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Completed Phase 2 Interventional

Phase 2b Study of ALN-RSV01 in Lung Transplant Patients Infected With Respiratory Syncytial Virus (RSV)

ClinicalTrials.gov ID: NCT01065935

Public ClinicalTrials.gov record NCT01065935. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 17, 2026, 7:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Multinational, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Aerosolized ALN-RSV01 Plus Standard of Care in Lung Transplant Patients Infected With Respiratory Syncytial Virus (RSV)

Study identification

NCT ID
NCT01065935
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Alnylam Pharmaceuticals
Industry
Enrollment
87 participants

Conditions and interventions

Interventions

  • ALN-RSV01 Drug
  • Normal Saline Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 31, 2010
Primary completion
Mar 31, 2012
Completion
Apr 30, 2012
Last update posted
Feb 4, 2018

2010 – 2012

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
Clinical Site Phoenix Arizona 85013
Clinical Site Los Angeles California 90033
Clinical Site Denver Colorado 80202
Clinical Site Tampa Florida 33606
Clinical Site Atlanta Georgia 30322
Clinical Site Chicago Illinois 60153
Clinical Site Chicago Illinois 60637
Clinical Site Boston Massachusetts 02114
Clinical Site Boston Massachusetts 02115
Clinical Site Ann Arbor Michigan 48109
Clinical Site St Louis Missouri 63110
Clinical Site New York New York 10032
Clinical Site Cleveland Ohio 44195
Clinical Site Philadelphia Pennsylvania 19104
Clinical Site Pittsburgh Pennsylvania 15213
Clinical Site Nashville Tennessee 37232
Clinical Site Dallas Texas 75390
Clinical Site Houston Texas 77030

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 15 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01065935, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 4, 2018 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01065935 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →