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ANG-3777 for Hemodialysis
Phase 1
Waitlist Available
Led By Daniel K. Ries, MD
Research Sponsored by Angion Biomedica Corp
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 day 1 and day 2
Awards & highlights
Study Summary
The purpose of this study is to evaluate the pharmacokinetics and safety of a single-dose of ANG-3777 in subjects with renal failure receiving maintenance hemodialysis.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ day 1 and day 2
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~day 1 and day 2
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Measure the pharmacokinetic (PK) parameters of a single dose of ANG-3777 including, but not limited to: AUC(0-last) and AUC(0-inf)
Measure the pharmacokinetic (PK) parameters of a single dose of ANG-3777 including, but not limited to: Cmax
Measure the pharmacokinetic (PK) parameters of a single dose of ANG-3777 including, but not limited to: Tmax
Side effects data
From 2007 Phase 3 trial • 330 Patients • NCT0003581562%
Depression
53%
Site reactions
33%
Respiratory failure
14%
Change in visual acuity
13%
Hypoglycemia
13%
Headache
11%
Thrombotic events
8%
Hepatotoxicity
6%
Abnormal blood chemistries (other than liver)
100%
80%
60%
40%
20%
0%
Study treatment Arm
IGF-1
Placebo
Trial Design
1Treatment groups
Experimental Treatment
Group I: ANG-3777Experimental Treatment1 Intervention
Administered IV as a single dose over 30 minutes on Day 1, greater than 24 hours before receiving scheduled hemodialysis (HD).
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Who is running the clinical trial?
Angion Biomedica CorpLead Sponsor
11 Previous Clinical Trials
946 Total Patients Enrolled
Nucleus Network LtdOTHER
11 Previous Clinical Trials
490 Total Patients Enrolled
Daniel K. Ries, MDPrincipal InvestigatorNucleus Network Ltd
1 Previous Clinical Trials
16 Total Patients Enrolled
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