Phase 4
N=41
Octaplas Pediatric Plasma Exchange Trial
Adverse Effects in the Therapeutic Use of Plasma Substitutes
Bottom Line
View on ClinicalTrials.gov: NCT01938378 ↗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
| Outcome | Result | p-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.
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.