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NCT06891742

Phase I Study of OriC902 in Treatment of Advanced HCC

Recruiting now Phase 1 Last updated 24 March 2025
What this trial tests

Phase 1 trial testing OriC902 in HCC in 44 participants. Currently enrolling.

Timeline
24 February 2025
Primary endpoint
31 December 2027
31 March 2028

Quick facts

Lead sponsorPeking University
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment44
Start date24 February 2025
Primary completion31 December 2027
Estimated completion31 March 2028
Sites2 locations across China

Drugs / interventions tested

Conditions studied

Sponsor

Peking University

Who can join

Adults 18 to 75, any sex, with HCC. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a Phase I clinical study evaluating the safety, pharmacokinetics, and initial efficacy of a GPC3-targeted chimeric antigen receptor autologous T cell injection (OriC902) in GPC3-positive advanced hepatocellular carcinoma (HCC) subjects

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HCC

Currently open trials in the same condition.

Other Peking University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06891742.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing