Autopsy report · NCT04677829

Safety and Tolerability of PNT001 in Patients With Acute Traumatic Brain Injury (TBI)

“The study was terminated due to administrative, non-safety related reasons.”

The sponsor’s own words in the registry.

Life of this trial

• Registered 4 months before it started.
• Ran for about 0 months before it stopped.
• 1 participant enrolled.
• No results are posted on the registry.

Vital statistics

Status

Terminated

Phase

Phase 1

Sponsor

Pinteon Therapeutics, Inc

Sponsor type

Industry

Conditions

Traumatic Brain Injury

Interventions

PNT001; %5 dextrose for infusion

Participants

1

Sites

1

Countries

United States

Trials that died the same way

• Satavaptan for the Prevention of Ascites Recurrence in Patients With Ascites Due to Cirrhosis of the Liver
  “Study was terminated due to safety reason.” (93% match in meaning)
• Study of KHK 4323 in Healthy Volunteers and Subjects With Atopic Dermatitis
  “The study terminated for safety reasons.” (90% match in meaning)
• An Efficacy and Safety of Flomoxef Versus Cefepime in the Treatment of Participants With Urinary Tract Infections
  “Study was prematurely terminated due to administrative and strategic reasons” (89% match in meaning)
• Safety of Buprenorphine Transdermal Patch (BTDS) in Osteoarthritis Pain: a 52-Week Extension Phase
  “This study was terminated early for administrative reasons.” (88% match in meaning)
• Measuring Relative Afferent Pupillary Defect
  “The study was terminated early for administrative reasons.” (87% 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.