Autopsy report · NCT03919162
A Trial to Evaluate the Efficacy and Safety of PQ912 in Patients With Early AD
Cause of deathFunding or business, also safety
“It has been made the strategic decision to terminate the study. This decision to terminate the study early is not being made for safety reasons.”
Life of this trial
- Registered 2 years 7 months before it started.
- Ran for about 2 years 9 months before it stopped.
- 112 participants enrolled.
- Results were posted on the registry 1 year 4 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Vivoryon Therapeutics N.V.
- Sponsor type
- Industry
- Conditions
- Alzheimer Disease
- Interventions
- PQ912; Placebo
- Participants
- 112
- Sites
- 22
- Countries
- United States
Trials that died the same way
- A Study of TCD601 (Siplizumab) in New Onset Type 1 Diabetes Patients
“The study has been early terminated due to business reasons. This decision is not related to any safety, efficacy, or regulatory concerns.” - Effects of JNJ-53718678 in Adult and Adolescent Participants Who Had a Hematopoietic Stem Cell Transplantation and Who Are Infected With Respiratory Syncytial Virus (RSV)
“A strategic decision was made to discontinue the study. The decision was not based on a safety concern.” - An Evaluation Of PF-03715455 In Moderate To Severe Uncontrolled Asthma
“The termination was due to business reasons. No safety or efficacy concerns contributed to the termination of the study” - Pre-operative Mocetinostat (MGCD0103) and Durvalumab (MEDI4736) (PRIMED) for Squamous Cell Carcinoma of the Oral Cavity
“The study has been terminated due to a change in internal prioritization and not due to any safety concerns.” - Surgical Treatment of Chronic Neuropathic Pain
“The study was terminated due to lower than expected enrollment. The decision to terminate the study was not based on any safety or efficacy concerns.”
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.