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NCT Number: NCT07309497

Pragmatic Geriatric Assessment Before CAR-T or Bispecific Antibody Therapy to Predict Side Effects and Outcomes in Older Patients (GA-ACT Trial)

CAR-T cell or bispecific antibody therapies are a new treatment option for adult patients with aggressive forms of lymphoma or so-called plasma cell diseases ('multiple myeloma', 'plasma cell myeloma') that could not be cured with other, less intensive approaches. However, these are intensive therapies that can be associated with severe and potentially life-threatening side effects. Although there is no age limit for these therapies, we know little about the short- and long-term side effects of these treatments in people of advanced age.

Although a small number of patients in the pivotal studies were even over 80 years old, their number was too small to be able to assess the tolerability and success specifically in people over 65. At present, the treating physicians decide whether and, if so, which patients are considered 'fit' enough for this therapy. An objective assessment of the kind we want to investigate in our study does not currently exist on a regular basis. In this study, we therefore want to use simple clinical methods to investigate the effects of these forms of therapy in different areas of everyday function that are important for people in older age (mobility, memory, self-care skills, nutrition). We want to find out whether these investigations help to predict the risk of severe and/or long-term side effects. Based on the results, a pragmatic geriatric assessment could be introduced as standard before these therapies. Older patients could thus expect an improvement in their quality of life thanks to more predictable risks and side effects. Standardized screening could lead to lower healthcare costs for treatment and aftercare for both forms of therapy.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • male or female patients age ≥ 65 years,
  • scheduled for CAR-T-cell or bsAB treatments
  • signed informed consent
  • sufficient knowledge of the German or French language

Exclusion criteria

  • inability to understand or sign informed consent
  • refuse to consent

Treatment and study plan

pragmatic geriatric assessment

Other

observational study

Primary outcomes

  1. treatment toxicity

    Time frame: From enrollment to 3 month after end of treatment

    primary endpoint will be the composite rate of death or any one of ≥ grade 3 toxicity

Secondary outcomes

  1. health related quality of life

    Time frame: From enrollment to 3 month after end of treatment

    Secondary endpoints will be the rate of transfer to intensive care units, the length of hospital stay, the discharge home versus to rehab or nursing-care facilities as well as changes in physical function, cognitive function, nutritional status, ability of self-care and the quality-of-life at discharge and three months after start of therapy. In addition premature CAR-T or bsAB discontinuation, the frequency of treatment-specific toxicities such as the cytokine-release syndrome (CRS) and the immune effector cell-associated neurotoxicity syndrome (ICANS) will be captured

Study contacts

Contact information is provided by the study sponsor or research team.

Wiebke Gagesch, PD Dr. med.

CONTACT

[email protected]

+4144 417 11 11

Wiebke Rösler, Dr. med.

CONTACT

[email protected]

+4144 255 11 11

Sponsors and collaborators

Lead sponsor

University of Zurich

Other

Collaborators

  • Insel Gruppe AG, University Hospital Bern
  • Swiss Cancer Institute
  • University Hospital, Zürich

Registry information

Official study title

Pragmatic Geriatric Assessment (pGA) Before Bispecific Antibody and CAR-T-Cell Therapy (GA-ACT Trial) for the Prediction of Toxicity and Outcomes in Older Patients Scheduled for Chimeric Antigen Receptor T-Cell Therapy (CAR-T-Cell-Therapy) or Bispecific Antibody (bsAB) Treatment

Acronym: GA-ACT

Important dates

Study start
2025
Primary completion
2027
Study completion
2028
First posted
Dec 30, 2025
Registry last updated
Dec 30, 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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