Surufatinib and Serplulimab Combined With AG Regimen Compare With AG Regimen as Conversion Therapy for Patients With Locally Advanced Pancreatic Cancer (SAGE)

Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorSun Yat-sen University

About this trial

This is a Phase II Randomized Controlled PILOT clinical study. The purpose of this study is to explore the efficacy and safety of surufatinib and serplulimab in combination with albumin-paclitaxel and gemcitabine in the conversion therapy for patients with unresectable locally advanced pancreatic cancer. Furthermore, it compares the efficacy of surufatinib and serplulimab in combination with albumin-paclitaxel and gemcitabine to the albumin-paclitaxel and gemcitabine regimen in the conversion therapy for patients with unresectable locally advanced pancreatic cancer.

Eligibility criteria

Qualifiers

Written informed consent obtained from the patient prior to treatment.

Pathologically confirmed unresectable locally advanced pancreatic cancer, received no surgical therapy.

Age between 18 and 75 years at the time of study entry.

Eastern Cooperative Oncology Group (ECOG) performance status ≤ 1.

Disqualifiers

Participants diagnosed pancreatic cancer with distant metastases.

Participation in other antineoplastic drug clinical trials within 4 weeks prior to enrollment;

Previous systemic antitumor therapy (chemotherapy, radiation, targeted or immunoth, etc.).

Diagnosis of any second malignancy, except for adequately treated basal cell skin cancer or in situ carcinoma of the cervix uteri.

Trial design

Treatments tested in this trial

  • Surufatinib + Serplulimab+Albumin-paclitaxel + Gemcitabine
  • Albumin-paclitaxel + Gemcitabine

Treatment groups

50 Participants
are divided into 2 treatment groups

Sponsors and collaborators