MK-2206 in Recurrent Nasopharyngeal Carcinoma (MC1079)
Primary Purpose
Recurrent Nasopharyngeal Carcinoma
Status
Completed
Phase
Phase 2
Locations
Hong Kong
Study Type
Interventional
Intervention
MK-2206
Sponsored by
About this trial
This is an interventional treatment trial for Recurrent Nasopharyngeal Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Aged > 18 year, able to give written informed consent.
- History of histologically or cytologically confirmed non-keratinizing NPC that has recurred at locoregional and/or distant sites, and is not amenable to potentially curative radiotherapy or surgery.
- Patients must have progressed within 24 months of receiving one or two prior line of chemotherapy for recurrent disease, of which at least one line must contain platinum drugs such as Cisplatin, Carboplatin or oxaliplatin.
- Adequate organ reserve: neutrophils >1.5x109/L, platelets ≥100 x109/L, hemoglobin ≥9 g/dL, serum alanine aminotransferase (ALT) < 2.5 x upper limit of normal (ULN) or ALT< 5 x ULN in the presence of liver metastases, serum bilirubin < 2.5 x ULN, serum creatinine < 1.5 x ULN.
- Presence of measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST ver 1.1).
Exclusion Criteria:
- Chemotherapy, radiotherapy (except to bone metastases) or investigational treatment within 4 weeks of enrollment.
- Patients with diabetes or in risk for hyperglycemia should not be excluded from trials with MK-2206, but the hyperglycemia should be well controlled before the patient enters the trial.
- Cardiovascular: baseline QTcF > 450 msec (male) or QTcF >470 msec (female) Left bundle branch block, 2nd or 3rd degree AV block, bifascicular block, sick sinus syndrome, Wolff-Parkinson-white syndrome, significant sinus bradycardia (< 50bpm) . However, patients with asymptomatic right bundle branch block or 1st degree AV block, in the absence of known cardiac disease (e.g. coronary, valvular) are NOT excluded..
- Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Sites / Locations
- Department of Clinical Oncology, Prince of Wales Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
MK-2206
Arm Description
Outcomes
Primary Outcome Measures
The proportion of patients alive and progression-free at 6 months along with the confirmed response rate as a dual primary endpoint
Secondary Outcome Measures
Adverse events
Overall survival
Progression-free survival
RECIST-based subjective response
Laboratory correlates: pharmacokinetics, plasma EBV DNA half-life
treatment tolerability
duration of response
Full Information
NCT ID
NCT01370070
First Posted
May 12, 2011
Last Updated
January 11, 2017
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT01370070
Brief Title
MK-2206 in Recurrent Nasopharyngeal Carcinoma
Acronym
MC1079
Official Title
Multicenter Phase II Study of MK-2206 in Previously Treated Patients With Recurrent and Metastatic Nasopharyngeal Carcinoma
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
July 2011 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
January 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
5. Study Description
Brief Summary
To evaluate the activity and safety of MK-2206 in patients with recurrent or metastatic nasopharyngeal carcinoma (NPC)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Recurrent Nasopharyngeal Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
MK-2206
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
MK-2206
Intervention Description
200mg weekly repeated q 28 days
Primary Outcome Measure Information:
Title
The proportion of patients alive and progression-free at 6 months along with the confirmed response rate as a dual primary endpoint
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Adverse events
Time Frame
2 Years
Title
Overall survival
Time Frame
3 years
Title
Progression-free survival
Time Frame
3 Years
Title
RECIST-based subjective response
Time Frame
3 Years
Title
Laboratory correlates: pharmacokinetics, plasma EBV DNA half-life
Time Frame
3 years
Title
treatment tolerability
Time Frame
2 years
Title
duration of response
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Aged > 18 year, able to give written informed consent.
History of histologically or cytologically confirmed non-keratinizing NPC that has recurred at locoregional and/or distant sites, and is not amenable to potentially curative radiotherapy or surgery.
Patients must have progressed within 24 months of receiving one or two prior line of chemotherapy for recurrent disease, of which at least one line must contain platinum drugs such as Cisplatin, Carboplatin or oxaliplatin.
Adequate organ reserve: neutrophils >1.5x109/L, platelets ≥100 x109/L, hemoglobin ≥9 g/dL, serum alanine aminotransferase (ALT) < 2.5 x upper limit of normal (ULN) or ALT< 5 x ULN in the presence of liver metastases, serum bilirubin < 2.5 x ULN, serum creatinine < 1.5 x ULN.
Presence of measurable disease as per Response Evaluation Criteria in Solid Tumors (RECIST ver 1.1).
Exclusion Criteria:
Chemotherapy, radiotherapy (except to bone metastases) or investigational treatment within 4 weeks of enrollment.
Patients with diabetes or in risk for hyperglycemia should not be excluded from trials with MK-2206, but the hyperglycemia should be well controlled before the patient enters the trial.
Cardiovascular: baseline QTcF > 450 msec (male) or QTcF >470 msec (female) Left bundle branch block, 2nd or 3rd degree AV block, bifascicular block, sick sinus syndrome, Wolff-Parkinson-white syndrome, significant sinus bradycardia (< 50bpm) . However, patients with asymptomatic right bundle branch block or 1st degree AV block, in the absence of known cardiac disease (e.g. coronary, valvular) are NOT excluded..
Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brigette Ma, MD, FRACP
Organizational Affiliation
Department of Clinical Oncology, Prince of Wales Hospital, The Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Clinical Oncology, Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
12. IPD Sharing Statement
Citations:
PubMed Identifier
26084990
Citation
Ma BB, Goh BC, Lim WT, Hui EP, Tan EH, Lopes Gde L, Lo KW, Li L, Loong H, Foster NR, Erlichman C, King AD, Kam MK, Leung SF, Chan KC, Chan AT. Multicenter phase II study of the AKT inhibitor MK-2206 in recurrent or metastatic nasopharyngeal carcinoma from patients in the mayo phase II consortium and the cancer therapeutics research group (MC1079). Invest New Drugs. 2015 Aug;33(4):985-91. doi: 10.1007/s10637-015-0264-0. Epub 2015 Jun 19.
Results Reference
derived
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MK-2206 in Recurrent Nasopharyngeal Carcinoma
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