Autopsy report · NCT02862600
Open-Label Study of Perhexiline in Patients With Hypertrophic Cardiomyopathy and Moderate to Severe Heart Failure
Cause of deathFutility
“Lack of Efficacy”
Life of this trial
- Ran for about 10 months before it stopped.
- 35 participants enrolled.
- Results were posted on the registry 3 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 2
- Sponsor
- Heart Metabolics Limited
- Sponsor type
- Industry
- Conditions
- Cardiomyopathy, Hypertrophic; Cardiomyopathy, Hypertrophic, Familial
- Interventions
- Perhexiline; Use of bioanalytical assay to monitor plasma levels of perhexiline
- Participants
- 35
- Sites
- 11
- Countries
- United States
Trials that died the same way
- Cross Linking for Treatment of Corneal Infection
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“lack of effectiveness” - Efficacy of the Infusion of Donor Plasma in COVID-19 Infection
“Lack of efficacy of treatment tested” - Study to Evaluate the Clinical Benefit Response in Cancer Patients With Advanced Disease With AMT2003 Versus Placebo
“Lack of efficacy. Stopped at first interim evaluation point”
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.