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NCT06389552
Long-term Observational Study to Evaluate the DFS and OS of Adjuvant FOLFIRINOX Regimen in Pancreatic Cancer Patients
Conditions: Adjuvant Chemotherapy
Sex: All
Ages: 19 Years – N/A
Healthy volunteers: No
Enrollment: 36
Sponsor: HK inno.N Corporation
Location: Seoul ST. Mary's Hospital Seoul
Summary
This study is designed to evaluate the safety and efficacy of adjuvant FOLFIRINOX regimen in pancreatic cancer patients after curative surgery.
Eligibility Criteria
Inclusion Criteria:
* Age over 19 at the time of obtaining the informed consent form
* Planning to FOLFIRINOX as adjuvant therapy after pancreatic cancer surgery
* ECOG 0 or 1
* Scheduled to RO or R1 resection
* Organ function capable of chemotherapy
Exclusion Criteria:
* FOLFIRINOX contraindications among the drug approval requirements
* Palliative Therapy
* Experienced toxic reactions or Hypersensitivity reactions of FOLFIRINOX
Source: ClinicalTrials.gov (NCT06389552). StuddyBuddy aggregates publicly available trial information.