Autopsy report · NCT00815516
Study to Compare the Efficacy and Safety of Micafungin Versus Conventional Amphotericin B for the Treatment of Neonatal Candidiasis
Cause of deathSlow enrollment
“It was decided to discontinue the study due to insufficient recruitment.”
Life of this trial
- Registered 4 years 2 months before it started.
- Ran for about 1 year 10 months before it stopped.
- 30 participants enrolled.
- Results were posted on the registry 9 months after it ended.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Astellas Pharma Global Development, Inc.
- Sponsor type
- Industry
- Conditions
- Candidiasis
- Interventions
- micafungin; amphotericin B deoxycholate
- Participants
- 30
- Sites
- 17
- Countries
- Brazil, Bulgaria, Canada, Colombia, Greece, Hungary, Israel, Philippines, Romania, Turkey (Türkiye), Ukraine, United States
Trials that died the same way
- Comparing Palliative Radiotherapy With or Without Carboplatin
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“Study was stopped due to insufficient recruitment.” - Jet Injection of 1% Buffered Lidocaine Versus Topical EMLA for Local Anesthesia Before Lumbar Puncture in Children
“Due to low recruitment numbers, the study was terminated.” - A Study of ANV419 Alone or in Combination With Approved Treatments in Patients With Multiple Myeloma (OMNIA-2)
“The study was ended due to a lack of recruitment” - To Determine the Objective Response Rate of 4 Cycles of Docetaxel + Anthracycline (Epirubicin or Doxorubicine) Followed by 4 Cycles of Docetaxel Single Agent
“the study was early terminated due to lack of recruitment.”
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.