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Completed Phase 2 Interventional

Efficacy of SBR759 in Lowering Serum Phosphate Levels in Chronic Kidney Disease Patients on Hemodialysis

ClinicalTrials.gov ID: NCT00704483

Public ClinicalTrials.gov record NCT00704483. 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, 9:30 PM EST

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

Official title

A 12-week, Open Label, Multicenter, Titration Study, With a 9-month Maintenance Treatment Extension, to Demonstrate Efficacy of SBR759 Compared to Sevelamer HCl in Lowering Serum Phosphate Levels in Chronic Kidney Disease Patients on Hemodialysis

Brief summary

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

This study will evaluate the efficacy of SBR759 compared to sevelamer HCl in lowering serum phosphate levels in Chronic Kidney Disease patients on hemodialysis

Study identification

NCT ID
NCT00704483
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
321 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
Jul 2008 (Type not available)
Primary completion
Aug 2010 (Actual)
Completion
Not listed
Last update posted
Dec 19, 2020

Started 2008

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Novartis Chula Vista California 91910 —
Novartis La Mesa California 91942 —
Novartis Whittier California 90602 —
Novartis Denver Colorado 80262 —
Novartis North Chicago Illinois 60064 —
Novartis Peoria Illinois 61602 —
Novartis Mishawaka Indiana 46545 —
Novartis Baltimore Maryland 21287 —
Novartis Fall River Massachusetts 02720 —
Novartis Springfield Massachusetts 01104 —
Novartis Investigative Site Omaha Nebraska 68144 —
Novartis New York New York 10032 —
Novartis Winston-Salem North Carolina 27157-1082 —
Novarits Fargo North Dakota 58103 —
Novartis Portland Oregon 97210 —
Novartis Pittsburgh Pennsylvania 15224 —
Novartis Investigative Site Houston Texas 77024 —
Novartis San Antonio Texas 78207 —
Novartis Fairfax Virginia 22031 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 47 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00704483, 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 Dec 19, 2020 · 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 NCT00704483 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →