-
CSR Summary Not yet available
-
NCT02195479
-
Primary Citation
-
Trial Information
Generic NameDaratumumabProduct NameDARZALEX®Therapeutic AreaEnrollment706% Female53.7%% White85.1%
Product ClassMonoclonal AntibodySponsor Protocol Number54767414MMY3007Data PartnerJohnson & JohnsonCondition StudiedMultiple MyelomaMean/Median Age (Years)71.4
Supporting Documentation
- Collected Datasets Available
- Data Definition Specification Available
- Protocol with Amendments Available
- Statistical Analysis Plan Available
- Clinical Study Report Available
Approved Data Requests Associated with this Trial
- 2025-0152 : Comparative Outcomes of DVMP, DRd, VMP, and Rd in Older High-Risk Cytogenetic Multiple Myeloma Patients: A Propensity Score Analysis
- 2025-0008 : Characterization of the trajectory of infections among patients with Multiple Myeloma treated with daratumumab
- 2024-0648 : Analysis of mutiple myeloma cell dynamics in response to different treatments.
- 2024-0032 : Thrombotic risk in patients with newly diagnosed multiple myeloma treated with a non-immunomodulatory drug containing quadruplet
- 2023-5316 : Prospective Assessment of ISS-R2 as a Prognostic Indicator in Patients with Newly Diagnosed Multiple Myeloma in the Anti-CD38 Era
- 2023-5195 : Predictive modeling of adverse events and symptoms patterns in large scale clinical trials
- 2023-5162 : Is minimal residual disease a valid surrogate endpoint for survival in multiple myeloma?
- 2022-5048 : Predictors of exposure, therapeutic and adverse effects of medicines used in the treatment of multiple myeloma
- 2021-4663 : Thromboembolism Prophylaxis and the Incidence of Venous Thromboembolism in Newly Diagnosed Multiple Myeloma Patients Enrolled on the MAIA trial
- 2021-4660 : Associations between response, progression, and overall survival in phase III daratumumab clinical trials in relapsed/refractory multiple myeloma