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Direct Lytic Agent
Exebacase for Staphylococcus Aureus Endocarditis (DISRUPT Trial)
Phase 3
Waitlist Available
Research Sponsored by ContraFect
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up day 60
Awards & highlights
DISRUPT Trial Summary
This trial will study whether exebacase is effective and safe in addition to standard of care antibiotics for treating patients with Staphylococcus aureus bloodstream infections.
Eligible Conditions
- Staph Bacteremia
- Staphylococcus Aureus Endocarditis
DISRUPT Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 60
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 60
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Clinical Responder Rate at Day 14 in the MRSA Population in the Microbiological Intent-to-treat (mITT) Analysis Set
Treatment-emergent Adverse Events (TEAEs) Through Day 60
Secondary outcome measures
30-day survival in the MRSA population
Clinical responder rate at Day 14 in all S. aureus patients
Clinical responder rate at Day 60 in all S. aureus patients
+2 moreDISRUPT Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: ExebacaseExperimental Treatment1 Intervention
Group II: PlaceboPlacebo Group1 Intervention
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Who is running the clinical trial?
ContraFectLead Sponsor
3 Previous Clinical Trials
141 Total Patients Enrolled
1 Trials studying Staphylococcus Aureus Endocarditis
121 Patients Enrolled for Staphylococcus Aureus Endocarditis
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