ID
44764
Description
Study ID: 109059 Clinical Study ID: OTB109059 Study Title: TXA107979:A Phase II Study to Evaluate: Delay in Intravaginal Ejaculatory Latency Time (IELT), Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Two Oral Doses of GSK557296 in a Randomized, Double Blind, Placebo-Controlled, Parallel Group Study in Men with Premature Ejaculation Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01021553 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: epelsiban Trade Name: Study Indication: Premature Ejaculation
Mots-clés
Versions (3)
- 13/11/2018 13/11/2018 -
- 13/04/2021 13/04/2021 - Dr. rer. medic Philipp Neuhaus
- 17/11/2021 17/11/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
17 novembre 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 4.0
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Delay in IELT, Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GSK557296 in Men with Premature Ejaculation, 109059
Liver Events
- StudyEvent: ODM
Description
Notification
Alias
- UMLS CUI-1
- C1556667
- UMLS CUI-2
- C0422202
Description
Email, last, Medical Monitor, Date in time, Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0013849
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C1708968
- UMLS CUI [1,4]
- C0011008
- UMLS CUI [1,5]
- C0040223
Description
Email, first, Medical Monitor, Date in time, Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0013849
- UMLS CUI [1,2]
- C0205435
- UMLS CUI [1,3]
- C1708968
- UMLS CUI [1,4]
- C0011008
- UMLS CUI [1,5]
- C0040223
Description
Email, Last, Clinical Trial Safety Documentation, Date in time, Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0013849
- UMLS CUI [1,2]
- C1517741
- UMLS CUI [1,3]
- C3899555
- UMLS CUI [1,4]
- C0011008
- UMLS CUI [1,5]
- C0040223
Description
Email, First, Clinical Trial Safety Documentation, Date in time, Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0013849
- UMLS CUI [1,2]
- C0205435
- UMLS CUI [1,3]
- C3899555
- UMLS CUI [1,4]
- C0011008
- UMLS CUI [1,5]
- C0040223
Description
Liver Dysfunction or Failure by Clinical Classification Adverse Event, Non-serious Adverse Event, Date in time, Time
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C1556667
- UMLS CUI [1,2]
- C1518404
- UMLS CUI [1,3]
- C0011008
- UMLS CUI [1,4]
- C0040223
Description
Liver Chemistry
Alias
- UMLS CUI-1
- C0232741
- UMLS CUI-2
- C0022885
Description
Medical History
Alias
- UMLS CUI-1
- C0262926
Description
Age
Type de données
boolean
Alias
- UMLS CUI [1]
- C0001779
Description
Pregnancy
Type de données
text
Alias
- UMLS CUI [1]
- C0032961
Description
Liver, Diagnostic Imaging; Hepatobiliary System, Diagnostic Imaging
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0023884
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [2,1]
- C1711359
- UMLS CUI [2,2]
- C0011923
Description
Liver, Diagnostic Imaging, Results; Hepatobiliary System, Diagnostic Imaging, Results
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0023884
- UMLS CUI [1,2]
- C0011923
- UMLS CUI [1,3]
- C1274040
- UMLS CUI [2,1]
- C1711359
- UMLS CUI [2,2]
- C0011923
- UMLS CUI [2,3]
- C1274040
Description
Biopsy of liver
Type de données
boolean
Alias
- UMLS CUI [1]
- C0193388
Description
Herbal medicine; Complementary Medicine; Alternative Medicine; Dietary Supplements; Illicit medication use
Type de données
boolean
Alias
- UMLS CUI [1]
- C2240391
- UMLS CUI [2]
- C1148474
- UMLS CUI [3]
- C0002346
- UMLS CUI [4]
- C0242295
- UMLS CUI [5]
- C0281875
Description
Fasting, Change in Diet
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0015663
- UMLS CUI [1,2]
- C3671772
Description
Investigational Product (Liver)
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0023884
Description
Liver Dysfunction or Failure by Clinical Classification Adverse Event, Experimental Drug
Type de données
text
Alias
- UMLS CUI [1,1]
- C1556667
- UMLS CUI [1,2]
- C0304229
Description
Experimental Drug, Start Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0808070
Description
Experimental Drug, End Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0806020
Similar models
Liver Events
- StudyEvent: ODM
C1519255 (UMLS CUI-2)
C1519255 (UMLS CUI [1,2])
C0422202 (UMLS CUI-2)
C1517741 (UMLS CUI [1,2])
C1708968 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
C0205435 (UMLS CUI [1,2])
C1708968 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
C1517741 (UMLS CUI [1,2])
C3899555 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
C0205435 (UMLS CUI [1,2])
C3899555 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0040223 (UMLS CUI [1,5])
C1518404 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0040223 (UMLS CUI [1,4])
C0022885 (UMLS CUI-2)
C0022885 (UMLS CUI [1,2])
C0011923 (UMLS CUI [1,2])
C1711359 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
C0011923 (UMLS CUI [1,2])
C1274040 (UMLS CUI [1,3])
C1711359 (UMLS CUI [2,1])
C0011923 (UMLS CUI [2,2])
C1274040 (UMLS CUI [2,3])
C1148474 (UMLS CUI [2])
C0002346 (UMLS CUI [3])
C0242295 (UMLS CUI [4])
C0281875 (UMLS CUI [5])
C3671772 (UMLS CUI [1,2])
C0023884 (UMLS CUI-2)
C0304229 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])