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RECRUITING
NCT07473973
PHASE3

ENERGY 2: Evaluation of the Efficacy and Safety of INZ-701 in Infants With ENPP1 Deficiency

Sponsor: Inozyme Pharma

View on ClinicalTrials.gov

Summary

The primary purpose of ENERGY 2 (Study INZ701-105) is to assess the efficacy and safety of INZ-701 in infants with ENPP1 Deficiency.

Official title: The ENERGY 2 Study: An Open-Label Phase 3 Study to Evaluate the Efficacy and Safety of INZ-701 in Infants With Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 (ENPP1) Deficiency

Key Details

Gender

All

Age Range

0 Years - 1 Year

Study Type

INTERVENTIONAL

Enrollment

12

Start Date

2025-03-26

Completion Date

2028-11-07

Last Updated

2026-03-18

Healthy Volunteers

No

Interventions

DRUG

INZ-701

Recombinant fusion protein that contains the extracellular domains of human ENPP1 coupled with an Fc fragment from an immunoglobulin gamma-1 (IgG1) antibody.

Locations (8)

Hospital Universitario Pedro Ernesto/Rio de Janeiro

Rio de Janeiro, Brazil

Hopital Necker - Enfants Malades

Paris, France

Gyermekgyogyaszat, DE

Debrecen, Hungary

Azienda Ospedaliera Universitaria Meyer

Florence, Italy

King Faisal Specialist Hospital and Research Center

Riyadh, Saudi Arabia

Hospital Sant Joan de Deu Edificio Consultas Externas. Unitat de Recerca

Barcelona, Esplugues de Llobregat, Spain

Umraniye Traiing and Research Hospital

Istanbul, Turkey (Türkiye)

Royal Manchester Children's Hospital

Manchester, United Kingdom