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NCT03672292 · ClinicalTrials.gov registry record · Phase 2

Evaluate Safety and Efficacy of the Coadministration of Ibrexafungerp With Voriconazole in Patients With Invasive Pulmonary Aspergillosis

A Phase 2 study, sponsored by Scynexis.

Terminated
Registry status
Phase 2
Development phase
22
Enrollment target

NCT03672292: Clinical Trial Phase 2 study, sponsored by Scynexis.

NCT03672292 is a Phase 2 study that was terminated before completion, run by Scynexis. The registered enrollment target is 22 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03672292, a Phase 2 study, was terminated before completion, sponsored by Scynexis.

TERMINATED
Registry status
Phase 2
Development phase
22 participants
Enrollment target

Study Summary

Study to evaluate the safety and efficacy of coadminstration of SCY-078 with a mold-active azole (voriconazole) compared to voriconazole in patients with invasive pulmonary aspergillosis.

Primary Outcome

Number of participants with treatment-emergent adverse events (TEAEs), drug-related adverse events (AEs), discontinuations due to AEs and deaths.

Interventions

  • DRUG Voriconazole
  • DRUG SCY-078
  • OTHER Oral Placebo Tablets

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2019-01-22
Est. Completion 2023-03-27
Phase Phase 2
Scynexis

13 total trials

Why NCT03672292 stopped before completion

NCT03672292 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 22 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 3 interventions - of which Voriconazole is the first listed.

NCT03672292 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03672292 about?

NCT03672292 is a clinical study titled "Evaluate Safety and Efficacy of the Coadministration of Ibrexafungerp With Voriconazole in Patients With Invasive Pulmonary Aspergillosis". Study to evaluate the safety and efficacy of coadminstration of SCY-078 with a mold-active azole (voriconazole) compared to voriconazole in patients with invasive pulmonary aspergillosis.

What is the current status of trial NCT03672292?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 22 participants. The study started on 2019-01-22. Estimated completion is 2023-03-27.

What interventions are being tested in trial NCT03672292?

The interventions under investigation include: Voriconazole (DRUG), SCY-078 (DRUG), Oral Placebo Tablets (OTHER).

Who is sponsoring clinical trial NCT03672292?

This trial is sponsored by Scynexis, which has 13 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03672292's enrollment target sits among peer trials

22 1790th of 2000 higher than 207 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03672292, the US trial registry maintained by the National Library of Medicine. NCT03672292 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.