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NCT01821859 · ClinicalTrials.gov registry record · Phase 2

Abraxane/Bevacizumab

A Phase 2 study, sponsored by OHSU Knight Cancer Institute.

Terminated
Registry status
Phase 2
Development phase
5
Enrollment target

NCT01821859: Clinical Trial Phase 2 study, sponsored by OHSU Knight Cancer Institute.

NCT01821859 is a Phase 2 study that was terminated before completion, run by OHSU Knight Cancer Institute. The registered enrollment target is 5 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01821859, a Phase 2 study, was terminated before completion, sponsored by OHSU Knight Cancer Institute.

TERMINATED
Registry status
Phase 2
Development phase
5 participants
Enrollment target

Study Summary

The protocol will study the effect of the combination of two drugs-Abraxane and Bevacizumab-on a subject's ovarian cancer, fallopian tube cancer, or primary peritoneal cancer. This study drug combination will be given to subjects who have already been treated for their cancer with other chemotherapy, and now their cancer has become worse or has come back again. Neither one of these study drugs has been approved by the FDA for treatment in these three types of cancer.

Primary Outcome

Using RECIST criteria, Complete Response (CR)= disappearance of all target lesions, Partial Response (PR)= At least a 30% decrease in the sum of the longest diameter of target lesions, and Stable Disease (SD)= neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify as progressive disease.

Interventions

  • DRUG Bevacizumab
  • DRUG Abraxane

Trial Details

FieldValue
Enrollment Target 5 participants
Start Date 2010-01
Est. Completion 2011-11
Phase Phase 2
OHSU Knight Cancer Institute

211 total trials

Why NCT01821859 stopped before completion

NCT01821859 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 5 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Bevacizumab is the first listed.

NCT01821859 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01821859 about?

NCT01821859 is a clinical study titled "Abraxane/Bevacizumab". The protocol will study the effect of the combination of two drugs-Abraxane and Bevacizumab-on a subject's ovarian cancer, fallopian tube cancer, or primary peritoneal cancer. This study drug combination will be given to subjects who have already been treated for their cancer with other chemotherapy...

What is the current status of trial NCT01821859?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 5 participants. The study started on 2010-01. Estimated completion is 2011-11.

What interventions are being tested in trial NCT01821859?

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

Who is sponsoring clinical trial NCT01821859?

This trial is sponsored by OHSU Knight Cancer Institute, which has 211 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01821859's enrollment target sits among peer trials

5 2000th of 2000 the lowest 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 NCT01821859, the US trial registry maintained by the National Library of Medicine. NCT01821859 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.