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Jiedu Granule in Advanced Hepatocellular Carcinoma as Second-line Treatment After Failure of Sorafenib

Jiedu Granule in Advanced Hepatocellular Carcinoma as Second-line Treatment After Failure of Sorafenib

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800017171
Enrollment
Unknown
Registered
2018-07-17
Start date
2018-08-01
Completion date
Unknown
Last updated
2019-11-18

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

Conditions

Hepatocellular carcinoma

Interventions

Case series:Jiedu Granule

Sponsors

Changhai Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Male or female aged older than 18 years; 2. Histologically diagnosed HCC, OR clinically diagnosed HCC; 3. Documented progression with or intolerance to first-line sorafenib monotherapy and sorafenib-based combination as first-line therapy for advanced HCC; 4. For patients who receive first-line sorafenib monotherapy or sorafenib-based combination, patients must have received at least 14 days of sorafenib treatment with the lowest dosage of 400 mg per day; 5. Stage is C according to the BCLC staging classification; 6. ECOG performance status 0 or 1.

Exclusion criteria

Exclusion criteria: 1. Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment; 2. Local treatment including radiotherapy (except palliative radiotherapy), percutaneous ethanol injection, radiofrequency ablation, transarterial embolization, or cryotherapy administered within 4 weeks prior to enrollment; 3. Had a solid organ transplant; 4. Presence of brain or leptomeningeal metastases; 5. Has had esophageal or gastric variceal bleeding within the last 6 months; 6. the researchers consider those who were not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Overall survival;Objective Response Rate;

Secondary

MeasureTime frame
Progression-free survival;Disease Control Rate;

Countries

China

Contacts

Public ContactXiaofeng Zhai

Changhai Hospital

zhxfch@163.com+86 021 31161950

Outcome results

None listed

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