Reset filter
Keywords
Clinical Chemistry Tests ×
Physical Examination ×
Show more Keywords
Table of contents
  1. 1. Clinical Trial
  2. 2. Routine Documentation
  3. 3. Registry/Cohort Study
  4. 4. Quality Assurance
  5. 5. Data Standard
  6. 6. Patient-Reported Outcome
  7. 7. Medical Specialty
Selected data models

You must log in to select data models for download or further analysis.

12 Search results.

Relevance Rating New first Old first

Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphomas NCT00996593 - Physical Examination, Laboratory Results Hematology/ Chemistry Follow- Up

- 1/31/22 - 1 form, 8 itemgroups, 44 items, 1 language
Itemgroups: Date of physical examination,Visit Week physical examination,B- Symptoms,Physical Examination,Organ/ System,Visit Week laboratory,Hematology,Chemistry
Study ID: 104507 Clinical Study ID: BEX104507 Study Title: Phase II Study of Iodine-131 Anti-B1 Antibody for Non Hodgkin’s Lymphoma Patients who have Previously Received Rituximab Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00996593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: tositumomab Trade Name: Bexxar Study Indication: Lymphoma, Non-Hodgkin

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - Cycle 1 Day 21 - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Urinalysis microscopy results; Serum beta-hCG Pregnancy Test; PK Sampling - Plasma Samples; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment

- 10/30/19 - 1 form, 19 itemgroups, 82 items, 1 language
Itemgroups: Administrative,Visit Date,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Results,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,PK Sampling - Plasma Samples,Study Treatment Compliance (Return) ,New Adverse Events and Concomitant Treatment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - SRT501, Monotherapy, Cycle __ Day 21 - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Urinalysis microscopy results; Serum beta-hCG Pregnancy Test; Radiographic Assessment; Disease Marker Assessment; Disease Response; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment

- 3/10/19 - 1 form, 23 itemgroups, 109 items, 1 language
Itemgroups: Administrative,Visit Date,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Result,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,Radiographic Assessment,Radiographic Assessment ,Disease Marker Assessment ,Disease Marker Assessment ,Disease Response,Study Treatment Compliance (Return) ,New Adverse Events and Concomitant Treatment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - SRT501 + Bortezomib Cycle __ Day 21 - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Urinalysis microscopy results; Serum beta-hCG Pregnancy Test; Radiographic Assessment; Disease Marker Assessment; Disease Response; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment

- 3/10/19 - 1 form, 23 itemgroups, 107 items, 1 language
Itemgroups: Administrative,Visit Date,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Result,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,Radiographic Assessment,Radiographic Assessment ,Disease Marker Assessment ,Disease Marker Assessment ,Disease Response,Study Treatment Compliance (Return) ,New Adverse Events and Concomitant Treatment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - Unscheduled - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Serum beta-hCG Pregnancy Test; Radiographic Assessment; Disease Marker Assessment

- 3/5/19 - 1 form, 19 itemgroups, 95 items, 1 language
Itemgroups: Administrative,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Result,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,Radiographic Assessment,Radiographic Assessment ,Disease Marker Assessment,Disease Marker Assessment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - Cycle 2 Day 21 - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Urinalysis microscopy results; Serum beta-hCG Pregnancy Test; Radiographic Assessment; Disease Marker Assessment; Disease Response; Study Treatment Compliance (Return); New Adverse Events and Concomitant Treatment

- 3/1/19 - 1 form, 23 itemgroups, 109 items, 1 language
Itemgroups: Administrative,Visit Date,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Result,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,Radiographic Assessment,Radiographic Assessment ,Disease Marker Assessment,Disease Marker Assessment ,Disease Response,Study Treatment Compliance (Return) ,New Adverse Events and Concomitant Treatment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma NCT00920556 - Screening - Physical Examination; Vital Signs; 12-Lead ECG; Hematology; Clinical Chemistry, Coagulation and Electrolytes; Urinalysis; Urinalysis microscopy results; Serum beta-hCG Pregnancy Test; Radiographic Assessment; Disease Marker Assessment

