Hematology ×
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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

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- 4/13/21 - 1 form, 18 itemgroups, 195 items, 2 languages
Itemgroups: Patient, Father, Mother, Living arrangement, Sibling, Medical history, Nursing support, Support device, Personal aids, School, Kindergarten, workshop, Therapies in school, kindergarten, workshop, Medication, Medication history, Therapy, Nutrition, Continence, Catheters and drainages, Other
- 4/7/21 - 1 form, 2 itemgroups, 7 items, 1 language
Itemgroups: Administrative Data, Log Status
- 4/1/21 - 1 form, 16 itemgroups, 59 items, 1 language
Itemgroups: Administrative, Physical Examination (Follow-Up), Physical Examination (Follow-Up), Laboratory Results - Hematology/ Chemistry (Follow-Up), Laboratory Results (Follow-Up) - Hematology, Laboratory Results (Follow-Up) - Hematology, Laboratory Results (Follow-Up) - Chemistry, Laboratory Results (Follow-Up) - Chemistry, Post-Treatment Response (Follow -Up), Post-Treatment Response (Follow-Up) - CT or other Radiological Imaging Results, Post-Treatment Response (Follow-Up) - Bone Marrow Biopsy, Post-Treatment Response (Follow-Up) - Measurable Lymphoma Disease, Post-Treatment Response (Follow-Up) - Non-Measurable Lymphoma Disease, Post-Treatment Response (Follow-Up) - Non-Measurable Lymphoma Disease, Post-Treatment Response (Follow-Up) - Response, Signature of Investigator
- 3/30/21 - 1 form, 2 itemgroups, 5 items, 1 language
Itemgroups: Administrative Data, Investigational Product Discontinuation
Study ID: 110921 Clinical Study ID: 110921 Study Title: A Phase II Trial of Ofatumumab in Subjects with Waldenstrom's Macroglobulinemia Patient Level Data: Study Listed on Identifier: NCT00811733 Link: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Ofatumumab Trade Name: N/A Study Indication: Waldenstrom Macroglobulinaemia The primary objective of this open-label, multi-center, Phase II study was to evaluate the safety and efficacy of Ofatumumab in subjects diagnosed with Waldenstrom Macroglobulinaemia. For the study, eligible subjects were enrolled to receive up to 3 cycles of treatment with Ofatumumab. The first cycle consisted of a single dose of 300 mg followed by 3 weekly doses of 1000 mg (Treatment Group A) or 4 weekly doses of 2000 mg (Treatment Group B) of Ofatumumab, with response assessment beginning at Week 12. Based on the Week 12-16 response, eligible subjects could receive up to 2 additional cycles of treatment. This form has to be filled out at the end of study/ end of treatment. Complete this Form when the subject permanently stops the investigational product (IP). If the subject decided to withdraw consent and stop participation in the study, also complete the End of Study Form. If the subject decided to permanently stop the investigational product but will be followed for disease progression or survival per protocol, do not complete the End of Study Form until follow-up is complete.
- 3/30/21 - 1 form, 5 itemgroups, 23 items, 1 language
Itemgroups: Administrative Data, Pregnancy information, End of study, End of study details, Signature