.g., males 0-16, males 17-99, females 0- 16, females 17-99 years).
Datentyp
date
Alias
- UMLS CUI [1,1]
- C0883335
- UMLS CUI [1,2]
- C0011008
Beschreibung
Age range low
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0001779
- UMLS CUI [1,2]
- C1514721
- UMLS CUI [1,3]
- C0205251
Beschreibung
Age range high
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0001779
- UMLS CUI [1,2]
- C1514721
- UMLS CUI [1,3]
- C0205250
Beschreibung
(tick one box) In the original paper-based version of this clinical study report, 'weeks' was pre-selected for this item.
Datentyp
integer
Alias
- UMLS CUI [1,1]
- C0001779
- UMLS CUI [1,2]
- C1519795
Beschreibung
In the original paper-based version of this clinical study report, 'Male and Female reference range' was pre-selected for this item.
Datentyp
integer
Alias
- UMLS CUI [1]
- C0079399
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 5 U/L.
Datentyp
integer
Maßeinheiten
- U/L
Alias
- UMLS CUI [1]
- C0008000
- UMLS CUI [2,1]
- C1272773
- UMLS CUI [2,2]
- C0201836
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 60 U/L.
Datentyp
integer
Maßeinheiten
- U/L
Alias
- UMLS CUI [1]
- C0008000
- UMLS CUI [2,1]
- C1299400
- UMLS CUI [2,2]
- C0201836
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 10 µmol/L.
Datentyp
integer
Maßeinheiten
- µmol/L
Alias
- UMLS CUI [1]
- C0008000
- UMLS CUI [2,1]
- C1272773
- UMLS CUI [2,2]
- C0201975
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 60 µmol/L.
Datentyp
integer
Maßeinheiten
- µmol/L
Alias
- UMLS CUI [1]
- C0008000
- UMLS CUI [2,1]
- C1299400
- UMLS CUI [2,2]
- C0201975
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 8.0 g/dL.
Datentyp
float
Maßeinheiten
- g/dL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1272773
- UMLS CUI [2,2]
- C0518015
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 18 g/dL.
Datentyp
float
Maßeinheiten
- g/dL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1299400
- UMLS CUI [2,2]
- C0518015
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 4.0 x 10^3/µL
Datentyp
float
Maßeinheiten
- 10^3/µL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1272773
- UMLS CUI [2,2]
- C0023508
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 17 x 10^3/µL
Datentyp
float
Maßeinheiten
- 10^3/µL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1299400
- UMLS CUI [2,2]
- C0023508
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 100 x 10^3/µL
Datentyp
integer
Maßeinheiten
- 10^3/µL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1272773
- UMLS CUI [2,2]
- C0005821
Beschreibung
In the original paper-based version of this clinical study report, this item was pre-filled with 800 x 10^3/µL
Datentyp
integer
Maßeinheiten
- 10^3/µL
Alias
- UMLS CUI [1]
- C0018941
- UMLS CUI [2,1]
- C1299400
- UMLS CUI [2,2]
- C0005821
Ähnliche Modelle
Laboratory Reference Ranges
- StudyEvent: ODM
C0600091 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C2347796 (UMLS CUI [2,1])
C0457083 (UMLS CUI [2,2])
C0011008 (UMLS CUI [1,2])
C1514721 (UMLS CUI [1,2])
C0205251 (UMLS CUI [1,3])
C1514721 (UMLS CUI [1,2])
C0205250 (UMLS CUI [1,3])
C1272773 (UMLS CUI [2,1])
C0201836 (UMLS CUI [2,2])
C1299400 (UMLS CUI [2,1])
C0201836 (UMLS CUI [2,2])
C1272773 (UMLS CUI [2,1])
C0201975 (UMLS CUI [2,2])
C1299400 (UMLS CUI [2,1])
C0201975 (UMLS CUI [2,2])
C1272773 (UMLS CUI [2,1])
C0518015 (UMLS CUI [2,2])
C1299400 (UMLS CUI [2,1])
C0518015 (UMLS CUI [2,2])
C1272773 (UMLS CUI [2,1])
C0023508 (UMLS CUI [2,2])
C1299400 (UMLS CUI [2,1])
C0023508 (UMLS CUI [2,2])
C1272773 (UMLS CUI [2,1])
C0005821 (UMLS CUI [2,2])
C1299400 (UMLS CUI [2,1])
C0005821 (UMLS CUI [2,2])