Double-blind, Randomized, Placebo-controlled, Prospective Phase III Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients With Chronic Lymphocytic Leukemia ("PRO-SID" Study)

Octapharma

Status and phase

Enrolling

Phase 3

Conditions

Hypogammaglobulinemia

Chronic Lymphocytic Leukemia

Treatments

Biological: Panzyga

Other: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT04502030

NGAM-12

Details and patient eligibility

About

Study Evaluating Efficacy and Safety of Panzyga in Primary Infection Prophylaxis in Patients with Chronic Lymphocytic Leukemia

Enrollment

240 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Treatment-naïve or relapsed/refractory CLL patients undergoing CLL antineoplastic treatment. Diagnosis of B-cell CLL established according to International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria and documented within medical records.
Hypogammaglobulinemia (IgG levels <5 g/L) as confirmed by the Central Laboratory.
≥18 years of age.
Voluntarily given, fully informed written and signed consent obtained before any study-related procedures are conducted.

Exclusion criteria

IgG treatment within 3 months prior to Screening.
Antibiotic prophylaxis and/or treatment within 7 days prior to Baseline (with the exception of trimethoprim-sulfamethoxazole [TMP/SMX], diaminodiphenyl sulfone [dapsone] and pentamidine inhalation).
Current major infection or >1 major infection in the previous 6 months before Baseline.
History of anaphylaxis or severe systemic response to immunoglobulin, blood or plasma-derived products or any Panzyga component.
History of a non-CLL malignancy or other medical condition with life-expectancy of less than two years.
Severe liver disease, with signs of ascites and/or hepatic encephalopathy.
Severe kidney disease (as defined by estimated glomerular filtration rate [eGFR] <30 mL/min/1.73 m2).
Body weight >140 kg.
Eastern Cooperative Oncology Group (ECOG) performance score of >2 (Appendix 1).
Female patients of childbearing potential unwilling to use a protocol-required method of contraception (as per protocol section 7.3.9 b) from the Screening Visit throughout the study treatment period and for 30 days following the last dose of study drug.
Human immunodeficiency virus (HIV) infection at Screening (defined for the study as positive HIV antibody test).
Patients found to be chronic carriers of hepatitis B virus (HBV), defined by positive surface antigen (HBsAg), positive Hepatitis B core antibodies (HBcAb) and/or low HBV titers, who will not receive targeted antiviral therapy while undergoing CLL therapy, and patients with active HBV, defined as high HBV titers.
Uncontrolled hepatitis C infection at Screening (defined for the study as positive hepatitis virus C [HCV] polymerase chain reaction [PCR]).
Pregnant and lactating women.
Subjects with a history of thromboembolic events (TEE) such as deep vein thrombosis, pulmonary embolism, myocardial infarction, ischemic stroke, transient ischemic attack, peripheral artery disease (Fontaine IV) within 6 months before Baseline.
Planned or ongoing immunosuppressive treatment (other than for CLL or corticosteroids) or other forbidden medication during the entire study duration after study enrollment.
Participation in another interventional clinical trial that is either blinded or involves an investigational (not approved) product within 3 months before Baseline or during the course of the clinical study. Participation in observational clinical trials or open-label trials involving an approved product may be permitted after consultation with the medical monitor.
Known IgA deficiency with antibodies to IgA.
Known blood hyperviscosity, or other hypercoagulable states.
Patients unable or unwilling to understand or comply with the study protocol.