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RO-6958688

Alternative Names: ro-6958688, ro6958688, ro 6958688
Latest Update: 2024-06-03
Latest Update Note: Clinical Trial Update

Product Description

A Novel T-cell Bispecific Antibody That Targets the Human Carcinoembryonic Antigen (CEA) on Tumor Cells and CD3 on T Cells (Sourced from: https://clinicaltrials.gov/ct2/show/NCT02324257)

Mechanisms of Action: CEA Binder,CD3 Binder

Novel Mechanism: Yes

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: Hoffmann-La Roche
Company Location: BASEL SWITZERLAND V8
Company CEO: Severin Schwan
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for RO-6958688

Countries in Clinic: Australia, France, Israel, Korea, Spain, Taiwan, United Kingdom, United States

Active Clinical Trial Count: 1

Highest Development Phases

Phase 2: Non-Small-Cell Lung Cancer

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Morpheus Lung

P2

Active, not recruiting

Non-Small-Cell Lung Cancer

2025-09-30

45%

Morpheus Lung

P2

Active, not recruiting

Non-Small-Cell Lung Cancer

2025-09-30

45%

Morpheus Lung

P2

Active, not recruiting

Non-Small-Cell Lung Cancer

2025-09-30

45%

Morpheus Lung

P2

Active, not recruiting

Non-Small-Cell Lung Cancer

2025-09-30

45%

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