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Clinical Trials/EUCTR2017-003399-30-AT
EUCTR2017-003399-30-AT
Active, not recruiting
Phase 1

A Prospective, Randomized, Double-Blind Comparison of LY900014 and Fiasp®, Both in Combination with Basal Insulin in Adults with Type 1 Diabetes, PRONTO-Compare - PRONTO-Compare

Eli Lilly and Company0 sites632 target enrollmentOctober 19, 2018
DrugsFiasp®

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Eli Lilly and Company
Enrollment
632
Status
Active, not recruiting
Last Updated
7 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 19, 2018
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • You are diagnosed with type 1 diabetes and have been using insulin continuously for at least 12 months
  • You are 18 years of age or older
  • You are already being treated with insulin allowed for study participation.
  • Your blood glucose levels are within allowed limits for study participation
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 581
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 51

Exclusion Criteria

  • You have had more than 1 emergency treatment for very low blood glucose or poor blood glucose control in the last 6 months.
  • You are taking certain diabetes medications that are not allowed for study participation.
  • You have major problems with your heart, kidneys, liver, or you have a blood disorder.
  • You have had, or are now being treated for, certain types of cancer.

Outcomes

Primary Outcomes

Not specified

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