Pegozafermin
drug drugOn this page
Also known as BIO89100PegozaferminaPegozafermineTEV-47948
Summary
Pegozafermin (CHEMBL4594466) is a phase-3 clinical-stage protein targeting FGFR1; indicated across 3 conditions including hypertriglyceridemia and metabolic dysfunction-associated steatohepatitis.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Protein
- Targets: 1 (FGFR1)
- Indications: 3 conditions
- Clinical trials: 7
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL4594466 |
| Name | Pegozafermin |
| Type | Protein |
| Max phase | 3 |
Also known as: BIO89100, Pegozafermin, Pegozafermina, Pegozafermine, TEV-47948, PEGOZAFERMIN
Targets
Targets
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| FGFR1 | fibroblast growth factor receptor 1 | Agonist | 9.22 | 11.5% | P11362 |
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
Aggregated over 1 target gene(s): FGFR1.
Top Reactome pathways
22 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| PI3K Cascade | 1 | FGFR1 |
| PIP3 activates AKT signaling | 1 | FGFR1 |
| Signaling by FGFR1 amplification mutants | 1 | FGFR1 |
| Signaling by activated point mutants of FGFR1 | 1 | FGFR1 |
| FGFR1b ligand binding and activation | 1 | FGFR1 |
| FGFR1c ligand binding and activation | 1 | FGFR1 |
| FGFR1c and Klotho ligand binding and activation | 1 | FGFR1 |
| Constitutive Signaling by Aberrant PI3K in Cancer | 1 | FGFR1 |
| NCAM signaling for neurite out-growth | 1 | FGFR1 |
| Signal transduction by L1 | 1 | FGFR1 |
| Phospholipase C-mediated cascade: FGFR1 | 1 | FGFR1 |
| Downstream signaling of activated FGFR1 | 1 | FGFR1 |
| SHC-mediated cascade:FGFR1 | 1 | FGFR1 |
| PI-3K cascade:FGFR1 | 1 | FGFR1 |
| FRS-mediated FGFR1 signaling | 1 | FGFR1 |
| Negative regulation of FGFR1 signaling | 1 | FGFR1 |
| Signaling by FGFR1 in disease | 1 | FGFR1 |
| RAF/MAP kinase cascade | 1 | FGFR1 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | 1 | FGFR1 |
| Signaling by plasma membrane FGFR1 fusions | 1 | FGFR1 |
| Epithelial-Mesenchymal Transition (EMT) during gastrulation | 1 | FGFR1 |
| Formation of paraxial mesoderm | 1 | FGFR1 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| negative regulation of transcription by RNA polymerase II | 1 |
| MAPK cascade | 1 |
| skeletal system development | 1 |
| angiogenesis | 1 |
| ureteric bud development | 1 |
| in utero embryonic development | 1 |
| organ induction | 1 |
| neuron migration | 1 |
| epithelial to mesenchymal transition | 1 |
| positive regulation of mesenchymal cell proliferation | 1 |
| chondrocyte differentiation | 1 |
| protein phosphorylation | 1 |
| sensory perception of sound | 1 |
| positive regulation of cell population proliferation | 1 |
| fibroblast growth factor receptor signaling pathway | 1 |
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 |
|---|---|---|---|
| hypertriglyceridemia | 3 | MONDO:0005347 | EFO:0004211 |
| metabolic dysfunction-associated steatohepatitis | 2 | MONDO:0007027 | EFO:1001249 |
| metabolic dysfunction-associated steatotic liver disease | 2 | MONDO:0013209 | EFO:0003095 |
Clinical trials
