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Completed Phase 3 Interventional

Phase 3 Study of Bavituximab Plus Docetaxel Versus Docetaxel Alone in Patients With Late-stage Non-squamous Non-small-cell Lung Cancer

ClinicalTrials.gov ID: NCT01999673

Public ClinicalTrials.gov record NCT01999673. 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 Oct 21, 2026, 2:11 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

SUNRISE: A Phase III, Randomized, Double-Blind, Placebo-Controlled Multicenter Trial of Bavituximab Plus Docetaxel Versus Docetaxel Alone in Patients With Previously Treated Stage IIIb/IV Non-Squamous Non Small-Cell Lung Cancer

Brief summary

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

The primary purpose of this research study is to see whether adding bavituximab (an investigational drug) to the standard chemotherapy drug docetaxel, will improve the results of the treatment for non-small-cell lung cancer.

Study identification

NCT ID
NCT01999673
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Peregrine Pharmaceuticals
Industry
Enrollment
582 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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 2013 (Type not available)
Primary completion
Mar 2017 (Actual)
Completion
Mar 2017 (Actual)
Last update posted
Apr 21, 2017

2013 – 2017

United States locations

U.S. sites
39
U.S. states
20
U.S. cities
37
Facility City State ZIP Site status
Peregrine Pharmaceuticals Investigational Site Huntsville Alabama 35805 —
Peregrine Pharmaceuticals Investigational Site Chandler Arizona 85224 —
Peregrine Pharmaceuticals Investigational Site Glendale Arizona 85306 —
Peregrine Pharmaceuticals Investigational Site Greenbrae California 94904 —
Peregrine Pharmaceuticals Investigational Site Los Angeles California 90048 —
Peregrine Pharmaceuticals Investigational Site Oceanside California 92056 —
Peregrine Pharmaceuticals Investigational Site Orange California 92868 —
Peregrine Pharmaceuticals Investigational Site West Hills California 91307 —
Peregrine Pharmaceuticals Investigational Site Fort Myers Florida 33916 —
Peregrine Pharmaceuticals Investigational Site St. Petersburg Florida 33705 —
Peregrine Pharmaceuticals Investigational Site Tampa Florida 33612 —
Peregrine Pharmaceuticals Investigational Site Athens Georgia 30607 —
Peregrine Pharmaceuticals Investigational Site Savannah Georgia 31404 —
Peregrine Pharmaceuticals Investigational Site Chicago Illinois 60637 —
Peregrine Pharmaceuticals Investigational Site Indianapolis Indiana 46254 —
Peregrine Pharmaceuticals Investigational Site Marrero Louisiana 70006 —
Peregrine Pharmaceuticals Investigational Site Shreveport Louisiana 71101 —
Peregrine Pharmaceuticals Investigational Site Baltimore Maryland 21201 —
Peregrine Pharmaceuticals Investigational Site Frederick Maryland 21701 —
Peregrine Pharmaceuticals Investigational Site Boston Massachusetts 02114 —
Peregrine Pharmaceuticals Investigational Site Lincoln Nebraska 68506 —
Peregrine Pharmaceuticals Investigational Site Lebanon New Hampshire 03756 —
Peregrine Pharmaceuticals Investigational Site Albuquerque New Mexico 87131 —
Peregrine Pharmaceuticals Investigational Site Winston-Salem North Carolina 27103 —
Peregrine Pharmaceuticals Investigational Site Cincinnati Ohio 45242 —
Peregrine Pharmaceuticals Investigational Site Middletown Ohio 45042 —
Peregrine Pharmaceuticals Investigational Site Portland Oregon 97213 —
Peregrine Pharmaceuticals Investigational Site Hershey Pennsylvania 17033 —
Peregrine Pharmaceuticals Investigational Site Pittsburgh Pennsylvania 15232 —
Peregrine Pharmaceuticals Investigational Site Chattanooga Tennessee 37404 —
Peregrine Pharmaceuticals Investigational Site Knoxville Tennessee 37909 —
Peregrine Pharmaceuticals Investigational Site Nashville Tennessee 37203 —
Peregrine Pharmaceuticals Investigational Site Nashville Tennessee 37323 —
Peregrine Pharmaceuticals Investigational Site Abilene Texas 79606 —
Peregrine Pharmaceuticals Investigational Site Dallas Texas 75201 —
Peregrine Pharmaceuticals Investigational Site Dallas Texas 75390 —
Peregrine Pharmaceuticals Investigational Site Fort Worth Texas 76104 —
Peregrine Pharmaceuticals Investigational Site Temple Texas 76508 —
Peregrine Pharmaceuticals Investigational Site Seattle Washington 98108 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 122 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01999673, 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 Apr 21, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01999673 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →