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Completed Phase 2 Interventional Results available

Phase II Study Assessing Safety and Efficacy of APL-2 in Glomerulopathies

ClinicalTrials.gov ID: NCT03453619

Public ClinicalTrials.gov record NCT03453619. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 6:31 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Study to Evaluate the Safety and Biologic Activity of APL- 2 in Patients With IgA Nephropathy, Lupus Nephritis, Primary Membranous Nephropathy, or C3 Glomerulopathy (C3 Glomerulonephritis and Dense Deposit Disease)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase II trial assessing the safety and preliminary efficacy of daily APL-2 subcutaneous infusion administered for 16 weeks with a 6 month safety follow up, in patients with glomerulopathies

Study identification

NCT ID
NCT03453619
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Apellis Pharmaceuticals, Inc.
Industry
Enrollment
21 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 26, 2018 (Actual)
Primary completion
Apr 16, 2020 (Actual)
Completion
Aug 26, 2023 (Actual)
Last update posted
Feb 13, 2025

2018 – 2023

United States locations

U.S. sites
17
U.S. states
14
U.S. cities
17
Facility City State ZIP Site status
Stanford University Stanford California 94305 —
Children's Hospital Colorado Aurora Colorado 80045 —
HealthONE Physician Care, Rocky Mountain Hospital for Children Denver Colorado 80205 —
Washington Nephrology Associates Washington D.C. District of Columbia 20037 —
Horizon Research Group Coral Gables Florida 33134 —
Emory University Atlanta Georgia 30322 —
American Research LLC Jeffersonville Indiana 47130 —
Northwest Louisiana Nephrology LLC Shreveport Louisiana 71101 —
Washington Nephrology Associates Takoma Park Maryland 20912 —
Clinical Research Consultants Kansas City Missouri 64111 —
Davita Clinical Research The Bronx New York 10461 —
Westchester Medical Center Valhalla New York 10595 —
Southeastern Nephrology Associates Wilmington North Carolina 28401 —
University Clinical Health Memphis Tennessee 38103 —
Washington Nephrology Associates Alexandria Virginia 22304 —
Davita Clinical Research Chesapeake Virginia 23320 —
Milwaukee Nephrologists Wauwatosa Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03453619, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 13, 2025 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03453619 live on ClinicalTrials.gov.

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