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Terminated Phase 2 Interventional

AG-858 in Patients Who Are Cytogenetically Positive After Treatment With Gleevec™

ClinicalTrials.gov ID: NCT00058747

Public ClinicalTrials.gov record NCT00058747. 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 10, 2026, 2:52 AM EST

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Official title

Phase II Exploratory Study Of AG-858 Plus Gleevec™ In Patients With Chronic Myelogenous Leukemia (CML) In Chronic Phase Who Are Cytogenetically Positive After Treatment With Gleevec™

Brief summary

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

This is a Phase II, exploratory, open-label study of the investigational product AG-858, in patients who are cytogenetically positive after treatment with Gleevec. The trial will consist of three independent Phase II evaluations of patient groups according to their cytogenetic status as defined in the eligibility criteria (Eligibility Criteria 4a, 4b, and 4c).

Study identification

NCT ID
NCT00058747
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Agenus Inc.
Industry
Enrollment
40 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
Mar 2003 (Type not available)
Primary completion
Apr 2006 (Actual)
Completion
Apr 2006 (Actual)
Last update posted
Sep 7, 2012

2003 – 2006

United States locations

U.S. sites
11
U.S. states
10
U.S. cities
11
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed La Jolla California — —
Not listed Los Angeles California — —
Not listed Denver Colorado — —
Not listed Farmington Connecticut — —
Not listed Chicago Illinois — —
Not listed Boston Massachusetts — —
Not listed St Louis Missouri — —
Not listed New York New York — —
Not listed Portland Oregon — —
Not listed Pittsburgh Pennsylvania — —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00058747, 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 7, 2012 · Synced Nov 10, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00058747 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →