Clinical trial · Interventional
A Phase I/II Study of Cediranib (AZD2171) in Japanese Metastatic Colorectal Cancer Patients in Combination With FOLFOX
A Two Part Study in Japanese Patients With mCRC, Consisting of an Open-label Phase I Part to Assess the Safety and Tolerability of Cediranib (AZD2171) in Combination With FOLFOX Followed by a Phase II, Randomised, Double-blind, Parallel Group Study to Assess the Efficacy of Cediranib (AZD2171) in Combination With FOLFOX
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Metastatic Colorectal Cancer | Malignant Colorectal Neoplasm | CURATED_BROADER | 0.80 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| AZD2171 | Drug | Cediranib | ALIAS |
| FOLFOX (5-fluorouracil, Leucovorin, Oxaliplatin) | Drug | FOLFOX Regimen | ALIAS |
| Placebo Cediranib | Drug | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- ACTIVE_COMPARATOR
- label
- FOLFOX + Cediranib 20 mg
- description
- FOLFOX + Cediranib 20 mg
- interventionNames
- Drug: AZD2171
- Drug: FOLFOX (5-fluorouracil, Leucovorin, Oxaliplatin)
- type
- ACTIVE_COMPARATOR
- label
- FOLFOX + Cediranib 30 mg
- description
- FOLFOX + Cediranib 30 mg
- interventionNames
- Drug: AZD2171
- Drug: FOLFOX (5-fluorouracil, Leucovorin, Oxaliplatin)
- type
- PLACEBO_COMPARATOR
- label
- FOLFOX + Placebo Cediranib
- description
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available