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Phase 4 N=41 Treatment

Octaplas Pediatric Plasma Exchange Trial

Adverse Effects in the Therapeutic Use of Plasma Substitutes

Enrolled (actual)
41
Serious AEs
2.4%
Results posted
Mar 2020
Primary outcome: Primary: Monitoring of Adverse Drug Reactions Caused by the Octaplas™Used for Plasma Exchange. — 0; 5; 3; 8 event

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Octaplas™ (Biological)
Age
Pediatric, Adult · 2+ yrs
Sex
All
Sponsor
Octapharma
Primary completion
Jan 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Monitoring of Adverse Drug Reactions Caused by the Octaplas™Used for Plasma Exchange.
0; 5; 3; 8
PRIMARY
Monitoring of TEs and TEEs Caused by the Octaplas™Used for Plasma Exchange.
0; 0; 0; 0
SECONDARY
Assessment of Blood Urea Nitrogen Levels
26.4; 25.2; -1.4; 27.3; 27.6; 1.2
SECONDARY
Assessment of Carbon Dioxide Levels
25.0; 26.9; 2.2; 27.3; 28.2; 0.5
SECONDARY
Assessment of Chloride Levels
105.0; 105.2; 0.5; 105.5; 105.4; 0.6
SECONDARY
Assessment of Creatinine Levels
1.7; 1.3; -0.4; 1.3; 1.2; -0.1
SECONDARY
Assessment of Glucose Levels
144.7; 135.2; -12.0; 138.2; 142.7; 12.5
SECONDARY
Assessment of Potassium Levels
3.9; 3.8; -0.1; 3.9; 4.0; 0.1
SECONDARY
Assessment of Sodium Levels
140.0; 141.6; 1.6; 141.2; 142.3; 1.5
SECONDARY
Assessment of Leukocyte Levels
12.8; 13.6; 0.9; 14.9; 15.3; 1.2
SECONDARY
Assessment of Erythrocyte Levels
4.0; 4.1; 0.1; 3.6; 3.7; 0.1
SECONDARY
Assessment of Hemoglobin Levels
11.5; 12.1; 0.4; 10.7; 11.0; 0.3
SECONDARY
Assessment of Hematocrit Levels
34.1; 35.6; 1.1; 31.7; 32.8; 0.8
SECONDARY
Assessment of Mean Corpuscular Volume Levels
86.4; 86.8; 0.2; 88.1; 90.0; 0.3
SECONDARY
Assessment of Mean Corpuscular Hemoglobin Levels
29.0; 29.4; 0.1; 29.6; 30.2; 0.1
SECONDARY
Assessment of Mean Corpuscular Hemoglobin Concentration Levels
33.6; 33.9; 0.1; 33.6; 33.6; 0
SECONDARY
Assessment of Mean Red Cell Distribution Width Levels
14.4; 13.9; 0.0; 14.6; 15.0; 0.1
SECONDARY
Assessment of Mean Ionized Calcium Levels
1.225; 1.129; -0.093; 1.194; -0.030; 1.212
SECONDARY
Investigator's Assessment of Overall Safety
37; 4; 0; 25; 1; 0

Summary

To assess the safety and tolerability of octaplas™ in the pediatric population by monitoring serious adverse drug reactions, adverse drug reactions (ADRs), thrombotic events (TEs), thromboembolic events (TEEs) and by measuring safety laboratory parameters in pediatric patients who require therapeutic plasma exchange.

Eligibility Criteria

Inclusion Criteria

  • Patients in whom therapeutic plasma exchange (TPE) is required.
  • Patient is male or female ≥ 2 years to ≤ 20 years of age.
  • Patient or patient's legal representative(s)/guardian(s) has /have given voluntarily written and signed informed consent before any study-related procedure is to be performed. If children are old enough (age usually deemed by each institution) to understand the risks and benefits of the study, they should also be informed and provide their written assent.

Exclusion Criteria

  • Patient with known homozygous congenital deficiency of Protein S.

Exclusion Criteria

  • Patient has a history of severe hypersensitivity reaction to plasma-derived products or to any excipient of the investigational product.
  • Patient has an already known IgA deficiency with documented antibodies against IgA.
  • Patient is currently participating in another interventional clinical study or has participated during the past 1 month prior to study inclusion. This is not applicable to non-interventional trials and does not exclude patients who have been exposed to Investigational Medicinal Product with a washout of at least 30 days from enrollment in LAS-213. Concurrent participation in a device study will be considered on a case by case basis.
  • Patient is pregnant.
  • Use of Angiotensin-Converting-Enzyme-inhibitors within 72 hours of the start of the first infusion episode or planned used of these medications while on study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01938378). 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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