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Recruiting NA INTERVENTIONAL NCT06478927

Backline Treatment of Advanced Hepatocellular Carcinoma With Palbociclib

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Currently, it has been demonstrated that CDK4 is highly expressed in hepatocellular carcinoma patients and is significantly associated with poor prognosis in hepatocellular carcinoma patients. Palbociclib is the world's first marketed inhibitor of the cell cycle protein-dependent kinase CDK4/6, which is capable of blocking cell cycle progression and inhibiting tumor cell proliferation. However, current evidence for the use of CDK4/6 inhibitors in patients with advanced hepatocellular carcinoma cells remains lacking. This study used palbociclib backline treatment for patients with advanced hepatocellular carcinoma, aiming to further validate the potential role of CDK4/6 inhibitors in the treatment of patients with advanced hepatocellular carcinoma.

Detailed Description

This study was a single arm, prospective, open clinical study. Twenty-two patients with advanced hepatocellular carcinoma were enrolled in this study and were simultaneously treated and observed with palbociclib. The efficacy and safety of palbociclib in patients with advanced hepatocellular carcinoma were evaluated by PFS, ORR, DCR, OS, and AE.

Interventions

Name: Palbociclib capsules
Type: DRUG
Description: Palbociclib capsules, oral, 125 mg/dose, qd, take 3 weeks and then stop for 1 week, 28d for one treatment cycle until disease progression or intolerable toxicity.

Primary Outcomes

Measure: Progression-free survival (PFS)
TimeFrame: up to approximately 2 years.
Description: PFS is defned as the time from randomization untlthe date of first occurence of investigator assessed radiolbgical disease progression or death due to any cause,whichever came first.

Trial Information

NCT ID

NCT06478927

Status

Recruiting

Study Type

INTERVENTIONAL

Phases

NA

Sponsor

Henan Cancer Hospital

Last Updated

December 15, 2025