A Study of LY3050258 in Healthy Participants
| Status: | Completed |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 30 - 80 |
| Updated: | 7/29/2018 |
| Start Date: | June 2014 |
| End Date: | December 2014 |
A Multiple-Dose, Dose Escalation, Safety, Tolerability, and Pharmacokinetic Study of LY3050258
This is a multiple dose study of LY3050258 in healthy men and postmenopausal women. This
study will evaluate the safety and how well the body tolerates LY3050258. It will last
approximately 14 weeks with a 2 week follow-up appointment after the last treatment with
study drug.
study will evaluate the safety and how well the body tolerates LY3050258. It will last
approximately 14 weeks with a 2 week follow-up appointment after the last treatment with
study drug.
Inclusion Criteria:
- Healthy males or healthy postmenopausal females, including Japanese participants
- Body mass index (BMI) of 18 and 35 kilograms per square meter (kg/m^2), inclusive
Exclusion Criteria:
- Abnormal siting blood pressure as determined by the investigator
- Abnormality in the 12-lead electrocardiogram (ECG) that, in the opinion of the
investigator, places the participant at an unacceptable risk for study participation
- Aspartate aminotransferase (AST) or alkaline phosphatase (ALT) greater than 2 times
the upper limit of normal (ULN)
- Skin condition that in the opinion of the investigator makes the participant
unsuitable for study participation
- Current use of statins within the last 3 months prior to dosing
- Current use or previous use of anabolic steroids in the preceding 6 months prior to
dosing
- Use of dehydroepiandrosterone, other potential over-the-counter steroidal supplements,
or other nutritional products intended to have weight-reduction and/or
performance-enhancing effects within 21 days prior to dosing
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