ID
38111
Beschrijving
Study ID: 105036 Clinical Study ID: 105036 Study Title: A single-blind, randomized, placebo-controlled study to investigate the safety, tolerability, and potential effects on betamethasone pharmacokinetics of a co-administered infusion of GSK221149A in healthy female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: betamethasone Trade Name: Retosiban Study Indication: Women's Health & Pregnancy - Other, pre-term labour
Trefwoorden
Versies (1)
- 18-09-19 18-09-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
18 september 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Betamethasone pharmacokinetics of a co-administered infusion of GSK221149A; 105036
Pharmacokinetics Blood
- StudyEvent: ODM
Beschrijving
Predose
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0439565
Beschrijving
0,5 Hour post dose
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0439568
- UMLS CUI-3
- C1442458
Beschrijving
6 Hours post dose
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0439568
- UMLS CUI-3
- C1292428
Beschrijving
12 Hours post dose
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0439568
- UMLS CUI-3
- C1292430
Beschrijving
24 Hours post dose
Alias
- UMLS CUI-1
- C0031328
- UMLS CUI-2
- C0439568
- UMLS CUI-3
- C1442770
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Pharmacokinetics Blood
- StudyEvent: ODM
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C0439568 (UMLS CUI-2)
C1292430 (UMLS CUI-3)
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C1292430 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0439568 (UMLS CUI-2)
C1442770 (UMLS CUI-3)
C0439568 (UMLS CUI [1,2])
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