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Completed Phase 1 Interventional

Efficacy and Safety Study of AVB-S6-500 in Patients With Platinum-Resistant Recurrent Ovarian Cancer

ClinicalTrials.gov ID: NCT03639246

Public ClinicalTrials.gov record NCT03639246. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 4:02 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1b/2 Randomized, Controlled Study of AVB-S6-500 in Combination With Pegylated Liposomal Doxorubicin (PLD) or Paclitaxel (Pac) in Patients With Platinum-resistant Recurrent Ovarian Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 1b/2 study of AVB-S6-500 in combination with pegylated liposomal doxorubicin (PLD) or paclitaxel (Pac) in patients with platinum resistant recurrent ovarian cancer. The phase 1b portion of the study is open label and patients will receive either AVB-S6-500+PLD or AVB-S6-500+ Pac. The Phase 2 portion of the study is randomized, double-blind, placebo-controlled study to compare efficacy and tolerability of AVB-S6-500 in combination with PLD or Pac versus placebo plus PLD or Pac.

Study identification

NCT ID
NCT03639246
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Aravive, Inc.
Industry
Enrollment
53 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 5, 2018
Primary completion
Jan 7, 2021
Completion
Dec 29, 2022
Last update posted
Feb 12, 2023

2018 – 2022

United States locations

U.S. sites
16
U.S. states
7
U.S. cities
15
Facility City State ZIP Site status
Arizona Oncology Phoenix Arizona 85016
Arizona Oncology Associates Tucson Arizona 85711
Kaiser Permanente Oakland Oakland California 94611
Kaiser Permanente Roseville Roseville California 95661
Kaiser Permanente San Francisco San Francisco California 94115
Kaiser Permanente Santa Clara Santa Clara California 95051
Kaiser Permanente Vallejo Vallejo California 94589
Kaiser Permanente Walnut Creek Walnut Creek California 94596
Massachusetts General Hospital Boston Massachusetts 02214
Dana Farber Cancer Institute Boston Massachusetts 02215
Washington University St Louis Missouri 63110
OUHSC-Stephenson Cancer Center Oklahoma City Oklahoma 73104
Willamette Valley Cancer Institute and Research Center Eugene Oregon 97401
Texas Oncology - Austin Central Austin Texas 78731
Texas Oncology - Fort Worth Fort Worth Texas 76104
Texas Oncology - San Antonio Medical Center San Antonio Texas 78240

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03639246, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 12, 2023 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03639246 live on ClinicalTrials.gov.

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