Total trials: 7.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 3 |
| PHASE2 | 2 |
| PHASE1/PHASE2 | 1 |
| PHASE1 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05852431 | PHASE3 | ACTIVE_NOT_RECRUITING | To Evaluate the Efficacy and Safety of Pegozafermin in Subjects With Severe Hypertriglyceridemia |
| NCT06318169 | PHASE3 | RECRUITING | A Study Evaluating the Efficacy and Safety of Pegozafermin in Participants With MASH and Fibrosis (ENLIGHTEN-Fibrosis) |
| NCT06419374 | PHASE3 | RECRUITING | A Study to Evaluate the Efficacy and Safety of Pegozafermin in Participants With Compensated Cirrhosis Due to MASH |
| NCT04048135 | PHASE1/PHASE2 | COMPLETED | A Multiple Ascending Dose Study of Pegozafermin in Participants With Biopsy Confirmed Nonalcoholic Steatohepatitis (NASH) or Nonalcoholic Fatty Liver Disease (NAFLD) and at High Risk of NASH |
| NCT04541186 | PHASE2 | COMPLETED | Study to Explore the Efficacy and Safety of BIO89-100 (Pegozafermin) in Participants With Severe Hypertriglyceridemia |
| NCT04929483 | PHASE2 | COMPLETED | Study Evaluating the Safety, Efficacy and Tolerability of BIO89-100 in Subjects With Biopsy-confirmed Nonalcoholic Steatohepatitis (NASH) |
| NCT05022693 | PHASE1 | COMPLETED | PK Study of Liquid Formulation of BIO89-100 in Subjects With NASH With Compensation Cirrhosis |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.
84 molecules share ≥1 primary target. Top 84 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| PAZOPANIB | ChEMBL + PubChem | Phase 4 (approved) | FGFR1 |
| REGORAFENIB | ChEMBL + PubChem | Phase 4 (approved) | FGFR1 |
| AXITINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| BRIGATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| CABOZANTINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| CAPIVASERTIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| DASATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| ENTRECTINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| ERDAFITINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| FEDRATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| FUTIBATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| INFIGRATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| LENVATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| MIDOSTAURIN | ChEMBL | Phase 4 (approved) | FGFR1 |
| NICLOSAMIDE | ChEMBL | Phase 4 (approved) | FGFR1 |
| NINTEDANIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| NINTEDANIB ESYLATE | ChEMBL | Phase 4 (approved) | FGFR1 |
| PEMIGATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| PONATINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| SORAFENIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| SUNITINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| TIVOZANIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| UPADACITINIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| VANDETANIB | ChEMBL | Phase 4 (approved) | FGFR1 |
| ADEFOVIR | ChEMBL | Phase 3 | FGFR1 |
| ALISERTIB | ChEMBL | Phase 3 | FGFR1 |
| BRIVANIB | ChEMBL | Phase 3 | FGFR1 |
| BRIVANIB ALANINATE | ChEMBL | Phase 3 | FGFR1 |
| CEDIRANIB | ChEMBL | Phase 3 | FGFR1 |
