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Completed Phase 2 Interventional

A Randomized Study of the Safety and Efficacy of FG-2216 in Subjects With Renal Anemia Not Requiring Dialysis and Not Receiving Recombinant Human Erythropoietin

ClinicalTrials.gov ID: NCT00456053

Public ClinicalTrials.gov record NCT00456053. 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 Nov 3, 2026, 9:25 PM EST

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

Brief summary

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

The purpose of this study is to test the safety and efficacy of FG-2216 in the treatment of patients with renal anemia who are not receiving erythropoietin and who are not on dialysis.

Study identification

NCT ID
NCT00456053
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kyntra Bio
Industry
Enrollment
145 participants

Conditions and interventions

Conditions

Interventions

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
Dec 2005 (Type not available)
Primary completion
Not listed
Completion
Jul 2007 (Actual)
Last update posted
Nov 6, 2007

2005 – 2007

United States locations

U.S. sites
27
U.S. states
16
U.S. cities
27
Facility City State ZIP Site status
Research Site Tucson Arizona — —
Research Site Little Rock Arkansas — —
3 Research Sites Los Angeles California — —
Research Site Oakland California — —
Research Site San Diego California — —
Research Site Santa Clara California — —
Research Site Lauderdale Lakes Florida — —
Research Site Miami Florida — —
Research Site Pembroke Pines Florida — —
Research Site Atlanta Georgia — —
Research Site South Holland Illinois — —
Research Site Shreveport Louisiana — —
Research Site Springfield Massachusetts — —
Research Site Kalamazoo Michigan — —
Research Site Pontiac Michigan — —
Research Site Flushing New York — —
Research Site Cincinnati Ohio — —
Research Site Columbus Ohio — —
Research Site Portland Oregon — —
Research Site Allentown Pennsylvania — —
Research Site Hershey Pennsylvania — —
Research Site Pittsburgh Pennsylvania — —
Research Site Orangeburg South Carolina — —
Research Site Houston Texas — —
Research Site San Antonio Texas — —
Research Site Chesapeake Virginia — —
Research Site Fairfax Virginia — —

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 NCT00456053, 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 Nov 6, 2007 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00456053 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →