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Clinical Trials/NCT02939118
NCT02939118
Completed
N/A

A One-Year, Multicenter, Observational, Follow-up Safety Study in Subjects Previously Implanted With VC-01™ Combination Product

ViaCyte0 sites51 target enrollmentNovember 7, 2016

Overview

Phase
N/A
Intervention
Not specified
Conditions
Type 1 Diabetes Mellitus
Sponsor
ViaCyte
Enrollment
51
Primary Endpoint
Incidence of adverse events reported during the study.
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this trial is to evaluate the long-term safety in subjects previously implanted with VC-01™ combination product.

Registry
clinicaltrials.gov
Start Date
November 7, 2016
End Date
February 8, 2024
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ViaCyte
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Previous implantation of VC-01™ combination product with subsequent explantation of all VC-01 units.

Exclusion Criteria

  • There are no exclusion criteria for this trial.

Outcomes

Primary Outcomes

Incidence of adverse events reported during the study.

Time Frame: 12 months

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