Mirabegron
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Also known as BetanisBetmigaMyrbetriqMyrbetriq granulesYM-178YM178MIRABEGRON (YM178)MirabegronÊMirabegronÂ
Summary
Mirabegron (CHEMBL2095212) is an approved small-molecule β-adrenergic agonist (ATC G04BD12) targeting ADRB1, ADRB2, and ADRB3; indicated across 16 conditions including overactive bladder and interstitial cystitis.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: G04BD12
- Targets: 3 (ADRB1, ADRB2, ADRB3)
- Indications: 16 conditions
- Clinical trials: 153
- Chemistry: 396.5 Da · C21H24N4O2S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2095212 |
| Name | Mirabegron |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 9865528 |
| ChEBI | CHEBI:65349 |
| ATC | G04BD12 |
| Molecular formula | C21H24N4O2S |
| Molecular weight | 396.5 |
| InChIKey | PBAPPPCECJKMCM-IBGZPJMESA-N |
SMILES: C1=CC=C(C=C1)[C@H](CNCCC2=CC=C(C=C2)NC(=O)CC3=CSC(=N3)N)O
IUPAC name: 2-(2-amino-1,3-thiazol-4-yl)-N-[4-[2-[[(2R)-2-hydroxy-2-phenylethyl]amino]ethyl]phenyl]acetamide
ChEBI definition: A monocarboxylic acid amide obtained by formal condensation of the carboxy group of 2-amino-1,3-thiazol-4-ylacetic acid with the anilino group of (1R)-2-{[2-(4-aminophenyl)ethyl]amino}-1-phenylethanol. Used for the treatment of overactive bladder syndrome.
Pharmacological roles (ChEBI): β-adrenergic agonist.
Also known as: Betanis, Betmiga, Mirabegron, Myrbetriq, Myrbetriq granules, YM-178, YM178, MIRABEGRON, mirabegron, MIRABEGRON (YM178), MirabegronÊ, Mirabegron (YM178)
Parent form; salt/anhydrous children: CHEMBL3542362
Patent coverage: 514 distinct patent families (1,038 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 |
|---|---|---|---|---|---|
| ADRB1 | β1-adrenoceptor | Agonist | 5 | 0% | P08588 |
| ADRB2 | β2-adrenoceptor | Agonist | 5 | 0.4% | P07550 |
| ADRB3 | β3-adrenoceptor | Agonist | 8.8 | 0.1% | P13945 |
Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Beta-3 adrenergic receptor.
Bioactivity
ChEMBL activities: 1 potent at pChembl ≥ 5 of 1 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| ADRB3 | 7.65 | EC50 | 22.4 | nM | CHEMBL_ACT_25708405 |
Target pathways
Aggregated over 3 target gene(s): ADRB1, ADRB2, ADRB3.
Top Reactome pathways
16 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Signal Transduction | 3 | ADRB1, ADRB2, ADRB3 |
| Signaling by GPCR | 3 | ADRB1, ADRB2, ADRB3 |
| Class A/1 (Rhodopsin-like receptors) | 3 | ADRB1, ADRB2, ADRB3 |
| Amine ligand-binding receptors | 3 | ADRB1, ADRB2, ADRB3 |
| GPCR downstream signalling | 3 | ADRB1, ADRB2, ADRB3 |
| Adrenoceptors | 3 | ADRB1, ADRB2, ADRB3 |
| G alpha (s) signalling events | 3 | ADRB1, ADRB2, ADRB3 |
| GPCR ligand binding | 3 | ADRB1, ADRB2, ADRB3 |
| Membrane Trafficking | 1 | ADRB2 |
| Metabolism of proteins | 1 | ADRB2 |
| Vesicle-mediated transport | 1 | ADRB2 |
| Deubiquitination | 1 | ADRB2 |
| Ub-specific processing proteases | 1 | ADRB2 |
| Post-translational protein modification | 1 | ADRB2 |
| Cargo recognition for clathrin-mediated endocytosis | 1 | ADRB2 |
| Clathrin-mediated endocytosis | 1 | ADRB2 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| diet induced thermogenesis | 3 |
| norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure | 3 |
| adenylate cyclase-activating G protein-coupled receptor signaling pathway | 3 |
| response to cold | 3 |
| heat generation | 3 |
| negative regulation of multicellular organism growth | 3 |
| positive regulation of MAPK cascade | 3 |
| brown fat cell differentiation | 3 |
| adenylate cyclase-activating adrenergic receptor signaling pathway | 3 |
| positive regulation of cold-induced thermogenesis | 3 |
