Status:

COMPLETED

Comparing the Efficacy, Safety, and Tolerability of Combination Antivirals (Amantadine, Ribavirin, Oseltamivir) Versus Oseltamivir for the Treatment of Influenza in Adults at Risk for Complications

Lead Sponsor:

National Institute of Allergy and Infectious Diseases (NIAID)

Conditions:

Influenza

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

Seasonal influenza is responsible for many hospitalizations and deaths each year, despite effective antiviral treatments. Some individuals have medical conditions such as heart or lung diseases that m...

Detailed Description

Seasonal influenza is responsible for approximately 226,000 excess hospitalizations annually and despite effective antivirals causes significant morbidity and mortality (estimated 24,000-50,000 deaths...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Enrollment (Screening)
  • Signed informed consent prior to initiation of any study procedures
  • Presence of an underlying medical condition(s) that might increase risk of complications from influenza
  • History of an influenza-like illness defined as:
  • One or more respiratory symptom (cough, sore throat, or nasal symptoms) AND
  • Either
  • Fever (subjective or documented \>38 degrees C) OR
  • 1 or more constitutional symptom (headache, malaise, myalgia, sweats/chills or fatigue)
  • Onset of illness no more than 96 hours before screening defined as when the subject experienced at least one respiratory symptom, constitutional symptom, or fever
  • Willingness to have samples stored
  • Randomization
  • Signed informed consent
  • Presence of a medical condition(s) that had been associated with increased risk of complications from influenza
  • Age 65 years of age or older
  • Asthma
  • Neurological and neuro-developmental conditions (including disorders of the brain, spinal cord, peripheral nerve, and muscle such as cerebral palsy, epilepsy \[seizure disorders\], stroke, moderate to severe developmental delay, muscular dystrophy, or spinal cord injury) \[though still able to provide informed consent per inclusion criteria #1\]
  • Chronic lung disease (such as COPD and cystic fibrosis)
  • Heart disease (such as congenital heart disease, congestive heart failure, and coronary artery disease)
  • Blood disorders (excluding genetic causes of anemia, as noted in the exclusion criteria)
  • Endocrine disorders (such as diabetes mellitus)
  • Kidney disorders
  • Liver disorders
  • Metabolic disorders (such as inherited metabolic disorders and mitochondrial disorders)
  • Weakened immune system due to disease or medication (such as people with HIV/AIDS, or cancer, chronic steroids or other medications causing immune suppression)
  • BMI ≥ 40(kg/m²)
  • Onset of illness no more than 96 hours before screening defined as when the subject experienced at least one respiratory symptom, constitutional symptom, or fever
  • Positive test for influenza (either rapid antigen or PCR)
  • \- Results from influenza testing obtained for clinical indications within 12 hours before screening/enrollment may be used if available. Randomization may proceed in cases of discrepant results (one positive and one negative)
  • One of the following to avoid pregnancy:
  • Females who were able to become pregnant (i.e., are not postmenopausal, have not undergone surgical sterilization, and are sexually active with men) must agree to use at least 2 effective forms of contraception from the date of informed consent through 6 months after the last dose of study drug. At least one of the methods of contraception should be a barrier method
  • Males who had not undergone surgical sterilization and are sexually active with women must agree to use condoms plus have a partner use at least one additional effective form of contraception from the date of informed consent through 6 months after the last dose of study drug
  • Willingness to have samples stored
  • EXCLUSION CRITERIA:
  • (for Enrollment or Randomization)
  • Women who were pregnant or breast-feeding, and men whose female partner(s) was pregnant
  • Inability to take oral medication or a history of gastrointestinal malabsorption that would preclude the use of oral medication.
  • Hemoglobin \< 10 g/dL
  • WBC \< 1.5 times 10(9)/L
  • Neutrophils \< 0.75 x 10(9)/L
  • Platelets \< 50 x 10(9)/L
  • History of genetic hemoglobinopathy (e.g., thalassemia major or sickle cell anemia) or autoimmune hemolytic anemia
  • Received more than 2 doses of any antiviral influenza medications since onset of influenza symptoms
  • Received stavudine (d4T), didanosine (ddI), zidovudine (AZT), or azathioprine within 30 days prior to study entry
  • Creatinine clearance less than 60 mL/min (estimated by the Cockcroft-Gault equation using serum creatinine)
  • History of autoimmune hepatitis
  • Uncompensated liver disease (defined as AST \> 3 times site upper limit of normal (ULN), ALT \> 3 times ULN, or Direct Bilirubin \> 2 times ULN)
  • Clinical signs of end-stage liver disease including jaundice, coagulopathy, portal hypertension, esophageal varices, ascites, peripheral edema, gastrointestinal bleeding, or encephalopathy
  • Chronic liver disease categorized as Child-Pugh class C (Child-Pugh score 10-15)
  • Known hypersensitivity to rimantadine, amantadine, ribavirin, oseltamivir, peramivir, or zanamivir
  • Received live attenuated virus vaccine (influenza or other) within 3 weeks prior to study entry
  • Use of any investigational drug within 30 days or 5 half-lives (whichever was longer) prior to study entry
  • Participation in other research protocols that would require more than 100 mL of blood to be drawn in any 4-week period that overlaps with this study.

Exclusion

    Key Trial Info

    Start Date :

    September 1 2010

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    March 30 2017

    Estimated Enrollment :

    881 Patients enrolled

    Trial Details

    Trial ID

    NCT01227967

    Start Date

    September 1 2010

    End Date

    March 30 2017

    Last Update

    February 4 2019

    Active Locations (91)

    Enter a location and click search to find clinical trials sorted by distance.

    Page 1 of 23 (91 locations)

    1

    Simon Williamson Clinic

    Birmingham, Alabama, United States, 35211

    2

    East Valley Family Physicians

    Chandler, Arizona, United States, 85224

    3

    Thomas Lenzmeier Family Practice

    Glendale, Arizona, United States, 85308

    4

    Central Phoenix Medical Center

    Phoenix, Arizona, United States, 85020

    Comparing the Efficacy, Safety, and Tolerability of Combination Antivirals (Amantadine, Ribavirin, Oseltamivir) Versus Oseltamivir for the Treatment of Influenza in Adults at Risk for Complications | DecenTrialz