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NCT00058747 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Agenus.

Terminated
Registry status
Phase 2
Development phase
40
Enrollment target

NCT00058747: Clinical Trial Phase 2 study, sponsored by Agenus.

NCT00058747 is a Phase 2 study that was terminated before completion, run by Agenus. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00058747, a Phase 2 study, was terminated before completion, sponsored by Agenus.

TERMINATED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

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).

Interventions

  • DRUG Autologous HSP-70 Protein-Peptide Complex (AG-858) Plus Gleevec™.

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2003-03
Est. Completion 2006-04
Phase Phase 2
Agenus

24 total trials

Why NCT00058747 stopped before completion

NCT00058747 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 1 intervention - of which Autologous HSP-70 Protein-Peptide Complex (AG-858) Plus Gleevec™. is the first listed.

NCT00058747 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00058747 about?

NCT00058747 is a clinical study titled "AG-858 in Patients Who Are Cytogenetically Positive After Treatment With Gleevec™". 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 ...

What is the current status of trial NCT00058747?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2003-03. Estimated completion is 2006-04.

What interventions are being tested in trial NCT00058747?

The interventions under investigation include: Autologous HSP-70 Protein-Peptide Complex (AG-858) Plus Gleevec™. (DRUG).

Who is sponsoring clinical trial NCT00058747?

This trial is sponsored by Agenus, which has 24 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00058747's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00058747, the US trial registry maintained by the National Library of Medicine. NCT00058747 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.