| signal transduction | 3 |
| G protein-coupled receptor signaling pathway | 3 |
| positive regulation of cardiac muscle cell apoptotic process | 2 |
| adenylate cyclase-modulating G protein-coupled receptor signaling pathway | 2 |
| negative regulation of smooth muscle contraction | 2 |
Indications & clinical
Indications
16 indications (4 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 |
|---|---|---|---|
| overactive bladder | 4 | MONDO:0006624 | EFO:1000781 |
| interstitial cystitis | 3 | MONDO:0018301 | EFO:1000869 |
| nephrolithiasis | 3 | MONDO:0008171 | EFO:0004253 |
| heart failure | 2 | MONDO:0005252 | EFO:0003144 |
| prediabetes syndrome | 2 | MONDO:0006920 | EFO:1001121 |
| intracerebral hemorrhage | 2 | MONDO:0013792 | EFO:0005669 |
| liver disorder | 1 | MONDO:0005154 | EFO:0001421 |
| polycystic ovary syndrome | 1 | MONDO:0008487 | EFO:0000660 |
| kidney disorder | 1 | MONDO:0005240 | EFO:0003086 |
7 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 153.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 38 |
| PHASE1 | 33 |
| PHASE3 | 28 |
| PHASE2 | 26 |
| Not specified | 18 |
| EARLY_PHASE1 | 5 |
| PHASE1/PHASE2 | 3 |
| PHASE2/PHASE3 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05051436 | PHASE4 | RECRUITING | The Effects of Mirabegron and Tadalafil on Glucose Tolerance in Prediabetics |
| NCT05362292 | PHASE4 | RECRUITING | TReating Incontinence for Underlying Mental and Physical Health |
| NCT05604222 | PHASE4 | ACTIVE_NOT_RECRUITING | Effect of Behavioral Sleep Intervention on Lower Urinary Tract Symptoms in Older Women |
| NCT06465576 | PHASE4 | RECRUITING | Strategy for Withdrawal of Pharmacological Treatment for Urinary Incontinence in Children (StayDry) |
| NCT06479720 | PHASE4 | RECRUITING | Efficacy of Solifenacin or Mirabegron With Local Estrogen Versus Combination Pharmacotherapy for Overactive Bladder |
| NCT07187466 | PHASE4 | NOT_YET_RECRUITING | Behavioral and/or Mirabegron to Treat Urinary Symptoms in Parkinson Disease |
| NCT07310797 | PHASE4 | NOT_YET_RECRUITING | Comparison of Mirabegron and Tamsulosin for Ureteral Stone Expulsion |
| NCT01745094 | PHASE4 | COMPLETED | A Study to Evaluate the Effect of Mirabegron + Solifenacin in Overactive Bladder Patients |
| NCT01964183 | PHASE4 | COMPLETED | Post-marketing Study to Evaluate the Effect of Mirabegron on the Plasma Concentration of Tolterodine |
| NCT02086188 | PHASE4 | COMPLETED | Study of Behavioral Modification Program and Mirabegron to Improve Urinary Urgency in Multiple Sclerosis |
| NCT02092181 | PHASE4 | COMPLETED | A Pilot Study of Mirabegron and Behavioral Modification Including Pelvic Floor Exercise for Overactive Bladder in Parkinson’s Disease (MAESTRO) |
| NCT02095665 | PHASE4 | COMPLETED | Ureteral Stent-related Pain and Mirabegron (SPAM) Trial |
| NCT02138747 | PHASE4 | COMPLETED | A Study to Evaluate Tolerability and Participants Preference Between Mirabegron and Tolterodine Extended Release (ER) in Participants With Overactive Bladder (OAB) |
| NCT02216214 | PHASE4 | COMPLETED | Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Older Adult Subjects With Overactive Bladder (OAB) |
| NCT02279615 | PHASE4 | UNKNOWN | Efficacy And Safety Of Combination Therapy For Treatment Of Overactive Bladder In Male Patients With Benign Prostatic Hyperplasia. |
| NCT02294396 | PHASE4 | COMPLETED | Postmarketing Study to Evaluate add-on Therapy With Anticholinergics in Patients With Overactive Bladder (OAB) on Mirabegron. |
| NCT02361502 | PHASE4 | UNKNOWN | MIrabegron With oveRACtive bLadder Symptoms in mEn |
| NCT02436889 | PHASE4 | COMPLETED | Treatment of Incontinence Without Memory Problems |
