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Completed Phase 1 Interventional

A Study of Anti-HIV Monoclonal Antibody KD-247

ClinicalTrials.gov ID: NCT00917813

Public ClinicalTrials.gov record NCT00917813. 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 Sep 5, 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

A Study of the Safety, Tolerability, and Pharmacokinetics of KD-247, a Humanized Monoclonal Antibody That Recognizes the Principal Neutralizing Determinant of HIV-1, in Asymptomatic HIV-1 Seropositive Individuals Who Are Not Receiving Concurrent Antiretroviral Therapy

Brief summary

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

The purpose of this study is to evaluate the safety and tolerability of 3 infusions of KD-247 over 2 weeks in HIV-1 seropositive individuals; to determine the pharmacokinetic parameters of KD-247 when administered as above; and to assess the effect of KD-247 infusions on plasma HIV-1 ribonucleic acid (RNA) load and on CD4+ T cell counts.

Study identification

NCT ID
NCT00917813
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
27 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 64 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
Aug 31, 2007
Primary completion
Not listed
Completion
Not listed
Last update posted
Nov 18, 2012

Started 2007

United States locations

U.S. sites
15
U.S. states
8
U.S. cities
15
Facility City State ZIP Site status
Pacific Oaks Medical Group Beverly Hills California 90211
Providence Clinical Research Burbank California 91505
Peter J. Ruane, MD, Inc. Los Angeles California 90036
Washington Hospital Center CAR Washington D.C. District of Columbia 20010
Gary Richmond, MD, PA Fort Lauderdale Florida 33316
Orlando Immunology Center Orlando Florida 32803-1851
Vita Research Solutions, Inc. Tamarac Florida 33319
AIDS Research Consortium of Atlanta Atlanta Georgia 30308
Northstar Medical Chicago Illinois 60657
Institute of Human Virology, University of Maryland Baltimore Maryland 21201
Albany Medical Center Albany New York 12208
Aaron Diamond AIDS Research Center (ADARC) New York New York 10016
Central Texas Clinical Research Austin Texas 78705
Therapeutic Concepts, P.A. Houston Texas 77004
DCOL Center for Clinical Research Longview Texas 75605

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 NCT00917813, 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 18, 2012 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00917813 live on ClinicalTrials.gov.

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