Autopsy report · NCT02881567
Efficacy and Safety of Daclizumab in Participants With RRMS Switching From Natalizumab
Cause of deathFunding or business
“Study terminated in line with Biogen decision to withdraw Zinbryta from the market and not to pursue further studies of daclizumab in MS.”
Life of this trial
- Registered 8 months before it started.
- Ran for about 1 year 5 months before it stopped.
- 41 participants enrolled.
- Results were posted on the registry 1 year after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Biogen
- Sponsor type
- Industry
- Conditions
- Relapsing-Remitting Multiple Sclerosis (RRMS)
- Interventions
- Daclizumab
- Participants
- 41
- Sites
- 11
- Countries
- Canada, Germany, Italy, Puerto Rico, United States
Trials that died the same way
- A Study of BMN 255 in Participants With Non-Alcoholic Fatty Liver Disease And Hyperoxaluria
“The study was withdrawn because BioMarin decided to end the overall development program. The study withdrawal was not due to any patient safety concerns.” - A Study of Atezolizumab Versus Observation as Adjuvant Therapy in Participants With High-Risk Muscle-Invasive Urothelial Carcinoma (UC) After Surgical Resection
“Sponsor decided to terminate the study early because the study did not meet its primary endpoint and because the study had met its goals of providing safety and additional exploratory efficacy information for atezolizumab monotherapy in MIBC.” - Study of Magrolimab Combinations in Patients With Relapsed/Refractory Multiple Myeloma
“This study was terminated early due to the Sponsor's decision to discontinue development of the investigational drug and close the program.” - Medication Use Among American Indians Adults
“The study has not been stopped. The study does not qualify as a clinical trial so it was withdrawn from clinicaltrials.gov.” - Safety and Efficacy of MAGE-A3/A6 T Cell Receptor Engineered T Cells (KITE-718) in HLA-DPB1*04:01 Positive Adults With Advanced Cancers
“The study was terminated due to the sponsor's decision to discontinue the clinical trial.”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.