| NCT02468375 | PHASE4 | COMPLETED | Prospective Study for Patient Perception of Treatment Satisfaction After Switching to Mirabegron in Patients With Overactive Bladder Who Were Unsatisfied With Efficacy of Antimuscarinic Therapy or Adverse Event. |
| NCT02495389 | PHASE4 | COMPLETED | Mirabegron and Urinary Urgency Incontinence |
| NCT02536976 | PHASE4 | COMPLETED | Mirabegron in Parkinson Disease and Impaired Cognition |
| NCT02540707 | PHASE4 | COMPLETED | Comparisons of the Effects of Solifenacin Versus Mirabegron on Autonomic System, Arterial Stiffness and Psychosomatic Distress and Clinical Outcomes |
| NCT02656173 | PHASE4 | COMPLETED | A Phase 4 Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Male Subjects With Overactive Bladder (OAB) Symptoms, While Taking the Alpha Blocker for Benign Prostatic Hypertrophy (BPH) |
| NCT02757768 | PHASE4 | COMPLETED | A Study to Evaluate the Efficacy, Safety, and Tolerability of Mirabegron in Men With OAB Symptoms While Taking Tamsulosin Hydrochloride for Lower Urinary Tract Symptoms (LUTS) Due to Benign Prostatic Hyperplasia (BPH) |
| NCT02981459 | PHASE4 | WITHDRAWN | Mirabegron for the Treatment of Pain Motivated Urinary Frequency and Urgency in Women |
| NCT03012113 | PHASE4 | UNKNOWN | Mirabegron and Brown Adipose Tissue |
| NCT03412513 | PHASE4 | UNKNOWN | Mirabegron for Treatment of Overactive Bladder Symptoms in Patients With Parkinson’s Disease |
| NCT03558919 | PHASE4 | COMPLETED | Efficacy and Safety of the Mirabegron Compared With Solifenacin in Treatment of Overactive Bladder |
| NCT03695822 | PHASE4 | WITHDRAWN | Impact of Beta-3 Agonist on Psychological Distress and Blood Flow of the Bladder in Women With Overactive Bladder Syndrome |
| NCT04501640 | PHASE4 | COMPLETED | A Study to Investigate the Effect of Food With Mirabegron in Healthy Chinese Participants |
| NCT04562090 | PHASE4 | COMPLETED | A Study With Mirabegron 50 mg and 25 mg in Chinese Participants With Overactive Bladder |
| NCT04907032 | PHASE4 | COMPLETED | Posterior Tibial Nerve Stimulation (PTNS) Plus Mirabegron to Treat Refractory OAB Symptoms (PTNS-M Study) |
| NCT04909255 | PHASE4 | UNKNOWN | Beta-3 Agonist and Anti-muscarinic Agent for Sjogren’s Syndrome With Overactive Bladder |
| NCT05188742 | PHASE4 | UNKNOWN | Sequencing and Combination of Mirabegron and TTNS in Overactive Bladder Syndrome: a Multicenter, Randomized, Open-label, Crossover Trial |
| NCT05452434 | PHASE4 | UNKNOWN | Mirabegron Combined With Behavioral Intervention for Overactive Bladder:a Prospective Multicenter Randomized Controlled Clinical Study |
| NCT05946902 | PHASE4 | UNKNOWN | Comparisons of the Impact of Monotherapy With Mirabegron or Tolterodine Versus Combined Treatment With Mirabegron and Tolterodine on Autonomic Function and Bladder Blow Flow in Women With Overactive Bladder Syndrome: a Randomized Controlled Study |
| NCT06124066 | PHASE4 | COMPLETED | THE EFFECTS OF MIRABEGRON AND TAMSULOSIN FOR PATIENTS WITH URETERAL STENTS |
| NCT07533565 | PHASE4 | COMPLETED | A Pilot Study of Mirabegron and Montelukast in Cirrhotic Patients |
| NCT05621616 | PHASE3 | ACTIVE_NOT_RECRUITING | A Study to Learn How Effective and Safe the Drug ‘Mirabegron’ is and How Long it Stays in the Body of Children Aged 6 Months to Less Than 3 Years of Age With Neurogenic Detrusor Overactivity |
| NCT06551246 | PHASE3 | RECRUITING | Efficacy of Solifenacin, Mirabegron and Combination Therapy in Children With Daytime Urinary Incontinence (BeDry) |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline, but PharmGKB curates 0 clinical and 8 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
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.
