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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 up to 7 days
Summary
This trial tests SRX246, a drug aimed at reducing fear and anxiety, on people who feel anxious or scared. It measures how the drug affects their startle response and emotion recognition.
Eligible Conditions
- Anxiety
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 7 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 7 days
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in startle reflex between SRX246 and Placebo
Secondary study objectives
Change in State Anxiety Scale between SRX246 and Placebo
Change in emotional expression recognition between SRX246 and Placebo
Side effects data
From 2016 Phase 1 & 2 trial • 97 Patients • NCT020556386%
Dry Mouth
6%
Diarrhea
6%
Headache
100%
80%
60%
40%
20%
0%
Study treatment Arm
SRX246
Placebo
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: SRX246Experimental Treatment1 Intervention
SRX246 oral dosage capsules, daily dose to be taken bid, for up to 7 days
Group II: PlaceboPlacebo Group1 Intervention
Placebo oral dosage capsules, daily dose to be taken bid, for up to 7 days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
SRX246
2009
Completed Phase 2
~280
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Azevan PharmaceuticalsLead Sponsor
7 Previous Clinical Trials
436 Total Patients Enrolled
National Institute of Mental Health (NIMH)NIH
2,907 Previous Clinical Trials
2,738,893 Total Patients Enrolled
90 Trials studying Anxiety
41,804 Patients Enrolled for Anxiety
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