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Completed Phase 2 Interventional Results available

Sym004 vs Standard of Care in Subjects With Metastatic Colorectal Cancer

ClinicalTrials.gov ID: NCT02083653

Public ClinicalTrials.gov record NCT02083653. 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 May 5, 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

Open-label, Randomized, Controlled, Multicenter Phase II Trial Investigating 2 Sym004 Doses Versus Investigator's Choice (Best Supportive Care, Capecitabine, 5-FU) in Subjects With Metastatic Colorectal Cancer and Acquired Resistance to Anti-EGFR Monoclonal Antibodies

Study identification

NCT ID
NCT02083653
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Symphogen A/S
Industry
Enrollment
254 participants

Conditions and interventions

Interventions

  • Best Supportive Care (BSC) Other
  • Capecitabine Drug
  • Fluorouracil (5-FU) Drug
  • Sym004 (12 mg/kg) Drug
  • Sym004 (9/6 mg/kg) Drug

Other · Drug

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
Mar 5, 2014
Primary completion
Oct 23, 2016
Completion
Apr 25, 2017
Last update posted
Apr 15, 2019

2014 – 2017

United States locations

U.S. sites
9
U.S. states
5
U.S. cities
9
Facility City State ZIP Site status
USC Norris Comprehensive Cancer Center Los Angeles California 90033
Sharp Memorial Hospital San Diego California 92123
Florida Cancer Specialists-Broadway Fort Myers Florida 33916
Hematology - Oncology Associates of Treasure Coast Port Saint Lucie Florida 34952
Florida Cancer Specialists St. Petersburg Florida 33705
Mercy Research Springfield Missouri 65807
Washington University School of Medicine St Louis Missouri 63110
Comprehensive Cancer Centers of Nevada Henderson Nevada 89074
Texas Oncology, P.A. Tyler Texas 75702

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 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02083653, 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 15, 2019 · Synced May 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02083653 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →