TELI COM - Telithromycin in Children With Otitis Media

Phase 3

Terminated

• Conditions: Otitis Media, Suppurative; Otitis Media, Purulent

• Registration Number: NCT00315003
• Lead Sponsor: Sanofi

Brief Summary

This is a multinational, randomized (1:1), double-blind, double-dummy, comparative, 2- treatmentgroup study in children (age range: ≥6 months and \<72 months \[\< 6 years of age\]) with AOM.Subjects will be randomized to receive either telithromycin (50 mg/mL) oral suspension 25 mg/kgonce daily for 5 days or azithromycin (40 mg/mL) oral suspension (10 mg/kg once on Day 1, followed by 5 mg/kg once daily on Days 2-5, not to exceed 500 mg onDay 1 and 250 mg/day from Days 2 - 5. Matching placebo suspensions for telithromycin and azithromycin will also be dispensed to provide blinding for the different treatment regimens.Assessments and reporting of safety will be carried out at all visits.

Detailed Description

Not available

Study Timeline

• Study Start: 2006-01
• Study First Submitted: 2006-04-13
• Study First Submitted QC: 2006-04-14
• Study First Posted: 2006-04-17
• Primary Completion: 2006-07
• Study Completion: 2006-07
• Status Verified: 2009-04
• Last Update Submitted: 2009-04-02
• Last Update Posted: 2009-04-03

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 1500

Inclusion Criteria

Subjects meeting all of the following criteria will be considered for enrollment into the study:

• Subjects ≥6 months and <72 months (< 6 years) of age;

• Recent (within the last 72 hours) and rapid onset of AOM symptoms and signs;

• The presence of MEF on otoscopy indicated by a bulging tympanic membrane;

• Otalgia or ear tugging or touching within the last 24 hours that interferes with or precludes normal activity or sleep;

• At least 1 of the following clinical findings not specific to AOM: fever, vomiting, diarrhea, anorexia, sleep disturbance, or irritability;

• Caregiver-reported AOM symptoms sufficient for entry according to protocol criteria.

• Caregiver-reported AOM symptoms diary

• Tympanometry exhibiting:

  • Type B curve or positive pressure peak curves.

Exclusion Criteria

Subjects presenting with any of the following will not be included in the study:

• Uncertain diagnosis of AOM or mild to moderate symptoms and signs of AOM that would make the subject a candidate for observation and analgesic therapy with observation for 2-3 days.
• Otorrhea or tympanostomy tube present in the ear to be evaluated;
• Otitis externa;
• Down syndrome, cleft palate, craniofacial disorders, cystic fibrosis/mucoviscidosis, immotile cilia syndrome, congenital immunodeficiency or acquired immunodeficiency syndrome with <25% CD4 count or requiring prophylaxis for Pneumocystis jiroveci (carinii) or requiring treatment for an opportunistic infection;
• Known congenital long QT syndrome;
• Known or suspected uncorrected hypokalemia (≤3 mmol/L [mEq/L]), hypomagnesemia, bradycardia (<50 bpm);
• Myasthenia gravis;
• Known impaired renal function, as shown by creatinine clearance ≤25 mL/min;
• History of hypersensitivity or intolerance to macrolides or azithromycin;
• Previous enrollment in this study or previous treatment with telithromycin;
• Children of the investigator or subinvestigator, research assistant, pharmacist, study coordinator, other staff, or relative thereof directly involved in the conduct of the protocol.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
The primary efficacy variables will be time to symptom resolution (TSR) and clinical cure at theposttherapy/TOC Visit 3.

Secondary Outcome Measures

Name	Time	Method
Adverse events (AEs) reported by subjects, their parents/legally authorized representative, orobserved by the investigators will be recorded throughout the study.

Trial Locations

Locations (1)

Sanofi-Aventis; 🇵🇪 Lima, Peru