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NCT00077961 · ClinicalTrials.gov registry record · Phase 1

Rituximab Plus CAMPATH in Patients With Relapsed/Refractory Low-Grade or Follicular, CD20-positive, B-cell NHL

A Phase 1 study, sponsored by Genzyme, a Sanofi Company.

Terminated
Registry status
Phase 1
Development phase
49
Enrollment target

NCT00077961 is a Phase 1 study that was terminated before completion, run by Genzyme, a Sanofi Company. The registered enrollment target is 49 participants.

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The verdict

NCT00077961, a Phase 1 study, was terminated before completion, sponsored by Genzyme, a Sanofi Company.

TERMINATED
Registry status
Phase 1
Development phase
49 participants
Enrollment target

Study Summary

The purpose of this study is to determine the optimal dose of subcutaneous CAMPATH when used in combination with rituximab for patients with relapsing or refractory, low-grade or follicular, CD-20-positive, B-Cell non-Hodgkin's Lymphoma. Safety will be the primary objective of phase I, while the primary objective of phase II will be to determine overall response.

Interventions

  • DRUG CAMPATH (alemtuzumab)

Trial Details

FieldValue
Enrollment Target 49 participants
Start Date 2003-12
Phase Phase 1

Sponsor

Genzyme, a Sanofi Company

196 total trials

What the Registry Record Tells You About NCT00077961

The ClinicalTrials.gov registry entry for NCT00077961 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 49 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Genzyme, a Sanofi Company, which has 196 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which CAMPATH (alemtuzumab) is the first listed.

NCT00077961 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00077961 about?

NCT00077961 is a clinical study titled "Rituximab Plus CAMPATH in Patients With Relapsed/Refractory Low-Grade or Follicular, CD20-positive, B-cell NHL". The purpose of this study is to determine the optimal dose of subcutaneous CAMPATH when used in combination with rituximab for patients with relapsing or refractory, low-grade or follicular, CD-20-positive, B-Cell non-Hodgkin's Lymphoma. Safety will be the primary objective of phase I, while the pri...

What is the current status of trial NCT00077961?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 49 participants. The study started on 2003-12.

What interventions are being tested in trial NCT00077961?

The interventions under investigation include: CAMPATH (alemtuzumab) (DRUG).

Who is sponsoring clinical trial NCT00077961?

This trial is sponsored by Genzyme, a Sanofi Company, which has 196 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.