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To explore the therapeutic effect of Nimotuzumab (trade name Taixinsheng) combined with PD1 and Tiggio combined with gemcitabine in locally advanced or metastatic pancreatic cancer

To explore the therapeutic effect of Nimotuzumab (trade name Taixinsheng) combined with PD1 and Tiggio combined with gemcitabine in locally advanced or metastatic pancreatic cancer

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100043290
Enrollment
Unknown
Registered
2021-02-09
Start date
2021-03-01
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

Pancreatic cancer

Interventions

experimental group:Nimotuzumab combined with PD-1, Tiggio, gemcitabine

Sponsors

Baotou Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. The first diagnosis of locally advanced or metastatic pancreatic cancer, and the need for puncture or biopsy is pathologically confirmed as pancreatic cancer, or pathological diagnosis cannot be obtained. After MDT discussion, the clinical diagnosis of pancreatic cancer is considered, with or without immunohistochemical examination of EGFR expression or Genetic testing of K-RAS mutations can be done. 2. Have not received special treatment such as radiotherapy and chemotherapy before. 3. Good physical condition: (1) ECOG score <= 2 points; (2) Pain control is good, pain numerical grading (NRS) evaluation value <= 3; (3) Biliary tract is unobstructed (such as obstructive jaundice, current bile duct stent implantation); (4) Stable weight. 4. Aged 18-80 years, voluntarily join the clinical trial and sign the informed consent form, with high compliance.

Exclusion criteria

Exclusion criteria: 1. Patients receiving any radiotherapy or chemotherapy or participating in other clinical trials; 2. Have a history of major surgery in the past 3 weeks; 3. Patients with severe underlying diseases: including severe cardiovascular and cerebrovascular diseases, abnormal liver, kidney, and respiratory functions; 4. Cannot tolerate the side effects of chemotherapy drugs. 5. Patients have poor compliance and cannot cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
Overall survival (OS);Progression-free survival (PFS);Objective response rate (ORR);Adverse reactions;

Countries

China

Contacts

Public ContactYa-Qin Tam, Jie Li

Baotou Cancer Hospital

tanyaqin@csco.ac.cn+86 15332726426

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026