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Tenex (GUANFACINE)
Tenex works by stimulating alpha-2 adrenergic receptors in the brain, which helps to reduce the activity of certain nerve cells.
Tenex (Guanfacine) is a central alpha-2 adrenergic agonist developed by Promius Pharma, targeting Nischarin. It was FDA-approved in 1986 for attention deficit hyperactivity disorder and hypertensive disorder. As an off-patent medication, Tenex is available from multiple generic manufacturers. Key safety considerations include its potential to cause dizziness, fatigue, and dry mouth. Tenex has a half-life of 15 hours and bioavailability of 81%.
At a glance
| Generic name | GUANFACINE |
|---|---|
| Sponsor | Promius Pharma |
| Drug class | Central alpha-2 Adrenergic Agonist |
| Target | Nischarin |
| Modality | Small molecule |
| Therapeutic area | Neuroscience |
| Phase | FDA-approved |
| First approval | 1986 |
Mechanism of action
Guanfacine is central alpha2A-adrenergic receptor agonist. Guanfacine is not central nervous system (CNS) stimulant. The mechanism of action of guanfacine in ADHD is not known.
Approved indications
- Attention deficit hyperactivity disorder
- Hypertensive disorder
Common side effects
- Somnolence
- Abdominal Pain
- Fatigue
- Irritability
- Nausea
- Dizziness
- Vomiting
- Hypotension
- Decreased Appetite
- Enuresis
- Headache
Key clinical trials
- ACE-D Aim 3 Clinical Cognitive Trial to Enhance Translation in Depression (PHASE2)
- Mechanistic Evaluation of Guanfacine on Drinking Behavior in Women and Men With Alcohol Use Disorders (PHASE2)
- Maximizing trEatment of Neurological Dysfunction Using INtravenous Guanfacine Study (PHASE2)
- Guanfacine for Hyperactivity in Children With Down Syndrome (HYPEbeGONE_DS) (PHASE2)
- Treating Young Children With Attention Deficit Hyperactivity Disorder (PHASE4)
- Effect of Guanfacine on the Reversal of Opioid-induced Hyperalgesia (OIH) (NA)
- Effect of Guanfacine on Opioid-induced Hyperalgesia (OIH) and Tolerance (PHASE4)
- AWARE: Management of ADHD in Autism Spectrum Disorder (PHASE4)
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 |