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NCT Number: NCT06513273

Observational Study on the Outcome of AML Patients Treated With New Drugs in Real-life (BoxTrial)

This multicenter, prospective and retrospective observational study aims to evaluate the use and efficacy of new drugs or their combinations in real-life in a population of adult AML patients.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Ematologia Ente Ecclesiastico Casa Sollievo Della Sofferenza, San Giovanni Rotondo, Italy

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About this study

This multicenter, prospective and retrospective observational study (model: case only) aims to evaluate the use and efficacy of new drugs or their combinations in real-life in a population of adult AML patients treated at Italian GIMEMA centers. No additional procedures or visits other than those required by normal clinical practice will be required. every patient will be followed for a minimum of 24 months.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged 18 years or older
  • AML diagnosis according to the ELN guidelines, excluding M3
  • Signed Informed consent, if applicable
  • Treatment initiation with novel drugs in monotherapy or combination, in accordance with the AIFA authorizations, from the AIFA registration up to 31.12.2027 with particular attention to:
  • patients affected by FLT3-mutated AML treated with gilteritinib.
  • patients affected by IDH-mutated AML treated with IDH inhibitors.
  • patients affected by AML in maintenance therapy with oral azacytidine.
  • patients affected by AML treated with glasdegib.
  • patients affected by AML treated with gemtuzumab ozogamicin.
  • other novel drugs or combination for the treatment of AML approved during the study period.

Exclusion criteria

Patients included in interventional clinical trials.

Treatment and study plan

Primary outcomes

  1. New therapies efficacy in terms of Overall survival

    Time frame: at 24 months

    evaluation of the efficacy of the new therapies or their combinations in the real-life for AML patients in terms of Overall Survival

Study contacts

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

Enrico Crea

CONTACT

[email protected]

0670390514

Paola Fazi

CONTACT

[email protected]

0670390528

Sponsors and collaborators

Lead sponsor

Gruppo Italiano Malattie EMatologiche dell'Adulto

Other

Registry information

Official study title

Observational GIMEMA Study on the Outcome of Acute Myeloid Leukemia (AML) Patients Treated With New Drugs in Real-life

Acronym: Box

Important dates

Study start
2025
Primary completion
2029
Study completion
2029
First posted
Jul 22, 2024
Registry last updated
Aug 13, 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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