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NCT00014560 · ClinicalTrials.gov registry record · Phase 1

Antibody Therapy in Treating Patients With Refractory or Relapsed Non-Hodgkin's Lymphoma or Chronic Lymphocytic Leukemia

A Phase 1 study, sponsored by Dartmouth-Hitchcock Medical Center.

Terminated
Registry status
Phase 1
Development phase
3
Enrollment target

NCT00014560: Clinical Trial Phase 1 study, sponsored by Dartmouth-Hitchcock Medical Center.

NCT00014560 is a Phase 1 study that was terminated before completion, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 3 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00014560, a Phase 1 study, was terminated before completion, sponsored by Dartmouth-Hitchcock Medical Center.

TERMINATED
Registry status
Phase 1
Development phase
3 participants
Enrollment target

Study Summary

RATIONALE: Antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. PURPOSE: Phase I trial to study the effectiveness of antibody therapy in treating patients who have refractory or relapsed non-Hodgkin's lymphoma or chronic lymphocytic leukemia.

Primary Outcome

This study was prematurely ended by the sponsor Medarex (supplier of BsAb) due to toxicities experienced at other sites on unrelated trials leading to the decision that Medarex would not be manufacturing the investigational product (BsAb).

Interventions

  • BIOLOGICAL sargramostim
  • BIOLOGICAL bispecific antibody 4G7xH22

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2000-09-28
Est. Completion 2003-02-14
Phase Phase 1
Dartmouth-Hitchcock Medical Center

427 total trials

Why NCT00014560 stopped before completion

NCT00014560 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (95% lower).

The record links to 0 conditions, and to 2 interventions - of which sargramostim is the first listed.

NCT00014560 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00014560 about?

NCT00014560 is a clinical study titled "Antibody Therapy in Treating Patients With Refractory or Relapsed Non-Hodgkin's Lymphoma or Chronic Lymphocytic Leukemia". RATIONALE: Antibodies can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. PURPOSE: Phase I trial to study the effectiveness of antibody therapy in treating patients who have refractory or relapsed non-Hodgkin's lymphoma or chronic ly...

What is the current status of trial NCT00014560?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 3 participants. The study started on 2000-09-28. Estimated completion is 2003-02-14.

What interventions are being tested in trial NCT00014560?

The interventions under investigation include: sargramostim (BIOLOGICAL), bispecific antibody 4G7xH22 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00014560?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00014560's enrollment target sits among peer trials

3 1999th of 2000 higher than 1 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT00014560, the US trial registry maintained by the National Library of Medicine. NCT00014560 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.