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Phase 2 N=137 Randomized Quadruple-blind Treatment

Evaluation of Efficacy and Safety of Peramivir in Adults With Acute Serious or Potentially Life-threatening Influenza

Influenza

Enrolled (actual)
137
Serious AEs
10.2%
Results posted
Feb 2015
Primary outcome: Primary: Time to Clinical Stability (Kaplan-Meier Estimate) — 23.7; 37.0; 28.1 hours — p=0.306

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Peramivir 200 mg (Drug); Peramivir 400 mg (Drug); Oseltamivir (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
BioCryst Pharmaceuticals
Primary completion
Sep 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Time to Clinical Stability (Kaplan-Meier Estimate)
23.7; 37.0; 28.1 0.306
SECONDARY
Change From Baseline in Scores of Symptoms of Influenza
1.3; 1.1; 1.2; -0.2; -0.3; -0.3 >0.05
SECONDARY
Time to Resumption of Ability to Perform Usual Activities (Kaplan-Meier Estimate)
8.8; 9.0; 13.7 0.276
SECONDARY
Incidence of Clinical Relapse of Influenza After Treatment (Number of Participants Experiencing Relapse During the Study)
0; 0; 0
SECONDARY
Time to Hospital Discharge (Kaplan-Meier Estimate)
4.0; 3.8; 4.0 0.994
SECONDARY
Change in Amount of Influenza Virus in Nose and Throat (Influenza A and B Combined)
3.6; 3.5; 3.4; -1.5; -1.6; -1.5 >0.05

Summary

This study has been designed as a randomized, double-blind, controlled, study to evaluate the efficacy and safety of two once daily intravenous peramivir regimens (200 mg and 400 mg) versus oral oseltamivir phosphate (75 mg twice daily) in hospitalized subjects with acute serious or potentially life threatening influenza. Study treatments will be provided for up to 5 consecutive days.

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years of age, male or female
  • Able to provide informed consent, or for whom consent may be provided by guardian
  • Presence of fever at time of screening of ≥38.0°C (≥ 100.0°F) taken orally, or ≥38.5°C (≥101.2°F) taken rectally. This requirement is waived if the subject has (1) a history of fever within 24 hours prior to screening and administered any antipyretic(s) in the 24 hours prior to screening, or (2) has no history of documented fever as defined above, but reports a symptom of feverishness at some time during 48 hours prior to screening
  • Presence of at least 1 respiratory symptom (cough, sore throat, nasal congestion/symptoms) of any severity (mild, moderate, severe)
  • Presence of at least 1 constitutional symptom (headache, myalgia, feverishness, malaise, fatigue) of any severity (mild, moderate, severe)
  • Onset of illness no more than 72 hours before presentation. Time of onset of illness defined as either (1) the time when temperature (oral or rectal) was elevated (at least 1°C of elevation-oral temperature), OR (2) the time when the subject experienced the presence of at least 1 respiratory symptom AND the presence of at least 1 constitutional symptom
  • Presence of 1 or more of the following factors in a subject willing to be hospitalized for inpatient observation and treatment:
  • Age ≥60 years
  • Presence of chronic obstructive pulmonary disease (COPD) or other chronic lung disease requiring daily pharmacotherapy
  • History of congestive heart failure with or without medically significant recent change in cardiac status, but without signs or symptoms compatible with NYHA Class IV functional status
  • Presence of diabetes mellitus, clinically stable or unstable
  • Transcutaneous oxygen saturation 1.6 mg/dL or a result >25% above the upper limit of normal for the laboratory performing the test
  • History of clinically significant proteinuria (≥1000 mg/24 hrs)
  • History of moderate or severe renal impairment and/or previous clinical laboratory data indicating an estimated creatinine clearance <50 mL/min during the previous 12 months
  • Electrocardiogram (ECG) at Screening visit showing evidence of acute ischemia, or presence of a medically significant dysrhythmia
  • Presence of cardiac signs or symptoms compatible with NYHA Class III or Class IV functional status for congestive heart failure or angina (see NYHA Appendix V)
  • Presence of diagnosed COPD or other chronic lung condition requiring either continuous or intermittent oxygen therapy as an outpatient. Note: Subjects who are determined to require acute supplemental oxygen therapy at the time of Screening and/or at hospital admission may be enrolled, if exclusion criteria #13 or #14 are not applicable.
  • History of organ transplantation during the previous 12 months
  • Known HIV infection with most recent CD4+ T-cell count ≤350 cells/mL
  • History of diagnosis of any type of cancer (hematologic or solid tumor), that has required chemotherapy or radiation therapy in the previous 12 months, excluding non-melanomatous localized skin cancer
  • Presence of ongoing requirement for chronic mechanical ventilation, either via oral or nasotracheal intubation or via tracheostomy, or chronic or intermittent requirement for BiPAP (bilevel positive airway pressure) at screening. Note: Subjects who require intermittent CPAP treatment for sleep apnea (without oxygen supplementation) may be enrolled
  • Subjects who require acute mechanical ventilatory support of any type at the time of screening.
  • History of alcohol abuse or drug addiction during the previous 12 months
  • Participation in a clinical study of an experimental medication or other treatment during the previous 4 weeks
  • Previous treatment with intravenous or intramuscular peramivir
  • Women who are pregnant (positive serum or urine pregnancy test), who are attempting to become pregnant, or who are breast-feeding
  • Subjects who have been hospitalized due to a condition other than acute influenza a
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00453999). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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