280 molecules share ≥1 primary target. Top 60 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| Crizotinib | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| Desloratadine | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| Dihydroergotamine | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| Pramipexole | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| RIFAMPIN | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| TEGASEROD | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| ARIPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| BISOPROLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| BROMOCRIPTINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| CARVEDILOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| CLOTRIMAZOLE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| EPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| FENOTEROL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| FORMOTEROL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| ISOPROTERENOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| LABETALOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| LEVOBUNOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| MONTELUKAST | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| NOREPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PHENYLEPHRINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PIMOZIDE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PINDOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PRACTOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PROPAFENONE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| PROPRANOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| SALMETEROL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| SOTALOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| TAMOXIFEN | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| THIORIDAZINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| TIMOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2, ADRB3 |
| ALPRENOLOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| BOPINDOLOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| CIMATEROL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| FLESTOLOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| LEVISOPRENALINE | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| LEVOPROPRANOLOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| MILVETEROL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| RAFABEGRON | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| SOLABEGRON | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| TRETOQUINOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| XAMOTEROL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| ZENIDOLOL | ChEMBL | Phase 2 | ADRB1, ADRB2, ADRB3 |
| Alogliptin | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Bosentan | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Fidaxomicin | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Glycopyrrolate | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Linagliptin | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Methotrexate | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Propoxyphene | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Pyrazinamide | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| Tiotropium Bromide Monohydrate | PubChem | Approved | ADRB1, ADRB2, ADRB3 |
| CLOZAPINE | ChEMBL + PubChem | Phase 4 (approved) | ADRB2, ADRB3 |
| OLANZAPINE | ChEMBL + PubChem | Phase 4 (approved) | ADRB2, ADRB3 |
| OLODATEROL | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2 |
| TAMSULOSIN | ChEMBL + PubChem | Phase 4 (approved) | ADRB1, ADRB2 |
| ACEBUTOLOL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2 |
| ALBUTEROL | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2 |
| AMIODARONE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB3 |
| AMITRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRB1, ADRB2 |
| AMLODIPINE | ChEMBL | Phase 4 (approved) | ADRB2, ADRB3 |
Related Atlas pages
- Genes: ADRB1, ADRB2, ADRB3
- Diseases: overactive bladder, interstitial cystitis, nephrolithiasis
- Drugs: Crizotinib, Desloratadine, Dihydroergotamine, Pramipexole, Rifampin, Tegaserod, Aripiprazole, Bisoprolol, Bromocriptine, Carvedilol, Clotrimazole, Epinephrine, Fenoterol, Formoterol, Isoproterenol, Labetalol, Levobunolol, Montelukast, Norepinephrine, Phenylephrine, Pimozide, Pindolol, Practolol, Propafenone, Propranolol, Salmeterol, Sotalol, Tamoxifen, Thioridazine, Timolol, Alogliptin, Bosentan, Fidaxomicin, Glycopyrrolate, Linagliptin, Methotrexate, Propoxyphene, Pyrazinamide, Clozapine, Olanzapine, Olodaterol, Tamsulosin, Acebutolol, Albuterol, Amiodarone, Amitriptyline, Amlodipine