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Clinical AML Registry and Biomaterial Database of the Study Alliance Leukemia (SAL)

T

Technische Universität Dresden

Status

Enrolling

Conditions

Acute Myeloid Leukemia (AML)

Study type

Observational

Funder types

Other

Identifiers

NCT03188874
SAL-AML-REG-BIO

Details and patient eligibility

About

This is a registry study in adult patients with newly diagnosed or refractory/relapsed acute myeloid leukemia.

Investigator's sites: 51 sites in Germany.

Primary objectives:

  • Identification of epidemiological data on AML: age, prognostic factors and subgroup distributions. Incidence and age distribution are compared with the data of population-related tumor registry.
  • Evaluation of the most important patient-relevant clinical endpoints (outcomes): relapse-free survival (RFS) / time to relapse (TTR), calculation of cumulative incidence of relapse (CIR) and overall survival (OS)
  • Documentation of treatment strategy

Full description

see brief summary

Enrollment

15,000 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • AML according to the WHO (World Health Organization) diagnostic criteria, including acute promyelocytic leukemia
  • Age ≥ 18 years. There is no upper age limit.
  • Signed written informed consent

Exclusion criteria

  • there are no exclusion criteria

Trial contacts and locations

51

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Central trial contact

Christoph Röllig, Prof. Dr.

Data sourced from clinicaltrials.gov

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