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GLP-1 Receptor Antagonist
Dose A for Hypoglycemia
Phase 1
Waitlist Available
Led By Tracey McLaughlin, MD
Research Sponsored by Tracey McLaughlin
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 0-180 minutes following initiation of ogtt
Awards & highlights
Study Summary
This study is designed to evaluate the safety, efficacy, and pharmacokinetic profile of single ascending doses of exendin 9-39 administered by subcutaneous route in subjects with post-bariatric hypoglycemia.
Eligible Conditions
- Hypoglycemia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 0-180 minutes following initiation of ogtt
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~0-180 minutes following initiation of ogtt
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Treatment effect on plasma glucose
Secondary outcome measures
Treatment effect on symptoms of hypoglycemia
Trial Design
4Treatment groups
Active Control
Group I: Dose AActive Control1 Intervention
Subcutaneous injection of Dose A of Exendin (9-39)
Group II: Dose CActive Control1 Intervention
Subcutaneous injection of Dose C of Exendin (9-39)
Group III: Dose DActive Control1 Intervention
Subcutaneous injection of Dose D of Exendin (9-39)
Group IV: Dose BActive Control1 Intervention
Subcutaneous injection of Dose B of Exendin (9-39)
Find a Location
Who is running the clinical trial?
Tracey McLaughlinLead Sponsor
2 Previous Clinical Trials
49 Total Patients Enrolled
2 Trials studying Hypoglycemia
49 Patients Enrolled for Hypoglycemia
Tracey McLaughlin, MDPrincipal InvestigatorStanford University
8 Previous Clinical Trials
520 Total Patients Enrolled
1 Trials studying Hypoglycemia
60 Patients Enrolled for Hypoglycemia
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