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Clinical Trials in China / NCT07272109
Starting soon Phase 3

Active Anti-diabetic Treatment Plus Chemotherapy for Pancreatic Cancer Related Diabetes

NCT07272109 · tracked via the Priya Life Science China tracker
Sponsor
Fudan University
Phase
Phase 3
Started
2026-01-01
Last updated
2025-12-15

Condition(s) studied

Pancreatic Cancer

Investigational drug(s) / intervention(s)

Nab-paclitaxel →Gemcitabine (1000 mg/m2) →Anti-DiabeticsActive treatment and monitoring

Nab-paclitaxel: 120 mg per square meter of body-surface area on days 1, 8, and 15 every 4 weeks

Gemcitabine (1000 mg/m2): (1000 mg per square meter) on days 1, 8, and 15 every 4 weeks

Anti-Diabetics: Metformin, insulin or other anti-diabetic treatments

Active treatment and monitoring: Attend follow-ups at designated endocrinology clinics, with proactive inquiry about hypoglycemic measures and medication implementation.

Study summary

The purpose of this study is to evaluate the efficacy of anti-diabetic treatment on improving the overall survival for metastatic pancreatic cancer patients complicated by diabetes receiving gemcitabine and nab-paclitaxel chemotherapy.

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * Ability to understand and the willingness to sign a written informed consent document. * Age ≥ 18 years and ≤ 80 years. * Eastern Cooperative Oncology Group (ECOG) performance status 0-2. * Histologically or cytologically confirmed metastatic pancreas adenocarcinoma. * History of diabetes mellitus, or newly diagnosed diabetes meeting the diagnostic criteria of the American Diabetes Association. * The expected survival ≥ 3 months. * Able to comply with study visit schedules and other protocol requirements. Exclusion Criteria: * • History of other malignancies requiring anti-cancer therapy within 2 years prior to enrollment (except treated Stage I prostate cancer, in situ cervical cancer, in situ breast cancer, etc.); * Non-primary pancreatic cancer patients; * Digestive tract inflammation, including biliary tract infection, gastrointestinal infection, pancreatitis, etc.; * Pregnant or lactating women.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Shanghai Cancer Center Shanghai China

More Fudan University trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07272109 on ClinicalTrials.gov ↗ ← All trials in China