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Vurolenatide

Alternative Names: Vurolenatide, nm-002, nm002, nm 002
Latest Update: 2022-12-20
Latest Update Note: Clinical Trial Update

Product Description

a long-acting injectable GLP-1 analogue for short bowel syndrome

Mechanisms of Action: GLP-1 Agonist

Novel Mechanism: No

Modality: Fusion Protein

Route of Administration: Subcutaneous

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: 9 Meters Biopharma
Company Location: RALEIGH NC 27615
Company CEO: John Temperato
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Vurolenatide

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Short Bowel Syndrome

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

NMSBS01-002

P2

Terminated

Short Bowel Syndrome

2022-08-05

24%

NMSBS01-001

P2

Unknown status

Short Bowel Syndrome

2020-12-11

24%

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