MedPath

Pharmacokinetics, Acceptability and Safety of Famciclovir in Infants (1 Month to Less Than 12 Months) With Herpes Simplex Infection

Phase 2
Completed
Conditions
Herpes Simplex
Interventions
Registration Number
NCT00448227
Lead Sponsor
Novartis
Brief Summary

This study will evaluate the acceptability and safety of famciclovir in infants with herpes simplex infection

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
18
Inclusion Criteria
  • Male and female patients from 1 month up to 1 year of age with herpes simplex infection
Exclusion Criteria
  • Patients with gestational age less than 32 weeks. Patients unable to swallow. Patients with history of malabsorption or previous gastrointestinal surgery.

Other protocol-defined inclusion/exclusion criteria may apply.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
FamciclovirfamciclovirFamciclovir was administered orally as a suspension in OraSweet® on Day 1. Patients received a single, individualized dose between 25-200 mg based on body weight.
Primary Outcome Measures
NameTimeMethod
Pharmacokinetics of Single Dose - TmaxPlasma samples were collected at 0.5, 1, 4 and 6 hours after dosing.

Measured by Tmax - The time after administration of a drug when the maximum plasma concentration is reached.

Pharmacokinetics of Single Dose - CmaxPlasma samples were collected at 0.5, 1, 4 and 6 hours after dosing.

Measured by Cmax - The maximum plasma concentration of study medication

Pharmacokinetics of Single Dose - AUC(0-tlast)Plasma samples were collected at 0.5, 1, 4 and 6 hours after dosing.

Measured by AUC(0-tlast) - Area under the plasma concentration time curve from time zero to the last quantifiable concentration-timepoint.

Pharmacokinetics of Single Dose - AUC(0-6h)Plasma samples were collected at 0.5, 1, 4 and 6 hours after dosing.

Measured by AUC(0-6h) - Area under the plasma concentration time curve from time zero up to 6 hours post dose (i.e. the time of the last sample).

Secondary Outcome Measures
NameTimeMethod
Safety Assessed by AEs, SAEs38 days

AEs and SAEs were collected during patient's stay in the clinic for PK sampling up to Hour 8, then at day 2 visit, 8 days(safety follow-up call) and 38 days (safety follow-up call) post dose.

Safety Assessed by Labs2 days

Samples for safety labs were obtained at baseline and Day 2 visit and samples were analyzed by local accredited laboratory.

Tolerability of of the Famciclovir Pediatric Formulation as Assessed by Study Personnel.30 minutes after dosing

Tolerability was assessed by the study personnel 30 minutes after dosing using the following scale:

1. Significant emesis occurred,

2. Infant spit out most of the dose ingesting less than half of what was administered,

3. Infant spit out some of the dose, but ingested at least 50% of what was administered,

4. Infant was able to ingest and retain the dose administered

Acceptability of the Famciclovir Pediatric Formulation as Assessed by the Patient's CaregiverImmediately after dosing

Assessed by the caregiver using a 5-point scale immediately after dosing:

1. Very badly accepted/unacceptable: infant showed great displeasure, compromising use of formulation

2. Badly but accepted: infant showed displeasure with dosing but could be coaxed to take complete dose

3. Neither good nor bad: infant showed no apparent displeasure and with little effort was coaxed to take complete dose

4. Well accepted: infant appeared to enjoy the formulation and with little coaxing ingested most of dose

5. Very well accepted: infant appeared eager and ingested most of dose without special coaxing

Acceptability of the Famciclovir Pediatric Formulation as Assessed by Study PersonnelImmediately after dosing

Assessed by the study personnel using a 5-point scale after dosing:

1. Very badly accepted/unacceptable: infant showed great displeasure, compromising use of formulation

2. Badly but accepted: infant showed displeasure with dosing but could be coaxed to take complete dose

3. Neither good nor bad: infant showed no apparent displeasure and with little effort was coaxed to take complete dose

4. Well accepted: infant appeared to enjoy the formulation and with little coaxing ingested most of dose

5. Very well accepted: infant appeared eager and ingested most of dose without special coaxing

Trial Locations

Locations (6)

Children's Memorial Hospital Chicago

🇺🇸

Chicago, Illinois, United States

Children's Hospital of Michigan

🇺🇸

Detroit, Michigan, United States

Archana Chatterjee

🇺🇸

Omaha, Nebraska, United States

University Hospital Cased Medical Center Rainbow Babies and Children's Hospital

🇺🇸

Cleveland, Ohio, United States

UT Southwestern Medical Center

🇺🇸

Dallas, Texas, United States

Pediatric Infectious Disease Of University of Alabama

🇺🇸

Birmingham, Alabama, United States

© Copyright 2025. All Rights Reserved by MedPath