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Immunotherapy Using HLA-A24-restricted Survivin-derived Peptide Mixed with IFA and IFN-alpha for Patients with Oral Cancer (Phase I clinical study)

Immunotherapy Using HLA-A24-restricted Survivin-derived Peptide Mixed with IFA and IFN-alpha for Patients with Oral Cancer (Phase I clinical study) - Phase I Clinical Study of Survivin-2B Peptide Vaccine Therapy Mixed with IFA and IFN -alpha

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000000999
Enrollment
12
Registered
2008-01-28
Start date
2007-01-01
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

Advanced or recurrent oral cancer

Interventions

Vaccination of survivin-2B peptide 1.0mg mixed with IFA every 2 weeks, and IFN-alpha 1,500,000 IU twice a week. Vaccination of survivin-2B peptide 1.0mg mixed with IFA every 2 weeks, and IFN-alpha 3,0

Sponsors

Department of Oral Surgery, Sapporo Medical University School of Medicine
Lead Sponsor
Department of Pathology, Sapporo Medical University School of Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically proven oral cancer, 2) HLA class I-positive and survivin-positive in the cancerous lesions by immunohistochemistry, 3) HLA-A*2402 positive, 4) unresectable advanced or recurrent oral cancer, 5) from 20-90 years old, 6) ECOG performance status between 0 and 3.

Exclusion criteria

Exclusion criteria: 1) prior cancer therapy, such as chemotherapy, radiation therapy, steroid therapy, or other immunotherapy within the past 4 weeks, 2) presence of other cancers that might influence the prognosis, 3) immunodeficiency or a history of splenectomy, 4) severe cadiac insufficiency, acute infection, or hematopoietic failure, 5) ongoing brest-feeding, 6) unsuitability for the trial based on clinical judgement.

Design outcomes

Primary

MeasureTime frame
Toxicity

Secondary

MeasureTime frame
Clinical and immunological responses. Clinical responses are evaluated by RECIST criteria and change of tumor marker levels. Immunological responses are evaluated by DTH, tetramer staining and ELISPOT assay.

Countries

Japan

Contacts

Public ContactAkihiro Miyazaki

Sapporo Medical University Department of Oral Surgery

amiyazak@sapmed.ac.jp011-611-2111(ext.3578)

Outcome results

None listed

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