Product Description
Mechanisms of Action: CB1 Antagonist
Novel Mechanism: Yes
Modality: Small Molecule
Route of Administration: Oral
FDA Designation: None *
Approval Status: Not Approved
Approved Countries: Brazil | Chile | Colombia | European Medicines Agency | Germany | Hungary | India | Ireland | Italy | Peru | Portugal | Slovenia | Sweden | United Kingdom
Approved Indications: None
Known Adverse Events: None
Company: Sanofi
Company Location: PARIS I0 75008
Company CEO: Paul Hudson
Additional Commercial Interests: None
Clinical Description
Countries in Clinic:
Active Clinical Trial Count:
Highest Development Phases
Phase 4: Obesity|Atherosclerosis|Healthy Volunteers|Insulin Resistance|Inflammation|Other|Dyslipidemia|Overweight|Obesity, Abdominal|Diabetes, Gestational|Alcoholism|Cocaine-Related Disorders
Phase 3: Obesity|Non-alcoholic Fatty Liver Disease|Fatty Liver, Alcoholic|Dyslipidemia|Other|Type 2 Diabetes|Prediabetic State|Glucose Intolerance|Weight Loss|Tobacco Use Disorder|Carotid Stenosis|Metabolic Syndrome X|Obesity, Abdominal|Arteriosclerosis|Albuminuria|Atherosclerosis|Smoking Cessation|Schizophrenia|Prader-Willi Syndrome|Spinal Cord Injuries|Weight Gain|Myocardial Infarction|Overweight|Non-alcoholic Steatohepatitis|Stroke|Myocardial Ischemia|Hepatitis, Alcoholic|Coronary Artery Disease
Phase 2: Alcoholic Intoxication|Obesity|Spinal Cord Injuries|Tobacco Use Disorder|Psychotic Disorders|Polycystic Ovary Syndrome|Schizophrenia|Hypertension|Marijuana Abuse|Affective Disorders, Psychotic
Phase 1: Marijuana Abuse
Trial |
Phase |
Trial Status |
Disease |
Primary Completion Date |
Probability of Success |
---|---|---|---|---|---|
2022-001522-30 | P3 |
Active, not recruiting |
Spinal Cord Injuries |
2024-09-29 |
|
RIMOFATSCI-2 | P2 |
Unknown status |
Spinal Cord Injuries |
2023-11-01 |
|
RIMOFATSCI-1 | P2 |
Completed |
Spinal Cord Injuries |
2022-06-07 |
|
Effec Acomplia gastric sensitivity | P4 |
Completed |
Healthy Volunteers |
2021-03-03 |