Autopsy report · NCT06302439
PROPEL - A Prospective Observational Patient Registry to Evaluate ENPP1 and ABCC6 Deficiency
Cause of deathFunding or business
“The study was terminated by the sponsor prior to planned completion based on a review of the data across indications and overall program considerations. Study termination was not related to participant safety.”
Life of this trial
- Registered 5 months before it started.
- Ran for about 2 years 1 month before it stopped.
- 54 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Sponsor
- Inozyme Pharma
- Sponsor type
- Industry
- Conditions
- Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 Deficiency; ATP-Binding Cassette Subfamily C Member 6 Deficiency
- Interventions
- No Intervention for this observational study
- Participants
- 54
- Sites
- 14
- Countries
- Canada, Germany, Italy, Japan, Oman, Spain, Turkey (Türkiye), United Kingdom, United States
Trials that died the same way
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“The study was terminated early due to sponsor decision unrelated to safety or efficacy findings” - Study of Ataluren (PTC124) in Hemophilia A and B
“Study was terminated early due to Sponsor decision and not reflective of adverse safety findings.” - Colorectal Lesion Evaluation and Appropriate Resolution (CLEAR) Study
“Study terminated per sponsor decision due to operational reasons. The termination was not a result of any participant safety concerns.” - Study of Obeldesivir to Treat Children With Respiratory Syncytial Virus (RSV) Infection
“Study was terminated by Sponsor; the decision was not due to any safety findings.” - A Study to Assess Recurrence of Actinic Keratosis in Participants Treated With Methyl Aminolevulinate Hydrochloride Cream or Vehicle Cream Who Achieved Complete Response to Treated Lesions in Earlier Study
“The study was terminated early as per Sponsor's decision”
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.