Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 1Phase 2 Interventional Results available

A Study Of PF-05212384 Plus FOLFIRI Versus Bevacizumab Plus FOLFIRI In Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT01937715

Public ClinicalTrials.gov record NCT01937715. 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 17, 2026, 9:08 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

An Open-Label, Multi-Center, Randomized Phase 1b/2 Study Of PF-05212384 Plus 5-Fluorouracil-Leucovorin-Irinotecan (FOLFIRI) Versus Bevacizumab Plus FOLFIRI In Metastatic Colorectal Cancer

Brief summary

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

This is a multicenter, open label Phase 1b/2 study in patients with metastatic colorectal carcinoma. The Phase 1b will identify the dose of the combination of PF-05212384 plus FOLFIRI. The randomized, two-arm Phase 2 portion will compare the efficacy and safety of PF-05212384 plus FOLFIRI to that of bevacizumab plus FOLFIRI. The study population will consist of patients with mCRC previously treated with an oxaliplatin-based regimen in the first line setting or who have progressed within 6 months of the end of an adjuvant oxaliplatin-based regimen.

Study identification

NCT ID
NCT01937715
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
18 participants

Conditions and interventions

Interventions

Drug · Biological

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
Feb 2014 (Type not available)
Primary completion
Aug 2015 (Actual)
Completion
Aug 2015 (Actual)
Last update posted
Aug 18, 2016

2014 – 2015

United States locations

U.S. sites
35
U.S. states
5
U.S. cities
18
Facility City State ZIP Site status
St. Jude Hospital Yorba Linda DBA St. Joseph Heritage Healthcare Fullerton California 92835 —
UCLA Hematology Oncology Irvine California 92604 —
Drug Management Only: UCLA West Medical Pharmacy, Attn Steven L. Wong, Pharm .D. Los Angeles California 90095-7349 —
Drug Management Only: UCLA West Medical Pharmacy Los Angeles California 90095-7349 —
UCLA West Medical Pharmacy, Att: Steven L. Wong, Pharm D. Los Angeles California 90095-7349 —
Ronald Reagan UCLA Medical Center Los Angeles California 90095 —
Ronald Regan UCLA Medical Center, Drug Information Center Los Angeles California 90095 —
TRIO-US Central Administration, Regulatory Management Only Los Angeles California 90095 —
TRIO-US Central Administration Los Angeles California 90095 —
TRIO_US Los Angeles California 90095 —
UCLA Hematology Oncology Administrative Address Los Angeles California 90095 —
Westwood Bowyer Clinic, Peter Morton Medical Building Los Angeles California 90095 —
West Valley Hematology/Oncology Med Group Northridge California 91328 —
UCLA/Pasadena Healthcare Pasadena California 91105 —
Central Coast Medical Oncology Corporation Santa Maria California 93454 —
UCLA Hematology Oncology Santa Monica California 90404 —
UCLA Santa Monica Medical Center & Orthopaedic Hospital Santa Monica California 90404 —
UCLA/Santa Clarita Valley Cancer Center Valencia California 91355 —
UCLA Cancer Center Westlake Village California 91361 —
Comprehensive Cancer Centers of Nevada Research Department Henderson Nevada 89014 —
Comprehensive Cancer Centers of Nevada Henderson Nevada 89052 —
Comprehensive Cancer Centers of Nevada Henderson Nevada 89074 —
Comprehensive Cancer Centers of NV Las Vegas Nevada 89128 —
COmprehensive Cancer Centers of Nevada Las Vegas Nevada 89148 —
Comprehensive Cancer Centers for Nevada Las Vegas Nevada 89169 —
Metrohealth Medical Center Cleveland Ohio 44109 —
Medical Group of the Carolinas - Hematology Spartanburg Spartanburg South Carolina 29303 —
Spartanburg Regional Medical Center Spartanburg South Carolina 29303 —
Kadlec Clinic Hematology and Oncology Kennewick Washington 99336 —
Kadlec Medical Center Richland Washington 99352 —
Outpatient Imaging Center Richland Washington 99352 —
Investigational Drug Services Seattle Washington 98101 —
Virginia Mason Medical Center Seattle Washington 98101 —
Medical Oncology Associates, PS Spokane Washington 99208 —
Spokane Valley Cancer Center Spokane Valley Washington 99216 —

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01937715, 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 Aug 18, 2016 · Synced Oct 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01937715 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →