AD HOC Trial: Artificial Intelligence-Based Drug Dosing In Hepatocellular Carcinoma
Eligible age
18–99 yrs
Accepts
All genders
Locations
1 state
Healthy volunteers
No
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About this study
This study will test the hypothesis that a novel combination of three drugs (sorafenib, sonidegib, and irinotecan), in conjunction with individually optimized doses, can be safely administered and lead to improved clinical outcomes in patients with hepatocellular carcinoma compared to standard of care. The main objective of this study is to establish safe dose ranges for the coadministration of sorafenib, sonidegib, and irinotecan in patients with hepatocellular carcinoma. Furthermore, we will collect data to inform the application of an artificial intelligence/computational approach to individual dosing of combination chemotherapy. Individualization of dosing will be achieved by using Phenotypic Personalized Medicine (PPM) to maximize treatment efficacy in patients with hepatocellular carcinoma, while minimizing toxicity. Drug efficacy will be assessed by measuring plasma circulating tumor DNA (ctDNA). Toxicity will be assessed by quantitating organ injury and patient tolerability. Recommended dosing for future studies will be based on the totality of the data.
Sponsor: University of Florida
You may qualify if…
- ✓ Adults ≥ eighteen years of age
- ✓ Biopsy proven advanced-stage hepatocellular carcinoma (HCC), as confirmed by pathological analysis; or confirmation of HCC from a LI-RADS 5 imaging score.
- ✓ Not eligible for, or had disease progression after, surgical or locoregional therapies when these treatments are intended as sole, definitive therapy aimed at curing the disease, rather than as part of a combination therapy approach
- ✓ Subjects must not have more than one active malignancy at the time of enrollment (Subjects with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen \[as determined by the treating physician and approved by the PI\] may be included).
- ✓ Eastern Cooperative Oncology Group (ECOG) performance status score of 2 or less.
- ✓ Child-Pugh liver function class A
- ✓ Life expectancy of 12 weeks or more
- ✓ At least one target lesion that could be measured in one dimension, according to the Response Evaluation Criteria in Solid Tumors (mRECIST).
You may not qualify if…
- ✕ Subjects of childbearing potential who are unwilling or unable to use an acceptable method to avoid pregnancy for the entire study period and for at least 20 months after the last dose of study drug.
- ✕ Subjects who are pregnant or breastfeeding.
- ✕ History of any other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of protocol therapy or that might affect the interpretation of the results of the study or that puts the subject at high risk for treatment complications or protocol noncompliance, in the opinion of the treating physician.
- ✕ Prisoners or subjects who are involuntarily incarcerated, or subjects who are compulsorily detained for treatment of either a psychiatric or physical illness.
- ✕ Inability to follow up with treatment center for up to 12 weeks after enrollment
- ✕ Anticipated major surgery during the time of planned study
- ✕ Homozygosity for UGT1A1\*28 via genotyping
Where it's recruiting
Gainesville
Source: ClinicalTrials.gov · NCT05669339 · last updated 2026-06-04