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Trial of Two Dosing Regimens of Micafungin Versus Caspofungin for the Treatment of Esophageal Candidiasis

COMPARATIVE STUDY OF PHASE III RANDOMIZED, DOUBLE-BLIND TWO REGIMES OF DOSE OF MICAFUNGIN (FK463) VERSUS CASPOFUNGIN FOR THE TREATMENT OF CANDIDIASTIC ESOPHAGITIS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REPEC
Registry ID
PER-046-04
Enrollment
51
Registered
2004-07-05
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Micafungin administered intravenously in daily dose Group name:micafungin Type of group
Endovenous micafungin is administered every other day with placebo.

Sponsors

FUJISAWA HEALTH CARE INC,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Esophageal candidiasis confirmed by endoscopy Negative pregnancy test for female patients of childbearing potential

Exclusion criteria

Exclusion criteria: Pregnant or nursing female patient Evidence of liver disease Another active opportunistic fungal infection and/or receiving acute systemic therapy for an opportunistic fungal infection Concomitant esophagitis caused by herpes simplex virus or cytomegalovirus Received an oral or topical antifungal agent within 48 hours or a systemic antifungal agent within 72 hours of first dose of study drug Known to be non-responsive to therapy in any prior systemic antifungal clinical trail Experienced > 2 episodes of esophageal candidiasis requiring systemic antifungal therapy History of anaphylaxis attributed to echinocandin class of antifungals

Design outcomes

Primary

MeasureTime frame
Outcome name:Comparative incidence of success, defined as the complete elimination of esophageal lesions Measure:Comparative incidence of success, defined as the complete elimination of esophageal lesions Timepoints:day 14

Secondary

MeasureTime frame
Outcome name:General therapeutic response Measure:General therapeutic response Timepoints:day 14

Countries

Argentina, Brazil, Peru, South Africa

Outcome results

None listed

Source: REPEC (via WHO ICTRP)