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NCT03441048CompletedPhase 1

Lintuzumab-Ac225 in Combination with Cladribine + Cytarabine + Filgastrim + Mitoxantrone (CLAG-M) for Relapsed/Refractory Acute Myeloid Leukemia

A Phase I Study of Lintuzumab-Ac225 in Combination with CLAG-M Chemotherapy in Patients with Relapsed/Refractory Acute Myeloid Leukemia

Source: ClinicalTrials.gov · Last updated 8 Oct 2024

Brief summary (registry, in English)

This is a prospective, single-center phase I clinical study aimed at determining the maximum-tolerated dose, recommended phase 2 dose and safety of Lintuzumab-Ac225 in combination with CLAG-M chemotherapy in the management of relapsed/refractory acute myeloid leukemia. This study uses a 3+3 design with a five-patient cohort at the recommended phase 2 dose.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
26 (actual)
First submitted
15 Feb 2018
Start date
22 May 2018
Primary completion date
22 May 2024
Lead sponsor
Medical College of Wisconsin
NCT number
NCT03441048

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 26
  • From 22 May 2018 to the primary completion date, 22 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior chemotherapy or radiotherapy within 14 days of study entry unless fully recovered from adverse effects due to treatment, at investigator's discretion.
  • Active malignancy within 2 years of entry, except previously treated melanoma grade 2 or less, non-melanoma skin cancer, carcinoma in situ, or cervical intraepithelial neoplasia, and organ confined prostate cancer with no evidence of progressive disease based on prostate-specific antigen (PSA) levels and are not on active therapy. Active malignancy is malignancy receiving treatment.

Other illness

  • Active severe infection not well controlled by antibacterial or antiviral therapy.
  • Known infection with human immunodeficiency virus.
  • Patients with documented pulmonary disease, with a diffusing capacity of the lungs for carbon monoxide (DLCO) and/or forced expiratory volume in one second (FEV1) \<65%, or history of dyspnea at rest, or requiring oxygen.

Other

  • Acute Promyelocytic Leukemia.
  • Pregnant or breast feeding women.

Who the study is looking for

  • Age ≥18 years at the time of informed consent.
  • Morphologically documented primary AML or secondary AML \[from prior conditions such as Myelodysplastic Syndrome (MDS), myeloproliferative neoplasm (MPN)\] or therapy related AML (t-AML), as defined by World Health Organization (WHO) criteria.
  • In first or subsequent relapse or refractory status after prior therapy, with or without prior hematopoietic stem cell transplant (HSCT). Patients with MDS and progression to AML on hypomethylating agents will also be included.
  • Eastern Cooperative Oncology Group (ECOG) performance score 0-2.
  • Greater than 25% of blasts must be CD33 positive on flow cytometry using Phycoerythrin (PE) labeled anti-CD33 antibody.
  • Patients must meet the following clinical laboratory criteria:
    • Total bilirubin ≤ 2 x the upper limit of the normal range (ULN)
    • Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 5 x ULN.
    • Calculated creatinine clearance ≥ 50 mL/min
    • Resting left ventricular ejection fraction (LVEF) \> 40%
  • Female patients must agree to avoid becoming pregnant, and male patients should avoid impregnating a female partner.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Froedtert Hospital and the Medical College of Wisconsin
Coordinator of this site? Confirm its status
MilwuakeeUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.