Dutogliptin

drug
On this page

Also known as DutogliptinaDutogliptinePhx1149

Summary

Dutogliptin (CHEMBL4296719) is a phase-3 clinical-stage small molecule; indicated across 2 conditions including type 2 diabetes mellitus and st-elevation myocardial infarction.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 2 conditions
  • Clinical trials: 10
  • Chemistry: 241.1 Da · C10H20BN3O3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4296719
NameDutogliptin
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID11253490
Molecular formulaC10H20BN3O3
Molecular weight241.1
InChIKeyDVJAMEIQRSHVKC-BDAKNGLRSA-N

SMILES: B([C@@H]1CCCN1C(=O)CN[C@@H]2CCNC2)(O)O

IUPAC name: [(2R)-1-[2-[[(3R)-pyrrolidin-3-yl]amino]acetyl]pyrrolidin-2-yl]boronic acid

Also known as: Dutogliptin, Dutogliptina, Dutogliptine, Phx1149, PHX1149, DUTOGLIPTIN

Parent form; salt/anhydrous children: CHEMBL4297203

Patent coverage: 493 distinct patent families (1,373 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: 4 (assay-derived). Sample: Dipeptidyl peptidase 4, Dipeptidyl peptidase 8, Prolyl endopeptidase FAP, Dipeptidyl peptidase 9.

Bioactivity

ChEMBL activities: 5 potent at pChembl ≥ 5 of 5 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
DPP47.64IC5023nMCHEMBL_ACT_15714350
DPP47.6IC5025nMCHEMBL_ACT_24689241
DPP96.18IC50663nMCHEMBL_ACT_15714344
FAP5.12IC507520nMCHEMBL_ACT_15714326
DPP85.07IC508427nMCHEMBL_ACT_15714339

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

2 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).

IndicationTrial phaseMONDOEFO
type 2 diabetes mellitus3MONDO:0005148MONDO:0005148
ST-elevation myocardial infarction3MONDO:0041656EFO:0008585

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE38
PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00850239PHASE3TERMINATEDSafety and Efficacy Study of Dutogliptin/PHX1149T in Subjects With Type 2 Diabetes Mellitus on a Background Medication of Metformin
NCT00865592PHASE3TERMINATEDLong-term Study to Evaluate the Safety of Dutogliptin/PHX1149T in Subjects With Type 2 Diabetes Mellitus
NCT00947557PHASE3TERMINATEDSafety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus (T2DM) on Background Therapy With Glimepiride With or Without Metformin
NCT00958269PHASE3TERMINATEDStudy to Evaluate Safety and Efficacy of Dutogliptin in Type 2 Diabetes Mellitus Subjects With Moderate and Severe Renal Impairment
NCT00970424PHASE3TERMINATEDSafety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus (T2DM) on Background Therapy With Pioglitazone
NCT00998686PHASE3TERMINATEDSafety and Efficacy Study of Dutogliptin in Subjects With Type 2 Diabetes Mellitus on a Background Medication of Metformin
NCT01089790PHASE3TERMINATEDSafety and Efficacy of Dutogliptin in Patients With Type 2 Diabetes Mellitus Receiving Background Treatment With Glimepiride Alone or in Combination With Metformin or With Pioglitazone Alone
NCT05881382PHASE3UNKNOWNDutogliptin in Co-administration With Filgrastim in Early Recovery Post-myocardial Infarction
NCT00530881PHASE2COMPLETEDRandomized, Double-Blind, Placebo-Controlled, With PHX1149 in Patients With Type 2 Diabetes Mellitus
NCT01101945PHASE2TERMINATEDLong-term Extension Study to Evaluate the Safety of Dutogliptin/PHX1149T in Subjects With Type 2 Diabetes Mellitus

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

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