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Clinical Trials in Australia / NCT07202065
Recruiting Phase 2/3

Role of Antibiotic Therapy or Immunoglobulin On iNfections in hAematoLogy Dosing Immunoglobulin (Dose Ig)

NCT07202065 · tracked via the Priya Life Science Australia tracker
Phase
Phase 2/3
Started
2025-04-28
Last updated
2025-10-07

Condition(s) studied

MyelomaNon Hodgkin's LymphomaLeukemia

Investigational drug(s) / intervention(s)

Immune Globulin Intravenous →

Immune Globulin Intravenous: Participants will be treated with intravenous immunoglobulin monthly (every 4 weeks ± 1 week).

Study summary

This study is being conducted to find out how safe and effective different strategies of infection prevention are in comparison to each other, for preventing infection in patients with blood cancers. The best way to find out this information is to directly compare the effect of different treatment strategies in patients with blood cancers. We want to know how these different treatments impact on your health and your use of healthcare services.

This research project uses an Adaptive Platform Design. This design allows the researchers to compare multiple infection prevention strategies within the same trial at the same time (rather than running separate trials), to analyse results as the trial occurs and to add new research questions during the course of the trial.

The treatments that you may receive as part of the study will be determined by which domain(s) of the platform you participate in. By combining data collected within each domain as part of the platform, the researchers can investigate and compare treatment strategies and infection outcomes across a broader range of participants.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. Patients must be receiving IVIg replacement at standard dose for prevention of bacterial infections due to hypogammaglobulinaemia for at least 6 consecutive months. 2. Patient is not eligible for trial of Ig cessation in the opinion of the treating clinician and local investigator. Exclusion Criteria: 1. Prior or planned allogeneic haematopoietic stem cell transplantation. 2. Major infection (Grade 3 or higher) in preceding 3 months, and or current active infection requiring systemic antimicrobial treatment. 3. Previous splenectomy. 4. Known history of bronchiectasis. 5. Previous participation in this domain. 6. Treating team deems enrolment in the domain is not in the best interest of the patient.

Primary outcome measure(s)

Trial sites (3)

FacilityCityRegionStatus
Royal Adelaide Hospital Adelaide South Australia Recruiting
Austin Hospital Melbourne Victoria Recruiting
Northern Health Melbourne Victoria Recruiting

More Monash University trials in Australia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07202065 on ClinicalTrials.gov ↗ ← All trials in Australia