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Not yet recruitingNCT02496988Updated Jul 14, 2015

Effect of Cytokine-induced Killer Cells for Advanced Malignant Gliomas

A Phase 4 interventional study of Temozolomide and CIK in Cytokine-Induced Killer Cells and Advanced Milignant Gliomas, sponsored by The First People's Hospital of Changzhou. Not yet recruiting. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2015-07-14.

Sponsored by The First People's Hospital of Changzhou · Phase 4 and Interventional

Phase
Phase 4
Study type
Interventional
Enrollment
120
Allocation
Non-randomized
Ages
18 Years to 80 Years
Sex
All
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Study summary

The purpose of this study is to determine whether combining of Temozolomide and cytokine-induced killer cells (CIK) transfusion can prolong survival of patients with Advanced Malignant Gliomas. The effectiveness and safety of CIK cells for the treatment of Malignant Glioma is also evaluated.

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Conditions studied

  • Cytokine-Induced Killer Cells
  • Advanced Milignant Gliomas

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Keywords

  • Cytokine-Induced Killer Cells
  • Milignant Gliomas
  • Temozolomide
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In context

Glioma

1,397 studies on the registry are indexed under Glioma; 351 are open to participants now.

This study's planned enrollment of 120 is above the median of 32 across 1,065 interventional studies indexed under Glioma.

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Lead sponsor

The First People's Hospital of Changzhou is the lead sponsor of 25 studies on the registry; 11 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Subjects with documented histologically confirmed primary grade 4 advanced malignant glioma.
  • No more than 3 prior relapses or prior systemic treatments.
  • Recurrent disease documented by MRI after prior therapy.
  • Must have at least one site of bidimensionally measurable disease:

archived tissue from the initial diagnosis of advanced malignant glioma or upon transformation to advanced malignant glioma are available for central review within approximately 4 weeks after enrollment.

  • Completed at least one full cycle of temozolomide of 200 mg/m2/day administered on Days 1-5 of a 28-day cycle, without unacceptable toxicity or progression.
  • Karnofsky performance status of 60 or more. Adequate organ and bone marrow function as defined by hematological and serum chemistry limits.
  • At least 18 years old.
  • Both men and women must practice adequate contraception.
  • Informed consent.

Exclusion criteria

Exclusion Criteria:

  • Progressed while on temozolomide.
  • Evidence of acute intracranial or intratumoral hemorrhage > Grade 1.
  • Not recovered from the toxic effects of prior therapy.
  • Pregnant or breast feeding.
  • History of diabetes mellitus.
  • Uncontrolled intercurrent illness.
  • Congestive heart failure, unstable angina, or a myocardial infarction within 3 months of entering the study.
  • HIV positive.
  • Diagnosis of another malignancy may exclude subject from study.
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Study design

Phase
Phase 4
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
120 participants (estimated)

Study arms

  • Other
    Temozolomide

    Capsules supplied in 5-mg, 20-mg, 100-mg, 140-mg, 180-mg, and 250-mg strengths; dosed at 200 mg/m2/day for 5 consecutive days, repeated every 28 days

    Drug: Temozolomide

  • Other
    Temozolomide+CIK

    Autologous cytokine-induced killer cells were transfer via venous one week after Temozolomide treat

    Biological: CIK

Interventions

  • DrugTemozolomide

    Capsules supplied in 5-mg, 20-mg, 100-mg, 140-mg, 180-mg, and 250-mg strengths; dosed at 200 mg/m2/day for 5 consecutive days, repeated every 28 days

  • BiologicalCIK

    The patients received autologous cytokine-induced killer cells transfusion one week after Temozolomide treat

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What researchers measure

Primary outcomes

  1. Overall survival

    Time frame: 5 years

Secondary outcomes

  1. Adverse events

    Time frame: 4 weeks

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 14, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02496988
Lead sponsor
The First People's Hospital of Changzhou
Responsible party
Sponsor
First posted
Jul 14, 2015
Start date
Jul 2015
Primary completion
Jul 2028 (estimated)
Completion
Jul 2030 (estimated)
Last update
Jul 14, 2015

Study contacts

Jingting Jiang, M.D
Contact
wcpjjt@163.com
8651968870978

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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