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Oral GW786034 treatment for ovarian cancer NCT00281632 - Screening

- 15-03-21 - 1 Formulier, 24 Itemgroepen, 129 Data-elementen, 2 Talen
Itemgroepen: Header, Eligibility Question, Demography, Physical examination, Disease Characteristics, Metastatic Disease Site, local laboratory, Residual toxicities related to previous therapy for cancer, Residual toxicities, Cancer related current medical conditions, Medical Conditions, non-cancer related medical conditions, Medical Conditions, Prior anti-cancer therapy, Prior anti-cancer therapy - medication, Prior anti-cancer therapy - radiotherapy, Vital signs, ECOG Performance Status Scale, 12 LEAD ECG, 12-lead ECG Abnormalities, Local Laboratory - Haematology, Local Laboratory - Clinical Chemistry, Urinalysis, Electronically transferred laboratory data
Study ID: 104450 Clinical Study ID: VEG104450 Study Title: This study is a non-randomized, open-label, multi-center Phase II study of GW786034 to evaluate the administration of oral GW786034 in subjects with ovarian cancer. Clinicaltrials.gov Identifier: NCT00281632 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: pazopanib Trade Name: Votrient Study Indication: Neoplasms, Ovarian CRF Pages: 722-853

GSK Ropinirole in Subjects with Restless Legs Syndrome 101468/191 Screening (Form 1)

- 30-08-17 - 1 Formulier, 19 Itemgroepen, 84 Data-elementen, 1 Taal
Itemgroepen: General Information, RLS Screen History, RLS Diagnostic Criteria, Demography, Vital signs, Orthostatic Vital Signs, Electrocardiogramm (12 Lead), Physical Examination, Laboratory Evaluation, Pregnancy Dipstick, Significant medical/surgical history and physical examination, List of diagnosis other than RLS or PLMS, Prior and Concomitant Medication, Details prior and concomitant medication, RLS Pharmacotherapy history, Details RLS pharmacotherapy history, Screening Inclusion Criteria, Screening Exclusion Criteria, Repeat Electrocardiogram
Study ID: 101468/191 Clinical Study ID: SKF-101468/191 Study Title:A 12 Week, Double-Blind, Placebo-Controlled, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Ropinirole in Subjects with Restless Legs Syndrome (RLS) Suffering from Periodic Leg Movements of Sleep (PLMS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Requip Study Indication: Restless Legs Syndrome

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