Trial of Atezolizumab and Bevacizumab With SRF388 or Placebo in Patients With Hepatocellular Carcinoma

Part of paid clinical trials in Tucson, Arizona.

Sponsor
Coherus Oncology, Inc.
Study ID
NCT05359861
Phase
PHASE2
Status
Completed

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • SRF388 — DRUG
    SRF388 will be administered by intravenous injection (IV)
  • Atezolizumab — DRUG
    Azezolizumab will be administered by IV
  • Bevacizumab — DRUG
    Bevacizumab will be administered by IV
  • Placebo — DRUG
    Placebo will be administered by IV

Study Details

This is a Phase 2 trial composed of an open label Lead-In followed by a Randomized Phase designed to evaluate the efficacy and safety of SRF388 in combination with atezolizumab plus bevacizumab compared to placebo (inactive substance) in combination with atezolizumab plus bevacizumab in patients with first-line advanced or metastatic HCC.

Key Dates

Start date
Apr 12, 2022
Status verified
Nov 2025
Primary completion
Jun 30, 2025
Completion
Jul 8, 2025

Study Design

Enrollment
30 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Lead-In
    A minimum of 6 patients and up to 30 patients will be enrolled in an open-label Lead-In to assess the preliminary safety and tolerability of SRF388 with atezolizumab plus bevacizumab.
  • Experimental: Arm A: SRF388 in Combination with atezolizumab plus bevacizumab
    Patients randomized to Arm A will receive SRF388 with atezolizumab plus bevacizumab.
  • Experimental: Arm B: Placebo in combination with atezolizumab plus bevacizumab
    Patients randomized to Arm B will receive placebo with atezolizumab plus bevacizumab.

Primary Outcome Measure

Nature, frequency, and severity of adverse events (AEs) per NCI CTCAE version 5.0 or higher [ Time Frame: Up to 2 years ]

Locations (15)

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