ASPECCT: A Study of Panitumumab Efficacy and Safety Compared to Cetuximab in Patients With KRAS Wild-Type Metastatic Colorectal Cancer
Status: | Completed |
---|---|
Conditions: | Colorectal Cancer, Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 12/27/2018 |
Start Date: | February 2, 2010 |
End Date: | March 7, 2017 |
A Randomized, Multicenter, Open-label, Phase 3 Study to Compare the Efficacy and Safety of Panitumumab and Cetuximab in Subjects With Previously Treated, Wild-type KRAS, Metastatic Colorectal Cancer
The primary objective of this study is to compare the effect of panitumumab versus cetuximab
on overall survival (OS) for chemorefractory metastatic colorectal cancer (mCRC) among
patients with wild-type Kirsten rat Sarcoma-2 virus (KRAS) tumors.
on overall survival (OS) for chemorefractory metastatic colorectal cancer (mCRC) among
patients with wild-type Kirsten rat Sarcoma-2 virus (KRAS) tumors.
Inclusion Criteria:
- Histologically or cytologically confirmed diagnosis of adenocarcinoma of the colon or
rectum, metastatic disease
- Wild-type KRAS tumor status
- Eastern Cooperative Oncology Group (ECOG) score of 0, 1 or 2
- Must have failed a prior regimen containing irinotecan for metastatic disease and a
prior regimen containing oxaliplatin for metastatic disease
- Must have previously received a thymidylate synthase inhibitor (eg, fluorouracil,
capecitabine, raltitrexed, or fluorouracil-uracil) at any point for treatment of
colorectal cancer (CRC)
- Adequate hematologic, renal, hepatic and metabolic function
Exclusion Criteria:
- Symptomatic brain metastases requiring treatment
- Prior anti-epidermal growth factor receptor (EGFr) antibody therapy (eg, panitumumab
or cetuximab) or treatment with small molecule EGFr inhibitors (eg, gefitinib,
erlotinib, lapatinib)
- Antitumor therapy (eg, chemotherapy, hormonal therapy, immunotherapy, antibody
therapy, radiotherapy), or investigational agent or therapy ≤ 30 days before
randomization.
- Clinically significant cardiovascular disease
- Active infection requiring systemic treatment or any uncontrolled infection ≤14 days
prior to randomization
We found this trial at
6
sites
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