Ozmosi | BA-1301 Drug Profile
Drug Profile
Using advanced filters...
Advanced Search [+]

BA-1301

Alternative Names: BA-1301, BA 1301, BA1301
Clinical Status: Active
Latest Update: 2025-04-15
Latest Update Note: Clinical Trial Update

Product Description

BA1301 for injection is the Group's first novel ADC candidate that targets Claudin 18.2. It employs a site-specific conjugation technology to connect the cytotoxic payload with a monoclonal antibody that targets Claudin 18.2. This enables the cytotoxic payload to be directed to the tumor site through the targeting characteristics of the antibody. Such design reduces the toxic side effects of the cytotoxic payload, thus improving the therapeutic window, while retaining its tumor-killing effect. (Sourced from: https://www.boan-bio.com/en/uploads/2023-01/11/_1673420140_37ahis.pdf)

Mechanisms of Action: CLDN18.2 Inhibitor

Novel Mechanism: No

Modality: Antibody Drug Conjugate

Route of Administration: Intravenous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Company: Shandong Boan Biotechnology Co., Ltd
Company Location:
Company Founding Year: None
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for BA-1301

Countries in Clinic: China

Active Clinical Trial Count: 1

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Oncology Solid Tumor Unspecified

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT06927349

BA1301/CT-CHN-101

P1

Recruiting

Oncology Solid Tumor Unspecified

2026-06-30

2025-04-16

Primary Endpoints

Recent News Events

Date

Type

Title