Autopsy report · NCT03358407
GSK2983559 First Time in Human Study
Cause of deathSafety
“Terminated due to non clinical toxicology findings and reduced safety margins.”
Life of this trial
- Registered 1 month before it started.
- Ran for about 1 year 1 month before it stopped.
- 31 participants enrolled.
- Results were posted on the registry 1 year 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 1
- Sponsor
- GlaxoSmithKline
- Sponsor type
- Industry
- Conditions
- Inflammatory Bowel Diseases
- Interventions
- GSK2983559; Placebo
- Participants
- 31
- Sites
- 1
- Countries
- United Kingdom
Trials that died the same way
- Vorinostat, Carboplatin and Gemcitabine in Women With Recurrent, Platinum-Sensitive Ovarian Cancer
“Terminated due to unacceptable toxicity” - Safety Study of Bevacizumab (Avastin) With Thoracic Radiation in Non-small Cell Cell Lung Cancer
“Study terminated due to toxicity” - A Dose-finding Study of Birabresib (MK-8628) in Participants With Recurrent Glioblastoma Multiforme (MK-8628-002)
“This study was terminated due to lack of clinical activity and not due to safety reasons.” - QUILT-3.031: AMG 337 in Subjects With Advanced or Metastatic Clear Cell Sarcoma
“Prematurely terminated due to lack of therapeutic effect” - A Phase II Study of Belinostat in Combination With Bortezomib in Patients With Relapsed, Refractory Multiple Myeloma
“Terminated due to dose limiting toxicity”
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.