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Lemuteporfin

Alternative Names: lemuteporfin
Latest Update: 2013-07-25
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: No Mechanism

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Topical,Injection

FDA Designation: None *

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
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Lemuteporfin

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 2: Lower Urinary Tract Symptoms|Prostatic Hyperplasia|Healthy Volunteers

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success
LTS ACN-05

P2

Completed

Healthy Volunteers

2013-03-01

32%
PLUS

P2

Terminated

Lower Urinary Tract Symptoms|Prostatic Hyperplasia

None

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