RecruitingPhase 3NCT05645107

A Study to Evaluate Efficacy, Safety, and PK of XEMBIFY®+Standard Medical Treatment (SMT) Compared to Placebo+SMT to Prevent Infections in Participants With HGG and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia, Multiple Myeloma, and Non-Hodgkin Lymphoma

Studying OBSOLETE: Other immunodeficiency syndrome with predominantly antibody defects

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Key facts

Sponsor
Grifols Therapeutics LLC
Intervention
Xembify(drug)
Enrollment
386 enrolled
Eligibility
18 years · All sexes
Timeline
20222026

Study locations (30)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT05645107 on ClinicalTrials.gov

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