| DOVITINIB | ChEMBL | Phase 3 | FGFR1 |
| ENZASTAURIN | ChEMBL | Phase 3 | FGFR1 |
| LESTAURTINIB | ChEMBL | Phase 3 | FGFR1 |
| LINIFANIB | ChEMBL | Phase 3 | FGFR1 |
| MOTESANIB | ChEMBL | Phase 3 | FGFR1 |
| OLVEREMBATINIB | ChEMBL | Phase 3 | FGFR1 |
| ORANTINIB | ChEMBL | Phase 3 | FGFR1 |
| RUBOXISTAURIN | ChEMBL | Phase 3 | FGFR1 |
| SEMAXANIB | ChEMBL | Phase 3 | FGFR1 |
| SURUFATINIB | ChEMBL | Phase 3 | FGFR1 |
| AG-13958 | ChEMBL | Phase 2 | FGFR1 |
| AT-9283 | ChEMBL | Phase 2 | FGFR1 |
| AZD-1480 | ChEMBL | Phase 2 | FGFR1 |
| BMS-754807 | ChEMBL | Phase 2 | FGFR1 |
| CENISERTIB | ChEMBL | Phase 2 | FGFR1 |
| CEP-11981 | ChEMBL | Phase 2 | FGFR1 |
| DANUSERTIB | ChEMBL | Phase 2 | FGFR1 |
| DERAZANTINIB | ChEMBL | Phase 2 | FGFR1 |
| DORAMAPIMOD | ChEMBL | Phase 2 | FGFR1 |
| E-7090 | ChEMBL | Phase 2 | FGFR1 |
| ENMD-2076 | ChEMBL | Phase 2 | FGFR1 |
| FEXAGRATINIB | ChEMBL | Phase 2 | FGFR1 |
| FGFR INHIBITOR DEBIO 1347 | ChEMBL | Phase 2 | FGFR1 |
| FISOGATINIB | ChEMBL | Phase 2 | FGFR1 |
| FORETINIB | ChEMBL | Phase 2 | FGFR1 |
| ILORASERTIB | ChEMBL | Phase 2 | FGFR1 |
| LIRAFUGRATINIB | ChEMBL | Phase 2 | FGFR1 |
| LUCITANIB | ChEMBL | Phase 2 | FGFR1 |
| MILCICLIB | ChEMBL | Phase 2 | FGFR1 |
| MK-2461 | ChEMBL | Phase 2 | FGFR1 |
| NARAZACICLIB | ChEMBL | Phase 2 | FGFR1 |
| OCIFISERTIB | ChEMBL | Phase 2 | FGFR1 |
| OSI-632 | ChEMBL | Phase 2 | FGFR1 |
| PEXMETINIB | ChEMBL | Phase 2 | FGFR1 |
| R-406 | ChEMBL | Phase 2 | FGFR1 |
| RAF-265 | ChEMBL | Phase 2 | FGFR1 |
| REBASTINIB | ChEMBL | Phase 2 | FGFR1 |
| RESIGRATINIB | ChEMBL | Phase 2 | FGFR1 |
| ROGARATINIB | ChEMBL | Phase 2 | FGFR1 |
| RX-518 | ChEMBL | Phase 2 | FGFR1 |
| SEGIGRATINIB | ChEMBL | Phase 2 | FGFR1 |
| SU-014813 | ChEMBL | Phase 2 | FGFR1 |
| TANDUTINIB | ChEMBL | Phase 2 | FGFR1 |
| TOCERANIB | ChEMBL | Phase 2 | FGFR1 |
| TOZASERTIB | ChEMBL | Phase 2 | FGFR1 |
| Afatinib | PubChem | Approved | FGFR1 |
| belumosudil | PubChem | Approved | FGFR1 |
| Binimetinib | PubChem | Approved | FGFR1 |
| Crizotinib | PubChem | Approved | FGFR1 |
| dacomitinib | PubChem | Approved | FGFR1 |
| Fostamatinib | PubChem | Approved | FGFR1 |
| Gefitinib | PubChem | Approved | FGFR1 |
| Idelalisib | PubChem | Approved | FGFR1 |
| Selumetinib | PubChem | Approved | FGFR1 |
| Trametinib | PubChem | Approved | FGFR1 |
Related Atlas pages
- Genes: FGFR1
- In clinical trials for: hypertriglyceridemia, metabolic dysfunction-associated steatohepatitis, metabolic dysfunction-associated steatotic liver disease
- Drugs: Pazopanib, Regorafenib, Axitinib, Brigatinib, Cabozantinib, Capivasertib, Dasatinib, Entrectinib, Erdafitinib, Fedratinib, Futibatinib, Infigratinib, Lenvatinib, Midostaurin, Niclosamide, Nintedanib, Pemigatinib, Ponatinib, Sorafenib, Sunitinib, Tivozanib, Upadacitinib, Vandetanib, Adefovir, Alisertib, Brivanib, Brivanib Alaninate, Cediranib, Dovitinib, Enzastaurin, Lestaurtinib, Linifanib, Motesanib, Olverembatinib, Orantinib, Ruboxistaurin, Semaxanib, Surufatinib, Afatinib, belumosudil, Binimetinib, Crizotinib, dacomitinib, Fostamatinib, Gefitinib, Idelalisib, Selumetinib, Trametinib