Autopsy report · NCT05601492
Adherence to Otezla
Cause of deathRegulatory or ethics
“Terminated IRB approval 6/26/2024, study was never initiated or activated”
Life of this trial
- Withdrawn before it enrolled anyone. Its dates are the sponsor's plans, not events that happened.
Vital statistics
- Status
- Withdrawn
- Phase
- Early Phase 1
- Sponsor
- Wake Forest University Health Sciences
- Sponsor type
- University, hospital or other
- Conditions
- Psoriasis
- Interventions
- Otezla - Standard Care; Reminder Text Intervention with apremilast; Extended Consultation for apremilast
- Participants
- 0
- Sites
- 1
- Countries
- United States
Trials that died the same way
- Simvastatin Nasal Rinses for the Treatment of COVID-19 Mediated Dysomsia
“Study halted prematurely; IRB approval not obtained” - Low-Level Transcutaneous Vagus Stimulation in ST Segment Elevation Myocardial Infarction: TREAT MI Study
“Study never initiated; withdrawn prior to receiving IRB approval” - Safety of Topical Tranexamic Acid in Total Joint Arthroplasty in High Risk Patients
“Study did not receive IRB approval, so did not start” - Study Comparing Intubation Via Video Laryngeal Mask Airways (VLMAs) Versus Video Laryngoscopy
“Study never approved by the IRB. Was not initiated” - Exhaled Breath Condensate pH in Patients With Cough Caused by Gastroesophageal Reflux
“IRB approval not renewed/approval lapsed. Prior status: insufficient enrollment; study suspended pending analysis”
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.