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Glioma-immunotherapy with fusions of dendritic and glioma cells.

Immunotherapy with fusions of glioma cells, glioma initiating cells,and dendritic cells for patients with malignant glioma - GLIM-FDG

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTc030190122
Enrollment
50
Registered
2019-10-23
Start date
2016-09-03
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Malignant glioma

Interventions

DCs are mixed with lethally irradiated (300 Gy) glioma cells. Fusion is started by polyethylene glycol, and is stopped by stepwise additionof serum-free RPMI medium. The fusion cells (FC) are cultured

Sponsors

Akasaki Yasuharu
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)A patient who requires a sugery against brain tumor regarded as malignant glioma (WHO grade 2 or 3 or 4) on an imaging examnination(CT or MRI) of brain. 2) A patient who is 15 year to under 75 year, at the time of entry for this trial. 3)A patient who is able to undergo a collection of peripheral blood mononuclear cells(PBMC) using an apehresis system. 4)A patient who preserves function of major organs, such as hart, liver, kidny, and bone marrow etc, with satisfying the standerds below. 5)A patient who is estimated 2 or less the Performance status(PS) grade. 6)A patient who is expected to be alive for 3 months and more. 7)A patient who has no other cancer.

Exclusion criteria

Exclusion criteria: 1) A patient who has an allergy against biological products 2) A patient who has past or current history of autoimmune disease 3) A patient who is a HBV carrier, testing positive for antibodies of HCV, HIV, and HTLV. 4) A patient who has an immune deficiency for some reasons. 5) A patient who is taking steroids for long time, and is hard to stop them. 6) A patient who has a sever infection. 7) A patient who has a sever respiratory disease(Hugh-Jones Class 3 or more). 8) A patient who has a sever hart disease(NYHA Class 3 or more). 9) A patient who has uncontrolable diabetes. 10) A pregnant or possibility of pregnant woman, and a breastfeeder. 11) A patient who has been registered in other clinical trial. 12) A patient who is judged as unsuitable subject for this trial in some reasons.

Design outcomes

Primary

MeasureTime frame
1) A group of patients with newly diagnosed grade 4 glioma (N-G4): 2-year ovaerall survival (OS) ratio 2) A group of patients with newly diagnosed grade 2/3 glioma (N-G2/3): 3-year OS ratio 3) A group of patients with recurrent glioma (R): 1-year OS ratio # An overall survival time is defined as the time from the date of entry until the date of death.

Secondary

MeasureTime frame
1) A group of N-GIV: 1-year progression free survival (PFS) ratio 2) A group of N-G2/3 glioma: 2-year PFS ratio 3) A group of R: 6-month PFS ratio # A progression free survival time is defined as the time from the date of entry until the first documented progression in MRI using The Revised Assessment in Neuro-Oncology, or the the first documented progression in the clinical symptom.

Countries

Japan

Contacts

Public ContactMutsunori Murahashi

The Jikei University

murahashi@jikei.ac.jp+81-3-3433-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026