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NCT00703664 · ClinicalTrials.gov registry record · Phase 2

Bortezomib and Vorinostat in Treating Patients With Recurrent Mantle Cell Lymphoma or Recurrent and/or Refractory Diffuse Large B-Cell Lymphoma

A Phase 2 study, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
65
Enrollment target

NCT00703664: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00703664 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 65 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00703664, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
65 participants
Enrollment target

Study Summary

This phase II trial studies how well bortezomib and vorinostat work in treating patients with recurrent mantle cell lymphoma or recurrent and/or refractory diffuse large B-cell lymphoma. Bortezomib and vorinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

Primary Outcome

ORR: Complete Response (CR) + Partial Response (PR) assessed according to the Revised Response Criteria for Malignant Lymphoma.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • DRUG Bortezomib
  • DRUG Vorinostat

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2008-07-09
Est. Completion 2017-12-01
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00703664 record still lists

NCT00703664 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 65 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (51% lower).

The record links to 0 conditions, and to 3 interventions - of which Laboratory Biomarker Analysis is the first listed.

NCT00703664 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00703664 about?

NCT00703664 is a clinical study titled "Bortezomib and Vorinostat in Treating Patients With Recurrent Mantle Cell Lymphoma or Recurrent and/or Refractory Diffuse Large B-Cell Lymphoma". This phase II trial studies how well bortezomib and vorinostat work in treating patients with recurrent mantle cell lymphoma or recurrent and/or refractory diffuse large B-cell lymphoma. Bortezomib and vorinostat may stop the growth of cancer cells by blocking some of the enzymes needed for cell gro...

What is the current status of trial NCT00703664?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 65 participants. The study started on 2008-07-09. Estimated completion is 2017-12-01.

What interventions are being tested in trial NCT00703664?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Bortezomib (DRUG), Vorinostat (DRUG).

Who is sponsoring clinical trial NCT00703664?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00703664's enrollment target sits among peer trials

65 987th of 2000 higher than 1,005 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 NCT00703664, the US trial registry maintained by the National Library of Medicine. NCT00703664 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.