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Panitumumab and Bortezomib for Patients With Advanced Colorectal Cancer

This study has been terminated.
(Low accrual--unable to meet accrual goals)
Sponsor:
Collaborator:
Millennium Pharmaceuticals, Inc.
Information provided by (Responsible Party):
Georgetown University
ClinicalTrials.gov Identifier:
NCT01504477
First received: December 14, 2011
Last updated: July 9, 2017
Last verified: July 2017
December 14, 2011
July 9, 2017
December 2011
February 2014   (Final data collection date for primary outcome measure)
Maximum tolerated dose [ Time Frame: 12 months ]
The maximum tolerated dose of bortezomib to be used in combination with panitumumab
Same as current
Complete list of historical versions of study NCT01504477 on ClinicalTrials.gov Archive Site
  • Disease control rate [ Time Frame: 16 weeks ]
    Stable disease after 2 cycles, partial response or complete response
  • Overall response rate [ Time Frame: 16 weeks ]
    Partial response plus complete response
  • Overall survival [ Time Frame: 4 years ]
    Time from study registration to death
  • Duration of disease control [ Time Frame: 2 years ]
    Time from study registration until progressive disease
  • Pharmacodynamic effects [ Time Frame: 3 weeks ]
    pharmacodynamic effects of panitumumab alone and in combination with bortezomib on the EGFR and proteosome pathways by phosphoprotein pathway analysis
Same as current
Not Provided
Not Provided
 
Panitumumab and Bortezomib for Patients With Advanced Colorectal Cancer
A Phase I/II Clinical Trial of the Anti-EGFR Monoclonal Antibody, Panitumumab, and the Proteosomal Inhibitor, Bortezomib, in Patients With Advanced, Refractory KRAS Wild-Type Colorectal Cancer
Panitumumab plus bortezomib for colon cancer

This study is for patients with colon cancer that cannot be fully removed by surgery and has come back after or not responded to standard chemotherapy treatment.

Subjects will be enrolled to either the first part of the study (Phase I) or the second part of the study (Phase II). Phase I will be completed before Phase II will start. The purpose of the Phase I part is to find the highest dose of bortezomib that can be given with panitumumab without causing severe side effects. The purpose of the Phase II part is to test the effects the two drugs have on subjects with colorectal cancer.

Panitumumab is a drug that targets a protein important for the growth of cancer cells known as EGFR. By blocking the activity of the protein, panitumumab can block cancer cell growth and even lead to their death. Panitumumab is given intravenously once every two weeks. Panitumumab is approved by the FDA for patients with colorectal cancer.

Bortezomib is a drug that targets a part of the cancer cell known as the proteosome. By inhibiting the proteosome, bortezomib can inhibit cancer cell growth and even lead to their death. Bortezomib is given intravenously, once a week, 3 out of every 4 weeks. Bortezomib is not FDA approved for the treatment of colorectal cancer.

As part of this study the investigators will be taking biopsies of patients' tumors before any treatment, after starting with the panitumumab alone, and after receiving both the panitumumab and bortezomib. The investigators want to investigate what markers inside tumors may relate to how well these two medications work. These biopsies are required as part of the study.

Interventional
Phase 1
Phase 2
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Colorectal Cancer
Drug: Panitumumab and bortezomib

Panitumumab 6 mg/kg IV over 60 minutes on Day -14 (first cycle only), then Day 1 and 15 of each 28-day cycle.

Bortezomib will be administered in escalating doses until the maximum tolerated dose is determined and then at the maximum tolerated dose as an IV bolus injection over 3-5 seconds on Day 1, 8, and 15 of each 28-day cycle.

Other Names:
  • Velcade
  • Vectibix
Experimental: Combination of Panitumumab and Bortezomib
IV panitumumab and bortezomib
Intervention: Drug: Panitumumab and bortezomib
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Terminated
6
February 2014
February 2014   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Histologically proven colorectal cancer with measurable or evaluable disease
  • KRAS wild-type colorectal cancer
  • Progression on, or intolerance of, or ineligibility for all standard therapies
  • Progression on prior anti-EGFR therapy
  • Lesion that is amenable to biopsy
  • ECOG performance status 0-2
  • LVEF >/= institutional normal
  • Corrected QT interval less then 500 milliseconds by EKG
  • Grade 2 or less peripheral neuropathy
  • Adequate hepatic, bone marrow, and renal function
  • Partial thromboplastin time must be </= 1.5 x upper limit of institution's normal range and INR < 1.5. Subjects on anticoagulants will be permitted to enroll as long as the INR is in the acceptable therapeutic range as determined by the investigator.
  • Subjects with no brain metastases or a history of previously treated brain metastases who have been treated by surgery or stereotactic radiosurgery at least 4 weeks prior to enrollment and have a baseline MRI that shows no evidence of active intracranial disease and have not had treatment with steroids within 1 week of study enrollment.
  • Life expectancy > 12 weeks
  • Subject is capable of understanding and complying with parameters of the protocol and able to sign and date the informed consent form.

Exclusion Criteria:

  • CNS metastases which do not meet the criteria above
  • Prior cancer chemotherapy, radiation therapy, or any investigational agent within three weeks before starting therapy
  • Active severe infection or known chronic infection with HIV or hepatitis B virus
  • Cardiovascular disease problems including unstable angina, therapy for life-threatening ventricular arrhythmia, or myocardial infarction, stroke, or congestive heart failure within the last 6 months
  • Peripheral neuropathy >/= Grade 2 at baseline or peripheral neuropathy >/= Grade 1 with neuropathic pain
  • Life-threatening visceral disease or other severe concurrent disease
  • Female subject is pregnant or lactating
  • Diagnosed or treated for another malignancy within 3 years of enrollment with the exception of complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, or low risk prostate cancer after curative therapy
  • Patient has hypersensitivity to bortezomib, boron, or mannitol
  • Clinically significant and uncontrolled major medical condition(s)
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT01504477
2011-033
X05374 ( Other Identifier: Millennium Pharmaceuticals )
Yes
Not Provided
Plan to Share IPD: No
Plan Description: There is no plan for this
Georgetown University
Georgetown University
Millennium Pharmaceuticals, Inc.
Principal Investigator: Michael Pishvaian, MD PhD Georgetown University
Georgetown University
July 2017

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP