Midodrine

drug
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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

FieldValue
ChEMBL IDCHEMBL1201212
NameMidodrine
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID4195
ChEBICHEBI:6933
ATCC01CA17
Molecular formulaC12H18N2O4
Molecular weight254.28
InChIKeyPTKSEFOSCHHMPD-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):

TargetpChemblTypeValueUnitActivity ID
ADRA1A5.3AC504990nMCHEMBL_ACT_25219361
ADRA1A5.14AC507300nMCHEMBL_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).

IndicationTrial phaseMONDOEFO
cardiovascular disorder4MONDO:0004995EFO:0000319
hypotensive disorder3MONDO:0005468EFO:0005251
toxic shock syndrome3MONDO:0001881EFO:0006834
spinal cord injury3MONDO:0043797MONDO:0043797
orthostatic hypotension2MONDO:0005469EFO:0005252
hepatopulmonary syndrome1MONDO:0004694EFO: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

PhaseTrials
Not specified25
PHASE418
PHASE210
PHASE38
PHASE17
PHASE2/PHASE34
PHASE1/PHASE23
EARLY_PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01456481PHASE4ACTIVE_NOT_RECRUITINGAssessment of Midodrine in the Prevention of Vasovagal Syncope: The Prevention of Syncope Trial IV
NCT05058612PHASE4RECRUITINGMidodrine for the Early Liberation of Vasopressor Support in the ICU (LIBERATE Multi-Site)
NCT05839652PHASE4RECRUITINGTreatment of Orthostatic Hypotension in SCI
NCT00046163PHASE4TERMINATEDA Phase IV Study in Subjects With Neurogenic Orthostatic Hypotension
NCT00046475PHASE4COMPLETEDA Study for Patients With Neurogenic Orthostatic Hypotension
NCT00108355PHASE4COMPLETEDVasoconstrictors as Alternatives to Albumin After Large-Volume Paracentesis (LVP) in Cirrhosis
NCT00555880PHASE4COMPLETEDStudy to Assess the Benefit of Midodrine in the Treatment of Patients With Neurogenic Orthostatic Hypotension
NCT00839358PHASE4COMPLETEDEffect of Midodrine and Albumine in the Prevention of Complications in Cirrhotic Patients Awaiting Liver Transplantation
NCT01822535PHASE4COMPLETEDBody Temperature in Persons With Tetraplegia When Exposed to Cold
NCT02308124PHASE4COMPLETEDTreatment and Prognosis of Neurogenic Orthostatic Hypotension : A Prospective Randomized Study
NCT02379156PHASE4COMPLETEDThermoregulation and Cognition During Cool Ambient Exposure in Tetraplegia
NCT02771158PHASE4WITHDRAWNMidodrine During Recovery From Septic Shock
NCT03080441PHASE4UNKNOWNMinimization of Intradialytic Hypotension Using Cardiography-Guided Intervention
NCT03350659PHASE4COMPLETEDEfficacy and Safety of Midodrine and Atomoxetine for Neurogenic OH
NCT03911817PHASE4COMPLETEDImpact of Midodrine Administration on the Clinical Outcome of Septic Shock Patients
NCT04440085PHASE4UNKNOWNRaGuS Trial by Postoperative Patients
NCT04489589PHASE4COMPLETEDMidodrine for the Early Liberation of Vasopressor Support in the ICU
NCT04668859PHASE4TERMINATEDMidodrine as Novel Treatment of Post-Cardiopulmonary Bypass Vasoplegic Syndrome
NCT06405555PHASE2/PHASE3NOT_YET_RECRUITINGMidodrine in Heart Failure With Reduced Ejection Fraction With Hypotension
NCT00240045PHASE2/PHASE3COMPLETEDThe Use of Drugs to Improve Kidney Function in Patients With Liver and Kidney Dysfunction
NCT01531959PHASE3COMPLETEDMidodrine for the Treatment of Refractory Hypotension
NCT01707953PHASE3COMPLETEDEfficacy of Midodrine for the Prevention of Orthostatic Hypotension During Early Mobilization After Fast-track Hip Arthroplasty
NCT02173288PHASE2/PHASE3COMPLETEDRole of Midodrine and Tolvaptan in Patients With Cirrhosis With Refractory or Recurrent Ascites
NCT02307565PHASE3COMPLETEDBlood Pressure, Cerebral Blood Flow and Cognition in Spinal Cord Injury
NCT02919917PHASE2/PHASE3COMPLETEDTreatment of Post-SCI Hypotension
NCT02990546PHASE3WITHDRAWNMidodrine in the Recovery Phase of Septic Shock
NCT03706053PHASE3TERMINATEDMidodrine Use in Septic Shock
NCT04595942PHASE3UNKNOWNMidodrine and Fludrocortisone for Vasovagal Syncope
NCT04621617PHASE3UNKNOWNMidodrine and Albumin in Patients With Refractory Ascites
NCT05240391PHASE3COMPLETEDMidodrine Versus Albumin for Prevention of Paracentesis Induced Circulatory Disturbance
NCT00262470PHASE1/PHASE2ACTIVE_NOT_RECRUITINGTreatment of Orthostatic Intolerance
NCT06319248PHASE2RECRUITINGMID-STEP (MIDodrine for Sepsis Treatment and Early vasoPressor Weaning) Trial
NCT00004268PHASE2COMPLETEDPhase II Study of Midodrine for Neurogenic Orthostatic Hypotension
NCT00227448PHASE2COMPLETEDInduced Hypertension for Acute Ischemic Stroke
NCT00426842PHASE2COMPLETEDA Dose Response Trial Using 5 and 10 Mg of Midodrine Hydrochloride
NCT00835224PHASE2COMPLETEDSafety and Efficacy of L-NAME and Midodrine to Increase MAP
NCT01587222PHASE2WITHDRAWNMidodrine, Octreotide and Albumin: Impact on Renal Function of Patients With Liver Cirrhosis and Renal Failure
NCT02893553PHASE2COMPLETEDThe Effects of Normalizing Blood Pressure on Cerebral Blood Flow in Hypotensive Individuals With Spinal Cord Injury
NCT03482297PHASE1/PHASE2COMPLETEDAutomated Abdominal Binder for Orthostatic Hypotension
NCT04048707PHASE2WITHDRAWNAngiotensin 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.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).