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Completed Phase 2 Interventional Results available

Sevelamer for Reducing Endotoxemia and Immune Activation

ClinicalTrials.gov ID: NCT01543958

Public ClinicalTrials.gov record NCT01543958. 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 Oct 20, 2026, 11:38 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

Sevelamer Carbonate for Reducing Endotoxemia and Immune Activation: A Proof of Concept Study

Brief summary

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

HIV-infected people can have an increase in inflammation in their body organs, even after taking anti-HIV medicines. Sevelamer carbonate is used to bind phosphate in dialysis patients. It can also bind endotoxin in the gut and lowers endotoxin levels in the blood of dialysis patients. Sevelamer carbonate decreases the inflammation endotoxin causes in dialysis patients. A5296 is a phase II, single-arm study to evaluate the effect of 8 weeks of sevelamer carbonate administration on markers of microbial translocation and T-cell activation in the blood in chronically HIV-infected subjects not receiving ART.

Study identification

NCT ID
NCT01543958
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
40 participants

Conditions and interventions

Interventions

Drug · Device

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
Nov 2011 (Type not available)
Primary completion
Sep 2012 (Actual)
Completion
Nov 2012 (Actual)
Last update posted
Oct 11, 2018

2011 – 2012

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Alabama Therapeutics CRS (5801) Birmingham Alabama 35294 —
UCLA CARE Center CRS (601) Los Angeles California 90095 —
Ucsf Aids Crs (801) San Francisco California 94110 —
Harbor-UCLA Med. Ctr. CRS (603) Torrance California 90502 —
University of Colorado Hospital CRS (6101) Aurora Colorado 80045 —
Univ. of Miami AIDS CRS (901) Miami Florida 33136 —
Northwestern University CRS (2701) Chicago Illinois 60611 —
Massachusetts General Hospital ACTG CRS (101) Boston Massachusetts 02114 —
Washington University CRS (2101) St Louis Missouri 63110 —
AIDS Care CRS (1108) Rochester New York 14642 —
Univ. of Rochester ACTG CRS (1101) Rochester New York 14642 —
Univ. of Cincinnati CRS (2401) Cincinnati Ohio 45267 —
Case CRS (2501) Cleveland Ohio 44106 —
Metro Health CRS (2503) Cleveland Ohio 44109 —
Hosp. of the Univ. of Pennsylvania CRS (6201) Philadelphia Pennsylvania 19104 —

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 NCT01543958, 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 11, 2018 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01543958 live on ClinicalTrials.gov.

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