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Phase 3 Completed N=81 Treatment

Study to Investigate Efficacy, Safety and Pharmacokinetics of BT595 in Subjects With PID

Primary Immunodeficiency Disease
Source: ClinicalTrials.gov NCT02810444 ↗
Enrolled (actual)
81
Serious AEs
13.4%
Results posted
Jul 2023
Primary outcomePrimary: Rate of Acute Serious Bacterial Infections — 0.015 SBI rate per subject-year
◆ Published Evidence
Emerging
7citations · ~2 / year
Efficacy, safety and pharmacokinetics of a new 10% normal human immunoglobulin for intravenous infusion, BT595, in children and adults with primary immunodeficiency disease.
Vox sanguinis · 2022 · Open access · High-confidence link

Summary

This Phase III clinical study is to test efficacy, safety and pharmacokinetics of BT595 in treating patients with Primary Immunodeficiency (PID)

Linked Publications (2)

  • Efficacy, safety and pharmacokinetics of a new 10% normal human immunoglobulin for intravenous infusion, BT595, in children and adults with primary immunodeficiency disease.
    Vox sanguinis · 2022 · 7 citations · Open access · High-confidence link
  • BT595, a 10% Human Normal Immunoglobulin, for Replacement Therapy of Primary Immunodeficiency Disease: Results of a Subcohort Analysis in Children.
    Journal of clinical immunology · 2023 · 4 citations · Open access · High-confidence link

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Acute Serious Bacterial Infections
0.015 —
SECONDARY
IgG Trough Levels (Total IgG) Before Each Infusion
8.467; 7.824; 7.824; 8.278; 8.246; 8.410 —
SECONDARY
Rate of Any Infections
2.80 —
SECONDARY
Rate of Nonserious Infections
2.74 —
SECONDARY
Time to Resolution of Infections
7.0 —
SECONDARY
Antibiotic Treatment Information
6.0 —
SECONDARY
Rate of Time Lost From School/Work Due to Infections
4.32 —
SECONDARY
Hospitalization / Hospitalization Due to Infection
0.70; 0.36 —
SECONDARY
Fever Episodes
1.69 —

Eligibility Criteria

Criteria for inclusion:

  • Written informed consent/assent obtained from subjects/subjects' parent(s) or legally acceptable representative indicating that they understood the purpose of, and procedures required for the study and are willing to participate in it.
  • Male or female, aged 2 through 75 years, inclusive.
  • Diagnosis of PID with impaired antibody production, ie:
  • Diagnosis of common variable immunodeficiency (CVID) as defined by the European Society for Immunodeficiencies (ESID)/Pan American Group for Immunodeficiency (PAGID) diagnostic criteria.

Or

  • X-linked agammaglobulinaemia (XLA) as defined by ESID/PAGID diagnostic criteria.
  • Established replacement therapy with any immunoglobulin for intravenous administration (IVIg) reference preparation during the previous 6 months, including documentation of IgG trough levels.
  • Established replacement therapy with a single IVIg reference preparation for ≥3 months prior to treatment start with BT595 at a 3 week (Q3W) or 4 week (Q4W) schedule with a constant IVIg dose that did not change by ±20% of the mean dose, regular dosage intervals, and at least 1 IgG trough level of ≥5 g/L during the previous 3 months.

Criteria for exclusion:

  • Pregnancy or unreliable contraceptive measures or lactation period (females only).
  • Known intolerance to immunoglobulins or comparable substances (eg, vaccination reaction).
  • Known intolerance to proteins of human origin or known allergic reactions to components of the study product.
  • Participation in another clinical study within 30 days before entering the study or during the study and/or previous participation in this study.
  • Employee or direct relative of an employee of the contract research organization, the study site, or Biotest.
  • Acquired medical conditions known to cause secondary immune deficiency, such as chronic lymphatic leukemia, lymphoma, multiple myeloma, as well as protein losing enteropathies and hypoalbuminemia.
  • Other medical condition, laboratory finding, or physical examination finding that precludes participation.
  • Recent febrile illness that precludes or delays participation.
  • Active infection and receiving antibiotic therapy for the treatment of this infection at the time of screening. Note: if the subject was deemed to be a screen failure due to a nonserious active infection requiring antibiotic therapy, the subject may have been rescreened after the initial screening.
  • Therapy with systemic steroids or other immunosuppressant drugs at the time of enrollment (current daily use of corticosteroids, ie, >10 mg prednisone equivalent/day for >30 days. Intermittent corticosteroid use during the study was allowable, if medically necessary).
  • History of thrombotic events (including myocardial infarction, cerebral vascular accident [including stroke], pulmonary embolism, and deep vein thrombosis) within the 6 months before treatment start with BT595 or the presence of significant risk factors for thrombotic events.
  • Therapy with live-attenuated virus vaccines within 3 months before start of the study.
  • Selective, absolute immunoglobulin A (IgA) deficiency or known antibodies to IgA.
  • Positive diagnosis of hepatitis B or hepatitis C.
  • Positive human immunodeficiency virus (HIV) test.
  • History of drug or alcohol abuse within the 12 months before treatment start with BT595.
  • Inability or lacking motivation to participate in the study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02810444) and the linked publication. 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. Informational only — not medical advice.

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