Autopsy report · NCT00810212

Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion

“Sponsor preferred a better study design”

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• Withdrawn before it enrolled anyone.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Withdrawn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, Phase 2

Sponsor

Mesoblast, Ltd.

Sponsor type

Industry

Conditions

Degenerative Disc Disease; Degenerative Spondylolisthesis; Spinal Stenosis

Interventions

PLF with autograft; PLF with NeoFuse; PLF with NeoFuse; PLF with NeoFuse

Participants

0

Sites

1

Countries

United States

Trials that died the same way

• Study of Efficacy on NT-proBNP of Recombinant Human Neuregulin-1 in Chronic Heart Failure Patients
  “Sponsor has designed another study with different endpoint to replace the current study” (76% match in meaning)
• Effectiveness and Tolerability of LabiaStick#01 in Subjects With Symptomatic Non-hypertrophic Chronic Vulvar Dermatoses
  “New study design will be made” (73% match in meaning)
• AndraTec PMCF Study : Investigating the AndraTec Guidewires,PTA Balloons and Stents in Iliac Disease.
  “Sponsor did not pusue with the study” (71% match in meaning)
• Safety Study of Intranasal Etripamil for the Termination of Spontaneous Episodes of Paroxysmal Supraventricular Tachycardia (PSVT). NODE-302
  “Study was stopped by the Sponsor” (70% match in meaning)
• A Study in Patients With Advanced Parkinson's Disease to Assess the Relative Bioavailability of Levodopa Administered as ND0612 Subcutaneous Infusion Versus Levodopa Administered as Carbidopa-Levodopa Enteral Suspension
  “Decision to change the study design” (70% 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.