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Study identifier: NCT07582432 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Clinical Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of Gamunex in Participants With Chronic Lymphocytic Leukemia, Multiple Myeloma, or Non-Hodgkin Lymphoma

Condition: Chronic Lymphocytic Leukemia, Multiple Myeloma, or Non-Hodgkin Lymphoma  ·  Sponsor: Grifols Biologicals, LLC

PhasePhase 3
Planned participants49
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The main goal of this study is to show that people with certain immune problems (from Chronic Lymphocytic Leukemia, Multiple Myeloma, or Non-Hodgkin Lymphoma) get fewer serious infections when they receive Gamunex C through an IV once every 4 weeks, along with their usual medical care, for one year. All participants will receive Gamunex-C 500 mg/kg once every 4 weeks (total 13 doses) starting Day 1 (Week 1) through Week 48 (end of Treatment Phase).

This description comes directly from the study's public registry record.

Talk to the study team

Judith Wessels-Kranz  ·  +49 6103 801-6395,  ·  judith.wesselskranz@external.grifols.com,

Marina Acosta Enslen  ·  +1 (919) 813 9725  ·  marina.acostaenslen@grifols.com

Always discuss trial participation with your own doctor first.

Locations (5)

Study Site 102St. Petersburg, Florida, United StatesNot Yet Recruiting
Study Site 101Fort Wayne, Indiana, United StatesRecruiting
Study Site 105Westbrook, Maine, United StatesNot Yet Recruiting
Study Site 104Columbus, Ohio, United StatesNot Yet Recruiting
Study Site 103Tacoma, Washington, United StatesNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07582432