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NCT03093155 · ClinicalTrials.gov registry record · Phase 2

Evaluation of Weekly Ixabepilone With or Without Biweekly Bevacizumab

A Phase 2 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, sponsored by Yale University.

Completed
Registry status
Phase 2
Development phase
78
Enrollment target
2
Study locations

NCT03093155: Completed Phase 2 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, sponsored by Yale University.

NCT03093155 is a Phase 2 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer that has completed, run by Yale University. The registered enrollment target is 78 participants, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (69% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03093155, a Phase 2 study of Fallopian Tube Cancer and Epithelial Ovarian Cancer, has completed, sponsored by Yale University.

COMPLETED
Registry status
Phase 2
Development phase
78 participants
Enrollment target
2
Study locations

Study Summary

This is a randomized, two-arm, open-label Phase II multicenter study designed to examine the effects of adding bevacizumab to ixabepilone for the treatment of patients who have recurrent or persistent platinum-resistant/refractory epithelial (non-mucinous) ovarian, fallopian tube, or primary peritoneal cancer. Its primary objective is to assess whether adding bevacizumab to ixabepilone improves progression-free survival in its target population. Study participants will be stratified by (a) study site and (b) previous receipt of bevacizumab prior to randomization.

Primary Outcome

Progression-free survival (PFS), the primary endpoint, will be defined as the length of time from randomization to disease recurrence, disease progression, or death for any reason. The timeframe was updated upon results entry.

Interventions

  • DRUG Bevacizumab
  • DRUG Ixabepilone

Study Locations (2)

Connecticut

  • Smilow Cancer Hospital at Yale New Haven - New Haven

Maryland

  • Marlene & Stewart Greenebaum Comprehensive Cancer Center, University of Maryland - Baltimore

Trial Details

FieldValue
Enrollment Target 78 participants
Start Date 2017-04-03
Est. Completion 2022-12-29
Phase Phase 2
Yale University

1,492 total trials

What the finished NCT03093155 record still lists

NCT03093155 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 78 participants, a relatively small participant target, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (69% lower).

The record links to 3 conditions, with Fallopian Tube Cancer appearing as the primary indexed condition, and to 2 interventions - of which Bevacizumab is the first listed.

NCT03093155 reports a single indexed study location in Connecticut, Maryland.

Frequently Asked Questions

What is clinical trial NCT03093155 about?

NCT03093155 is a clinical study titled "Evaluation of Weekly Ixabepilone With or Without Biweekly Bevacizumab". This is a randomized, two-arm, open-label Phase II multicenter study designed to examine the effects of adding bevacizumab to ixabepilone for the treatment of patients who have recurrent or persistent platinum-resistant/refractory epithelial (non-mucinous) ovarian, fallopian tube, or primary periton...

What is the current status of trial NCT03093155?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 78 participants. The study started on 2017-04-03. Estimated completion is 2022-12-29.

What conditions does trial NCT03093155 study?

This clinical trial studies the following conditions: Fallopian Tube Cancer, Epithelial Ovarian Cancer, Primary Peritoneal Cancer.

What interventions are being tested in trial NCT03093155?

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

Who is sponsoring clinical trial NCT03093155?

This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03093155 being conducted?

This trial has 2 study locations across Connecticut, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Fallopian Tube Cancer

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT03093155's enrollment target sits among peer trials

78 40th of 85 higher than 46 of 85 other Fallopian Tube Cancer trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Fallopian Tube Cancer 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 NCT03093155, the US trial registry maintained by the National Library of Medicine. NCT03093155 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.