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Completed Phase 2 Interventional Results available

Dose Finding Study to Treat High Phosphate Levels in the Blood.

ClinicalTrials.gov ID: NCT02081534

Public ClinicalTrials.gov record NCT02081534. 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 23, 2026, 4:01 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

A Phase 2b, Randomized, Double Blind, Placebo-controlled, Parallel Group, Multicentre Dose Finding Study to Evaluate the Efficacy, Safety and Tolerability of AZD1722 to Treat Hyperphosphatemia in End-Stage Renal Disease Patients on Hemodialysis (ESRD-HD)

Study identification

NCT ID
NCT02081534
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ardelyx
Industry
Enrollment
162 participants

Conditions and interventions

Interventions

  • AZD1722 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 85 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
Feb 28, 2014
Primary completion
Oct 31, 2014
Completion
Oct 31, 2014
Last update posted
Sep 13, 2020

2014

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Research Site Downey California
Research Site Los Angeles California
Research Site Sacramento California
Research Site Whittier California
Research Site Denver Colorado
Research Site Pembroke Pines Florida
Research Site Tampa Florida
Research Site Winter Park Florida
Research Site Springfield Massachusetts
Research Site Detroit Michigan
Research Site Voorhees Township New Jersey
Research Site Flushing New York
Research Site Maspeth New York
Research Site Charlotte North Carolina
Research Site Cincinnati Ohio
Research Site 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 25 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02081534, 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 Sep 13, 2020 · Synced Jul 23, 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 NCT02081534 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →