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Bortezomib in Intrahepatic Cholangiocellular Carcinoma

Use of Bortezomib to treat Cholangiocellular Carcinoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035916
Enrollment
Unknown
Registered
2020-08-20
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-24

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

Conditions

cholangiocarcinoma

Interventions

GB:gemcitabine+bortezomib
control:GP/GEMOX

Sponsors

Oriental Hepatobiliary Surgery Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Pathological or cytological diagnosis of cholangiocarcinoma; 2. Measurable evaluation according to RECIST standard; 3. Aged 18 to 75 years; 4. WHO/ECOG physical strength score is 0-2; 5. Evaluation as progress according to RECIST criteria; 6. Blood routine examination: white blood cell > 3.0 x10^9/L, platelet > 100 x10^9/L; 7. Adequate liver reserve (bilirubin 60 ml/min; Creatinine < 120 mol/L); 9. Centerless dysfunction, chest pain (not medically controllable).No myocardial infarction occurred within 12 months prior to study initiation; 10. signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Secondary malignant tumor or other tumor accompanied within 3 years prior to the start of the study; 2. There is a brain or meningeal metastasis; 3. Contraindication of bortezomib; 4. Chronic diarrhea or colorectal inflammatory conditions, or untreated obstructions or subobstructions affecting systemic administration; 5. Active infections or other severe infections that may prevent the patient from receiving the planned treatment.For example, chronic, uncontrolled cholangitis that destroys branches of the biliary tract and cholangitis that has occurred twice or more in the past six months.Other active or uncontrolled infections, cirrhosis, or chronic active hepatitis should also be excluded; 6. Cardiac insufficiency, unstable angina pectoris, congestive heart failure, failure myocardial infarction and severe uncontrolled arrhythmia within 6 months before enrollment; 7. Participated in other clinical trials for research; 8. Pregnant and lactating women; 9. Individuals undergoing calibration monitoring or monitoring.

Design outcomes

Primary

MeasureTime frame
survival time;

Countries

China

Contacts

Public ContactHongyang Wang

Oriental Hepatobiliary Surgery Hospital

hywangk@vip.sina.com+86 021 81875361

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 29, 2026