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Riferminogene pecaplasmid

Alternative Names: riferminogene pecaplasmid, XRP-0038, XRP0038, XRP 0038
Latest Update: 2017-06-08
Latest Update Note: Clinical Trial Update

Product Description

Mechanisms of Action: Angiogenesis Activator

Novel Mechanism: Yes

Modality: Large Molecule

Route of Administration: Intramuscular

FDA Designation: None *

Approval Status: Not Approved

Approved Countries: None

Approved Indications: None

Known Adverse Events: None

Company: Sanofi
Company Location: PARIS I0 75008
Company CEO: Paul Hudson
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Riferminogene pecaplasmid

Countries in Clinic:

Active Clinical Trial Count:

Highest Development Phases

Phase 3: Peripheral Vascular Diseases|Peripheral Arterial Disease

Phase 2: Peripheral Vascular Diseases|Arterial Occlusive Diseases|Peripheral Arterial Disease|Intermittent Claudication

Phase 1: Peripheral Arterial Disease|Arterial Occlusive Diseases

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

2006-006277-24

P3

Completed

Unknown

2012-08-08

TAMARIS

P3

Completed

Peripheral Vascular Diseases|Peripheral Arterial Disease

2010-08-01

TALISMAN 211

P2

Completed

Peripheral Arterial Disease|Intermittent Claudication|Arterial Occlusive Diseases

2005-08-01

TALISMAN202

P2

Completed

Peripheral Arterial Disease

2005-07-01

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