Midodrine
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Also known as MidodrinaST 1085ST-1085MIDODRINE HYDROCHLORIDE
Summary
Midodrine (CHEMBL1201212) is an approved small-molecule prodrug (ATC C01CA17); indicated across 8 conditions including cardiovascular disorder and hypotensive disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: C01CA17
- Indications: 8 conditions
- Clinical trials: 76
- Chemistry: 254.28 Da · C12H18N2O4
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1201212 |
| Name | Midodrine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 4195 |
| ChEBI | CHEBI:6933 |
| ATC | C01CA17 |
| Molecular formula | C12H18N2O4 |
| Molecular weight | 254.28 |
| InChIKey | PTKSEFOSCHHMPD-UHFFFAOYSA-N |
SMILES: COC1=CC(=C(C=C1)OC)C(CNC(=O)CN)O
IUPAC name: 2-amino-N-[2-(2,5-dimethoxyphenyl)-2-hydroxyethyl]acetamide
ChEBI definition: An aromatic ether that is 1,4-dimethoxybenzene which is substituted at position 2 by a 2-(glycylamino)-1-hydroxyethyl group. A direct-acting sympathomimetic with selective α-adrenergic agonist activity, it is used (generally as its hydrochloride salt) as a peripheral vasoconstrictor in the treatment of certain hypotensive states. The main active moiety is its major metabolite, deglymidodrine.
Pharmacological roles (ChEBI): prodrug, α-adrenergic agonist, sympathomimetic agent, vasoconstrictor agent.
Also known as: Midodrina, Midodrine, ST 1085, ST-1085, midodrine, MIDODRINE, MIDODRINE HYDROCHLORIDE
Parent form; salt/anhydrous children: CHEMBL1200461
Patent coverage: 2,773 distinct patent families (5,482 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 5,478 (100%) of the total. 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: 2 (assay-derived). Sample: Alpha-1A adrenergic receptor, Adenosine receptor A3.
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 |
|---|---|---|---|---|---|
| ADRA1A | 5.3 | AC50 | 4990 | nM | CHEMBL_ACT_25219361 |
| ADRA1A | 5.14 | AC50 | 7300 | nM | CHEMBL_ACT_25230345 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
8 indications (1 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 |
|---|---|---|---|
| cardiovascular disorder | 4 | MONDO:0004995 | EFO:0000319 |
| hypotensive disorder | 3 | MONDO:0005468 | EFO:0005251 |
| toxic shock syndrome | 3 | MONDO:0001881 | EFO:0006834 |
| spinal cord injury | 3 | MONDO:0043797 | MONDO:0043797 |
| orthostatic hypotension | 2 | MONDO:0005469 | EFO:0005252 |
| hepatopulmonary syndrome | 1 | MONDO:0004694 | EFO:1001346 |
2 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 76.
Phase distribution
| Phase | Trials |
|---|---|
| Not specified | 25 |
| PHASE4 | 18 |
| PHASE2 | 10 |
| PHASE3 | 8 |
| PHASE1 | 7 |
| PHASE2/PHASE3 | 4 |
| PHASE1/PHASE2 | 3 |
| EARLY_PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01456481 | PHASE4 | ACTIVE_NOT_RECRUITING | Assessment of Midodrine in the Prevention of Vasovagal Syncope: The Prevention of Syncope Trial IV |
| NCT05058612 | PHASE4 | RECRUITING | Midodrine for the Early Liberation of Vasopressor Support in the ICU (LIBERATE Multi-Site) |
| NCT05839652 | PHASE4 | RECRUITING | Treatment of Orthostatic Hypotension in SCI |
| NCT00046163 | PHASE4 | TERMINATED | A Phase IV Study in Subjects With Neurogenic Orthostatic Hypotension |
| NCT00046475 | PHASE4 | COMPLETED | A Study for Patients With Neurogenic Orthostatic Hypotension |
| NCT00108355 | PHASE4 | COMPLETED | Vasoconstrictors as Alternatives to Albumin After Large-Volume Paracentesis (LVP) in Cirrhosis |
| NCT00555880 | PHASE4 | COMPLETED | Study to Assess the Benefit of Midodrine in the Treatment of Patients With Neurogenic Orthostatic Hypotension |
