Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00203502 · ClinicalTrials.gov registry record · Phase 2

Primary Systemic Therapy in Operable/Locally Advanced Breast Cancer

A Phase 2 study, sponsored by University of Arkansas.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT00203502: Completed Phase 2 study, sponsored by University of Arkansas.

NCT00203502 is a Phase 2 study that has completed, run by University of Arkansas. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00203502, a Phase 2 study, has completed, sponsored by University of Arkansas.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

The main purpose of this study is to find out what effects taking the drug bevacizumab together with two chemotherapeutic agents, docetaxel and cyclophosphamide followed by doxorubicin alone before surgery will on breast cancer. Bevacizumab will be given for twelve weeks in combination with chemotherapy then it ill be held during the administration of doxorubicin. Twenty-eight to fifty-six days after undergoing surgery, all patients will receive nine three-weekly infusions of bevacizumab.

Primary Outcome

Pathological complete response was defined as the absence of residual invasive and in situ cancer on hematoxylin and eosin evaluation of the resected breast.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Bevacizumab
  • DRUG Docetaxel

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2005-09
Est. Completion 2015-02
Phase Phase 2
University of Arkansas

318 total trials

What the finished NCT00203502 record still lists

NCT00203502 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

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

NCT00203502 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00203502 about?

NCT00203502 is a clinical study titled "Primary Systemic Therapy in Operable/Locally Advanced Breast Cancer". The main purpose of this study is to find out what effects taking the drug bevacizumab together with two chemotherapeutic agents, docetaxel and cyclophosphamide followed by doxorubicin alone before surgery will on breast cancer. Bevacizumab will be given for twelve weeks in combination with chemothe...

What is the current status of trial NCT00203502?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2005-09. Estimated completion is 2015-02.

What interventions are being tested in trial NCT00203502?

The interventions under investigation include: Cyclophosphamide (DRUG), Bevacizumab (DRUG), Docetaxel (DRUG).

Who is sponsoring clinical trial NCT00203502?

This trial is sponsored by University of Arkansas, which has 318 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00203502's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01306019 · 40 participants · Phase 1

    Lentiviral Gene Transfer for Treatment of Children Older Than Two Years of Age With X-Linked Severe Combined Immunodeficiency (XSCID)

  • NCT01608152 · 40 participants

    Development of a Video Game for the Improvement of Outcomes in Stem Cell Transplant Survivors

  • NCT01668082 · 40 participants · NA

    An Investigation of Brain Tumor Metabolism in Patients Undergoing Surgical Resection

  • NCT02015013 · 40 participants · Phase 2

    Hematopoietic Stem Cell Mobilization in Idiopathic CD4 Lymphocytopenia Patients and Healthy Controls for the Study of T Cell Maturation and Trafficking in Murine Models

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00203502, the US trial registry maintained by the National Library of Medicine. NCT00203502 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.