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3000-mg cohort for Campylobacteriosis
Phase 2
Waitlist Available
Led By Mohamed Al-Ibrahim, MB,ChB, FACP
Research Sponsored by Lumen Bioscience, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 14 days
Awards & highlights
Study Summary
This trial tests a new drug, LMN-101, to see if it can prevent or reduce the severity of an infection with the bacteria Campylobacter jejuni.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 14 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~14 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Frequency of solicited or unsolicited adverse events
Secondary outcome measures
Campylobacter
Proportion of subjects with specific solicited adverse events
Trial Design
2Treatment groups
Active Control
Placebo Group
Group I: 3000-mg cohortActive Control1 Intervention
LMN-101, six 500-mg capsules orally three times daily for 14 days (n=21)
Group II: Placebo cohortPlacebo Group1 Intervention
Placebo, six 500-mg capsules orally three times daily for 14 days (n=21)
Find a Location
Who is running the clinical trial?
Naval Medical Research CenterFED
33 Previous Clinical Trials
2,858 Total Patients Enrolled
University of MarylandOTHER
160 Previous Clinical Trials
302,241 Total Patients Enrolled
Lumen Bioscience, Inc.Lead Sponsor
4 Previous Clinical Trials
443 Total Patients Enrolled
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