Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Cumberland Pharmaceuticals
Age
18–75
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Weighs at least 45 kg and body mass index of 18 to 40 kg/m2, inclusive
An estimated creatinine clearance value based on Cockcroft-Gault method of:
* \>80 mL/min for subjects with normal renal function
* \<30 mL/min for subjects with severe renal impairment
* receiving hemodialysis three times a week for subjects with end stage renal impairment
If female, the subject is at least 2 years postmenopausal, surgically sterile or practicing effective birth control, and is not pregnant or lactating
Good venous access
You may not be if
History of any clinically significant acute illness (other than renal disease and conditions related to the renal disease in renal impairment subjects, such as stable diabetes or hypertension)
Has had a kidney transplant that is still functioning
History of unexplained syncope, cardiac arrest, unexplained cardiac arrythmia or torsade de pointes, structural heart disease, prolonged QT interval, or family history of long QT syndrome
Known hypersensitivity to telavancin or any of the excipients in the formulation, or a history of severe allergic or anaphylactic reactions
History of consuming more than 7 units of alcoholic beverages per week, or history of alcoholism or substance abuse within past 2 years
Known to be positive for human immunodeficiency virus antibody
For subjects with normal renal function, has had treatment with prescription or non-prescription drugs, including complementary and alternative medicines or over-the counter medications, with the exception of oral contraceptives, hormone replacement therapy, daily aspirin, and occasional use of acetaminophen within the past 14 days
For subjects with renal impairment, has not been on a stable dose of concomitant medications for at least 2 weeks prior to study start or is taking any medication that would interfere with the evaluation of televancin in this study
Has received an experimental agent within 30 days or ten half-lives, whichever is longer, prior to study drug administration
Has had any significant blood loss, donated one unit (450 mL) of blood or more, or received a transfusion of any blood or blood products within 60 days or donated plasma within 7 days prior to admission
Clareo Health | A Study to Evaluate the Effect of Renal Function on the Biological Activity of Telavancin
