Viewing Study NCT05918445



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Last Modification Date: 2024-10-26 @ 3:01 PM
Study NCT ID: NCT05918445
Status: RECRUITING
Last Update Posted: 2023-06-27
First Post: 2023-05-30

Brief Title: PM8002 in the Treatment of Patients With Advanced Solid Tumors
Sponsor: Biotheus Inc
Organization: Biotheus Inc

Study Overview

Official Title: Phase IbIIa Safety and Efficacy of PM8002 a Bispecific Antibody Targeting PD-L1 and VEGF-A as a Monotherapy in Patients With Advanced Solid Tumors
Status: RECRUITING
Status Verified Date: 2023-05
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 study is to characterize the safety tolerability pharmacokinetics PK immunogenicity pharmacodynamics PD and anti-tumor activity of PM8002 a PD-L1VEGF bispecific antibody as a single agent in adult subjects with advanced solid tumors
Detailed Description: None

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?: None