Ozmosi | LY-2405319 Drug Profile
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LY-2405319

Alternative Names: ly-2405319, ly2405319, ly 2405319
Clinical Status: Inactive
Latest Update: 2023-08-04
Latest Update Note: PubMed Publication

Product Description

an Engineered FGF21 Variant

Mechanisms of Action: FGF21 Analogue

Novel Mechanism: Yes

Modality: Peptide/Protein

Route of Administration: Subcutaneous

FDA Designation: *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Eli Lilly
Company Location: INDIANAPOLIS IN 46285
Company CEO: David A. Ricks
Additional Commercial Interests: None

Clinical Description

Countries in Clinic:

Active Clinical Trial Count:

Recent & Upcoming Milestones

Highest Development Phases

Phase 1: Type 2 Diabetes

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT01869959

I1K-MC-GLUG

P1

Completed

Type 2 Diabetes

2009-06-01

2019-03-19

Treatments

NCT00481117

I1K-MC-GLUD

P1

Completed

Type 2 Diabetes

None

2019-03-21

Treatments