HRS-4642 in Combination With AG for Neoadjuvant and Adjuvant Treatment of Pancreatic Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-80
SponsorRuijin Hospital

About this trial

To evaluate the safety and efficacy of HRS-4642 in Combination With AG for Neoadjuvant and Adjuvant Treatment of Pancreatic Cancer

Eligibility criteria

Qualifiers

Age: ≥18 and ≤80 years old, male or female;

Pathologically or cytologically confirmed ductal adenocarcinoma of the pancreas; and subjects must have at least one measurable lesion as defined by RECIST v1.1;

Imaging evaluation met the NCCN guidelines definition of resectable pancreatic cancer (including high-risk resectable) and borderline resectable pancreatic cancer.

Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1;

Disqualifiers

Previously received any anti-tumor therapy;

the presence of distant metastatic lesions diagnosed by imaging;

Known hypersensitivity to the study drug or any of its components;

previous or concurrent other malignant tumors;

Trial design

Treatments tested in this trial

  • HRS-4642+AG

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators

Ruijin Hospital

Lead sponsor

Jiangsu HengRui Medicine Co., Ltd.

Collaborator