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Phase I clinical trial of WT1 peptide-based vaccine combined with Temozoromide for patients with malignant glioma.

Phase I clinical trial of WT1 peptide-based vaccine combined with Temozoromide for patients with malignant glioma. - Phase I clinical trial of WT1 peptide-based vaccine combined with Temozoromide for patients with malignant glioma.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003504
Enrollment
3
Registered
2010-04-19
Start date
2010-04-01
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

The patient is intradermally injected with 3 mg of the HLA-A*2402-restricted, modified 9-mer WT1 peptide (p235-243:CYTWNQMNL) emulsified with Montanide ISA51 adjuvant. The WT1 vaccination was schedule

Sponsors

Department of Cancer immunotherapy, Osaka University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Diagnosed as malignant glioma 2. Informed about his diagnosis 3. WT1 expression in malignant cells 4. HLA-A*2402 positive 5. Require no evaluable diaseas 6. Aged 15 and over, and 79 and under 7. Performance Status (ECOG) 0-2 8. Followed by Operation, Radiation and Temozolomide 9. Meet the following criteria for organ functions 1)Neutrophil more than 1,000/microliter, Platelet more than 50,000/microliter, Hemoglobin more than 8g/dl 2) Serum creatinine less than 2.0 mg/dL 3) Serum bilirubin less than 1.5 folds of the upper normal limit 4) Serum AST/GOT less than 4 folds of the upper normal limit 5) Serum Albumin more than 2.5g/dl 6) Arterial oxygen saturation more than 94% in room air 10. Pleural effusion, ascites and pericardial effusion are not detected or controlled. 11. Survival period is expected more than 3 months 12. Informed consent has been obtained

Exclusion criteria

Exclusion criteria: 1. There is deep-seated active infection. 2,3 There are severe complications including malignant hypertention, cardiac failure, liver cirrhosis, severe DM, severe lung fiblosis, active interstitial pneumonitis.Patients who have complications that are considered inappropriate for the trial. 4. Dependent on total parenteral nutrition(TPN) 5. There are other malignancies. 6. There are hematopoietic stem cell disorders such as myelodisplastic syndorome(MDS) and myeloproliferative disorders (MPD). 7. Post allogeneic hematopoietic stem cell transplantation 8. Pregnant or lactating woman 9. There is severe psychiatric disorder. 10. Responsible doctors judged the patient inappropriate for the trial

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
1. Relapse-free survival time 2. Immune response to WT1

Countries

Japan

Contacts

Public ContactAkihiro Tsuboi

Osaka University Graduate School of Medicine Department of Cancer Immunotherapy

tsuboi@cit.med.osaka-u.ac.jp06-6879-3676

Outcome results

None listed

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