Mirogabalin
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Also known as MirogabalinaMirogabaline
Summary
Mirogabalin (CHEMBL3545125) is a phase-3 clinical-stage small molecule (ATC N02BF03) targeting SLC15A1 and SLC15A2; indicated across 4 conditions including fibromyalgia and neuralgia.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: N02BF03
- Targets: 2 (SLC15A1, SLC15A2)
- Indications: 4 conditions
- Clinical trials: 6
- Chemistry: 209.28 Da · C12H19NO2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL3545125 |
| Name | Mirogabalin |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 59509752 |
| ATC | N02BF03 |
| Molecular formula | C12H19NO2 |
| Molecular weight | 209.28 |
| InChIKey | FTBQORVNHOIASH-CKYFFXLPSA-N |
SMILES: CCC1=C[C@@H]2[C@H](C1)C[C@@]2(CC(=O)O)CN
IUPAC name: 2-[(1R,5S,6S)-6-(aminomethyl)-3-ethyl-6-bicyclo[3.2.0]hept-3-enyl]acetic acid
Also known as: Mirogabalin, Mirogabalina, Mirogabaline, MIROGABALIN
Parent form; salt/anhydrous children: CHEMBL3545257
Patent coverage: 91 distinct patent families (172 SureChEMBL compound mentions), from 1 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
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| SLC15A1 | Peptide transporter 1 | 0% | P46059 | ||
| SLC15A2 | Peptide transporter 2 | 0% | Q16348 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 2 target gene(s): SLC15A1, SLC15A2.
Top Reactome pathways
4 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Transport of small molecules | 1 | SLC15A1 |
| R-HSA-425393 | 1 | SLC15A1 |
| SLC-mediated transmembrane transport | 1 | SLC15A1 |
| Proton/oligopeptide cotransporters | 1 | SLC15A1 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| protein transport | 2 |
| dipeptide import across plasma membrane | 2 |
| tripeptide import across plasma membrane | 2 |
| oligopeptide transport | 2 |
| peptide transport | 2 |
| transmembrane transport | 2 |
| proton transmembrane transport | 2 |
| monoatomic ion transport | 1 |
| peptidoglycan transport | 1 |
| xenobiotic transport | 1 |
| dipeptide transport | 1 |
| renal absorption | 1 |
| regulation of nucleotide-binding domain, leucine rich repeat containing receptor signaling pathway | 1 |
| antibacterial innate immune response | 1 |
| transport across blood-brain barrier | 1 |
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 |
|---|---|---|---|
| fibromyalgia | 3 | MONDO:0005546 | EFO:0005687 |
| neuralgia | 3 | MONDO:0021667 | EFO:0005762 |
| diabetic neuropathy | 2 | MONDO:0006626 | EFO:1000783 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 6.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 3 |
| PHASE3 | 2 |
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT07451431 | PHASE4 | RECRUITING | Efficacy and Safety of Mirogabalin in Diabetic Peripheral Neuropathic Pain |
| NCT03901352 | PHASE3 | COMPLETED | Study of Mirogabalin for Central Neuropathic Pain |
| NCT04094662 | PHASE3 | COMPLETED | A Phase 3 Multicenter, Randomized, Double-blind, Placebo-controlled 14-week Study of DS-5565 in Chinese Patients With Diabetic Peripheral Neuropathic Pain |
| NCT06328062 | Not specified | RECRUITING | Comparing Efficiency of Mirogabalin and Pregabalin in Primary TKA |
