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Spots Global Cancer Trial Database for A Study to Evaluate Efficacy, Safety, and Pharmacokinetics of XEMBIFY® Plus Standard Medical Treatment (SMT) Compared to Placebo Plus SMT to Prevent Infections in Participants With Hypogammaglobulinemia and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia

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Trial Identification

Brief Title: A Study to Evaluate Efficacy, Safety, and Pharmacokinetics of XEMBIFY® Plus Standard Medical Treatment (SMT) Compared to Placebo Plus SMT to Prevent Infections in Participants With Hypogammaglobulinemia and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia

Official Title: A Multi-Center, Parallel, Double-Blinded, Placebo-Controlled Clinical Trial to Evaluate Efficacy, Safety, and Pharmacokinetics of XEMBIFY® Plus Standard Medical Treatment Compared to Placebo Plus Standard Medical Treatment to Prevent Infections in Patients With Hypogammaglobulinemia and Recurrent or Severe Infections Associated With B-cell Chronic Lymphocytic Leukemia

Study ID: NCT05645107

Interventions

Xembify
Placebo

Study Description

Brief Summary: The primary purpose of the study is to evaluate whether weekly administered XEMBIFY® plus Standard Medical Treatment (SMT) over a one-year period will reduce the rate of major bacterial infections per participant per year in participants with hypogammaglobulinemia (HGG) associated with B-cell chronic lymphocytic leukemia (CLL) in comparison to the Placebo plus SMT group.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

GC2202 Study Site 107, Miami, Florida, United States

GC2202 Study Site 105, Canton, Ohio, United States

GC2202 Study Site 102, Columbus, Ohio, United States

GC2202 Study Site 101, Pittsburgh, Pennsylvania, United States

GC2202 Study Site 110, Rockville, South Carolina, United States

GC2202 Study Site 108, Harlingen, Texas, United States

GC2202 Study Site 202, Burgas, , Bulgaria

GC2202 Study Site 210, Plovdiv, , Bulgaria

GC2202 Study Site 205, Ruse, , Bulgaria

GC2202 Study Site 209, Sofia, , Bulgaria

GC2202 Study Site 201, Sofia, , Bulgaria

GC2202 Study Site 206, Sofia, , Bulgaria

GC2202 Study Site 207, Sofia, , Bulgaria

GC2202 Study Site 204, Sofia, , Bulgaria

GC2202 Study Site 208, Sofia, , Bulgaria

GC2202 Study Site 403, Legnica, Dolnośląskie, Poland

GC2202 Study Site 406, Wałbrzych, Dolnośląskie, Poland

GC2202 Study Site 402, Toruń, Kujawsko-pomorskie, Poland

GC2202 Study Site 401, Kraków, Małopolskie, Poland

GC2202 Study Site 405, Słupsk, Pomorskie, Poland

GC2202 Study Site 503, Brasov, RO, Romania

GC2202 Study Site 504, Bucuresti, RO, Romania

GC2202 Study Site 506, Cluj-Napoca, RO, Romania

GC2202 Study Site 502, Timisoara, RO, Romania

GC2202 Study Site 602, Belgrade, , Serbia

GC2202 Study Site 601, Kragujevac, , Serbia

GC2202 Study Site 606, Nis, , Serbia

GC2202 Study Site 603, Sremska Kamenica, , Serbia

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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