To evaluate the safety,tolerability and antiviral activitity of ALN-RSV01 in RSV infected lung transplant patients
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
24
administered by nebulization once daily for 3 days
administered by nebulization once daily for 3 days
Clinical Site
San Diego, California, United States
Clinical Site
San Francisco, California, United States
Clinical Site
Denver, Colorado, United States
Assess safety and tolerability of aerosolized ALN-RSV01 versus placebo in lung transplant patients infected with RSV
Time frame: Day 30
Evaluate effects of ALN-RSV01 on clinical and virologic endpoints
Time frame: Throughout Trial
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Clinical Site
Gainesville, Florida, United States
Clinical Site
Atlanta, Georgia, United States
Clinical Site
Chicago, Illinois, United States
Clinical Site
Boston, Massachusetts, United States
Clinical Site
Minneapolis, Minnesota, United States
Clinical Site
Cleveland, Ohio, United States
Clinical Site
Nashville, Tennessee, United States
...and 3 more locations