Anti-PD-1/PD-L1 Combined With Anti-angiogenic Agents as First-line Therapy for Unresectable Hepatocellular Carcinoma: a Multicenter, Randomized, Open-label Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

This is a multicenter, randomized, open-label clinical study to evaluate the efficacy and safety of Adebrelimab plus Apatinib (cohort 1), or Adebrelimab plus Bevacizumab (cohort 2), or Camrelizumab plus Apatinib (cohort 3) as first-line treatment of unresectable HCC.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Locally advanced or metastatic and/or unresectable Hepatocellular Carcinoma (HCC)

• No prior systemic therapy for HCC. Previous use of herbal therapies/traditional Chinese medicines with anti-cancer activity included in the label is allowed.

• BCLC stage B or C, and not suitable for surgical or local therapy, or has progressed following surgical and/or local therapy

• At least one measurable lesion per RECIST v1.1

• ECOG Performance Status of 0 or 1

• Child-Pugh class of A5 to B7

• Adequate organ function

Locations
Other Locations
China
Beijing Cancer Hospital
RECRUITING
Beijing
Contact Information
Primary
Jun Zhou
Joelbmu@126.com
13366152815
Time Frame
Start Date: 2024-01-01
Estimated Completion Date: 2028-03-31
Participants
Target number of participants: 111
Treatments
Experimental: 1
Adebrelimab(1200mg iv q3w) plus Apatinib(250mg po qd)
Experimental: 2
Adebrelimab(1200mg iv q3w)plus Bevacizumab(15mg/kg iv q3w)
Experimental: 3
Camrelizumab (200mg iv q2w) plus Apatinib(250mg po qd)
Related Therapeutic Areas
Sponsors
Leads: Peking University Cancer Hospital & Institute

This content was sourced from clinicaltrials.gov