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Suspended No phase listed Observational

CANscriptTM Clinical Outcomes in a Real-World Setting (ANCERS)-2

ClinicalTrials.gov ID: NCT03253575

Public ClinicalTrials.gov record NCT03253575. 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 27, 2026, 2:15 PM EDT

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

Official title

CANscriptTM Clinical Outcomes in a Real-World Setting (ANCERS)-2: A Prospective, Multicenter, Observational Study Examining the Clinical Utility of CANscriptTM in Routine Clinical Practice

Brief summary

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

The purpose of this study is to test the CANscript™ sensitivity assay, which is a new and different assay developed to test the sensitivity of different cancer types to physician selected therapies (both drugs and/or drug combinations) indicated for the stage and type of cancer for treatment. CANscript™ tests how a patients specific tumor reacts to the therapies being considered by the treating physician. CANscript™ test results have been shown to closely correspond with actual clinical results, providing physicians with information that may help him/her develop a more personalized cancer treatment and care plan based on the patients specific condition. The researchers want to see if CANscript™ test results are helpful in selecting the treatments prescribed and provided. There will be about 800 people taking part in this study, across 5 different tumor types. The study is designed to assess the decision impact of the CANscript™ test results in informing physicians in therapy selection.

Study identification

NCT ID
NCT03253575
Recruitment status
Suspended
Study type
Observational
Phase
Not listed
Lead sponsor
Mitra RxDx, Inc.
Industry
Enrollment
800 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Not listed

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

Study timeline

Start date
Jul 13, 2017 (Actual)
Primary completion
Jul 31, 2019 (Estimated)
Completion
Dec 15, 2019 (Estimated)
Last update posted
Apr 8, 2019

2017 – 2019

United States locations

U.S. sites
30
U.S. states
14
U.S. cities
26
Facility City State ZIP Site status
Banner MD Anderson Cancer Center Gilbert Arizona 85234 —
University of Colorado School of Medicine-Denver Aurora Colorado 80045 —
Eastern CT Hematology and Oncology Associates Norwich Connecticut 06360 —
Lynn Cancer Institute Boca Raton Florida 33486 —
Broward Oncology Associates Fort Lauderdale Florida 33308 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
University of Miami-Sylvester Comprehensive Cancer Center Miami Florida 33136 —
The Center for Gyencologic Oncology Miramar Florida 33027 —
Florida Hospital Cancer Institute Orlando Florida 32804 —
Tallahassee Memorial Cancer Center Tallahassee Florida 32308 —
Memorial Health University Medical Center- Savannah Health Services Savannah Georgia 31404 —
Joliet Oncology Associates Joliet Illinois 60435 —
Edward Elmhurst Healthcare Naperville Illinois 60540 —
Community Hospital Munster Indiana 46321 —
Ochsner Health System New Orleans Louisiana 70121 —
Southcoast Centers for Cancer Care Fairhaven Massachusetts 02719 —
Michigan Center of Medical Research -MHP Farmington Hills Michigan 48334 —
St John Hospital and Medical Center (Great Lakes Cancer Managment Specialists) Grosse Pointe Woods Michigan 48236 —
War Memorial Hematology/Oncology Sault Ste. Marie Michigan 49783 —
Mercy Hospital St Louis Missouri 63141 —
University of Rochester/Wilmot Cancer Institute Rochester New York 14642 —
Saint Thomas Health Nashville Tennessee 37205 —
Austin Cancer Centers Austin Texas 78758 —
Doctors Hospital at Renaissance-DHR Health Edinburg Texas 78539 —
University of Texas Medical Branch at Galveston(UTMB) Galveston Texas 77550 —
Oncology Consultants Houston Texas 77024 —
Baylor College of Medicine Hemtology/Oncology Houston Texas 77030 —
Houston Methodist Medical Center Houston Texas 77030 —
The University of Texas Health Science Center at Houston- Hermann Houston Texas 77030 —
Invesclinic US McAllen Oncology McAllen Texas 78577 —

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 NCT03253575, 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 8, 2019 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03253575 live on ClinicalTrials.gov.

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