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Clinical Trials/NL-OMON36630
NL-OMON36630
Completed
Not Applicable

Study of the Safety, Tolerability, Pharmacokinetics and Effect on Renal Potassium Clearance after Multiple Oral Dosing of LY2623091 in Healthy Volunteers - LY2623091 MAD study

Eli Lilly0 sites32 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
chronic kidney disease
Sponsor
Eli Lilly
Enrollment
32
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
Eli Lilly

Eligibility Criteria

Inclusion Criteria

  • \- Healthy males and/or healthy females (postmenopausal/sterilized)
  • \- 18\-65 years, inclusive
  • \- BMI: 19\.0\-32\.5 kg/m2, inclusive
  • \- non\-smoking, or smoking a maximum of10 cigarettes/day

Exclusion Criteria

  • Suffering from: hepatitis B, cancer or HIV/AIDS. In case of participation in another drug study within 60 days before the start of this study or being a blood donor within 60 days from the start of the study. In case of donating more than 1\.5 liters of blood (for men) / more than 1\.0 liters of blood (for women) in the 10 months prior the start of this study.

Outcomes

Primary Outcomes

Not specified

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