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AZD6244 vs. Capecitabine (Xeloda®) in Patients With Advanced or Metastatic Pancreatic Cancer, Who Have Failed First Line Gemcitabine Therapy

A Phase II, Open, Randomised Study to Assess the Efficacy and Safety of AZD6244 vs. Capecitabine (Xeloda®) in Patients With Advanced or Metastatic Pancreatic Cancer, Who Have Failed First Line Gemcitabine Therapy

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00372944
Enrollment
70
Registered
2006-09-07
Start date
2006-08-31
Completion date
2008-10-31
Last updated
2014-08-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic Cancer

Keywords

advanced pancreatic cancer, metastatic pancreatic cancer, AZD6244

Brief summary

The purpose of this study is to assess the efficacy and safety of AZD6244 (ARRY-142886)versus capecitabine in patients with advanced or metastatic pancreatic cancer who have failed first-line therapy with gemcitabine. Following baseline assessments, a minimum of 64 patients in approximately 5-6 centers from the US will be treated with either AZD6244 or capecitabine. Treatment will be continued for as long as the patients receive clinical benefit. The status of all patients will be checked (whether they are still taking treatment or not) approximately 3 months after the last patient has entered the study.

Interventions

DRUGAZD6244

oral capsule

DRUGcapecitabine

oral tablet

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Confirmed with pancreatic cancer * Have failed first line gemcitabine therapy

Exclusion criteria

* Previous therapy with EGFR inhibitor, MEK inhibitor or capecitabine. * Any recent surgery, unhealed surgical incision or severe condition such as uncontrolled cardiac disease or chronic gastrointestinal diseases.

Design outcomes

Primary

MeasureTime frameDescription
Median time to death (TTD)Data cut off for this analysis was 5th April 2008.The TTD (days) was calculated as the interval from date of randomisation to date of patient death (from any cause). Patients who had not died at the time of the final analysis were censored at the last date the patient was known to be alive. Median TTD in days is presented here.

Secondary

MeasureTime frameDescription
Progression event countThe mandatory tumour assessment visit (MTAV) occurred on 27th February 2008 (+/-3days)The number of patients with a progression event occurring on or before MTAV where an event is defined as Objective and/or clinical disease progression as measured using RECIST criteria, or death from any cause
To assess the safety and tolerability of AZD6244 in the treatment of advanced or metastatic pancreatic cancer by review of adverse events (AEs) and laboratory parameters.Review of AEs for duration of study, from First Subject in August 2006 to Last Subject Last visit October 2008

Countries

Australia, Bulgaria, Hungary, Romania, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026