MK-2206 in Recurrent Nasopharyngeal Carcinoma (MC1079)

This study is currently recruiting participants.
Verified April 2013 by Chinese University of Hong Kong
Sponsor:
Information provided by (Responsible Party):
CCTU, Chinese University of Hong Kong
ClinicalTrials.gov Identifier:
NCT01370070
First received: May 12, 2011
Last updated: April 2, 2013
Last verified: April 2013

May 12, 2011
April 2, 2013
July 2011
May 2014   (final data collection date for primary outcome measure)
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 ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT01370070 on ClinicalTrials.gov Archive Site
  • Adverse events [ Time Frame: 2 Years ] [ Designated as safety issue: Yes ]
  • Overall survival [ Time Frame: 3 years ] [ Designated as safety issue: No ]
  • Progression-free survival [ Time Frame: 3 Years ] [ Designated as safety issue: No ]
  • RECIST-based subjective response [ Time Frame: 3 Years ] [ Designated as safety issue: No ]
  • Laboratory correlates: pharmacokinetics, plasma EBV DNA half-life [ Time Frame: 3 years ] [ Designated as safety issue: No ]
  • treatment tolerability [ Time Frame: 2 years ] [ Designated as safety issue: No ]
  • duration of response [ Time Frame: 3 years ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
MK-2206 in Recurrent Nasopharyngeal Carcinoma
Multicenter Phase II Study of MK-2206 in Previously Treated Patients With Recurrent and Metastatic Nasopharyngeal Carcinoma

To evaluate the activity and safety of MK-2206 in patients with recurrent or metastatic nasopharyngeal carcinoma (NPC)

Not Provided
Interventional
Phase 2
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Recurrent Nasopharyngeal Carcinoma
Drug: MK-2206
200mg weekly repeated q 28 days
Experimental: MK-2206
Intervention: Drug: MK-2206
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
45
May 2014
May 2014   (final data collection date for primary outcome measure)

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.
Both
18 Years and older
No
Contact: Brigette Ma, MD, FRACP 2632 ext 1042 brigette@clo.cuhk.edu.hk
Contact: Rosalie HO, RN 2632 1135 rosalie@clo.cuhk.edu.hk
Hong Kong
 
NCT01370070
NPC024
Not Provided
CCTU, Chinese University of Hong Kong
Chinese University of Hong Kong
Not Provided
Principal Investigator: Brigette Ma, MD, FRACP Department of Clinical Oncology, Prince of Wales Hospital, The Chinese University of Hong Kong
Chinese University of Hong Kong
April 2013

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