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Clinical Trials/JPRN-UMIN000039854
JPRN-UMIN000039854
Completed
未知

Phase 1/2 clinical trial of the intratumoral administration of oncolytic virus for unresectable pancreatic cancer - Intratumoral administration of oncolytic virus for unresectable pancreatic cancer

Kagoshima University0 sites24 target enrollmentApril 1, 2020

Overview

Phase
未知
Intervention
Not specified
Conditions
Pancreatic cancer
Sponsor
Kagoshima University
Enrollment
24
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 1, 2020
End Date
March 31, 2022
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Patients with the following complications: Severe heart disease, severe respiratory disease, severe digestive disease, severe liver disease, uncontrolled diabetes, and infection requiring continuous treatment 2\) Patients with a history of penicillin or allergy to pigs or cattle (including milk). 3\) Patients with a disease that requires the administration of systemic immunosuppressants or steroids. 4\) For patients judged to have failed the primary therapy of radiation or chemoradiation, the interval after the therapy is \<\= 1 month (patients are still eligible if the reason for primary therapy failure is progression of pancreatic cancer). 5\) Patients with other currently active cancers (patients are still eligible if the other cancers are basal cell carcinoma, carcinoma in situ, superficial bladder cancer, or malignancies without metastasis or recurrence for more than five years and have been treated appropriately) 6\) Patients with an uncontrollable fever or pain due to the tumor. 7\) Patients with a history of gastroduodenal surgery or gastroduodenal stricture. 8\) Patients who are pregnant, breast\-feeding, or have a positive pregnancy test within one year after menopause. 9\) Patients who received any other unapproved drug within four weeks before giving their consent. 10\) Patients deemed inappropriate to include in the trial by the investigator.

Outcomes

Primary Outcomes

Not specified

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