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Study of Safety and Pharmacokinetics of MK-8242 in Participants With Advanced Solid Tumors (P07650 AM1)

This study is currently recruiting participants.
Verified March 2013 by Merck
Sponsor:
Information provided by (Responsible Party):
Merck
ClinicalTrials.gov Identifier:
NCT01463696
First received: October 28, 2011
Last updated: March 11, 2013
Last verified: March 2013
History of Changes

October 28, 2011
March 11, 2013
December 2011
October 2014   (final data collection date for primary outcome measure)
Number of participants with dose limiting toxicities (DLTs) [ Time Frame: Cycle 1 (21 days) ] [ Designated as safety issue: Yes ]
Same as current
Complete list of historical versions of study NCT01463696 on ClinicalTrials.gov Archive Site
  • Maximum observed plasma concentration (Cmax) of MK-8242 [ Time Frame: Cycle 1, Day 1 pre-dose and through 24 hours post dose; Cycle 1 Day 7 pre-dose and through 48 hours post dose ] [ Designated as safety issue: No ]
  • Time to maximum plasma concentration (Tmax) of MK-8242 [ Time Frame: Cycle 1, Day 1 pre-dose and through 12 hours postdose; Cycle 1 Day 7 pre-dose and through 48 hours post dose ] [ Designated as safety issue: No ]
  • Area under the concentration time curve from Hour 0 to Hour 12 (AUC0-12) for MK-8242 [ Time Frame: Cycle 1, Day 1 and Day 7, Hour 0 through Hour 12 ] [ Designated as safety issue: No ]
  • AUC from time 0 to the time of final quantifiable sample (AUCtf) for MK-8242 [ Time Frame: Cycle 1, Day 1 pre-dose and through 12 hours post dose; Cycle 1 Day 7 pre-dose and through 48 hours post dose ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Study of Safety and Pharmacokinetics of MK-8242 in Participants With Advanced Solid Tumors (P07650 AM1)
A Phase I Study to Evaluate the Safety and Tolerability and Pharmacokinetic/Pharmacodynamics of MK-8242 in Patients With Advanced Solid Tumors

This study is being done to evaluate the safety and pharmacokinetic profile of MK-8242 in participants with advanced solid tumors. In Part 1 of the study, the study drug dose will be escalated to determine the maximum tolerated dose (MTD). In Part 2 of the study, the MTD will be confirmed and the recommended Phase 2 dose (RPTD) established; the effect of MK-8242 on liposarcoma and other tumor types will also be evaluated.
Not Provided
Interventional
Phase 1
Allocation: Non-Randomized
Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Solid Tumors
Drug: MK-8242
MK-8242 capsules will be administered orally twice a day (BID) in Cycle1 and once in the morning (QD) on Day 7 of a 21-day cycle to accommodate pharmacokinetic (PK) sampling. In Cycle 2 and subsequent cycles, MK-8242 will be administered orally twice a day (BID) on Days 1-7 in a 21-day cycle.
Other Name: SCH 900242
  • Experimental: Part 1: MK-8242 dose escalation
    Intervention: Drug: MK-8242
  • Experimental: Part 2: MK-8242 dose confirmation
    Intervention: Drug: MK-8242
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
132
August 2015
October 2014   (final data collection date for primary outcome measure)

Inclusion criteria:

  • Histologically confirmed advanced solid tumor for which there are no effective standard therapy options
  • Willing to provide tumor tissue for p53 wild type gene analysis Eastern Cooperative Oncology Group (ECOG) performance status of ≤1
  • Adequate organ function
  • Female participants and male participants and their partners who are of childbearing potential must agree to abstain from sexual intercourse or to use an acceptable method of contraception during the study and for 90 days following the last dose of study therapy
  • At least one measurable lesion
  • In Part 2, participants with liposarcoma must have a confirmed well-differentiated or de-differentiated histology

Exclusion criteria:

  • Known treated or untreated leptomeningeal metastases, or metastatic central nervous system disease
  • History of recent myocardial infarction (within the past year); or with unstable or uncontrolled angina, New York Heart Association (NYHA) Class III or IV congestive heart failure, uncontrolled hypertension, clinically significant cardiac dysrhythmia or clinically significant electrocardiogram (ECG) abnormality
  • Uncontrolled active infection on optimal systemic treatment
  • Clinically significant hepatitis or hepatitis C antibody positive, hepatitis B surface antigen positive, or human immunodeficiency virus (HIV) seropositive
  • Persistent, unresolved common terminology criteria for adverse events (CTCAE v4.0) ≥Grade 2 drug-related toxicity associated with previous treatment except for alopecia
  • Radiation therapy or other loco-regional therapy within 2 weeks prior to study
  • Use of moderate and strong Cytochrome P450 inhibitors or inducers within 1 week prior to study
  • Chemotherapy or any investigational drug(s) within 4 weeks prior to study
  • Known hypersensitivity to MK-8242 or its components
  • Nursing, pregnant, or intention to become pregnant during the study
  • Initiating bisphosphonate therapy or adjusting the bisphosphonate dose or regimen within 30 days of Cycle 1 Day 1
Both
18 Years and older
No
Contact: Toll Free Number 1-888-577-8839
United States,   United Kingdom
 
NCT01463696
P07650, 2011-001346-15
No
Merck
Merck
Not Provided
Not Provided
Merck
March 2013

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