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Phase 3 N=1,579 Randomized Double-blind Treatment

Safety and Efficacy of Pagibaximab Injection in Very Low Birth Weight Neonates for Prevention of Staphylococcal Sepsis

Staphylococcal Sepsis

Enrolled (actual)
1,579
Serious AEs
35.7%
Results posted
Oct 2011
Primary outcome: Primary: The Number of Participants With Staphylococcal Sepsis From Study Days 0 to 35. — 85; 79 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Placebo (Drug); Pagibaximab 50 mg/mL (Drug)
Age
Pediatric
Sex
All
Sponsor
Biosynexus Incorporated
Primary completion
May 2011

Outcome Measures

OutcomeResultp-value
PRIMARY
The Number of Participants With Staphylococcal Sepsis From Study Days 0 to 35.
85; 79

Summary

Evaluate the safety, PK and efficacy comparing Pagibaximab Injection to placebo in preventing staphylococcal sepsis in very low birth weight infants. 1550 infants will be enrolled prior to 48 hours of life and will be randomized 1:1 to receive active drug or placebo on study days 0, 1, 2, 9, 16, and 23.

Eligibility Criteria

Inclusion Criteria

  • In-patient at a Neonatal Intensive Care Unit (NICU)
  • Informed consent obtained from the legally authorized representative
  • Less than 48 hours old at the time of first infusion
  • Birth weight between 600 grams and 1200 grams
  • Estimated gestation age ≤33 weeks

For multiple gestations, twins may be enrolled if they each meet the entry criteria. They will both be assigned to the same treatment group.

Exclusion Criteria

  • Infants with history of a hypersensitivity or severe vasomotor reaction to any antibody preparation.
  • Infants with proven staphylococcal infection prior to randomization.
  • Infants with a concomitant infection or other medical condition, whose participation, in the opinion of the Investigator and/or medical advisor, may create an unacceptable additional risk.
  • Immunodeficiency other than due to prematurity.
  • Currently receiving, recently received, or planned to receive other investigational agents that could interfere with conduct or results of this study.
  • Severe congenital or chromosomal anomaly that would limit life expectancy or required corrective measures during the period of this study
  • Uncontrolled seizures
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00646399). 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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