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Completed Phase 2 Interventional Results available

Ferric Citrate in Managing Serum Phosphorus and Iron Deficiency in Anemic Chronic Kidney Disease (CKD) Subjects Not on Dialysis

ClinicalTrials.gov ID: NCT01736397

Public ClinicalTrials.gov record NCT01736397. 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 Jul 22, 2026, 2:28 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 of KRX-0502 (Ferric Citrate) in Managing Serum Phosphorus and Iron Deficiency in Anemic Subjects With Stage III to V Chronic Kidney Disease Not on Dialysis

Study identification

NCT ID
NCT01736397
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Keryx Biopharmaceuticals
Industry
Enrollment
149 participants

Conditions and interventions

Interventions

  • Ferric Citrate Drug
  • Placebo Drug

Drug

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
Oct 31, 2012
Primary completion
Oct 31, 2013
Completion
Nov 30, 2013
Last update posted
Oct 19, 2017

2012 – 2013

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
20
Facility City State ZIP Site status
Not listed Tempe Arizona
Not listed La Mesa California
Not listed Sacramento California
Not listed Denver Colorado
Not listed Edgewater Florida
Not listed Miami Florida
Not listed Meridian Idaho
Not listed Evergreen Park Illinois
Not listed Bethesda Maryland
Not listed Springfield Massachusetts
Not listed Detroit Michigan
Not listed Pontiac Michigan
Not listed Reno Nevada
Not listed Great Neck New York
Not listed Mineola New York
Not listed Asheville North Carolina
Not listed Wilmington North Carolina
Not listed Orangeburg South Carolina
Not listed Houston Texas
Not listed San Antonio Texas

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 NCT01736397, 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 Oct 19, 2017 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01736397 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →