Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Avigen
Age
18–65
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Non-smoking
Body mass index between 18.5 and 29.9 kg/m2 or body mass index greater than 29.9 kg/m2 with good to excellent body fat percentage
You may not be if
Known hypersensitivity to lidocaine or non-steroidal anti-inflammatory agents (NSAIDS)
History of clinically significant cardiovascular, pulmonary, endocrine, neurological, metabolic, or psychiatric disease
History of HIV or Hepatitis B
History of symptomatic hypotension
History of mental illness, drug addiction, drug abuse or alcoholism
History of cancer
History of inflammatory arthritis (rheumatoid, lupus, psoriatic arthritis)
Current use of immunosuppressive therapy (systemic steroids, cyclosporine) or use of nasal or topical steroids
History of gastric or duodenal ulcer disease
History of severe physical injury, direct impact trauma or neurological trauma within 6 months of Study Day 1
Female subjects who are pregnant or nursing
Have donated blood within 90 days of Study Day -1
Have received an investigational drug within 90 days of Screening
Require regular use of antihistamines, H2 blockers (such as cimetidine, ranitidine), TCAs or SSRIs or who have taken these medications witin 14 days of Study Day 1
