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Trials
To Evaluate Safety and Efficacy of FB-1603 in Hepatocellular Carcinoma Patient Receiving Transarterial Chemoembolization

trialsTrialRecruiting

To Evaluate Safety and Efficacy of FB-1603 in Hepatocellular Carcinoma Patient Receiving Transarterial Chemoembolization

A phase 1/2 trial of Placebo in hepatocellular carcinoma, run by Febico Biomedical Corp., now recruiting.

Also called: FECHT

Overview Connected2

Overview

To Evaluate Safety and Efficacy of FB-1603 in Hepatocellular Carcinoma Patient Receiving Transarterial Chemoembolization is a phase 1/2 interventional study registered as NCT06478719 by Febico Biomedical Corp., with 120 participants planned, started 2024-06-24 and due to reach its primary completion in 2028-06-07. Interventions recorded: Placebo and FB-1603.

Setting

A Phase I/II Randomized, Double-blinded Study of FB-1603 to Evaluate the Safety and Efficacy in Hepatocellular Carcinoma Patients Receiving Transarterial Chemoembolization (FECHT Trial)

Phase

Phase 1/2

Sponsor

Febico Biomedical Corp.

Registry

Started

2024-06-24

Enrolled

120 enrolled

Connected

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cancers

Hepatocellular carcinoma Intermediate hepatocellular carcinoma (BCLC B)

Evidence strength18/100 · Preliminary

How much and what kind of evidence, not how big the benefit. Click for the breakdown.

Phase 1/2+8
120 enrolled+10
No structured primary endpoint0
Result: recruiting0
No independent replication recorded0

Formula disclosed on the evidence page.

ProvenanceLast edited 2026-09-18 · Jude Gomila · Trial acronyms for registry records · diff · file

Sources & links

ClinicalTrials.gov NCT06478719

Data

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Hepatocellular carcinoma
Intermediate hepatocellular carcinoma (BCLC B)

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