Viewing Study NCT05864105


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Ignite Modification Date: 2025-12-26 @ 2:02 AM
Study NCT ID: NCT05864105
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-03-12
First Post: 2023-05-09
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: PM8002 in Combination With Chemotherapy as First Line Therapy in Hepatocellular Carcinoma
Sponsor: Biotheus Inc.
Organization:

Study Overview

Official Title: A Phase II Study to Evaluate the Efficacy, Safety and Pharmacokinetics of PM8002 Injection in Combination With Standard Chemotherapy as First Line Therapy in Unresectable Hepatocellular Carcinoma
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This is a multicenter, single-arm, open-label phase II study to evaluate the efficacy and safety of PM8002 in combination with chemotherapy in the first-line treatment of subjects with inoperable HCC.
Detailed Description: PM8002 is a Bispecific Antibody Targeting PD-L1 and VEGF.

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: