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A Single-Arm, Open-Label, Single-Center Study Evaluating the Efficacy and Safety of Low-Dose Radiotherapy Combined with Pemetplimab and Standard Therapy in Patients with Advanced Pancreatic Cancer

An open-label, single-center, single-arm study evaluating the efficacy and safety of low-dose radiotherapy combined with ptilimab and standard treatment in patients with advanced pancreatic cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118369
Enrollment
Unknown
Registered
2026-02-04
Start date
2025-12-15
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pancreatic cancer

Interventions

Therapy group:Low-dose radiotherapy (2Gy per dose, once a week) combined with ptilimab (200mg, intravenous drip, every 3 weeks) and standard chemotherapy regimens (AG or FOLFIRINOX)

Sponsors

Zhejiang Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Age: 18-75 years old, gender not limited. 2. The ECOG score ranges from 0 to 1. 3. Patients with malignant pancreatic tumors confirmed by histology or cytology; 4. Has not received previous treatment with PD-1 or PD-L1 inhibitors; 5. Have target lesions that can be radiotherapy-treated; 6. The subjects voluntarily joined this study and signed the informed consent form voluntarily.

Exclusion criteria

Exclusion criteria: 1. Has received radiotherapy in the past; 2. There are uncontrolled chronic infectious and non-infectious diseases, including but not limited to: heart failure that cannot be controlled by medication, hypertension that is difficult to control, etc. 3. Severe infections that are in the active stage or have poor clinical control; 4. Those with a history of abuse of psychotropic drugs and unable to quit, or patients with mental disorders; 5. Pregnant or lactating women, and patients with fertility who are unwilling or unable to take effective contraceptive measures; 6. The researcher judges other circumstances that may affect the progress of clinical research and the determination of research results.

Design outcomes

Primary

MeasureTime frame
Objective Response Rate;

Secondary

MeasureTime frame
Overall Survival;Progression-free survival;Disease control rate;

Countries

China

Contacts

Public ContactYang Liu

Zhejiang Provincial People's Hospital

yangliuqq2003@163.com+86 136 6660 1475

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026