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Efficacy and Safety of Temodal vs Semustine in Subjects With Recurrent Glioblastoma or Anaplastic Astrocytoma (Study P03644)

Primary Purpose

Glioblastoma, Astrocytoma

Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Temozolomide
Semustine
Sponsored by
Merck Sharp & Dohme LLC
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Prior histologic confirmation of glioblastoma, anaplastic astrocytoma. Evidence of tumor progression or recurrence. Age >=18 years. Karnofsky performance status >=60%. Absolute neutrophil count >=1,500/mm^3, platelet count >=100,000/mm^3, hemoglobin >=8g/dL. Serum BUN and creatinine <1.5 times upper normal limit of testing laboratory (ULN). Total bilirubin and direct bilirubin <1.5 times ULN. SGOT, SGPT <3 times ULN; alkaline phosphatase <2 times ULN. Life expectancy greater than 3 months. Informed consent obtained. If palliative radiation is needed, agree to give it prior to initiating chemotherapy with study drug. If palliative radiation is required during treatment with study drug, the patient should be permanently discontinued from further treatment with study drug. Women of childbearing potential must use a medically accepted, effective method of contraception. Women of childbearing potential must have a negative serum pregnancy test 24 hours prior to administration of study drug. Exclusion Criteria: Chemotherapy (excluding nitrosourea, mitomycin C or vincristine), biologic therapy or immunotherapy within 4 weeks, inclusive, prior to study drug administration. Nitrosourea or mitomycin C administration within 6 weeks, inclusive, prior to study drug administration. Vincristine within 2 weeks prior to study drug administration. Completion of radiation therapy, interstitial brachytherapy or radiosurgery within 4 weeks prior to study drug administration. Surgery within 3 weeks, inclusive, prior to study drug administration. Acute infection requiring intravenous antibiotics. Frequent vomiting or medical condition that could interfere with oral medication intake (eg, partial bowel obstruction). Previous or concurrent malignancies at other sites with the exception of surgically cured carcinoma in-situ of the cervix and basal or squamous cell carcinoma of the skin. Known HIV positive or AIDS-related illness. Pregnant or nursing women. Men who are not advised to use an effective method of contraception.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    Temodal group

    Semustine group

    Arm Description

    Subjects treated with temozolomide.

    Subjects treated with semustine.

    Outcomes

    Primary Outcome Measures

    Progression-free survival

    Secondary Outcome Measures

    Overall survival
    Objective response
    Scoring of health-related quality of life

    Full Information

    First Posted
    June 6, 2006
    Last Updated
    May 12, 2017
    Sponsor
    Merck Sharp & Dohme LLC
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00335075
    Brief Title
    Efficacy and Safety of Temodal vs Semustine in Subjects With Recurrent Glioblastoma or Anaplastic Astrocytoma (Study P03644)
    Official Title
    A Multicenter, Open-Label, Randomized, Active-Controlled Parallel Groups Study Comparing the Efficacy and Safety of Temodal vs Semustine in the Treatment of Subjects With Recurrent Glioblastoma or Anaplastic Astrocytoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    March 2, 2005 (Actual)
    Primary Completion Date
    February 23, 2006 (Actual)
    Study Completion Date
    February 23, 2006 (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
    The primary purpose of the study is to evaluate the efficacy and safety of temozolomide compared to semustine in the treatment of patients with glioblastoma multiforme or anaplastic astrocytoma.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Glioblastoma, Astrocytoma

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    151 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Temodal group
    Arm Type
    Experimental
    Arm Description
    Subjects treated with temozolomide.
    Arm Title
    Semustine group
    Arm Type
    Active Comparator
    Arm Description
    Subjects treated with semustine.
    Intervention Type
    Drug
    Intervention Name(s)
    Temozolomide
    Other Intervention Name(s)
    Temodal, Temodar, SCH 052365
    Intervention Description
    Temozolomide orally for 5 consecutive days (Day 1 through Day 5) every 28 days, at a dose of 150 mg/m2/day for subjects previously treated with chemotherapy, or 200 mg/m2/day for subjects who have not received previous chemotherapy.
    Intervention Type
    Drug
    Intervention Name(s)
    Semustine
    Other Intervention Name(s)
    Methyl-CCNU
    Intervention Description
    Semustine orally once every 28 days at a dose of 150 mg/m2/day.
    Primary Outcome Measure Information:
    Title
    Progression-free survival
    Time Frame
    2 months, 3 months, and 6 months
    Secondary Outcome Measure Information:
    Title
    Overall survival
    Time Frame
    6 months
    Title
    Objective response
    Time Frame
    6 months
    Title
    Scoring of health-related quality of life
    Time Frame
    6 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Prior histologic confirmation of glioblastoma, anaplastic astrocytoma. Evidence of tumor progression or recurrence. Age >=18 years. Karnofsky performance status >=60%. Absolute neutrophil count >=1,500/mm^3, platelet count >=100,000/mm^3, hemoglobin >=8g/dL. Serum BUN and creatinine <1.5 times upper normal limit of testing laboratory (ULN). Total bilirubin and direct bilirubin <1.5 times ULN. SGOT, SGPT <3 times ULN; alkaline phosphatase <2 times ULN. Life expectancy greater than 3 months. Informed consent obtained. If palliative radiation is needed, agree to give it prior to initiating chemotherapy with study drug. If palliative radiation is required during treatment with study drug, the patient should be permanently discontinued from further treatment with study drug. Women of childbearing potential must use a medically accepted, effective method of contraception. Women of childbearing potential must have a negative serum pregnancy test 24 hours prior to administration of study drug. Exclusion Criteria: Chemotherapy (excluding nitrosourea, mitomycin C or vincristine), biologic therapy or immunotherapy within 4 weeks, inclusive, prior to study drug administration. Nitrosourea or mitomycin C administration within 6 weeks, inclusive, prior to study drug administration. Vincristine within 2 weeks prior to study drug administration. Completion of radiation therapy, interstitial brachytherapy or radiosurgery within 4 weeks prior to study drug administration. Surgery within 3 weeks, inclusive, prior to study drug administration. Acute infection requiring intravenous antibiotics. Frequent vomiting or medical condition that could interfere with oral medication intake (eg, partial bowel obstruction). Previous or concurrent malignancies at other sites with the exception of surgically cured carcinoma in-situ of the cervix and basal or squamous cell carcinoma of the skin. Known HIV positive or AIDS-related illness. Pregnant or nursing women. Men who are not advised to use an effective method of contraception.

    12. IPD Sharing Statement

    Available IPD and Supporting Information:
    Available IPD/Information Type
    CSR Synopsis
    Available IPD/Information URL
    http://www.merck.com/clinical-trials/policies-perspectives.html

    Learn more about this trial

    Efficacy and Safety of Temodal vs Semustine in Subjects With Recurrent Glioblastoma or Anaplastic Astrocytoma (Study P03644)

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