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Antiviral
AT-752 for Dengue Fever
Phase 1
Waitlist Available
Research Sponsored by Atea Pharmaceuticals, 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 day 2 until 28 days post virus inoculation
Awards & highlights
Study Summary
This trial will study whether AT-752 is safe and effective in healthy people who are infected with dengue virus.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 2 until 28 days post virus inoculation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 2 until 28 days post virus inoculation
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Mean quantitative RNAemia (peak and duration and area under the plasma concentration versus time curve [AUC])
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: AT-752Experimental Treatment1 Intervention
AT-752 administered orally for 14 days
Group II: PlaceboPlacebo Group1 Intervention
Matching placebo administered orally for 14 days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
AT-752
2021
Completed Phase 1
~70
Find a Location
Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Atea Pharmaceuticals, Inc.Lead Sponsor
27 Previous Clinical Trials
3,812 Total Patients Enrolled
1 Trials studying Dengue Fever
21 Patients Enrolled for Dengue Fever
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Who else is applying?
What state do they live in?
California
North Carolina
Virginia
Other
What site did they apply to?
Atea Study Site
What portion of applicants met pre-screening criteria?
Met criteria
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