Recruiting NCT06726161
Study of the Theranostic Pair RYZ811 (Diagnostic) and RYZ801 (Therapeutic) to Identify and Treat Subjects With GPC3+ (Glypican-3) Unresectable HCC
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: RYZ811, RYZ801.
- Who it may be relevant to
- Registry conditions: Hepatocellular Carcinoma (HCC). Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Phase 1/2 Randomized, Controlled, Open-label Trial of Theranostic Pair RYZ811 (Diagnostic) and RYZ801 (Therapeutic) to Identify and Treat Subjects With GPC3+ Unresectable Hepatocellular Carcinoma (HCC)
Overview
Phase 1/2 randomized, controlled, open-label trial of theranostic pair RYZ811 (diagnostic) and RYZ801 (therapeutic) to identify and treat subjects with GPC3+ unresectable hepatocellular carcinoma (HCC)
Interventions
- Diagnostic test RYZ811
Ga-68 - Drug RYZ801
Ac-225
Primary outcome measures
- Therapeutic - RYZ801 [Time frame: Rate of DLTs during the first 42 days of study treatment]
- Therapeutic - RYZ801 [Time frame: From enrollment for up to three months or study discontinuation, whichever occurs first.]
- Therapeutic - RYZ801 [Time frame: From enrollment to 3months after randomization or study discontinuation, whichever occurs first.]
- Diagnostic - RYZ811 [Time frame: Baseline, pre-injection and post-injection up to 6 days post injection.]
- Diagnostic - RYZ811 [Time frame: RYZ811 biodistribution to be assessed on the day of injection.]
Eligibility criteria
Inclusion criteria
- Age of at least 18 years at the time of signing the informed consent form (ICF)
- Histologically/cytologically confirmed diagnosis of HCC.
- Barcelona Clinic Liver Cancer (BCLC) Stage C or BCLC Stage B not amenable to locoregional therapy
- Child-Pugh A
- Eastern Cooperative Oncology Group (ECOG) performance status (PS 0-1)
- Disease progression after 1 prior systemic therapy for unresectable HCC
- Measurable disease per RECIST v1.1
- Sufficient renal function
- Adequate hematologic function
- Adequate hepatic function
- The subject must have recovered from toxicities related to prior treatments to ≤Grade 1, unless clinically nonsignificant and/or stable on supportive therapy
- If HBV or HCV infection: Disease managed per local practice; antiviral treatment is allowed.
- Gastric or esophageal varices previously treated with endoscopic therapy according to institutional standards are permitted if no clinically significant bleeding
- For women of childbearing potential (WOCBP):
- Negative serum pregnancy test within 48 hours prior to the first dose of RYZ811
- Agreement to use barrier contraception and a second form of highly effective contraception
- For sexually active males:
- Must use a condom during intercourse
- Male subjects whose sexual partners are WOCBP must also agree to use a second form of highly effective contraception
- A condom is required to be used also by vasectomized men
Exclusion criteria
- Subjects with fibrolamellar carcinoma, sarcomatoid HCC or combined hepatocellular cholangiocarcinoma
- Prior liver transplantation
- Known hypersensitivity to 68Ga, 225Ac or any of the excipients of RYZ811 or RYZ801
- Portal vein tumor thrombosis classified as Vp4
- Documented hepatic encephalopathy within 6 months of enrollment
- Clinically meaningful ascites within 6 months of enrollment
- Prior EBRT to the liver within 12 weeks prior to receiving RYZ811
- Prior liver radioembolization
- Previously treated central nervous system (CNS) metastasis without recovery from acute side effects
- Documented history of idiopathic pulmonary fibrosis (IPF), interstitial lung disease (ILD) or pneumonitis
- Uncontrolled significant intercurrent illness including, but not limited to:
- QT interval corrected for heart rate using Fridericia's formula (QTcF) >470 ms
- Hemoglobin A1c (Hgb A1c) ≥8%
- Uncontrolled hypertension
- Dose Expansion only: Prior treatment with lenvatinib is exclusionary
- Significant cardiovascular disease or heart failure
- History of clinically significant bleeding
- Prior participation in any interventional clinical study
- Current somatic or psychiatric disease/condition that may interfere with the objectives and assessments of the study
- Have a history of primary malignancy within the past 3 years other than (1) HCC, (2) adequately treated carcinoma in situ or non-melanoma carcinoma of the skin, (3) any other curatively treated malignancy that is not expected to require treatment for recurrence during participation in the study, or (4) an untreated cancer on active surveillance that may not affect the subject's survival status for >3 years
- Subject requires other treatment that in the opinion of the Investigator would be more appropriate than what is offered in the study
- Pregnancy or breastfeeding
Note: Additional criteria may apply and will be assessed by the study site
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Sequential
- Masking
- Single blind
- Primary purpose
- Treatment
Study locations
United States · 13 centers
- Research Facility — Birmingham
- Research Facility — Phoenix
- Research Facility — Tucson
- Research Facility — Orange
- Research Facility — Jacksonville
- Research Facility — Lexington
- Research Facility — Baltimore
- Research Facility — Rochester
- … and 5 more centers
Identifiers
NCT: NCT06726161 · RYZ801-101