A Phase 2a Study to Evaluate Orally Administered ALS-008176 in Adults Hospitalized With a Respiratory Syncytial Virus

Completed · Phase 2 · Has a placebo group

Conditions studied: Respiratory Syncytial Virus Infections

In brief

This study is being to see how effective and safe ALS-008176 is in treating adults in the hospital with a Respiratory Syncytial Virus-Related Illness.

Key facts

Study ID: NCT02673476
Run by: Alios Biopharma Inc.
People needed: 9
Starts: 2016-02-29
Expected to finish: 2016-10-31
Last updated by the study team: 2025-02-04

Who can join

Age: 50 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subject is ≥50 years of age.
Female subjects of non-childbearing potential (i.e., surgically sterilized, post-menopausal [amenorrhea for 1 year confirmed by negative hormone panel]) who also have a negative pregnancy test at screening.
Male subjects must be either surgically sterilized (e.g., post-vasectomy or orchiectomy) or willing to adhere to the study's contraceptive requirements. Male subjects'female partner(s) must be surgically sterilized or post-menopausal (amenorrhea for 1 year) or their female partner(s) of child-bearing potential must be willing and able to adhere to the contraceptive requirements.
Each subject or their legal guardian must sign an informed consent form (ICF) indicating that he or she understands the purpose of and procedures required for the study and is willing to participate in the study before starting any screening activities.
Subject has a positive RT-PCR test result for RSV at the time of screening. NOTE: Co-infection with other acute viruses or bacteria is permitted.
Subject has been, or will be, admitted to the hospital for an acute respiratory illness with signs and symptoms consistent with a viral infection (e.g., fever, cough, nasal congestion, runny nose, sore throat, myalgia, lethargy, shortness of breath, or wheezing) with onset <7 days from the anticipated time of randomization.

You may not qualify if…

Subject is undergoing peritoneal dialysis, hemodialysis or hemofiltration or has an estimated glomerular filtration rate (GFR, determined by Cockcroft-Gault Formula) <30 mL/min.
Subject has presence of any concurrent illness, including laboratory, vital sign, ECG, or physical exam findings, or medical history that, in the opinion of the investigator, would place the subject at an unreasonably increased risk as a result of participation in this study.
Subject reports receiving an investigational drug or vaccine within 30 days, or 5 half-lives (whichever is longer) prior to the planned first dose of study drug.
Subject has a known history of human immunodeficiency virus (HIV) or chronic, active hepatitis infection.
ALT >3×ULN AND bilirubin >2×ULN (direct >35%) OR ALT>5×ULN
Subjects who have been hospitalized for >72 hours at the time of randomization.
Subjects anticipated to be hospitalized for <24 hours after randomization.
Subjects who are not expected to survive for <48 hours.
Recent (<5 half-lives) use, or anticipated use during conduct of the study, of concomitant medications (prescription and non-prescription) which are inhibitors of the OAT3 transporter.
Treatment of the current illness with drugs specifically targeting the RSV infection itself (e.g., RSV immunoglobulin, ribavirin, palivizumab). Medications treating the sequelae of the RSV infection or any concurrent illness are permitted if not otherwise excluded.
Subjects unwilling to undergo regular nasal swab procedures or with any physical abnormality which limits the ability to collect regular nasal specimens.
Subjects that are considered by the investigator to be immunocompromised over the past 12 months, whether due to underlying medical condition or medical therapy.
Subjects unable to take medications enterally (e.g., orally or via nasogastric or PEG tube) or a known gastrointestinal-related condition that may interfere with study drug absorption.
Female subject that is pregnant or breastfeeding
In the investigator's opinion, the subject is unwilling or unable to comply with protocol requirements, instructions, and protocol stated restrictions, and is unlikely to complete the study as planned.
Subject has known or suspected hypersensitivity to the study drug or its excipients (microcrystalline cellulose, mannitol, croscarmellose sodium, magnesium stearate, polyethylene glycol, polyvinyl alcohol, talc, titanium dioxide).

Where it is running

Lake Internal Med. Assoc. — Eustis, Florida, United States
The Research Center, Inc. — Hialeah, Florida, United States
JDH Medical Group LLC — Miami, Florida, United States
St Lucie Medical Center — Port Saint Lucie, Florida, United States
Tampa Genereal Hospital — Tampa, Florida, United States
Infectious Disease Specialists of Atlanta — Atlanta, Georgia, United States
Kentucky Lung Clinic, PSC — Hazard, Kentucky, United States
Bronson Methodist Hosp. Ped — Kalamazoo, Michigan, United States
William Beaumont Hospital — Troy, Michigan, United States
University of Missouri- Clinical Research Center — Columbia, Missouri, United States
Washington Univ School of Med — St Louis, Missouri, United States
Westmead Hospital — Northmead, New South Wales, Australia
Cairns Hospital — Cairns, Queensland, Australia
Mater Adult Hospital — South Brisbane, Queensland, Australia
Princess Alexandra Hospital — Woolloongabba, Queensland, Australia
The Queen Elizabeth Hospital — Woodville South, South Australia, Australia
Monash Heal.-Monash Lung&Sleep — Clayton, Victoria, Australia
The Royal Melbourne Hospital — Parkville, Victoria, Australia
Wellington Regional Hospital — Newtown, Wellington Region, New Zealand
Raffles Hospital — Singapore, Singapore
Taipei Med. Uni-Shuang Ho Hosp — New Taipei City, Taiwan

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.