ID
37735
Beschrijving
Study ID: 104864/627 Clinical Study ID: 104864/627 Study Title: An Open-label, Multicenter, Non-Comparative Phase II Study of the Combination of Intravenous Topotecan and Gemcitabine Administered Once Weekly for Three Weeks Every 28 Days as Second-line Treatment in Patients With Recurrent Platinum Sensitive Ovarian Cancer Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00061308 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Topotecan, Gemcitabine Study Indication: Peritoneal Cancer, Ovarian Cancer, Neoplasms, Ovarian, Fallopian Tube Cancer
Trefwoorden
Versies (1)
- 20-08-19 20-08-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
20 augustus 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Intravenous Topotecan and Gemcitabine as Second-line Treatment in Patients With Ovarian Cancer NCT00061308
Eligibility Criteria
- StudyEvent: ODM
Beschrijving
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Beschrijving
The same contraceptive method should be used throughout the study and continue for at least 4 weeks after the end of the study. A woman will be considered to be of childbearing potential if she is not surgically sterile or post—menopausal (i.e., documented absence of menses for one year prior to entry into the study).
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1960468
- UMLS CUI [1,2]
- C0700589
- UMLS CUI [2]
- C0009905
- UMLS CUI [3,1]
- C0042241
- UMLS CUI [3,2]
- C0037862
- UMLS CUI [4]
- C1706306
Beschrijving
Pregnancy; Breast Feeding
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0032961
- UMLS CUI [1,2]
- C0006147
Beschrijving
Histopathologic Grade | Borderline; Carcinoma; epithelial | Low Grade Malignant Neoplasm; Carcinoma; epithelial
Datatype
boolean
Alias
- UMLS CUI [1]
- C0919553
- UMLS CUI [2,1]
- C0205189
- UMLS CUI [2,2]
- C0007097
- UMLS CUI [2,3]
- C0221908
- UMLS CUI [3,1]
- C1334425
- UMLS CUI [3,2]
- C0007097
- UMLS CUI [3,3]
- C0221908
Beschrijving
Prior Chemotherapy; Chemotherapy Regimen; Numbers
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1514457
- UMLS CUI [1,2]
- C0237753
Beschrijving
Comorbidity; Malignant Neoplasms | Basal cell carcinoma; Treating; Adequate | Squamous cell carcinoma of skin; Treating; Adequate | Carcinoma in situ of uterine cervix | Incidental Findings; Carcinoid Tumor | Disease; Free of (attribute)
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0006826
- UMLS CUI [2,1]
- C0007117
- UMLS CUI [2,2]
- C1522326
- UMLS CUI [2,3]
- C0205411
- UMLS CUI [3,1]
- C0553723
- UMLS CUI [3,2]
- C1522326
- UMLS CUI [3,3]
- C0205411
- UMLS CUI [4]
- C0851140
- UMLS CUI [5,1]
- C0743997
- UMLS CUI [5,2]
- C0007095
- UMLS CUI [6,1]
- C0012634
- UMLS CUI [6,2]
- C0332296
Beschrijving
Communicable Diseases; Requirement; Antibiotic therapy
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009450
- UMLS CUI [1,2]
- C1514873
- UMLS CUI [1,3]
- C0338237
Beschrijving
Comorbidity; Severe (severity modifier); Malignant Neoplasms; Unrelated (finding) | Compliance behavior | Risk; Extreme | Life Expectancy
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0009488
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [1,3]
- C0006826
- UMLS CUI [1,4]
- C0445356
- UMLS CUI [2]
- C1321605
- UMLS CUI [3,1]
- C0035647
- UMLS CUI [3,2]
- C0205403
- UMLS CUI [4]
- C0023671
Beschrijving
Therapeutic radiology procedure | Bone Marrow
Datatype
boolean
Alias
- UMLS CUI [1]
- C1522449
- UMLS CUI [2]
- C0005953
Beschrijving
Concomitant Agent; Chemotherapeutic agent | Immunotherapy | Hormone Therapy | Therapeutic radiology procedure | Operative Surgical Procedures | cancer treatment
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347852
- UMLS CUI [1,2]
- C0729502
- UMLS CUI [2]
- C0021083
- UMLS CUI [3]
- C0279025
- UMLS CUI [4]
- C1522449
- UMLS CUI [5]
- C0543467
- UMLS CUI [6]
- C0920425
Beschrijving
Prior Therapy | Topotecan | gemcitabine
Datatype
boolean
Alias
- UMLS CUI [1]
- C1514463
- UMLS CUI [2]
- C0146224
- UMLS CUI [3]
- C0045093
Beschrijving
Camptothecin; Hypersensitivity | Nucleoside Analogs; Hypersensitivity | Compound (substance); Relationships
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0006812
- UMLS CUI [1,2]
- C0020517
- UMLS CUI [2,1]
- C1579410
- UMLS CUI [2,2]
- C0020517
- UMLS CUI [3,1]
- C1706082
- UMLS CUI [3,2]
- C0439849
Beschrijving
INVESTIGATIONAL AGENTS; Before; Clinical Trial Period
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1875319
- UMLS CUI [1,2]
- C0332152
- UMLS CUI [1,3]
- C2347804
Beschrijving
Did the patient meet all inclusion and exclusion criteria?
