Vorinostat (MK-0683) Phase I Study in Cutaneous T-Cell Lymphoma (CTCL) Patients (MK-0683-089 EXT1)
Primary Purpose
Lymphoma
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
vorinostat
Sponsored by
About this trial
This is an interventional treatment trial for Lymphoma
Eligibility Criteria
Inclusion Criteria (Parts I & II):
- Patients With CTCL Who Have Progressive, Persistent Or Recurrent Disease Subsequent To At Least One Prior Therapy
- Eastern Cooperative Oncology Group (ECOG) Performance Status Must Be 0-2
- Patients Have Adequate Bone Marrow, Liver Function And Renal Function
Exclusion Criteria (Parts I & II):
- Patients Had Prior Therapy Within 3 Weeks Before Registration, Or Have Not Recovered From Toxicities Of Prior Therapy
- Patients Have Uncontrolled Intercurrent Illness
- Pregnant Or Women Have A Will To Be Pregnant And Lactating Woman
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Vorinostat
Arm Description
Outcomes
Primary Outcome Measures
Parts I & II: Number of Participants Experiencing Clinical or Laboratory Adverse Experiences (AE)
A laboratory AE is defined as any unfavorable & unintended change in the chemistry of the body temporally associated with the use of study product, whether or not considered related to the use of the product. A clinical AE is defined similarly but also includes changes in structure or function of the body.
Part I: Number of Participants Experiencing Dose Limiting Toxicity (DLT)
A DLT was defined as any of the following (per Common Terminology Criteria for Adverse Events [CTCAE] version 3.0):
Grade 3 (severe)-4 (life-threatening) neutropenia with fever ≥ 38.5ºC
Grade 3-4 neutropenia with an infection requiring antibiotic or antifungal treatment
Grade 4 neutropenia lasting at least 5 days
Grade 4 thrombocytopenia
Other Grade 4 hematologic toxicity, including a decrease in hemoglobin, only at the discretion of the principal investigator
Grade 3 or 4 non-hematologic event, except which are manageable by supportive care or non-prohibited therapies
Secondary Outcome Measures
Part I: Total Drug Exposure (Area Under the Concentration Curve, AUC[0-24 Hours])
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Part I: Maximum Drug Concentration (Cmax)
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Part I: Time at Which Cmax Occurs (Tmax)
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Part I: The Amount of Time it Takes for the Drug Concentration to Decrease by Half (T1/2)
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00771472
Brief Title
Vorinostat (MK-0683) Phase I Study in Cutaneous T-Cell Lymphoma (CTCL) Patients (MK-0683-089 EXT1)
Official Title
Phase I Clinical Study of MK-0683 in Patients With Relapsed or Refractory Cutaneous T-Cell Lymphoma (CTCL)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2015
Overall Recruitment Status
Completed
Study Start Date
August 2008 (undefined)
Primary Completion Date
July 2011 (Actual)
Study Completion Date
July 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Merck Sharp & Dohme LLC
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Part I evaluates the safety, tolerability and pharmacokinetics (PK) of vorinostat in Japanese patients with relapsed or refractory CTCL. Part II evaluates the safety of vorinostat in Japanese pts. with relapsed or refractory CTCL. Relapsed or refractory CTCL patients will be newly enrolled in Part II.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lymphoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
10 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vorinostat
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
vorinostat
Other Intervention Name(s)
MK-0683, Zolinza
Intervention Description
Parts I & II: Vorinostat (400 mg) Oral, daily (QD). Treatment period is 28 days per cycle.
Primary Outcome Measure Information:
Title
Parts I & II: Number of Participants Experiencing Clinical or Laboratory Adverse Experiences (AE)
Description
A laboratory AE is defined as any unfavorable & unintended change in the chemistry of the body temporally associated with the use of study product, whether or not considered related to the use of the product. A clinical AE is defined similarly but also includes changes in structure or function of the body.
Time Frame
Day 1 up until 30 days post study completion or early termination (up to approximately 506 days)
Title
Part I: Number of Participants Experiencing Dose Limiting Toxicity (DLT)
Description
A DLT was defined as any of the following (per Common Terminology Criteria for Adverse Events [CTCAE] version 3.0):
Grade 3 (severe)-4 (life-threatening) neutropenia with fever ≥ 38.5ºC
Grade 3-4 neutropenia with an infection requiring antibiotic or antifungal treatment
Grade 4 neutropenia lasting at least 5 days
Grade 4 thrombocytopenia
Other Grade 4 hematologic toxicity, including a decrease in hemoglobin, only at the discretion of the principal investigator
Grade 3 or 4 non-hematologic event, except which are manageable by supportive care or non-prohibited therapies
Time Frame
Day 1 to Day 28
Secondary Outcome Measure Information:
Title
Part I: Total Drug Exposure (Area Under the Concentration Curve, AUC[0-24 Hours])
Description
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Time Frame
Days 1 & 28 of Cycle 1
Title
Part I: Maximum Drug Concentration (Cmax)
Description
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Time Frame
Days 1 & 28 of Cycle 1
Title
Part I: Time at Which Cmax Occurs (Tmax)
Description
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Time Frame
Days 1 & 28 of Cycle 1
Title
Part I: The Amount of Time it Takes for the Drug Concentration to Decrease by Half (T1/2)
Description
Blood samples taken as follows:
Day 1 & Day 28 of Cycle 1: pre dose, and 0.25, 0.5, 1.0, 1.5, 2.0, 3.0, 4.0, 6.0, 8.0, 10, 12 and 24 hours after dosing of vorinostat.
Time Frame
Days 1 & 28 of Cycle 1
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria (Parts I & II):
Patients With CTCL Who Have Progressive, Persistent Or Recurrent Disease Subsequent To At Least One Prior Therapy
Eastern Cooperative Oncology Group (ECOG) Performance Status Must Be 0-2
Patients Have Adequate Bone Marrow, Liver Function And Renal Function
Exclusion Criteria (Parts I & II):
Patients Had Prior Therapy Within 3 Weeks Before Registration, Or Have Not Recovered From Toxicities Of Prior Therapy
Patients Have Uncontrolled Intercurrent Illness
Pregnant Or Women Have A Will To Be Pregnant And Lactating Woman
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Medical Monitor
Organizational Affiliation
Merck Sharp & Dohme LLC
Official's Role
Study Director
12. IPD Sharing Statement
Citations:
PubMed Identifier
22506596
Citation
Wada H, Tsuboi R, Kato Y, Sugaya M, Tobinai K, Hamada T, Shimamoto T, Noguchi K, Iwatsuki K. Phase I and pharmacokinetic study of the oral histone deacetylase inhibitor vorinostat in Japanese patients with relapsed or refractory cutaneous T-cell lymphoma. J Dermatol. 2012 Oct;39(10):823-8. doi: 10.1111/j.1346-8138.2012.01554.x. Epub 2012 Apr 16.
Results Reference
result
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Vorinostat (MK-0683) Phase I Study in Cutaneous T-Cell Lymphoma (CTCL) Patients (MK-0683-089 EXT1)
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