Phase 2 Study of ALN-RSV01 in Lung Transplant Patients Infected With Respiratory Syncytial Virus (RSV)
Completed · Phase 2
Conditions studied: Respiratory Syncytial Virus Infections
In brief
To evaluate the safety,tolerability and antiviral activitity of ALN-RSV01 in RSV infected lung transplant patients
Key facts
- Study ID
- NCT00658086
- Run by
- Alnylam Pharmaceuticals
- People needed
- 24
- Starts
- 2008-04-01
- Expected to finish
- 2009-06-01
- Last updated by the study team
- 2018-01-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Single or bilateral lung transplant recipients
- Confirmed RSV infection
- Greater than 90 days post current lung transplant
- Rejection free for a minimum of 1 month
You may not qualify if…
- Antimicrobial therapy for known viral, bacterial, or fungal respiratory co-infection at the time of diagnosis
- Bronchiolitis obliterans syndrome (BOS) Grade 3 or any state BOS with FEV1 that has not been stable for at least 3 months
- Use of alemtuzumab within 9 months prior to screening; anti-thymocyte globulin(ATG) or thymoglobulin within 3 months of screening: concurrent use of >= 0.3 mg/kg/day prednisone or equivalent as maintenance therapy
- active treament for acute graft rejection
Where it is running
- Clinical Site — San Diego, California, United States
- Clinical Site — San Francisco, California, United States
- Clinical Site — Denver, Colorado, United States
- 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
- Clinical Site — Sydney, New South Wales, Australia
- Clinical Site — Brisbane, Queensland, Australia
- Clinical Site — Perth, Western Australia, Australia
Full record on ClinicalTrials.gov
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