Alias
- UMLS CUI-1
- C1512693
- UMLS CUI-2
- C0680251
Similar models
Eligibility Criteria
- StudyEvent: ODM
C0001779 (UMLS CUI [2])
C0011900 (UMLS CUI [1,2])
C0677886 (UMLS CUI [2])
C0238122 (UMLS CUI [3])
C1514428 (UMLS CUI [4])
C0206627 (UMLS CUI [5])
C0392920 (UMLS CUI [2,1])
C1514162 (UMLS CUI [2,2])
C0079083 (UMLS CUI [3])
C0008838 (UMLS CUI [4])
C0277554 (UMLS CUI [5])
C1513040 (UMLS CUI [1,2])
C1705052 (UMLS CUI [1,3])
C0040405 (UMLS CUI [2])
C0024485 (UMLS CUI [3])
C0332324 (UMLS CUI [1,2])
C1512288 (UMLS CUI [2])
C1272706 (UMLS CUI [3,1])
C0012634 (UMLS CUI [3,2])
C0332296 (UMLS CUI [3,3])
C0521982 (UMLS CUI [4,1])
C0032207 (UMLS CUI [4,2])
C1522449 (UMLS CUI [2])
C1513041 (UMLS CUI [3,1])
C0450429 (UMLS CUI [3,2])
C0700589 (UMLS CUI [1,2])
C0009905 (UMLS CUI [2])
C0042241 (UMLS CUI [3,1])
C0037862 (UMLS CUI [3,2])
C1706306 (UMLS CUI [4])
C0006147 (UMLS CUI [1,2])
C0205189 (UMLS CUI [2,1])
C0007097 (UMLS CUI [2,2])
C0221908 (UMLS CUI [2,3])
C1334425 (UMLS CUI [3,1])
C0007097 (UMLS CUI [3,2])
C0221908 (UMLS CUI [3,3])
C0237753 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,2])
C0007117 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
C0205411 (UMLS CUI [2,3])
C0553723 (UMLS CUI [3,1])
C1522326 (UMLS CUI [3,2])
C0205411 (UMLS CUI [3,3])
C0851140 (UMLS CUI [4])
C0743997 (UMLS CUI [5,1])
C0007095 (UMLS CUI [5,2])
C0012634 (UMLS CUI [6,1])
C0332296 (UMLS CUI [6,2])
C1514873 (UMLS CUI [1,2])
C0338237 (UMLS CUI [1,3])
C0205082 (UMLS CUI [1,2])
C0006826 (UMLS CUI [1,3])
C0445356 (UMLS CUI [1,4])
C1321605 (UMLS CUI [2])
C0035647 (UMLS CUI [3,1])
C0205403 (UMLS CUI [3,2])
C0023671 (UMLS CUI [4])
C0005953 (UMLS CUI [2])
C0729502 (UMLS CUI [1,2])
C0021083 (UMLS CUI [2])
C0279025 (UMLS CUI [3])
C1522449 (UMLS CUI [4])
C0543467 (UMLS CUI [5])
C0920425 (UMLS CUI [6])
C0146224 (UMLS CUI [2])
C0045093 (UMLS CUI [3])
C0020517 (UMLS CUI [1,2])
C1579410 (UMLS CUI [2,1])
C0020517 (UMLS CUI [2,2])
C1706082 (UMLS CUI [3,1])
C0439849 (UMLS CUI [3,2])
C0332152 (UMLS CUI [1,2])
C2347804 (UMLS CUI [1,3])
C0680251 (UMLS CUI-2)
C0680251 (UMLS CUI [1,2])