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NCT Number: NCT07202078

Role of Antibiotic Therapy or Immunoglobulin On iNfections in hAematoLogy: Starting Immunoglobulin (Start Ig)

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.

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Key information

Conditions

Myeloma Hematologic Diseases Hemic and Lymphatic Diseases Immune System Diseases Immunoproliferative Disorders Infections Leukemia Lymphatic Diseases Lymphoma Lymphoproliferative Disorders Neoplasms Neoplasms by Histologic Type Neoplasms, Plasma Cell Non Hodgkin's Lymphoma

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Royal Adelaide Hospital, Adelaide, South Australia, Australia

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About this study

This is a domain within the RATIONAL Platform Trial to test the effectiveness and safety of prophylactic antibiotics as an alternative Ig replacement in patients who have not yet commenced Ig replacement therapy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • None.

Exclusion criteria

  • Prior or planned allogeneic haematopoietic stem cell transplantation.
  • Already receiving systemic antibiotic prophylaxis for the purpose of preventing bacterial infection (NB: patients may receive antiviral, antifungal and PJP prophylaxis).
  • Received immunoglobulin replacement in the preceding three months.
  • Objection to receiving immunoglobulin products.
  • Known history of IgA deficiency with anti-IgA.
  • History of severe allergy to immunoglobulin products.
  • Current active infection requiring systemic antibiotics.
  • Allergy or intolerance of all domain antibiotic options.
  • Pregnant or breastfeeding.
  • Severe renal impairment (estimated or measured creatinine clearance of < 30 mL/min).
  • Previous splenectomy.
  • Previous participation in this domain.
  • Treating team deems enrolment in the domain is not in the best interest of the patient.

Treatment and study plan

Trimethoprim / Sulfamethoxazole

Drug

Once daily trimethoprim-sulfamethoxazole (co-trimoxazole) 160mg/800mg. NB: Doxycycline 100mg daily as an alternative for patients with hypersensitivity to co-trimoxazole.

Other names: Co-Trimoxazole

Immune Globulin Intravenous

Biological

IVIg every 4 weeks ± 1 week at a dose of 0.4g/kg, modified to achieve an IgG trough level of at least lower limit of age-specific serum IgG reference range; or SCIg, weekly, may be used in patients who meet local criteria for home-based self-administration in centres with established SCIg programs. Dosing is usually given at 100mg/kg/week, modified to achieve an IgG steady state level of at least the lower limit of the serum reference range. A loading IVIg dose may be given in the first month if required.

Other names: Immune Globulin Subcutaneous

Primary outcomes

  1. Event-free survival (EFS).

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Defined as time from randomisation (or, in domains with a single treatment arm, time from registration) until occurrence of a Grade 3 or higher infection (as defined by CTCAE Version 5), or death from any cause.

Secondary outcomes

  1. Occurrence of at least one Grade 3 or higher infection(s) from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Occurrence of at least one Grade 3 or higher infection(s) from randomisation to 12 months.

  2. Occurrence of one or more clinically documented infections (symptoms/signs of infection requiring antimicrobial treatment) from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Occurrence of one or more clinically documented infections (symptoms/signs of infection requiring antimicrobial treatment) from randomisation to 12 months.

  3. Number of clinically documented infections (symptoms/signs of infection requiring antimicrobial treatment) from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Number of clinically documented infections (symptoms/signs of infection requiring antimicrobial treatment) from randomisation to 12 months.

  4. Occurrence of one or more microbiologically documented infections from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Occurrence of one or more microbiologically documented infections from randomisation to 12 months.

  5. Number of microbiologically documented infections from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Number of microbiologically documented infections from randomisation to 12 months.

  6. All-cause mortality at 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    All-cause mortality at 12 months.

  7. Infection-related mortality at 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Infection-related mortality at 12 months.

  8. Time free from hospitalisation with antimicrobial administration with therapeutic intent from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Time free from hospitalisation with antimicrobial administration with therapeutic intent from randomisation to 12 months.

  9. Occurrence of one or more treatment-related adverse events.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Occurrence of one or more treatment-related adverse events.

  10. Number of treatment-related adverse events.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Number of treatment-related adverse events.

  11. Isolation of fluoroquinolone resistant organisms, co-trimoxazole resistant organisms, extended spectrum beta lactamases or multidrug resistant organisms from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Isolation of fluoroquinolone resistant organisms, co-trimoxazole resistant organisms, extended spectrum beta lactamases or multidrug resistant organisms from randomisation to 12 months.

  12. Number of infections with fluoroquinolone resistant organisms, co-trimoxazole resistant organisms, extended spectrum beta lactamases or multidrug resistant organisms isolated from randomisation to 12 months.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Number of infections with fluoroquinolone resistant organisms, co-trimoxazole resistant organisms, extended spectrum beta lactamases or multidrug resistant organisms isolated from randomisation to 12 months.

  13. Quality of Life (QoL) measured at randomisation then 3, 6, 9 and 12 months, using different questionnaire.

    Time frame: Randomisation, Month 3, Month 6, Month 9 and Month 12.

    Quality of Life (QoL) measured at randomisation then 3, 6, 9 and 12 months, using different questionnaire.

  14. Costs associated with allocated treatment arm and infections during study.

    Time frame: 12 months following randomisation (or, in domains with a single treatment arm, time from registration).

    Costs of infections and trial interventions will be estimated based on trial treatment and adverse event data within the hospital medical record, as well as linked data obtained from the Medicare Benefits Scheme (MBS), Pharmaceutical Benefits Scheme (PBS) and Australian Immunisation Register (AIR). Data from the quality of life questionnaires will be used to calculate quality adjusted life years.

Sponsors and collaborators

Lead sponsor

Monash University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Oct 1, 2025
Registry last updated
Oct 7, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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