Autopsy report · NCT04450342

REGENETEN™ Bioinductive Implant System in Full-thickness Tears

“Sponsor decision not related to safety.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 5 months before it started.
• Ran for about 2 years 11 months before it stopped.
• 119 participants enrolled.
• Results were posted on the registry 1 year 7 months after it ended.

Vital statistics

Status

Terminated

Phase

Na

Sponsor

Smith & Nephew, Inc.

Sponsor type

Industry

Conditions

Rotator Cuff Injuries

Interventions

Arthroscopic rotator cuff repair with REGENETEN™ Bioinductive Implant augmentation; Arthroscopic rotator cuff repair; Arthroscopic rotator cuff repair for revision surgery

Participants

119

Sites

30

Countries

Australia, Canada, France, Hong Kong, Singapore, Switzerland, United Kingdom, United States

Trials that died the same way

• Long-term Safety and Efficacy Evaluation of Subcutaneous Amlitelimab in Adult Participants With Moderate-to-severe Asthma Who Completed Treatment Period of Previous Amlitelimab Asthma Clinical Study
  “Sponsor decision; the decision is not related to any safety concern.” (96% match in meaning)
• Long-Chain Fatty Acid Oxidation Disorders Online Disease Monitoring Program
  “Sponsor decision not related to safety concerns” (92% match in meaning)
• Effect of Lixisenatide on Postprandial Lipid Profile in Obese Type 2 Diabetic Patients
  “Sponsor decision not related to safety reasons” (89% match in meaning)
• Double-blind, Randomized, Placebo-controlled Study Evaluating Efficacy and Safety of IgPro20 in Post-COVID-19 POTS
  “Sponsor decision, not for safety reasons.” (88% match in meaning)
• Study of Safety and Efficacy of Novel Immunotherapy Combinations in Patients With Triple Negative Breast Cancer (TNBC).
  “This was a sponsor decision and was not a consequence of any safety concern” (88% 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.