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RNA Therapy

ARCT-810 for Urea cycle disorder

Phase 1
Waitlist Available
Research Sponsored by Arcturus Therapeutics, Inc.
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 4 weeks

Summary

This trial tests ARCT-810, a new treatment for patients with a specific condition, to see if it is effective and well-tolerated. The treatment aims to help the body better process waste products.

Eligible Conditions
  • Urea cycle disorder

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 weeks for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Incidence, severity and dose-relationship of adverse events (AEs)
Secondary study objectives
AUC0-inf after single dose of ARCT-810
AUCExtrap after single dose of ARCT-810
CL after single dose of ARCT-810
+6 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: ARCT-810Experimental Treatment1 Intervention
Ascending single doses of ARCT-810 administered intravenously
Group II: PlaceboPlacebo Group1 Intervention
Single doses of 0.9% Saline administered intravenously
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
ARCT-810
2020
Completed Phase 1
~50

Find a Location

Who is running the clinical trial?

Arcturus Therapeutics, Inc.Lead Sponsor
12 Previous Clinical Trials
22,435 Total Patients Enrolled
~3 spots leftby Nov 2025