Colorectal Cancer Clinical Trial
Official title:
The Correlation Between the Moment of Bevacizumab theRapy initiatiOn and the Efficacy in patieNt With cOlorectal Cancer Treated With AvaStin Based First Line Regimens (CRONOS 1)
Verified date | September 2016 |
Source | Hoffmann-La Roche |
Contact | n/a |
Is FDA regulated | No |
Health authority | Romania: Ministry of Health |
Study type | Observational |
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.
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 |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Hoffmann-La Roche |
Romania,
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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