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Clinical Trials in Canada / NCT06408311
Active, not recruiting Phase 1

Safety of ENC-201-CED ENCRT

NCT06408311 · tracked via the Priya Life Science Canada tracker
Sponsor
Encellin
Phase
Phase 1
Started
2024-05-01
Last updated
2026-03-11

Condition(s) studied

Diabetes Mellitus, Type 1

Investigational drug(s) / intervention(s)

ENC-201-CED hPI

ENC-201-CED hPI: macro-encapsulated human primary islets

Study summary

The purpose of the study is to evaluate the safety and tolerability of ENC-201-CED in a subcutaneous space in patients with Type I diabetes.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Candidates must satisfy site's eligibility for standard of care islet infusion. Exclusion Criteria: * Candidates are excluded based on the site's criteria for standard of care islet infusion.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
UHN Toronto Ontario
McGill University Health Centre Montreal Quebec

More Encellin trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06408311 on ClinicalTrials.gov ↗ ← All trials in Canada