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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01277120
Other study ID # ML25178
Secondary ID
Status Terminated
Phase N/A
First received January 13, 2011
Last updated September 14, 2016
Start date April 2010
Est. completion date April 2016

Study information

Verified date September 2016
Source Hoffmann-La Roche
Contact n/a
Is FDA regulated No
Health authority Romania: Ministry of Health
Study type Observational

Clinical Trial Summary

This single arm, prospective, observational study will assess the correlation between the time from start of chemotherapy to the start of Avastin (bevacizumab) treatment with progression-free survival in patients with previously untreated metastatic colorectal cancer. Patients will be followed for up to 12 months after progressive disease occurs.


Recruitment information / eligibility

Status Terminated
Enrollment 174
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients, >/= the 18 years of age

- Previously untreated metastatic colorectal cancer

- Scheduled to start 1st line chemotherapeutic treatment

- ECOG performance status 0-1

Exclusion Criteria:

- Any conditions included in contraindication list for Avastin

- Prior chemotherapy for metastatic colorectal cancer

- Adjuvant/neoadjuvant chemotherapy or radio-chemotherapy of non-metastatic colorectal cancer completed <6 months prior to treatment start

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Hoffmann-La Roche

Country where clinical trial is conducted

Romania, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation of the time from the start of chemotherapy to the start of Avastin treatment with progression-free survival 60 months No
Secondary Overall survival 60 months No
Secondary Safety: Incidence of adverse events 60 months No
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