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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


Phase 3
18 Years
N/A
Not Enrolling
Both
Glioblastoma, Astrocytoma

Thank you

Trial Information

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


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.

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Progression-free survival

Outcome Time Frame:

2 months, 3 months, and 6 months

Safety Issue:

No

Authority:

China: Food and Drug Administration

Study ID:

P03644

NCT ID:

NCT00335075

Start Date:

March 2005

Completion Date:

February 2006

Related Keywords:

  • Glioblastoma
  • Astrocytoma
  • Astrocytoma
  • Glioblastoma

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