Autopsy report · NCT05614245

Safety, Tolerability, and Immunogenicity of Trivalent Coronavirus Vaccine Candidate VBI-2901e With E6020 Adjuvant

“Study was halted prematurely prior to enrollment of first participant based on study sponsor's decision to prioritize clinical development of VBI-2901a.”

The sponsor’s own words in the registry.

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• Withdrawn before it enrolled anyone.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Withdrawn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

Phase 1

Sponsor

VBI Vaccines Inc.

Sponsor type

Industry

Conditions

COVID-19; Coronavirus Infections

Interventions

VBI-2901e

Participants

0

Sites

4

Countries

Canada

Trials that died the same way

• High Cut Off Dialysis in Systemic Inflammatory Response Syndrome Patients After Cardiac Surgery
  “Study halted prematurely, prior to enrollment of first patient, due to recruiting problems.” (75% match in meaning)
• Cancer and Mild Cognitive Impairment a Patient-Caregiver Behavioral Intervention
  “Study halted prematurely, prior to enrollment of first participant” (75% match in meaning)
• Ribociclib vs. Palbociclib in Patients With Advanced Breast Cancer Within the HER2-Enriched Intrinsic Subtype
  “The study was prematurely halted because enrollment was significantly delayed compared with the original projections due to the evolving therapeutic landscape.” (74% match in meaning)
• Tiotropium Handihaler vs. Tiotropium Respimat in COPD
  “Study halted prematurely due to funding, prior to enrollment of first participant” (72% match in meaning)
• The Performance and Safety of Petit Drill in the French Paediatric Population: a Post-market Clinical Follow-up Study
  “Due to difficulty in recruiting patients, the Sponsor decided to prematurely stop the study” (69% match in meaning)

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.