| NCT06711978 | Not specified | NOT_YET_RECRUITING | Comparison of the Efficacy and Safety of Mirogabalin and Duloxetine in Chemotherapy-induced Peripheral Neuropathy in a Randomized Controlled Trial: a Quality of Life Study in Cancer Survivors |
| NCT07157852 | Not specified | RECRUITING | The Efficacy and Safety of Pregabalin and Mirogabalin in Patients With Fibromyalgia |
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
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
42 molecules share ≥1 primary target. Top 42 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| Ampicillin | ChEMBL + PubChem | Phase 4 (approved) | SLC15A1, SLC15A2 |
| cefaclor | ChEMBL + PubChem | Phase 4 (approved) | SLC15A1, SLC15A2 |
| Cefadroxil | ChEMBL + PubChem | Phase 4 (approved) | SLC15A1, SLC15A2 |
| Ceftibuten | ChEMBL + PubChem | Phase 4 (approved) | SLC15A1, SLC15A2 |
| cephalexin | ChEMBL + PubChem | Phase 4 (approved) | SLC15A1, SLC15A2 |
| aminolevulinic acid | PubChem | Approved | SLC15A1, SLC15A2 |
| Amoxicillin | PubChem | Approved | SLC15A1, SLC15A2 |
| Captopril | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefdinir | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefepime | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefixime | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefotaxime | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefpodoxime | PubChem | Approved | SLC15A1, SLC15A2 |
| Cefuroxime | PubChem | Approved | SLC15A1, SLC15A2 |
| Cephapirin | PubChem | Approved | SLC15A1, SLC15A2 |
| Cloxacillin | PubChem | Approved | SLC15A1, SLC15A2 |
| Dicloxacillin | PubChem | Approved | SLC15A1, SLC15A2 |
| Enalapril | PubChem | Approved | SLC15A1, SLC15A2 |
| Oseltamivir | PubChem | Approved | SLC15A1, SLC15A2 |
| oseltamivir acid | PubChem | Approved | SLC15A1, SLC15A2 |
| Oxacillin | PubChem | Approved | SLC15A1, SLC15A2 |
| Penicillin G | PubChem | Approved | SLC15A1, SLC15A2 |
| Valacyclovir | PubChem | Approved | SLC15A1, SLC15A2 |
| CEPHRADINE | ChEMBL | Phase 4 (approved) | SLC15A1 |
| CYCLACILLIN | ChEMBL | Phase 4 (approved) | SLC15A2 |
| CARNOSINE | ChEMBL | Phase 3 | SLC15A2 |
| LEVULINIC ACID | ChEMBL | Phase 3 | SLC15A2 |
| Cefazolin | PubChem | Approved | SLC15A1 |
| Cefoxitin | PubChem | Approved | SLC15A1 |
| Ceftazidime | PubChem | Approved | SLC15A1 |
| Ceftriaxone | PubChem | Approved | SLC15A1 |
| enalaprilat dihydrate | PubChem | Approved | SLC15A1 |
| Floxuridine | PubChem | Approved | SLC15A1 |
| Fosinopril | PubChem | Approved | SLC15A2 |
| Glycine | PubChem | Approved | SLC15A1 |
| Levodopa | PubChem | Approved | SLC15A1 |
| lisinopril | PubChem | Approved | SLC15A1 |
| Methyldopa | PubChem | Approved | SLC15A1 |
| Penicillin V | PubChem | Approved | SLC15A1 |
| prezatide | PubChem | Approved | SLC15A2 |
| valine | PubChem | Approved | SLC15A1 |
| zinc sulfate, unspecified form | PubChem | Approved | SLC15A1 |
Related Atlas pages
- Genes: SLC15A1, SLC15A2
- Diseases: fibromyalgia, neuralgia
- Drugs: Ampicillin, cefaclor, Cefadroxil, Ceftibuten, cephalexin, aminolevulinic acid, Amoxicillin, Captopril, Cefdinir, Cefepime, Cefixime, Cefotaxime, Cefpodoxime, Cefuroxime, Cephapirin, Cloxacillin, Dicloxacillin, Enalapril, Oseltamivir, Oxacillin, Penicillin G, Valacyclovir, Cephradine, Cyclacillin, Carnosine, Cefazolin, Cefoxitin, Ceftazidime, Ceftriaxone, Floxuridine, Fosinopril, Glycine, Levodopa, lisinopril, Methyldopa, Penicillin V