ClinConnect ClinConnect Logo
Search / Trial NCT00638612

AdV-tk Therapy With Surgery and Chemoradiation for Pancreas Cancer (PaTK01)

Launched by CANDEL THERAPEUTICS, INC. · Mar 13, 2008

Trial Information

Current as of October 08, 2025

Completed

Keywords

Immunotherapy Gene Therapy Cytotoxicity Tumor Vaccine Radiation Surgery Chemoradiation

ClinConnect Summary

The AdV-tk vector is injected into the tumor or tumor bed at the time of biopsy or standard tumor surgery after which valacyclovir pills are taken for 14 days. Two courses of AdV-tk, each followed by valacyclovir, are given as adjuvant to standard of care therapies (surgery and/or chemoradiation) which have been shown to work cooperatively with AdV-tk to kill tumor cells. Arm A is for resectable tumors in which the first course is given prior to surgery and the second is at the time of surgery. Arm B is for locally advanced disease in which both AdV-tk injections are administered by needle ...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Must have presumed pancreatic adenocarcinoma based on clinical and radiologic evaluation with identifiable tumor accessible for injection (pathologic diagnosis of pancreatic adenocarcinoma must be made prior to AdV-tk injection
  • For Arm A, resectable disease. Arm B for locally advanced disease has completed accrual.
  • Performance status must be ECOG 0-2
  • SGOT (AST)\<3x upper limit of normal
  • Serum creatinine\<2mg/dl and calculated creatinine clearance \>10ml/min
  • Platelets\>100,000/mm3 and WBC\>3000/mm3 and ANC\>1500/mm3
  • Must give study specific informed consent prior to enrollment
  • Exclusion Criteria:
  • Primary hepatic dysfunction including active hepatitis but not to exclude patients due to obstructive jaundice. If obstructive jaundice is clinically significant, bilirubin should be stable or decreasing prior to enrollment.
  • Evidence of clinically significant pancreatitis as determined by the investigator.
  • Patients on corticosteroids or other immunosuppressive drugs
  • Known HIV+ patients
  • Patients with acute infections (viral, bacterial or fungal infections requiring therapy)
  • Pregnant or breast-feeding patients. Female patients of childbearing age must have negative serum or urine pregnancy test within 1 week of beginning therapy
  • Evidence of distant metastatic disease at the time of enrollment or other malignancy (except squamous or basal cell skin cancers) and no prior abdominal radiation therapy or prior treatment for pancreatic cancer
  • Other serious co-morbid illness or compromised organ function

About Candel Therapeutics, Inc.

Candel Therapeutics, Inc. is a clinical-stage biotechnology company dedicated to advancing innovative therapies for patients with cancer. The company specializes in developing oncolytic virus therapies, harnessing the power of engineered viruses to selectively target and destroy cancer cells while stimulating the immune system. With a focus on both solid tumors and hematological malignancies, Candel Therapeutics is committed to transforming the treatment landscape through its robust pipeline of clinical programs and strategic collaborations. The company's mission is to improve patient outcomes and quality of life by delivering safe and effective therapeutic options in oncology.

Locations

Duarte, California, United States

Columbus, Ohio, United States

La Jolla, California, United States

Patients applied

0 patients applied

Trial Officials

Mark Bloomston, MD

Principal Investigator

Ohio State University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials