Autopsy report · NCT03400956
Assess Safety and Efficacy of Vilaprisan in Subjects With Uterine Fibroids (ASTEROID 4)
Cause of deathFunding or business
“Due to a change in the development program, the study was closed prematurely.”
Life of this trial
- Ran for about 3 years 5 months before it stopped.
- 103 participants enrolled.
- Results were posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Bayer
- Sponsor type
- Industry
- Conditions
- Uterine Fibroids
- Interventions
- Vilaprisan (BAY1002670); Placebo
- Participants
- 103
- Sites
- 87
- Countries
- Czechia, Japan, Russia, Ukraine, United States
Trials that died the same way
- Treosulfan-Based Versus Clofarabine-Based Conditioning Before Donor Hematopoietic Stem Cell Transplant for the Treatment of Myelodysplastic Syndromes or Acute Myeloid Leukemia
“The study was closed due to the end of funding.” - An Evaluation of a Novel Food Product in Adults Residing in an Area Endemic for Helminths
“Due to a business decision to stop the project, the study was terminated early.” - Human IL-15 (rhIL-15) and Obinutuzumab for Relapsed and Refractory Chronic Lymphocyte Leukemia
“The study was closed after \> 1 year of inactivity.” - Laryngeal Pacing Study
“The study was halted early as grant funding was awarded for a new study, which was opened in place of this one.” - COVID-19 Booster Vaccine in Autoimmune Disease Non-Responders
“The study was closed due to continued enrollment hurdles.”
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.