Skip to main content
Clinical Trials/JPRN-UMIN000029428
JPRN-UMIN000029428
Completed
Phase 1

Phase I investigator initiated clinical trial using a novel WT1 peptide vaccine for patients with metastatic pancreatic cancer - Phase I clinical trial using WT1 peptide vaccine for patients with metastatic pancreatic cancer.

Wakayama Medical University0 sites6 target enrollmentOctober 10, 2017

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
pancreatic cancer
Sponsor
Wakayama Medical University
Enrollment
6
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 10, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • (1\) Interstitial pneumonia or pulmonary fibrosis (2\) Comfirmed or suspicious brain metastatis (3\) Pleural effusion, ascites fluid, or pericardial fluid in need of drainage. (4\) Severe infection or being suspected (5\) Positive for serum HBs Ag or HBV\-DNA (6\) Positive for anti\-HCV or anti\-HIV ab (7\) Patients who require systemic administration of Corticosteroid (8\) Prior DSP\-7888, other WT1 peptides, or WT1 immunotherapy (9\) History of severe allergies to oil products (10\) History of hypersensitivity to paclitaxel, albumin, and gemcitabine (11\) Active another cancer to define the pprognosis (12\) Severe mental disorders (13\) Peripheral neuropathy \>\=CTCAE ver.4\.0JCOG Grade 2 (14\) Uncontrolled heart disease, pulmonary disease, kidney disease, or liver disease. (15\)Myocardial infarction, severe unstable angina pectoris, colonary or peripheral artery bypass, congestive heart failure, cerebrovascular disease, pulmonary embolization, deep vein thrombosis or other severe thromboembolism within 12 months (16\) Bleeding tendency or severe coagulation disorder (17\) Current participation in other clinical trials. (18\) Pregnant females or nursing mothers who can not stop lactation after the recruitment. Patients or partners, who don't attempt to doing contraception during the study period. (19\) The subject who was determined by investigator that being not adequate to participate in the trial.

Outcomes

Primary Outcomes

Not specified

Similar Trials