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Efficacy and safety of tiggol combined with amlotinib hydrochloride in the treatment of metastatic pancreatic cancer

Efficacy and safety of tiggol combined with amlotinib hydrochloride in the treatment of metastatic pancreatic cancer

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032669
Enrollment
Unknown
Registered
2020-05-06
Start date
2020-06-01
Completion date
Unknown
Last updated
2020-05-11

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

Conditions

Pancreatic cancer

Interventions

Case series:Tiggio 40-60mg/d amlotinib 8mg/d

Sponsors

Cancer Hospital Affiliated to Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years old; 2. Patients with ECoG score =1.5x10^9/L; (2) Platelet >=80x10^9/L; (3) Hemoglobin >=80g/L; (4) Creatinine <=1.5 ULN; (5) Child liver function grade A or B.

Exclusion criteria

Exclusion criteria: 1. Patients who are allergic to androtinib or tegio; 2. Patients with various factors affecting oral medication (including dysphagia, chronic diarrhea, intestinal obstruction, etc.); 3. Patients with abnormal coagulation (INR > 1.5, APTT > ULN); 4. Patients with severe heart disease include: (1) Angina pectoris; (2) Arrhythmias that need to be treated with drugs or have clinical significance (including significant abnormalities in baseline ECG, QTc interval > 450 ms in men and 470 MS in women); (3) Myocardial infarction; (4) Heart failure; (5) Left ventricular ejection fraction (LVEF) 140 mmHg, diastolic blood pressure > 90 mmHg) and patients with positive urine protein were also included; 6. Patients with other serious medical diseases, including cerebrovascular disease, uncontrolled infection, active peptic ulcer, etc; 7. Patients with central nervous system metastasis; 8. Pregnant and lactating women; 9. Patients who have been diagnosed with other tumors in the past 5 years; 10. Patients with mental illness or a history of psychoactive substance abuse; 11. The subjects that the researchers think should not participate in the experiment;

Design outcomes

Primary

MeasureTime frame
OS;

Countries

China

Contacts

Public ContactXiaoli Liao

Cancer Hospital Affiliated to Guangxi Medical University

nllxl@163.com+86 13978627806

Outcome results

None listed

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