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Study of continuous vaccination with epitope peptides for unresectable pancreatic cancer

Study of continuous vaccination with epitope peptides for unresectable pancreatic cancer - Study of continuous vaccination with epitope peptides for unresectable pancreatic cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000009053
Enrollment
60
Registered
2012-10-09
Start date
2012-07-01
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

Unresectable Pancreatic Cancer

Interventions

multicenter HLA-blinded study: patients will be vaccinated biweekly with peptide vaccine

Sponsors

Yamaguchi University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Continuous administration the peptide vaccine for patients who dropped out the VENUS-PC study (2)ECOG Performance Status must be 0,1,2 or 3 (3)Measureable region evaluable according to the RECIST(ver.1.1) (4)Patient's condition is keeping within grade 3 hematological toxicity and within grade2 non-hematological toxicity . (CTCAE ver. 4.0) (5)Patients must have signed the consent form.

Exclusion criteria

Exclusion criteria: (1) Active double cancer (include asynchronous double cancer with disease-free duration <=1 year) except carcinoma in situ or intramucosal cancer. (2) Interstitial pneumonia or pulmonary fibrosis. (3) Severe nervous disorder or mental disorder. (4)History of myocardial infarction, severe unstable angina pectoris, CABG, congestive heart failure, cerebrovascular accident, pulmonary embolism, deep-vein thrombosis, or other severe thromboembolism within 12 months (5) Allergy for using epitope peptides (6)Unhealed traumatic lesion, including traumatic fracture. (7)Pregnant females or nursing mothers who can not stop lactation after the recruitment. (8)The subject who was determined by investigator that being not adequate to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Safety

Countries

Japan

Contacts

Public ContactNobuaki Suzuki

Yamaguchi University Hospital Department of Surgery II

geka2dm@yamaguchi-u.ac.jp0836-22-2264

Outcome results

None listed

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