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GR-1901

Alternative Names: GR-1901, GR 1901, GR1901
Latest Update: None
Latest Update Note: None

Product Description

Mechanisms of Action: CD123 Inhibitor,CD3 Inhibitor

Novel Mechanism: No

Modality: Bispecific Antibody

Route of Administration: Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Chongqing Zhixiang Jintai Biopharmaceutical Co., Ltd./Zhixiang (Shanghai) Pharmaceutical Technology Co., Ltd.
Company Location:
Company CEO:
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for GR-1901

Countries in Clinic: China

Active Clinical Trial Count: 1

Highest Development Phases

Phase 1: Acute Myeloid Leukemia

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
CTR20222311

P1

Recruiting

Acute Myeloid Leukemia

None

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