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NCT00774202 · ClinicalTrials.gov registry record · Phase 2

Higher Dose of Rituxan Versus Standard Doses of Rituxan With Cyclophosphamide, Vincristine, and Prednisone in Subjects With Chronic ITP

A Phase 2 study, sponsored by Weill Medical College of Cornell University.

Completed
Registry status
Phase 2
Development phase
17
Enrollment target

NCT00774202: Completed Phase 2 study, sponsored by Weill Medical College of Cornell University.

NCT00774202 is a Phase 2 study that has completed, run by Weill Medical College of Cornell University. The registered enrollment target is 17 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00774202, a Phase 2 study, has completed, sponsored by Weill Medical College of Cornell University.

COMPLETED
Registry status
Phase 2
Development phase
17 participants
Enrollment target

Study Summary

This study is designed to compare the efficacy and safety of higher doses of Rituxan with a regimen combining standard doses of Rituxan + CVP in patients with chronic ITP who did not respond to or relapsed after standard doses of Rituxan. Patients eligible for this protocol will be stratified into two subgroups according to their initial response to Rituxan.

Primary Outcome

Outcome measure was determined by comparing the study participants' historical responses to their initial treatment of rituximab at standard dose/regimen without "enhancement" (based on duration of response and type of response) to the participants response to their study treatment responses. Thus each patient was his or her own control although all study treatments included standard dose rituximab treatments (one at double the dose and one with additional treatments).

Interventions

  • DRUG Rituxan, Cyclophosphamide, Vincristine, Prednisone
  • DRUG Higher Dose of Rituximab

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2003-11
Est. Completion 2008-02
Phase Phase 2

What the finished NCT00774202 record still lists

NCT00774202 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 17 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 2 interventions - of which Rituxan, Cyclophosphamide, Vincristine, Prednisone is the first listed.

NCT00774202 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00774202 about?

NCT00774202 is a clinical study titled "Higher Dose of Rituxan Versus Standard Doses of Rituxan With Cyclophosphamide, Vincristine, and Prednisone in Subjects With Chronic ITP". This study is designed to compare the efficacy and safety of higher doses of Rituxan with a regimen combining standard doses of Rituxan + CVP in patients with chronic ITP who did not respond to or relapsed after standard doses of Rituxan. Patients eligible for this protocol will be stratified into t...

What is the current status of trial NCT00774202?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 17 participants. The study started on 2003-11. Estimated completion is 2008-02.

What interventions are being tested in trial NCT00774202?

The interventions under investigation include: Rituxan, Cyclophosphamide, Vincristine, Prednisone (DRUG), Higher Dose of Rituximab (DRUG).

Who is sponsoring clinical trial NCT00774202?

This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00774202's enrollment target sits among peer trials

17 1903rd of 2000 higher than 93 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 NCT00774202, the US trial registry maintained by the National Library of Medicine. NCT00774202 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.