Reboxetine
Regulatory activity · MHRAAlso known as Reboxetina.
Recent clinical, regulatory, research and industry developments relating to this drug.
Studying the Role of Brain Molecules for Decision Making
Noradrenaline, Acetylcholine and Dynamic Learning in Healthy Humans
Pharmacovigilance in Gerontopsychiatric Patients
Drug Safety Update: Reboxetine: benefit-risk balance reviewed
International Committee of Medical Journal Editors
Chronic antidepressant treatment increases neurogenesis in adult rat hippocampus.
Profile
Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.
Regulatory timeline
The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.
Contains public sector information from the Medicines and Healthcare products Regulatory Agency (MHRA) licensed under the Open Government Licence (OGL v3).
Clinical trials
The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.
Late-stage studies
Phase III+ trials still open or recently active — where late-stage evidence is being generated.
Phase 3 Reboxetine Treatment in Depressed Children and Adolescents an 8-Week, Open Study
Pharmacovigilance in Gerontopsychiatric Patients
Recent completions
Trials that read out recently, adding to the completed evidence base.
Research activity
Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.
Journals, researchers & institutions
- The Journal of neuroscience : the official journal of the Society for Neuroscience1
- Duman RS1
- Eisch AJ1
- Malberg JE1
- Nestler EJ1
- Laboratory of Molecular Psychiatry1
Related drugs
Drugs sharing diseases, protein targets and literature with this one. Ranked by graph evidence (shared targets + diseases weighted above co-mentions).
- RxNorm (U.S. National Library of Medicine) — drug identity
- ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
- Europe PMC — research literature
- ClinicalTrials.gov — clinical trials
- Regulatory event sources are credited in the Regulatory Timeline above.