Trial Information
Summary: A Study of Tamiflu (Oseltamivir) for Treatment of Influenza in Immunocompromised Patients.
Status: Recruiting
Protocol Number: NV20234
Sponsor: Hoffmann-La Roche
Company Division: Pharmaceutical
Official Scientific Title: A randomized, double-blind trial evaluating conventional and high dose Tamiflu in the treatment of influenza in immunocompromised patients
Brief Summary: This 2 arm study will investigate the efficacy and safety of twice daily conventional and high dose Tamiflu for the treatment of immunocompromised patients (as represented by transplant recipients). Eligible transplant recipients suffering from symptoms of an influenza-like illness will be randomized to receive either conventional dose (30mg-75mg twice daily po, depending on age and weight) or high dose (60mg-150mg twice daily po depending on age and weight) Tamiflu for 10 days. Nasal and throat swabs will be taken, and safety evaluations made, at intervals during the study. The anticipated time on study treatment is <3 months, and the target sample size is 100-500 individuals. Target sample size is
250.
Study Phase: IV
Study Design / Study Details:
- Purpose: Treatment
- Allocation: Randomized
- Masking: Double Blind
- Control: Active
- Assignment: Parallel
- Endpoints: Safety/Efficacy
Study Type:
Interventional
Condition: Influenza
Intervention Type: Drug
Intervention Name: oseltamivir [Tamiflu]
Primary Outcome: 1. Time to alleviation of all clinical influenza symptoms Time frame: Event driven
Key Secondary Outcomes: 1. Virus shedding and viral load Time frame: Days 1, 2, 6, 8, 11, 15 and 40
2. Time to resolution of fever Time frame: Event driven
3. Development of secondary illnesses, antibiotic use and hospitalizations. Time frame: Event driven
4. AEs, lab parameters, vital signs. Time frame: Throughout study
Inclusion Criteria:
- male and female patients, >=1 year of age;
- rapid diagnostic test positive for influenza in 24h prior to first dose;
- immunocompromised patients (liver and/or kidney transplant recipient, or allogenic HSCT);
- receiving immunosuppressant treatment, or not immune reconstituted;
- symptoms suggestive of influenza-like illness.
Exclusion Criteria:
- influenza vaccination in 2 weeks prior to randomization;
- antiviral treatment for influenza in 2 weeks prior to randomization;
- >48h between illness onset and first dose of study drug;
- SOT other than liver and/or kidney.
Gender: Males or Females
Age Limits: Min: 1 year Years
Accepts Healthy Volunteers: No
Anticipated Start Date: February, 2008
Trial Registration Date: 10/15/2007
Date Last Updated: 04/16/2008
Link To Trial Results
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Contact:
Research Site:
Located In:
Szeged, Hungary, 2724
Telephone: 973-235-5000 or 800-526-6367
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Trial listings updated: May 13, 2008 at 1:58:16 PM