Phase 2
Completed N=172
A Phase I/II Study of Cediranib (AZD2171) in Japanese Metastatic Colorectal Cancer Patients in Combination With FOLFOX
Source: ClinicalTrials.gov NCT00494221 ↗Enrolled (actual)
172
Serious AEs
32.6%
Results posted
Jun 2012
Primary outcomePrimary: Progression Free Survival — 10.23; 8.85; 8.32 Months
Summary
This Study is in two parts, the first part is to make sure that combining a potential new treatment, cediranib (AZD2171), with a standard treatment (FOLFOX) for metastatic colorectal cancer is safe. Once this part is complete and it is decided that it is safe to continue the Study will the go on to look at the efficacy of the two drugs together. This will be done by studying two treatment options. One will be the standard treatment alone (FOLFOX) + dummy cediranib (AZD2171) tablets and the other will be the standard treatment (FOLFOX) + real cediranib (AZD2171) tablets. Using dummy tablets means the study is 'blinded' and that non-one can tell the difference between the two treatment groups. This kind of study design is done to try to avoid the chance that the results might be biased in some way. The overall aim of the second part of the study is to see if adding cediranib (AZD2171) to a standard treatment for Metastatic Colorectal Cancer (mCRC), in this case FOLFOX, gives better results. That is, it's better than giving standard treatment alone in helping to prevent progression of mCRC.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Progression Free Survival |
10.23; 8.85; 8.32 | — |
| SECONDARY Objective Tumour Response Rate |
31; 39; 31 | — |
| SECONDARY Best Percentage Change in Tumour Size |
-36.56; -43.99; -40.22 | — |
| SECONDARY Duration of Response |
13.26; 8.12; 10.42 | — |
| SECONDARY Overall Survival |
NA; 20.07; 19.51 | — |
Eligibility Criteria
Inclusion Criteria
- Metastatic colorectal cancer
- WHO performance status 0-1
- Life expectancy is 12 weeks or longer
Exclusion Criteria
- Patient with uncontrolled brain metastases
- Patient with inappropriate laboratory tests values
- Patient with poorly controlled hypertension
Data sourced from ClinicalTrials.gov (NCT00494221). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.