drugset / Trial / NCT04190693

IMCY-T1D-002: Long-term Follow-up Study of T1D Patients Previously Treated With IMCY-0098 or Placebo

NCT04190693 ↗

Phase 1 Completed 30 enrolled Imcyse SA
RandomizedParallel-groupTriple-blindOther

Summary

This study is the follow-up of study IMCY-T1D 001 (EudraCT: 2016-003514-27, NCT03272269) in which patients with recent onset T1D have been treated with IMCY-0098 or placebo. At the end of the primary 6 month study, patients will be proposed to enter this follow-up study to evaluate up to 12 months (V3 - Week 48) the safety, the immune responses and the clinical parameters. The study involves a follow-up of 6 months after the end of the initial participation to the IMCY-T1D-001 study. Subjects will undergo visits at 24 weeks, 36 weeks and 48 weeks post first study product administration in study IMCY-T1D-001. For each patient, the study comprises a total of 3 visits occurring over a period of approximately 24 weeks (from study entry). The patients will undergo planned assessments and procedures as outlined in the table of study procedures.

Timeline

Start
2019-02-14
Primary completion
2019-10-08
Completion
2019-11-18

Drugs

EvaluationDrugModalityDoseRoute
Subject IMCY-0098 Peptide 25 ug —
Subject IMCY-0098 Peptide 75 ug —
Subject IMCY-0098 Peptide 225 ug —