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CN-201

Alternative Names: cn-201, cn 201, cn201
Latest Update: 2025-01-09
Latest Update Note: News Article

Product Description

CN-201 is being developed by Curon Biopharmaceutical (Shanghai) Co.,Ltd for the treatment of Acute Lymphoblastic Leukemia. (Sourced from: https://clinicaltrials.gov/ct2/show/NCT05579132?term=CN-201&draw=2&rank=1)

Mechanisms of Action: CD19 Inhibitor,CD3 Inhibitor

Novel Mechanism: No

Modality: Bispecific Antibody

Route of Administration: Oral,Intravenous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Merck
Company Location: KENILWORTH NJ 07033
Company CEO: Robert M. Davis
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for CN-201

Countries in Clinic: China

Active Clinical Trial Count: 3

Highest Development Phases

Phase 2: Acute Lymphoid Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma

Phase 1: Lymphoma, B-Cell|Lymphoma, Non-Hodgkin

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

CN201-101

P1

Recruiting

Lymphoma, B-Cell|Lymphoma, Non-Hodgkin

2025-06-01

CN201-103

P2

Recruiting

Acute Lymphoid Leukemia|Precursor Cell Lymphoblastic Leukemia-Lymphoma

2025-05-31

CTR20210029

P1

Not yet recruiting

Lymphoma, B-Cell|Lymphoma, Non-Hodgkin

None

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