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ANG-3070 for Proteinuria

Phase 2
Waitlist Available
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 week 12
Awards & highlights

Study Summary

This trial is testing a new drug to see if it is safe and effective in treating patients with a primary glomerular disease who have persistent proteinuria.

Eligible Conditions
  • Proteinuria
  • Glomerulonephritis

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~week 12
This trial's timeline: 3 weeks for screening, Varies for treatment, and week 12 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Percentage change in 24-hour urinary protein excretion at Week 12

Trial Design

4Treatment groups
Experimental Treatment
Placebo Group
Group I: 400 mg QDExperimental Treatment1 Intervention
400 mg of ANG-3070 will be taken once daily for 12 weeks
Group II: 300 mg BIDExperimental Treatment1 Intervention
300 mg of ANG-3070 will be taken twice a day for 12 weeks.
Group III: 200 mg QDExperimental Treatment1 Intervention
200 mg of ANG-3070 will be taken once daily for 12 weeks.
Group IV: PlaceboPlacebo Group1 Intervention
Placebo capsules will be taken once or twice daily for 12 weeks.

Find a Location

Who is running the clinical trial?

Angion Biomedica CorpLead Sponsor
11 Previous Clinical Trials
862 Total Patients Enrolled
John Neylan, MDStudy DirectorAngion Biomedica
3 Previous Clinical Trials
628 Total Patients Enrolled
~29 spots leftby May 2025