Autopsy report · NCT07457632

Integrative Liver-Targeted Therapy for Diabetic Macular Edema: Using "Tauroursodeoxycholate" or Traditional Chinese Medicine.

“The study was terminated due to additional regulatory requirements that could not be completed within the established academic timeline. As a result, continuation of the study was not feasible.”

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• Withdrawn before it enrolled anyone.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Withdrawn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 2

Sponsor

University of Alabama at Birmingham

Sponsor type

University, hospital or other

Conditions

Diabetic Macular Edema (DME)

Interventions

Tauroursodeoxycholate (TUDCA); Traditional Chinese Medicine (mQJDHW); placebo capsule

Participants

0

Trials that died the same way

• Intranasal Challenge of Healthy Adults With Respiratory Syncytial Virus (RSV)
  “The study was terminated as it was determined to not be feasible to complete enrollment and the study within the required timeline and budget.” (88% match in meaning)
• Therapeutic Exercise in Patients With Hemophilia
  “The Study was terminated due to lack of funding for continuing” (83% match in meaning)
• Utility of Hyperpolarized 13C-pyruvate Metabolic Magnetic Resonance Imaging
  “"Study terminated due to institutional resource constraints, including limited availability of specialized equipment and technical support. Termination was not related to participant safety, data quality, study conduct, or the investigational product” (82% match in meaning)
• Adherence to Antidepressant Treatment in Subjects With Depression
  “The study was terminated early based on the planned interim analysis that did not meet criteria for continuation.” (82% match in meaning)
• Safety, Pharmacokinetics and Efficacy Study of QCC374 in PAH Patients
  “Study was terminated early for strategic reasons. Only Part I of the study was completed.” (82% 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.