Pomaglumetad Methionil Anhydrous
drug drugOn this page
Also known as LY-2140023Ly2140023POMAGLUMETAD METHIONIL
Summary
Pomaglumetad Methionil Anhydrous (CHEMBL2110730) is a phase-3 clinical-stage small molecule; indicated across 4 conditions including post-traumatic stress disorder and methamphetamine dependence.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Indications: 4 conditions
- Clinical trials: 23
- Chemistry: 366.4 Da · C12H18N2O7S2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2110730 |
| Name | Pomaglumetad Methionil Anhydrous |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 25195354 |
| Molecular formula | C12H18N2O7S2 |
| Molecular weight | 366.4 |
| InChIKey | VOYCNOJFAJAILW-CAMHOICYSA-N |
SMILES: CSCC[C@@H](C(=O)N[C@]1(CS(=O)(=O)[C@@H]2[C@H]1[C@H]2C(=O)O)C(=O)O)N
IUPAC name: (1R,4S,5S,6S)-4-[[(2S)-2-amino-4-methylsulfanylbutanoyl]amino]-2,2-dioxo-2lambda6-thiabicyclo[3.1.0]hexane-4,6-dicarboxylic acid
Also known as: LY-2140023, Ly2140023, LY2140023, Pomaglumetad methionil anhydrous, POMAGLUMETAD METHIONIL ANHYDROUS, POMAGLUMETAD METHIONIL
Parent form; salt/anhydrous children: CHEMBL2105707
Patent coverage: 78 distinct patent families (194 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
No target linkage available.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
3 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| post-traumatic stress disorder | 1 | MONDO:0005146 | EFO:0001358 |
| methamphetamine dependence | 1 | MONDO:0005419 | EFO:0004701 |
| psychotic disorder | 1 | MONDO:0005485 | EFO:0005407 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 23.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 12 |
| PHASE2 | 6 |
| PHASE3 | 4 |
| PHASE2/PHASE3 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT01129674 | PHASE2/PHASE3 | TERMINATED | A Long-Term, Open-Label, Study on Schizophrenia |
| NCT01307800 | PHASE3 | TERMINATED | A Study of LY2140023 in Patients With Schizophrenia |
| NCT01328093 | PHASE3 | TERMINATED | A Comparison Study of LY2140023 and Aripiprazole in Schizophrenia Patients |
| NCT01452919 | PHASE3 | COMPLETED | A Physical Dependence Study in Schizophrenia |
| NCT01487083 | PHASE3 | TERMINATED | A Long-Term Study in Schizophrenia |
| NCT00149292 | PHASE2 | COMPLETED | Study of LY2140023 in Schizophrenia Comparing LY2140023, Olanzapine, and Placebo |
| NCT00520923 | PHASE2 | COMPLETED | A Study for Patients With Schizophrenia |
| NCT00845026 | PHASE2 | COMPLETED | A Safety Study Comparing LY2140023 to Atypical Antipsychotic Standard Treatment in Schizophrenic Patients |
| NCT01052103 | PHASE2 | COMPLETED | A Study of LY2140023 in Schizophrenia Patients With Prominent Negative Symptoms |
| NCT01086748 | PHASE2 | COMPLETED | A Study in Schizophrenia Patients |
| NCT01125358 | PHASE2 | TERMINATED | A Study in Schizophrenic Patients |
| NCT01354353 | PHASE1 | COMPLETED | A Study of Safety and Tolerability in Subjects With Schizophrenia |
| NCT01440478 | PHASE1 | COMPLETED | The Effects of Urinary pH Changes on an Investigational Compound in Healthy Subjects |
| NCT01475136 | PHASE1 | COMPLETED | A Study of LY2140023 in Hepatically-Impaired Participants |
| NCT01524237 | PHASE1 | COMPLETED | A Study of LY2979165 and LY2140023 in Healthy Volunteers |
| NCT01591330 | PHASE1 | COMPLETED | A Study of LY2140023 in Healthy Males and Females |
| NCT01606436 | PHASE1 | COMPLETED | A Study Measuring Effect of LY2140023 (Pomaglumetad Methionil) on Electrocardiographs in Participants With Schizophrenia |
| NCT01609218 | PHASE1 | COMPLETED | A Study of LY2140023 in Healthy Participants |
| NCT01637142 | PHASE1 | COMPLETED | A Study of LY2140023 in Healthy Participants |
| NCT01659177 | PHASE1 | WITHDRAWN | A Study of LY2140023 in Healthy Participants |
| NCT02234687 | PHASE1 | TERMINATED | A mGlu2/3 Agonist in the Treatment of PTSD |
| NCT03106571 | PHASE1 | TERMINATED | Study of Pomaglumetad and Methamphetamine |
| NCT03321617 | PHASE1 | COMPLETED | Glutamate Reducing Interventions in Schizophrenia |
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).
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.