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NCT00321685 · ClinicalTrials.gov registry record · Phase 2

Bevacizumab, Radiation Therapy, and Combination Chemotherapy in Treating Patients Who Are Undergoing Surgery for Locally Advanced Nonmetastatic Rectal Cancer

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

Completed
Registry status
Phase 2
Development phase
57
Enrollment target

NCT00321685: Completed Phase 2 study, sponsored by National Cancer Institute (NCI).

NCT00321685 is a Phase 2 study that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 57 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (57% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00321685, a Phase 2 study, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
57 participants
Enrollment target

Study Summary

This phase II trial studies how well giving bevacizumab, radiation therapy, and combination chemotherapy works in treating patients who are undergoing surgery for locally advanced nonmetastatic rectal cancer. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some find tumor cells and kill them or carry tumor-killing substances to them. Others interfere with the ability of tumor cells to grow and spread. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Radiation therapy uses high-energy x-rays to kill tumor cells. Drugs, such as capecitabine, may make tumor cells more sensitive to radiation therapy. Drugs used in chemotherapy, such as capecitabine, oxaliplatin, fluorouracil, and leucovorin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving bevacizumab together with radiation therapy and combination chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving bevacizumab together with combination chemotherapy after surgery may kill any tumor cells that remain after surgery.

Primary Outcome

Pathologic complete response to preoperative therapy was determined at the time of surgical resection. Pathologic complete response (pCR) is defined as no evidence of invasive cells on pathologic examination of the primary rectal cancer (or tissue from the area where the tumor had been if there is a complete clinical response). Pathologic complete response rate is calculated as number of patients achieving pathologic complete response divided by all eligible and treated patients

Interventions

  • DRUG Capecitabine
  • DRUG Fluorouracil
  • DRUG Oxaliplatin
  • BIOLOGICAL Bevacizumab
  • DRUG Leucovorin Calcium

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2006-07-25
Est. Completion 2019-02-11
Phase Phase 2
National Cancer Institute (NCI)

3,257 total trials

What the finished NCT00321685 record still lists

NCT00321685 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 57 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (57% lower).

The record links to 0 conditions, and to 5 interventions - of which Capecitabine is the first listed.

NCT00321685 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00321685 about?

NCT00321685 is a clinical study titled "Bevacizumab, Radiation Therapy, and Combination Chemotherapy in Treating Patients Who Are Undergoing Surgery for Locally Advanced Nonmetastatic Rectal Cancer". This phase II trial studies how well giving bevacizumab, radiation therapy, and combination chemotherapy works in treating patients who are undergoing surgery for locally advanced nonmetastatic rectal cancer. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some ...

What is the current status of trial NCT00321685?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 57 participants. The study started on 2006-07-25. Estimated completion is 2019-02-11.

What interventions are being tested in trial NCT00321685?

The interventions under investigation include: Capecitabine (DRUG), Fluorouracil (DRUG), Oxaliplatin (DRUG), Bevacizumab (BIOLOGICAL), Leucovorin Calcium (DRUG).

Who is sponsoring clinical trial NCT00321685?

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 NCT00321685's enrollment target sits among peer trials

57 1141st of 2000 higher than 855 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 NCT00321685, the US trial registry maintained by the National Library of Medicine. NCT00321685 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.