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NCT03373786 · ClinicalTrials.gov registry record · Phase 1

A Study of RG-012 in Subjects With Alport Syndrome

A Phase 1 study of Alport Syndrome, sponsored by Genzyme, a Sanofi Company.

Completed
Registry status
Phase 1
Development phase
4
Enrollment target
7
Study locations

NCT03373786 is a Phase 1 study of Alport Syndrome that has completed, run by Genzyme, a Sanofi Company. The registered enrollment target is 4 participants, below the 618-participant average among 5 other Alport Syndrome trials with a reported enrollment target (99% lower). The trial reports 7 study locations across 5 states.

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The verdict

NCT03373786, a Phase 1 study of Alport Syndrome, has completed, sponsored by Genzyme, a Sanofi Company.

COMPLETED
Registry status
Phase 1
Development phase
4 participants
Enrollment target
7
Study locations

Study Summary

This is a Phase 1, open-label, multi-center study of the safety, pharmacodynamics, and pharmacokinetics of RG-012 administered to subjects with Alport syndrome.

Conditions Studied

Interventions

  • DRUG RG012

Study Locations (7)

California

  • eStudySite - La Mesa
  • Academic Medical Research Institute - Los Angeles
  • Apex Research of Riverside - Riverside

Florida

  • Eminence Medical & Clinical Research - Tampa

Texas

  • Houston Nephrology Research - Cypress

Utah

  • Utah Kidney Research Institute - Salt Lake City

Wisconsin

  • Allegiance Research Specialists, LLC - Wauwatosa

Trial Details

FieldValue
Enrollment Target 4 participants
Start Date 2017-12-22
Est. Completion 2019-05-20
Phase Phase 1

Sponsor

Genzyme, a Sanofi Company

196 total trials

What the Registry Record Tells You About NCT03373786

The ClinicalTrials.gov registry entry for NCT03373786 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 4 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 618-participant average among 5 other Alport Syndrome trials with a reported enrollment target (99% lower). The listed sponsor is Genzyme, a Sanofi Company, which has 196 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Alport Syndrome appearing as the primary indexed condition, and to 1 intervention - of which RG012 is the first listed.

NCT03373786 reports 7 study locations spanning 5 distinct geographic areas - top geographies include California, Florida, Texas.

Frequently Asked Questions

What is clinical trial NCT03373786 about?

NCT03373786 is a clinical study titled "A Study of RG-012 in Subjects With Alport Syndrome". This is a Phase 1, open-label, multi-center study of the safety, pharmacodynamics, and pharmacokinetics of RG-012 administered to subjects with Alport syndrome.

What is the current status of trial NCT03373786?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 4 participants. The study started on 2017-12-22. Estimated completion is 2019-05-20.

What conditions does trial NCT03373786 study?

This clinical trial studies the following conditions: Alport Syndrome.

What interventions are being tested in trial NCT03373786?

The interventions under investigation include: RG012 (DRUG).

Who is sponsoring clinical trial NCT03373786?

This trial is sponsored by Genzyme, a Sanofi Company, which has 196 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03373786 being conducted?

This trial has 7 study locations across California, Florida, Texas, Utah, Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Alport Syndrome

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.