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An Observational Study of First-Line Bevacizumab (Avastin) With Fluoropyrimidine-Based Chemotherapy in Participants With Metastatic Colorectal Cancer

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Roche

Status

Completed

Conditions

Colorectal Cancer

Treatments

Drug: Bevacizumab
Drug: Chemotherapy

Study type

Observational

Funder types

Industry

Identifiers

NCT01712347
ML28233

Details and patient eligibility

About

This multicenter observational study will evaluate the efficacy and safety of first-line bevacizumab (Avastin) in combination with fluoropyrimidine-based chemotherapy in participants with metastatic colorectal cancer (mCRC). Participants for whom the treating physician has decided to initiate first-line fluoropyrimidine based chemotherapy in combination with bevacizumab will be observed for approximately 4 years.

Enrollment

351 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participants with histologically confirmed metastatic colorectal cancer who will receive bevacizumab in combination with first-line fluoropyrimidine-based chemotherapy

Exclusion criteria

  • Participants not qualified for bevacizumab treatment according to the local label

Trial design

351 participants in 1 patient group

mCRC Participants
Description:
mCRC participant will receive bevacizumab as per approved label with the approved first-line fluoropyrimidine based chemotherapy, as per physician discretion. The protocol does not specify the chemotherapy regimen to be used, the choice of chemotherapy will be at the discretion of treating physician.
Treatment:
Drug: Chemotherapy
Drug: Bevacizumab

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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