Centanafadine
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Also known as CentanafadinaDOV 216,419DOV 216,419 free baseDOV-216419EB-1020EB-1020 free base
Summary
Centanafadine (CHEMBL3301621) is a phase-3 clinical-stage small molecule; indicated across 4 conditions including attention deficit-hyperactivity disorder and eating disorder.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Indications: 4 conditions
- Clinical trials: 12
- Chemistry: 209.29 Da · C15H15N
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3301621 |
| Name | Centanafadine |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 16095349 |
| Molecular formula | C15H15N |
| Molecular weight | 209.29 |
| InChIKey | HKHCSWPSUSWGLI-CABCVRRESA-N |
SMILES: C1[C@H]2[C@@]1(CNC2)C3=CC4=CC=CC=C4C=C3
IUPAC name: (1R,5S)-1-naphthalen-2-yl-3-azabicyclo[3.1.0]hexane
Also known as: Centanafadina, Centanafadine, DOV 216,419, DOV 216,419 free base, DOV-216419, EB-1020, EB-1020 free base, CENTANAFADINE
Parent form; salt/anhydrous children: CHEMBL3301615
Patent coverage: 53 distinct patent families (187 SureChEMBL compound mentions), from 2 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 3 (assay-derived). Sample: Sodium-dependent noradrenaline transporter, Sodium-dependent serotonin transporter, Sodium-dependent dopamine transporter.
Bioactivity
ChEMBL activities: 2 potent at pChembl ≥ 5 of 3 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| SLC6A2 | 8 | IC50 | 10 | nM | CHEMBL_ACT_29194894 |
| SLC6A3 | 7.22 | IC50 | 60 | nM | CHEMBL_ACT_29194903 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
4 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| attention deficit-hyperactivity disorder | 3 | MONDO:0007743 | EFO:0003888 |
| eating disorder | 2 | MONDO:0005451 | EFO:0005203 |
| major depressive disorder | 2 | MONDO:0002009 | MONDO:0002009 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 12.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 6 |
| PHASE2 | 4 |
| PHASE3 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05428033 | PHASE3 | COMPLETED | A Trial of Centanafadine Efficacy and Safety in Children With Attention-deficit/ Hyperactivity Disorder (ADHD) |
| NCT06973577 | PHASE3 | COMPLETED | P3b Short-term Study of CTN in Patients With ADHD and Comorbid Anxiety |
| NCT04081363 | PHASE2 | COMPLETED | Open-label, Single-dose Trial to Assess the Pharmacokinetics of Centanafadine Extended-release Capsules in Pediatric Participants With Attention-deficit Hyperactivity Disorder (ADHD) |
| NCT05066724 | PHASE2 | COMPLETED | Efficacy of Centanafadine SR as a Potential Smoking Cessation Treatment |
| NCT05113953 | PHASE2 | COMPLETED | A Trial of Centanafadine Efficacy, Safety, and Tolerability in Adult Subjects With Binge Eating Disorder |
| NCT05536414 | PHASE2 | COMPLETED | Trial of Centanafadine Efficacy and Safety as Monotherapy or as Adjunct to SSRI in Adults With Major Depressive Disorder |
| NCT01744808 | PHASE1 | COMPLETED | A Study to Evaluate the Safety, Tolerance, and Pharmacokinetic and Pharmacodynamic Profile Of 1 SR Formulation of EB-1020 |
| NCT02144415 | PHASE1 | COMPLETED | A Study to Evaluate the Abuse Potential of EB-1020 Immediate-Release in Healthy Recreational Stimulant Users |
| NCT04398225 | PHASE1 | COMPLETED | A Trial to Assess the Pharmacokinetics, Safety, and Tolerability of Centanafadine in Pediatric Subjects With Attention-deficit/Hyperactivity Disorder |
| NCT04786730 | PHASE1 | COMPLETED | A Trial to Assess the Pharmacokinetics, Safety, and Tolerability of Centanafadine Capsules in Pediatric Subjects With Attention-deficit Hyperactivity Disorder |
| NCT07314333 | PHASE1 | COMPLETED | A Trial to Assess How Centanafadine Interacts With Stimulants in the Body |
| NCT07486895 | PHASE1 | COMPLETED | Trial to Demonstrate the Equivalence of Two Different Strengths of Oral Centanafadine Capsules in Healthy Subjects |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: attention deficit-hyperactivity disorder