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Azilect (RASAGILINE)
Azilect (RASAGILINE) is a small molecule monoamine oxidase inhibitor (MAOI) developed by TEVA and approved by the FDA in 2006 for the treatment of Parkinson's disease. It targets the 5-hydroxytryptamine receptor 6 and has a bioavailability of 36%. Azilect is commercially available as a branded and generic medication, with multiple generic manufacturers. Key safety considerations include potential interactions with other medications and dietary restrictions. As a MAOI, Azilect can have significant effects on various neurotransmitter systems.
At a glance
| Generic name | RASAGILINE |
|---|---|
| Sponsor | Teva |
| Drug class | Monoamine Oxidase Inhibitor |
| Target | 5-hydroxytryptamine receptor 6 |
| Modality | Small molecule |
| Therapeutic area | Metabolic |
| Phase | FDA-approved |
| First approval | 2006 |
Approved indications
- Parkinson's disease
Common side effects
- Hallucination
- Dyskinesia
- Impulse-control disorder
- On and off phenomenon
- Fall
- Freezing phenomenon
- Serotonin syndrome
- Hypersexuality
- Gambling disorder
- Orthostatic hypotension
- Delusion
- Bradykinesia
Drug interactions
- Alpha/Beta Agonists
- Amphetamines
- Indirectly Acting Sympathomimetic Amines
- Selective Serotonin Reuptake Inhibitors
- Serotonin/Norepinephrine Reuptake Inhibitors
- Tricyclic Antidepressants
- amitriptyline
- amoxapine
- buspirone
- ciprofloxacin
- citalopram
- clomipramine
Key clinical trials
- Effect of Rasagiline on Balance in Parkinson's Disease as Measured by Computerized Posturography (PHASE4)
- Relative Bioavailability Study of HNC364 Injectable Suspension (PHASE1)
- Efficacy and Safety of Rasagiline in Prodromal Parkinson's Disease (PHASE2,PHASE3)
- A Study to Evaluate the Safety, Tolerability, PK and PD of HNC364 Injectable Suspension (PHASE1)
- An Observational Study on Safinamide, Rasagiline and Other Standard of Care in PD
- Overnight Switch From Rasagiline To Safinamide (PHASE4)
- Rasagiline Tablets Special Drug Use-Results Survey "Survey on Long-term Safety"
- Image Parkinson's Disease Progression Study (PHASE2)
Patents
| Patent | Expiry | Type |
|---|---|---|
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| FDA label | Mechanism, indications, dosing, boxed warnings, drug interactions |
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
| FDA Orange Book | Patents + exclusivity |