IgPro20: Clinical Trials

11 trials of IgPro20, newest first

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6 completed, 3 recruiting, 2 terminated. 6 Phase 3, 2 Phase 2, 2 Phase 4.

By phase and status

PhaseTrialsStatus
Phase 36Completed 3, Terminated 2, Recruiting 1
Phase 22Completed 1, Recruiting 1
Phase 42Completed 2

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Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Single-arm Study of IgPro20 in Adults With Secondary Immune Deficiencies Due to Hematologic Malignancies Treated With B-cell Targeting Chimeric Antigen Receptor T-cell and T-cell Redirecting Therapies
IgPro20 - Secondary Immune Deficiency
Phase 3RecruitingCSL Behring632026-09-152026-10-14
Study of IgPro20 to Prevent Infection in People With Multiple Myeloma and Hypogammaglobulinemia
IgPro20 - Multiple Myeloma, Hypogammaglobulinemia
Phase 2RecruitingMemorial Sloan Kettering Cancer Center1002025-05-082026-10-05
Double-blind, Randomized, Placebo-controlled Study Evaluating Efficacy and Safety of IgPro20 in Post-COVID-19 POTS
IgPro20, Placebo - Post-COVID Postural Orthostatic Tachycardia Syndrome
Phase 3TerminatedCSL Behring162024-08-282026-04-13
Hizentra® in Inflammatory Neuropathies - pHeNIx Study
Hizentra - Chronic Inflammatory Demyelinating Polyneuropathy
RecruitingCSL Behring1002022-06-102025-01-07
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of IgPro20 in Adults With Dermatomyositis (DM)
human immunoglobulin G, Placebo - Dermatomyositis
Phase 3TerminatedCSL Behring1342019-10-212025-12-09
Safety and Pharmacokinetics of IgPro20 and IgPro10 in Adults With Systemic Sclerosis (SSc)
IgPro20, IgPro10 - Diffuse Cutaneous Systemic Sclerosis
Phase 2CompletedCSL Behring272019-09-192024-02-05
Safety and Tolerability of Higher Infusion Parameters of IgPro20 (Hizentra) in Subjects With Primary Immunodeficiency (PID)
IgPro20 - Primary Immunodeficiency
Phase 4CompletedCSL Behring492017-02-012020-03-25
Study of Immune Deficiency Patients Treated With Subcutaneous Immunoglobulin (IgPro20, Hizentra®) on Weekly and Biweekly Schedules
Subcutaneous Immune Globulin (Human) (Hizentra) - Primary Immune Deficiency, Secondary Immune Deficiency
Phase 4CompletedCSL Behring262016-03-152018-02-26
Extension Study of Maintenance Treatment With Subcutaneous Immunoglobulin (IgPro20) for Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
IgPro20 - Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), Polyradiculoneuropathy, Chronic Inflammatory Demyelinating
Phase 3CompletedCSL Behring822014-07-302018-10-02
Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy (EU Extension Study)
IgPro20 - Primary Immunodeficiency (PID)
Phase 3CompletedCSL Behring402008-08-012014-04-02
Extension Study of Subcutaneous Immunoglobulin Human in Patients With Primary Immunodeficiency (PID)
IgPro20 - Primary Immune Deficiency
Phase 3CompletedCSL Behring212008-06-012014-04-02

Conditions studied

Primary Immunodeficiency Diseases (4)  ·  Agammaglobulinemia (2)  ·  Multiple Myeloma (2)  ·  Polyradiculoneuropathy, Chronic Inflammatory Demyelinating (2)  ·  Burkitt Lymphoma (1)  ·  Common Variable Immunodeficiency (1)  ·  Dermatomyositis (1)  ·  Hematologic Neoplasms (1)  ·  Leukemia, Lymphocytic, Chronic, B-Cell (1)  ·  Scleroderma, Diffuse (1)

Sponsors

CSL Behring (10)  ·  Memorial Sloan Kettering Cancer Center (1)

Countries

United States (7)  ·  Canada (5)  ·  France (5)  ·  Germany (5)  ·  Italy (4)  ·  Poland (4)  ·  Spain (4)  ·  United Kingdom (4)  ·  Australia (2)  ·  Belgium (2)  ·  Czechia (2)  ·  Japan (2)  ·  Switzerland (2)  ·  Argentina (1)  ·  Denmark (1)

Top investigators

Elie Haddad, MD (1)  ·  Zainab Shahid, MBBS (1)

Results publications

PMID 24412910, PMID 33025378, PMID 33409867, PMID 39909490

NIH funding

2018 (2), 2023 (2), 2008 (1), 2015 (1), 2016 (1)