| NCT00839358 | PHASE4 | COMPLETED | Effect of Midodrine and Albumine in the Prevention of Complications in Cirrhotic Patients Awaiting Liver Transplantation |
| NCT01822535 | PHASE4 | COMPLETED | Body Temperature in Persons With Tetraplegia When Exposed to Cold |
| NCT02308124 | PHASE4 | COMPLETED | Treatment and Prognosis of Neurogenic Orthostatic Hypotension : A Prospective Randomized Study |
| NCT02379156 | PHASE4 | COMPLETED | Thermoregulation and Cognition During Cool Ambient Exposure in Tetraplegia |
| NCT02771158 | PHASE4 | WITHDRAWN | Midodrine During Recovery From Septic Shock |
| NCT03080441 | PHASE4 | UNKNOWN | Minimization of Intradialytic Hypotension Using Cardiography-Guided Intervention |
| NCT03350659 | PHASE4 | COMPLETED | Efficacy and Safety of Midodrine and Atomoxetine for Neurogenic OH |
| NCT03911817 | PHASE4 | COMPLETED | Impact of Midodrine Administration on the Clinical Outcome of Septic Shock Patients |
| NCT04440085 | PHASE4 | UNKNOWN | RaGuS Trial by Postoperative Patients |
| NCT04489589 | PHASE4 | COMPLETED | Midodrine for the Early Liberation of Vasopressor Support in the ICU |
| NCT04668859 | PHASE4 | TERMINATED | Midodrine as Novel Treatment of Post-Cardiopulmonary Bypass Vasoplegic Syndrome |
| NCT06405555 | PHASE2/PHASE3 | NOT_YET_RECRUITING | Midodrine in Heart Failure With Reduced Ejection Fraction With Hypotension |
| NCT00240045 | PHASE2/PHASE3 | COMPLETED | The Use of Drugs to Improve Kidney Function in Patients With Liver and Kidney Dysfunction |
| NCT01531959 | PHASE3 | COMPLETED | Midodrine for the Treatment of Refractory Hypotension |
| NCT01707953 | PHASE3 | COMPLETED | Efficacy of Midodrine for the Prevention of Orthostatic Hypotension During Early Mobilization After Fast-track Hip Arthroplasty |
| NCT02173288 | PHASE2/PHASE3 | COMPLETED | Role of Midodrine and Tolvaptan in Patients With Cirrhosis With Refractory or Recurrent Ascites |
| NCT02307565 | PHASE3 | COMPLETED | Blood Pressure, Cerebral Blood Flow and Cognition in Spinal Cord Injury |
| NCT02919917 | PHASE2/PHASE3 | COMPLETED | Treatment of Post-SCI Hypotension |
| NCT02990546 | PHASE3 | WITHDRAWN | Midodrine in the Recovery Phase of Septic Shock |
| NCT03706053 | PHASE3 | TERMINATED | Midodrine Use in Septic Shock |
| NCT04595942 | PHASE3 | UNKNOWN | Midodrine and Fludrocortisone for Vasovagal Syncope |
| NCT04621617 | PHASE3 | UNKNOWN | Midodrine and Albumin in Patients With Refractory Ascites |
| NCT05240391 | PHASE3 | COMPLETED | Midodrine Versus Albumin for Prevention of Paracentesis Induced Circulatory Disturbance |
| NCT00262470 | PHASE1/PHASE2 | ACTIVE_NOT_RECRUITING | Treatment of Orthostatic Intolerance |
| NCT06319248 | PHASE2 | RECRUITING | MID-STEP (MIDodrine for Sepsis Treatment and Early vasoPressor Weaning) Trial |
| NCT00004268 | PHASE2 | COMPLETED | Phase II Study of Midodrine for Neurogenic Orthostatic Hypotension |
| NCT00227448 | PHASE2 | COMPLETED | Induced Hypertension for Acute Ischemic Stroke |
| NCT00426842 | PHASE2 | COMPLETED | A Dose Response Trial Using 5 and 10 Mg of Midodrine Hydrochloride |
| NCT00835224 | PHASE2 | COMPLETED | Safety and Efficacy of L-NAME and Midodrine to Increase MAP |
| NCT01587222 | PHASE2 | WITHDRAWN | Midodrine, Octreotide and Albumin: Impact on Renal Function of Patients With Liver Cirrhosis and Renal Failure |
| NCT02893553 | PHASE2 | COMPLETED | The Effects of Normalizing Blood Pressure on Cerebral Blood Flow in Hypotensive Individuals With Spinal Cord Injury |
| NCT03482297 | PHASE1/PHASE2 | COMPLETED | Automated Abdominal Binder for Orthostatic Hypotension |
| NCT04048707 | PHASE2 | WITHDRAWN | Angiotensin 2 for Hepatorenal Syndrome |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).