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AVOVA-1 for Fallopian Tube Cancer
Study Summary
This trial is a double-blind study in which approximately 99 study patients will be randomized in a 2:1 ratio to receive either AVOVA-1 or MC. The primary endpoint of this trial is death from any cause with the metric of OS from the date of randomization. PFS will be a secondary endpoint and will be calculated as the time from the date of randomization for treatment until subjective tumor progression or death.
- Fallopian Tube Cancer
- Ovarian Cancer
- Peritoneal Carcinoma
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Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Trial Design
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Frequently Asked Questions
Does AVOVA-1 pose any risk to human health?
"There are preliminary safety data for AVOVA-1, resulting in a score of 2. Unfortunately there is no existing clinical evidence that supports the efficacy of this drug yet."
Are there any vacancies still available in this trial for participants?
"According to clinicaltrials.gov, this medical experiment is no longer recruiting participants; it was initially posted on November 18th, 2017 with its last update occurring in April 21st 2022. Although inactive for new patients, there are 2894 other trials accepting participants at present."
How many venues are presently hosting this research endeavor?
"As part of this medical trial, 6 different healthcare facilities are operational. These include Scripps Health in La Jolla, Hoag Memorial Hospital Presbyterian in Newport Beach and University of Colorado Hospital - Cancer Center Aurora, as well as 3 more locations."
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