CompletedPhase 1NCT06283589

The SEAPORT 1 Study: Evaluation of the Safety and Tolerability of INZ-701 in Adults With End-Stage Kidney Disease Undergoing Hemodialysis

Studying Calciphylaxis

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Key facts

Sponsor
Inozyme Pharma
Principal Investigator
Kurt Gunter, MD
Inozyme Pharma
Intervention
INZ-701(drug)
Enrollment
11 enrolled
Eligibility
18-69 years · All sexes
Timeline
20242024

Study locations (2)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06283589 on ClinicalTrials.gov

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