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Completed Phase 2 Interventional Results available

20-Week Repeat Oral Dose Study of AKB-6548 in Participants With Chronic Kidney Disease and Anemia

ClinicalTrials.gov ID: NCT01906489

Public ClinicalTrials.gov record NCT01906489. 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 21, 2026, 10:16 PM EDT

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

Official title

Phase 2b Randomized, Double-Blind, Placebo-Controlled Study to Assess the Pharmacodynamic Response, Safety, and Tolerability to 20 Weeks of Oral Dosing of AKB-6548 in Participants With Anemia Secondary to Chronic Kidney Disease (CKD), GFR Categories G3a-G5 (Stages 3, 4, AND 5) (Pre-Dialysis)

Study identification

NCT ID
NCT01906489
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Akebia Therapeutics
Industry
Enrollment
210 participants

Conditions and interventions

Interventions

  • AKB-6548 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 82 Years
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
Jul 22, 2013
Primary completion
Sep 2, 2014
Completion
Sep 2, 2014
Last update posted
Jul 20, 2022

2013 – 2014

United States locations

U.S. sites
47
U.S. states
19
U.S. cities
47
Facility City State ZIP Site status
Not listed Glendale Arizona
Not listed Tucson Arizona
Not listed Azusa California
Not listed Chula Vista California
Not listed Downey California
Not listed El Centro California
Not listed La Mesa California
Not listed Long Beach California
Not listed Riverside California
Not listed Sacramento California
Not listed San Diego California
Not listed Arvada Colorado
Not listed Westminster Colorado
Not listed Lauderdale Lakes Florida
Not listed Port Charlotte Florida
Not listed Tampa Florida
Not listed Augusta Georgia
Not listed Macon Georgia
Not listed Meridian Idaho
Not listed Evergreen Park Illinois
Not listed Lafayette Louisiana
Not listed Shreveport Louisiana
Not listed Detroit Michigan
Not listed Lansing Michigan
Not listed Petoskey Michigan
Not listed Pontiac Michigan
Not listed Farmington Missouri
Not listed Kansas City Missouri
Not listed Las Vegas Nevada
Not listed Albuquerque New Mexico
Not listed Flushing New York
Not listed Mineola New York
Not listed New Rochelle New York
Not listed Rosedale New York
Not listed Asheville North Carolina
Not listed Charlotte North Carolina
Not listed Rocky Mount North Carolina
Not listed Wilmington North Carolina
Not listed Cincinnati Ohio
Not listed Columbia South Carolina
Not listed Knoxville Tennessee
Not listed Arlington Texas
Not listed Austin Texas
Not listed Edinburg Texas
Not listed Houston Texas
Not listed San Antonio Texas
Not listed St. George Utah

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 NCT01906489, 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 Jul 20, 2022 · Synced Jul 21, 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 NCT01906489 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →