A Study of LY2216684 in Healthy Participants Receiving Albuterol or Propanolol

Inclusion Criteria:

- Are overtly healthy, as determined by medical history and physical examination.

- Male participants - Agree to use a reliable method of birth control during the study
and for 1 month following the last dose of study drug.

- Female participants - Are women of child-bearing potential who test negative for
pregnancy at the time of enrollment, have used a reliable method of birth control for
6 weeks prior to administration of study drug, and agree to use a reliable method of
birth control during the study and for 1 month following the last dose of study drug;
or Women not of child-bearing potential due to surgical sterilization (hysterectomy or
bilateral oophorectomy or tubal ligation) or menopause [at least 1 year without menses
or 6 months without menses and a follicle stimulating hormone (FSH) >40
milli-international units per milliliter (mIU/mL)].

- Have a body weight >50 kilograms (kg).

- Have clinical laboratory test results within normal reference range for the population
or investigator site, or results with acceptable deviations that are judged to be not
clinically significant by the investigator.

- Have venous access sufficient to allow blood sampling as per the protocol.

- Have normal blood pressure and pulse rate (sitting position) as determined by the
investigator.

- Are reliable and willing to make themselves available for the duration of the study
and are willing to follow study procedures.

- Have given written informed consent approved by Lilly and the ethical review board
(ERB) governing the site.

Exclusion Criteria:

- Are currently enrolled in, or discontinued within the last 30 days from, a clinical
trial involving an investigational drug or device or off-label use of a drug or device
other than the study drug, or are concurrently enrolled in any other type of medical
research judged not to be scientifically or medically compatible with this study.

- Have known allergies to LY2216684, albuterol (Group 1 only), propranolol (Group 2
only), or related compounds.

- Are persons who have previously completed or withdrawn from this study or any other
study investigating LY2216684 within 6 months prior to screening.

- Have an abnormality in the 12-lead electrocardiogram (ECG) that, in the opinion of the
investigator, increases the risks associated with participating in the study.

- Have a history of or current cardiovascular, respiratory, hepatic, renal,
gastrointestinal, endocrine, hematological, or neurological disorders capable of
significantly altering the absorption, metabolism, or elimination of drugs; of
constituting a risk when taking the study medication; or of interfering with the
interpretation of data.

- Have a history of or current asthma, including exercise induced asthma.

- Have a history or show evidence of significant active neuropsychiatric disease or have
a history of suicide attempt or ideation.

- Regularly use known drugs of abuse and/or show positive findings on urinary drug
screening.

- Show evidence of human immunodeficiency virus (HIV) and/or positive human HIV
antibodies.

- Show evidence of hepatitis C and/or positive hepatitis C antibody.

- Show evidence of hepatitis B and/or positive hepatitis B surface antigen.

- Are women with a positive pregnancy test or women who are lactating.

- Intend to use over-the-counter or prescription medication (including hormonal
contraceptives) within 14 days prior to dosing unless deemed acceptable by the
investigator and Sponsor's medical monitor

- Have donated blood of more than 500 milliliters (mL) within the last month.

- Have an average weekly alcohol intake that exceeds 14 units per week, or are unwilling
to stop alcohol consumption 48 hours prior to check-in in each period and while
resident at the Clinical Research Unit (CRU) [1 unit = 12 ounces (oz) or 360 mL of
beer; 5 oz or 150 mL of wine; 1.5 oz or 45 mL of distilled spirits].

- Consume 5 or more cups of coffee (or other beverages of comparable caffeine content)
per day, on a habitual basis, or any participants unwilling to adhere to study
caffeine restrictions.

- Have used any tobacco-containing or nicotine-containing products (including but not
limited to cigarettes, pipes, cigars, chewing tobacco, nicotine patches, nicotine
lozenges, or nicotine gum) within 6 months prior to enrollment.

- Have consumed grapefruit or grapefruit-containing products 7 days prior to enrollment
and during the study.

- Have a documented or suspected history of glaucoma.

- Participants determined to be unsuitable by the investigator for any reason.