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A Longitudinal Multi-Center Molecular Biomarker Discovery Registry for Patients With Hematologic Malignancies

A Longitudinal Multi-Center Molecular Biomarker Discovery Registry for Patients With Hematologic Malignancies

Recruiting
All
Phase N/A

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Overview

The TEMPUS AQUARIUS Study is a non-interventional, longitudinal observational study focused on hematological malignancies. It will collect rich molecular (multi-omic) and clinical data from patient cohorts through serial blood draws and the acquisition of leftover tissue and/or bone marrow aspirates during their routine therapy and disease monitoring. The primary goal is to understand the association between biomarkers and real-world clinical outcomes in these patient populations.

Eligibility

All Cohorts Inclusion Criteria:

  1. Willing and able to participate in the research and provide biospecimens
  2. Willing and able to provide informed consent

Cohort 001 Inclusion:

  1. Have documented diagnosis of AML according to the World Health Organization (WHO) classification
  2. Secondary AML is allowed

Cohort 002 Inclusion:

  1. Histologically confirmed diagnosis of Follicular Lymphoma (Subgroups A-D)
  2. Submission of baseline sample representative of current disease per laboratory manual (Subgroups A-D)
  3. 002A (Newly Diagnosed Active Observation): On active observation for 6 more or less, or intended for active observation
  4. 002B (Newly Diagnosed, High Risk): Intended for first line treatment
  5. 002B (Newly Diagnosed, High Risk): Meets the criteria for high risk by any of the following: Follicular Lymphoma Inernational Prognostic Index (FLIPI) High Risk, Groupe d'Etude des Lymphomes Follicularies (GELF) High Tumor Burden, Lactate Dehydrogenase (LDH) above the upper limit of normal (ULN)
  6. 002C (Relapsed / Refractory High Risk POD24 FL): Documented progression of disease within 24 months (POD24) of first line follicular lymphoma treatment, prior to second line treatment
  7. 002D (Transformed FL): Pathologically confirmed transformation

All Cohorts Exclusion Criteria:

1\. Not willing or able to adhere with the study procedures

Cohort 001:

1\. Have received any prior therapy intended for standard of care (SoC) treatment of AML

Cohort 002:

  1. 002A: Received prior treatment for follicular lymphoma
  2. 002A: Diagnosed with High Risk follicular lymphoma by any of the following definitions: FLIPI High Risk, GELF High Tumor Burden, LDH above ULN
  3. 002A: Resected patients with NED
  4. 002B: Intended for active observation
  5. 002B: Received prior treatment for follicular lymphoma

Study details
    Acute Myeloid Leukaemia (AML)
    Follicular Lymphoma ( FL)

NCT07154823

Tempus AI

15 May 2026

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