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NotablePrimary endpoints: details revised at 2 of 2 entriesShow 4 more changesShow less
Study sites: 22 to 23
Eligibility criteria expanded, about 40 words
Secondary endpoints: details revised at 2 of 3 entries
Publications: details revised at 44 of 56 entries
MinorStudy sites: 21 to 22v14
MinorStudy sites: 20 to 21v13
Show 2 earlier versionsHide 2 earlier versions
MinorStudy sites: 19 to 20v12
MinorStudy sites: 18 to 19v11
MinorTrial sites expanded: 15 → 18 locationsv10
MinorTrial sites expanded: 12 → 15 locationsv9
MinorStudy sites: 11 to 12v8
MinorStudy sites: 9 to 11v7
MinorStudy sites: 8 to 9v6
MinorStudy sites: 6 to 8v5
MinorEnrollment reduced: 80 → 60 participantsv4Show 9 more changesShow less
Trial sites expanded: 2 → 6 locations
Primary and study completion pushed from Nov 2026 to Dec 2026
Start date changed from estimate of Feb 2026 to Feb 13, 2026
Interventions: Antifungal Comparator (Drug), EL219 (Drug) to Active Comparator- IV Antifungal (LAmB or voriconazole) (Drug), EL219 (Drug)
Secondary endpoints: 6 to 3
Study description expanded, about 8 words
Publications: 44 to 56
Eligibility criteria expanded, about 5 words
Study title shortened, about 3 words
NotableStart date: Dec 2025 to Feb 2026
Study sites: 1 to 2
v3
NotableTrial status: Not Yet Recruiting to Recruiting
Study sites: 0 to 1
Start date: Nov 2025 to Dec 2025
v2
MinorStudy First Submitted
Stopped: an ongoing trial was terminated, suspended or withdrawn.
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The purpose of this study is to determine if EL219 is safe and effective compared to liposomal amphotericin B (LAmB) or voricanozole for early treatment of invasive mould infections