- 3/1/19 - 1 form, 19 itemgroups, 97 items, 1 language
Itemgroups: Administrative,Was a physical examination performed?,Physical Examination,Vital Signs,12-Lead ECG,ECG Results,ECG Findings,Hematology,Hematology ,Clinical Chemistry, Coagulation and Electrolytes,Clinical Chemistry, Coagulation and Electrolytes ,Urinalysis dipstick results,Urinalysis microscopy results,Urinalysis microscopy results ,Serum beta-hCG Pregnancy Test,Radiographic Assessment,Radiographic Assessment ,Disease Marker Assessment,Disease Marker Assessment
Study ID: 113222 Clinical Study ID: 113222 Study Title: A Phase II, Open Label, Clinical Study to Assess the Safety and Activity of SRT501 Alone or in Combination with Bortezomib in Patients with Multiple Myeloma Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00920556 Sponsor: GlaxoSmithKline Phase: Phase 2 Study Recruitment Status: Completed Generic Name:5.0g SRT501 Trade Name: Bortezomib Study Indication: Multiple Myeloma

Pharmacokinetics of an oral contraceptive co-administered with Albiglutide in women - 107032 - Early Term Data: Vital Signs, Physical Examination, ECG, Laboratory Tests

- 12/28/18 - 1 form, 9 itemgroups, 55 items, 1 language
Itemgroups: Administrative data,Vital Signs - Duplicate 1,Vital Signs - Duplicate 2,Physical Examination,Electrocardiogram,Overall Interpretation of ECG,Hematologic Test,Chemistry Test,UA / Urine Chemistry Test
Study ID: 107032 Clinical Study ID: GLP107032 Study Title: An open-label study to evaluate the pharmacokinetics of an oral contraceptive containing Norethindrone and Ethinyl Estradiol when co-administered with GSK716155 in healthy adult female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01077505 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Pharmacokinetics of an oral contraceptive co-administered with Albiglutide in women - 107032 - Follow-Up: Vital Signs, Electrocardiogram, Laboratory Tests

- 12/28/18 - 1 form, 9 itemgroups, 56 items, 1 language
Itemgroups: Administrative data,Vital Signs - Duplicate 1,Duplicate 2,Physical Examination,Electrocardiogram,Overall Interpretation of ECG,Hematologic Test,Chemistry Test,UA / Urine Chemistry Test
Study ID: 107032 Clinical Study ID: GLP107032 Study Title: An open-label study to evaluate the pharmacokinetics of an oral contraceptive containing Norethindrone and Ethinyl Estradiol when co-administered with GSK716155 in healthy adult female subjects Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT01077505 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Subcutaneous injections of GSK 716155 in healthy volunteers; Study ID: 105229 - Screening

- 11/6/18 - 1 form, 14 itemgroups, 67 items, 1 language
Itemgroups: Demography,Childbearing Potential,Physical Examination,Medical Conditions,Vital Signs,12-lead ECG,Holter Electrocardiography,Clinical Chemistry,Hematology finding,Urinalysis,Immunogenicity Study; Blood,Urine drug screening,Ethanol measurement, Urine; Ethanol measurement, breath,HIV Seropositivity, hepatitis b serology, hepatitis C serology test
Study ID: 105229 Clinical Study ID: GLP105229 Study Title: A double-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous injections of GSK 716155 in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Subcutaneous injections of GSK 716155 in healthy volunteers; Study ID: 105229 - Final Follow-Up

- 10/9/18 - 1 form, 9 itemgroups, 30 items, 1 language
Itemgroups: 12-lead ECG,Vital Signs,Physical Examination,Clinical Chemistry,Hematology finding,Urinalysis,Fructosamine measurement,Immunogenicity Study; Blood,Pharmacokinetic aspects; Blood
Study ID: 105229 Clinical Study ID: GLP105229 Study Title: A double-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous injections of GSK 716155 in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Subcutaneous injections of GSK 716155 in healthy volunteers; Study ID: 105229 - Day 13

- 10/9/18 - 1 form, 14 itemgroups, 51 items, 1 language
Itemgroups: 12-lead ECG,Vital Signs,Physical Examination,Clinical Chemistry,Hematology finding,Urinalysis,Free Fatty Acids measurement,Fructosamine measurement,Capillary Blood Glucose measurement,drug biological activity, Collection of blood specimen for laboratory procedure,Pharmacokinetic aspects; Blood,Antidiabetics; Tolerability Study,Adverse event,Antidiabetics; Tolerability Study; Worksheet
Study ID: 105229 Clinical Study ID: GLP105229 Study Title: A double-blinded, randomized, placebo-controlled, staggered-parallel, escalating dose study to investigate the safety, tolerability, pharmacokinetics and pharmacodynamics of subcutaneous injections of GSK 716155 in healthy volunteers. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: albiglutide Trade Name: Tanzeum,Eperzan Study Indication: Diabetes Mellitus, Type 2

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial