Dersimelagon
drugOn this page
Also known as Mt-7117
Summary
Dersimelagon (CHEMBL4802160) is a phase-3 clinical-stage small molecule; indicated across 5 conditions including erythropoietic protoporphyria and diffuse scleroderma.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- Indications: 5 conditions
- Clinical trials: 11
- Chemistry: 675.8 Da · C36H45F4N3O5
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4802160 |
| Name | Dersimelagon |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 126736894 |
| Molecular formula | C36H45F4N3O5 |
| Molecular weight | 675.8 |
| InChIKey | MUNWOYRHJPWQNE-GMFUQMJFSA-N |
SMILES: COC[C@H]1CN(C[C@@H]1C2=C(C=C(C=C2)C(F)(F)F)N3CCC(CC3)C(=O)O)C(=O)[C@@]4(CN(C[C@H]4C5=CC=C(C=C5)OC)C6CCCC6)F
IUPAC name: 1-[2-[(3S,4R)-1-[(3R,4R)-1-cyclopentyl-3-fluoro-4-(4-methoxyphenyl)pyrrolidine-3-carbonyl]-4-(methoxymethyl)pyrrolidin-3-yl]-5-(trifluoromethyl)phenyl]piperidine-4-carboxylic acid
Also known as: Dersimelagon, Mt-7117, MT-7117, DERSIMELAGON
Parent form; salt/anhydrous children: CHEMBL4802244
Patent coverage: 21 distinct patent families (69 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
5 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).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| erythropoietic protoporphyria | 3 | MONDO:0001676 | MONDO:0001676 |
| diffuse scleroderma | 2 | MONDO:0005019 | EFO:0000404 |
| liver disorder | 1 | MONDO:0005154 | EFO:0001421 |
| kidney disorder | 1 | MONDO:0005240 | EFO:0003086 |
| phototoxic dermatitis | 1 | MONDO:0006598 | EFO:1000753 |
Clinical trials
Total trials: 11.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 8 |
| PHASE3 | 2 |
| PHASE2 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05005975 | PHASE3 | RECRUITING | Extension Study to Evaluate Safety and Tolerability of Oral Dersimelagon (MT-7117) in Subjects With Erythropoietic Protoporphyria (EPP) or X-Linked Protoporphyria (XLP) |
| NCT06144840 | PHASE3 | ACTIVE_NOT_RECRUITING | INcreased Sun Exposure Without Pain In Research Participants With EPP or XLP |
| NCT04440592 | PHASE2 | COMPLETED | Study to Evaluate Efficacy, Safety, and Tolerability of MT-7117 in Subjects With Diffuse Cutaneous Systemic Sclerosis |
| NCT02834442 | PHASE1 | COMPLETED | A Study to Investigate the Safety, Tolerability and Pharmacokinetics of MT-7117 in Healthy Subjects |
| NCT03503266 | PHASE1 | COMPLETED | Mass Balance Study With MT-7117 |
| NCT03688022 | PHASE1 | COMPLETED | Relative Bioavailability and Drug-drug Interaction Study With MT-7117 and a Proton Pump Inhibitor |
| NCT04116476 | PHASE1 | COMPLETED | Study to Assess Pharmacokinetics, Safety, and Tolerability of MT-7117 in Subjects With Normal and Impaired Hepatic Function |
| NCT04656795 | PHASE1 | COMPLETED | PK Study in Subjects With Renal Impairment (Severe and if Required Mild & Moderate) Compared to Subjects With Normal Renal Function |
| NCT04793295 | PHASE1 | COMPLETED | Study to Investigate Drug-Drug Interaction Between MT-7117 and Test Drugs in Healthy Subjects |
| NCT05241535 | PHASE1 | COMPLETED | Study to Evaluate the Effect of a Single Oral Dose of MT-7117 on the QT/QTc Interval in Healthy Subjects |
| NCT06994286 | PHASE1 | COMPLETED | The Purpose of This Study is to Investigate the Safety, Tolerability and Pharmacokinetics of MT-7117 in Healthy Subjects. |
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
- Diseases: erythropoietic protoporphyria