An open label, prospective, multicenter study investigating clinical efficacy, safety, and pharmacokinetic properties of the human normal immunoglobulin for intravenous administration BT595 as replacement therapy in patients with primary immunodeficiency disease (PID)

Phase 1

• Conditions: Replacement therapy in patients with primary immunodeficiency disease (PID); MedDRA version: 19.0Level: PTClassification code 10064859Term: Primary immunodeficiency syndromeSystem Organ Class: 10010331 - Congenital, familial and genetic disorders; Therapeutic area: Diseases [C] - Immune System Diseases [C20]

• Registration Number: EUCTR2015-003652-52-GB
• Lead Sponsor: Biotest AG

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2016-08-08
• Last Update Posted: 20 July 2020

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

a) Written informed consent/assent obtained from subjects/subjects’ parent(s) or legally acceptable representative indicating that they understand the purpose of and procedures required for the study and are willing to participate in it.
b) Male or female, aged 2 through 75 years.
c) Diagnosis of PID with impaired antibody production, i.e.:
- 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 agammaglobulinemia (XLA) as defined by ESID/PAGID diagnostic criteria.
d) Established replacement therapy with any intravenous immunoglobulin (IVIg) reference preparation during the previous 6 months, including documentation of immunoglobulin G (IgG) trough levels.
e) Established replacement therapy with a single IVIg reference preparation for at least 3 months prior to treatment start with BT595 at a 3 or 4 week 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.

Are the trial subjects under 18? yes
Number of subjects for this age range: 20
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 35
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 5

Exclusion Criteria

a) Pregnancy or unreliable contraceptive measures or lactation period (females only).
b) Known intolerance to immunoglobulins or comparable substances (e.g., vaccination reaction).
c) Known intolerance to proteins of human origin or known allergic reactions to components of the study product.
d) Participation in another clinical study within 30 days before entering the study or during the study and/or previous participation in this study.
e) Employee or direct relative of an employee of the Contract Research Organization, the study site, or Biotest.
f) 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.
g) Other medical condition, laboratory finding, or physical examination finding that precludes participation.
h) Recent febrile illness that precludes or delays participation.
i) Active infection and receiving antibiotic therapy for the treatment of this infection at the time of screening. Note: if the subject is deemed to be a screen failure due to a nonserious active infection requiring antibiotic therapy, the subject may be rescreened after the initial screening.
j) Therapy with systemic steroids or other immunosuppressant drugs at the time of enrollment (current daily use of corticosteroids, i.e., >10 mg prednisone equivalent/day for >30 days. Intermittent corticosteroid use during the study is allowable, if medically necessary).
k) 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.
l) Therapy with live attenuated virus vaccines within 3 months before start of the study.
m) Selective, absolute immunoglobulin A (IgA) deficiency or known antibodies to IgA.
n) Positive diagnosis of hepatitis B or hepatitis C.
o) Positive HIV test.
p) History of drug or alcohol abuse within the 12 months before treatment start with BT595.
q) Inability or lacking motivation to participate in the study.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified