Trospium
drugOn this page
Also known as Trospium cationTrospium ionSID50112692Trospium chloride (Sanctura)
Summary
Trospium (CHEMBL1888176) is an approved small-molecule muscarinic antagonist (ATC G04BD09); indicated across 3 conditions including overactive bladder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: G04BD09
- Indications: 3 conditions
- Clinical trials: 15
- Chemistry: 392.5 Da · C25H30NO3+
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1888176 |
| Name | Trospium |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 5284632 |
| ChEBI | CHEBI:145791 |
| ATC | G04BD09 |
| Molecular formula | C25H30NO3+ |
| Molecular weight | 392.5 |
| InChIKey | OYYDSUSKLWTMMQ-AIZNXBIQSA-N |
SMILES: C1CC[N+]2(C1)[C@@H]3CC[C@H]2CC(C3)OC(=O)C(C4=CC=CC=C4)(C5=CC=CC=C5)O
IUPAC name: [(1R,5S)-spiro[8-azoniabicyclo[3.2.1]octane-8,1’-azolidin-1-ium]-3-yl] 2-hydroxy-2,2-diphenylacetate
ChEBI definition: A carboxylic ester resulting from the formal condensation of the carboxy group of hydroxy(diphenyl)acetic acid with the hydroxy group of (1S,3R,5R)-3-hydroxy-8λ5-azaspiro[bicyclo[3.2.1]octane-8,1’-pyrrolidin]-8-ylium. Its chloride salt is used to treat overactive bladder.
Pharmacological roles (ChEBI): muscarinic antagonist, antispasmodic drug.
Also known as: Trospium, Trospium cation, Trospium ion, trospium, SID50112692, TROSPIUM, Trospium chloride (Sanctura)
Parent form; salt/anhydrous children: CHEMBL3084748
Patent coverage: 12 distinct patent families (17 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
Broader ChEMBL bioactivity targets: 5 (assay-derived). Sample: Muscarinic acetylcholine receptor M2, Muscarinic acetylcholine receptor M1, Histamine H1 receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Muscarinic acetylcholine receptor M3.
Bioactivity
ChEMBL activities: 6 potent at pChembl ≥ 5 of 7 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| CHRM1 | 8.57 | AC50 | 2.7 | nM | CHEMBL_ACT_25210763 |
| CHRM2 | 8.21 | AC50 | 6.1 | nM | CHEMBL_ACT_25213378 |
| CHRM3 | 8.05 | AC50 | 8.9 | nM | CHEMBL_ACT_25136328 |
| CHRM2 | 7.58 | AC50 | 26 | nM | CHEMBL_ACT_25195170 |
| CHRM1 | 7.55 | AC50 | 28 | nM | CHEMBL_ACT_25135066 |
| KCNH2 | 6.2 | AC50 | 630 | nM | CHEMBL_ACT_25117296 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
3 indications (2 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 | 1 | MONDO:0006624 | EFO:1000781 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 15.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 4 |
| Not specified | 4 |
| PHASE3 | 3 |
| PHASE1/PHASE2 | 2 |
| PHASE1 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT06923891 | PHASE4 | NOT_YET_RECRUITING | An Open-Label Study to Evaluate the Efficacy and Tolerability of Xanomeline/Trospium In First Episode/Early Phase Schizophrenia Patients |
| NCT00932022 | PHASE4 | COMPLETED | Trospium Chloride XR in Obese Female Patients With Overactive Bladder |
| NCT04090190 | PHASE4 | COMPLETED | Inflammation in Women With Urgency Urinary Incontinence Treated With Anticholinergics |
| NCT04227184 | PHASE4 | COMPLETED | Investigation of Brain Mechanisms Involved in Urgency Urinary Incontinence |
| NCT07011732 | PHASE3 | RECRUITING | A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer’s Disease (ADAGIO-1) |
| NCT07011745 | PHASE3 | RECRUITING | A Phase 3 Study to Evaluate the Safety and Efficacy of KarXT + KarX-EC for the Treatment of Agitation Associated With Alzheimer’s Disease (ADAGIO-2) |
| NCT07084831 | PHASE3 | NOT_YET_RECRUITING | A Study Evaluating the Efficacy of Xanomeline/Trospium (XT) on Cognitive Impairment After 24 and 52 Weeks of Treatment in Adult Participants With Schizophrenia |
| NCT07423546 | PHASE1/PHASE2 | NOT_YET_RECRUITING | A PET/MRI Study of Cobenfy on Dopamine Transmission in Schizophrenia |
| NCT00465959 | PHASE1/PHASE2 | COMPLETED | Study of Trospium Chloride Inhalation Powder (TrIP) in Patients With Chronic Obstructive Pulmonary Disease |
| NCT07063342 | PHASE1 | RECRUITING | A Study to Evaluate Novel KarX and KarT Prototypes Versus the KarXT and KarX-EC Reference Following Single Doses, and to Explore the Effect of Food After Multiple Doses of Selected Prototypes in Healthy Adult Participants |
| NCT00986401 | PHASE1 | COMPLETED | Safety and Tolerability of Trospium Chloride and Metformin Hydrochloride in Healthy Subjects |
| NCT07379827 | Not specified | RECRUITING | Effectiveness and Adverse-effect Switch Evaluation of Xanomeline and Trospium Chloride (KarXT) |
| NCT01499069 | Not specified | COMPLETED | Urinary Nerve Growth Factor (NGF), Prostaglandin E2 (PGE2)and Adenosine Triphosphate (ATP): Potential Biomarkers in Overactive Bladder Patients |
| NCT03572231 | Not specified | COMPLETED | A Registry Study of Patients Initiating a Course of Drug Therapy for Overactive Bladder in Taiwan, Korea and China |
| NCT03602508 | Not specified | COMPLETED | Treatment Persistence Among Patients With Overactive Bladder: A Retrospective Secondary Data Analysis in Asia Oceania |
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
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.