Overview

Safety and Efficacy Study of Nitazoxanide in the Treatment of Acute Uncomplicated Influenza

Status:
Completed
Trial end date:
2011-05-01
Target enrollment:
0
Participant gender:
All
Summary
This is a randomized clinical trial designed to evaluate the safety/efficacy of two dosing regimens of oral nitazoxanide compared to placebo in the treatment of acute uncomplicated influenza in adults and adolescents. The investigators hypothesize that treatment with Nitazoxanide will reduce the duration of symptoms in patients with confirmed influenza infection. Secondarily, the investigators hypothesize that treatment with nitazoxanide will reduce the complications of influenza, severity of symptoms, time lost from work, time to return to normal daily activities.
Phase:
Phase 2/Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Romark Laboratories L.C.
Treatments:
Nitazoxanide
Criteria
INCLUSION CRITERIA

- age 12 to 65 years

- Presence of clinical signs, respiratory symptoms and constitutional symptoms
compatible with influenza infection:

1. fever,

2. at least one of the following respiratory symptoms: cough, sore throat, nasal
discharge, nasal congestion, sneezing.

3. At least one of the following constitutional symptoms: headache, myalgia, seats,
chills, fatigue of any severity (mild, moderate, severe)

- Confirmation of Influenza A or B infection in the local community

- Onset of illness no more than 48 hours before presentation. Time of onset of illness
is defined as either the earlier of (1) the time when the temperature was first
measured as elevated, or (2) the time when the patient experienced the presence of at
least one respiratory symptom AND the presence of at least one constitutional symptom.

- willing and able to comply with protocol requirements and provide informed consent

EXCLUSION CRITERIA:

- severity of illness requiring or anticipated to require in-hospital care

- High risk of complications from influenza as follows:

1. persons with asthma or other chronic pulmonary diseases

2. persons with hemodynamically significant cardiac disease

3. persons who have immunosuppressive disorders or receiving immunosuppressive
therapy

4. persons infected with Human Immunodeficiency Virus (HIV)

5. persons with sickle cell anemia or other hemoglobinopathies

6. persons with diseases requiring long-term aspirin therapy

7. persons with chronic renal dysfunction

8. persons with liver disorders

9. Persons with cancer

10. Persons with chronic metabolic disease such as diabetes and inherited
mitochondrial disorders

11. Persons with neuromuscular disorders, seizure disorders, or cognitive dysfunction

12. Residents of any age of nursing homes or long-term institutions.

- Females of child bearing age who are pregnant, breastfeeding or sexually active
without birth control

- vaccination for influenza or H1N1 (Swine Flu) on or after August 1, 2010

- treatment with antiviral medication such as oseltamivir, zanamivir, amantadine, or
rimantadine within 30 days of screening.

- Prior treatment with nitazoxanide within 30 days prior to screening.

- subjects with active respiratory allergies or expected to require anti-allergy
medications during the study period.

- known sensitivity to nitazoxanide

- subjects unable to take oral medication

- subjects with chronic kidney or liver disease

- Presence of any other pre-existing chronic infection that is undergoing or requiring
medical therapy