INZ-701

drug
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Summary

Inz-701 (CHEMBL4650401) is a phase-3 clinical-stage unknown.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Unknown
  • Clinical trials: 8

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4650401
NameINZ-701
TypeUnknown
Max phase3

Also known as: Inz-701, INZ-701

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

0 indications (0 at ChEMBL trial phase 4).

Clinical trials

Total trials: 8.

Phase distribution

PhaseTrials
PHASE32
PHASE1/PHASE22
PHASE22
PHASE12

Top trials by phase / activity

NCTPhaseStatusTitle
NCT06046820PHASE3ACTIVE_NOT_RECRUITINGThe ENERGY 3 Study: Evaluation of Efficacy and Safety of INZ-701 in Children With ENPP1 Deficiency
NCT07473973PHASE3RECRUITINGENERGY 2: Evaluation of the Efficacy and Safety of INZ-701 in Infants With ENPP1 Deficiency
NCT06462547PHASE2RECRUITINGADAPT Study: Long-term Safety Study of INZ-701 in Patients With ENPP1 Deficiency and ABCC6 Deficiency
NCT04686175PHASE1/PHASE2COMPLETEDEvaluation of Safety, Tolerability, and Efficacy of INZ-701 in Adults With ENPP1 Deficiency
NCT05030831PHASE1/PHASE2COMPLETEDEvaluation of Safety, Tolerability, and Efficacy of INZ-701 in Adults With ABCC6 Deficiency Causing PXE
NCT06739980PHASE2WITHDRAWNThe ENABLE Study: Safety and Efficacy Study of INZ-701 in Patients With ENPP1 Deficiency
NCT05734196PHASE1RECRUITINGThe ENERGY Study: Evaluation of Safety and Tolerability of INZ-701 in Infants With ENPP1 Deficiency or ABCC6 Deficiency
NCT06283589PHASE1COMPLETEDThe SEAPORT 1 Study: Evaluation of the Safety and Tolerability of INZ-701 in Adults With End-Stage Kidney Disease Undergoing Hemodialysis

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).

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.