47 Participants NeededMy employer runs this trial

Cedazuridine + Decitabine + Filgrastim for Acute Myeloid Leukemia

Recruiting at 11 trial locations
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial tests a new treatment option for children with high-risk acute myeloid leukemia (AML) that has returned or resisted previous treatments. It combines two medicines, cedazuridine and decitabine, to target leukemia cells, along with filgrastim to boost white blood cells and prevent infections. The trial aims to determine the safest and most effective dose of this treatment. Children who have undergone a stem cell transplant and have their AML in remission may qualify for this trial. As a Phase 1 trial, the research focuses on understanding how the treatment works in people, offering participants the chance to be among the first to receive this new treatment.

Do I have to stop taking my current medications for the trial?

The trial requires that you do not take certain medications that are metabolized by cytidine deaminase (like cytarabine and gemcitabine) on days when ASTX727 is given and for 24 hours after. If you're on other anti-cancer drugs or investigational drugs, you cannot participate. Always discuss with your doctor before making any changes to your medication.

Is there any evidence suggesting that this treatment is likely to be safe for humans?

Research has shown that the combination of cedazuridine and decitabine, known as ASTX727, has a safety profile similar to other treatments for acute myeloid leukemia (AML). Studies indicate that patients generally tolerate this combination well, with most side effects being manageable and not severe.

Additionally, researchers have combined ASTX727 with venetoclax for older or less fit patients. These studies found it safe for most participants, suggesting the treatment might suit different groups of people with AML.

Filgrastim, another component of this trial, helps increase white blood cell production. It is widely used and has a well-known safety record, with most people experiencing only mild side effects like bone pain.

Although this trial is in its early stages, the data so far suggest these treatments could be safe and tolerable for patients with high-risk AML.12345

Why are researchers excited about this trial's treatments?

Researchers are excited about this treatment for Acute Myeloid Leukemia because it combines cedazuridine and decitabine in a novel way. This combination allows for the oral administration of decitabine, which is typically given intravenously, making it more convenient for patients. Cedazuridine acts to enhance the effectiveness of decitabine by preventing its breakdown in the body, potentially improving treatment outcomes. Additionally, the inclusion of filgrastim helps stimulate white blood cell production, which can aid in recovery and reduce infection risk. This approach represents a promising advance in making leukemia treatment more patient-friendly while possibly increasing its efficacy.

What evidence suggests that this treatment might be an effective treatment for acute myeloid leukemia?

Research has shown that the combination of two drugs, cedazuridine and decitabine, known as ASTX727, yields promising results for treating acute myeloid leukemia (AML). In one study, 67% of patients responded well to this treatment, with 40% achieving complete remission, meaning no signs of cancer were found. Another study found that ASTX727 improved survival rates for patients with AML and myelodysplastic syndromes (MDS) after a stem cell transplant. Cedazuridine extends the effectiveness of decitabine in the body. In this trial, participants will receive ASTX727 along with Filgrastim, which may enhance the treatment's effectiveness. These findings suggest that ASTX727 could be a strong option for patients with high-risk, recurring, or hard-to-treat AML.12345

Who Is on the Research Team?

ML

Maria Luisa Sulis

Principal Investigator

Pediatric Early Phase Clinical Trial Network

Are You a Good Fit for This Trial?

This trial is for children and young adults (up to age 21) with high-risk acute myeloid leukemia that has come back or not responded to treatment, who have had a stem cell transplant. Participants must meet certain health requirements and cannot join if they have had prior solid organ transplants, are pregnant, or can't swallow tablets.

Inclusion Criteria

My body surface area is at least 1 square meter.
My acute myeloid leukemia is in complete remission.
My bilirubin levels are within 1.5 times the normal range for my age.
See 17 more

Exclusion Criteria

Patients who have received a prior solid organ transplantation
Patients currently receiving other anti-cancer agents
Known or suspected hypersensitivity to filgrastim, decitabine or cedazuridine (ASTX727)
See 12 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Patients receive filgrastim and ASTX727, with cycles repeating every 28 days for 12 cycles

336 days
Daily visits for administration on days 1-6 of each cycle

Follow-up

Participants are monitored for safety and effectiveness after treatment, including bone marrow aspiration and biopsy

1 year post-transplant

What Are the Treatments Tested in This Trial?

Interventions

  • Cedazuridine
  • Decitabine
  • Filgrastim

Trial Overview

The study is testing the safety and best dose of a drug combo called ASTX727 (cedazuridine plus decitabine) together with filgrastim after stem cell transplant in kids with high-risk AML. The goal is to see how well these drugs work together and what side effects may occur.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Treatment (ASTX727, diecitabine, filgrastim)Experimental Treatment8 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

National Cancer Institute (NCI)

Lead Sponsor

Trials
14,080
Recruited
41,180,000+

Citations

Phase II trial of 10-day ASTX727 (decitabine/cedazuridine ...

In this prospective clinical trial, we investigate the efficacy of a novel 10-day induction regimen with fully oral combination therapy for pts with R/R AML.

Fully Oral Combination of Decitabine/Cedazuridine (ASTX727 ...

The median follow-up time was 20 months. The ORR was 40/60 (67%), including 24 (40%) complete remission (CR), 13 (22%) CR with incomplete count ...

3.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/38452788/

Oral decitabine and cedazuridine plus venetoclax for older or ...

ASTX727 plus venetoclax is an active fully oral regimen and safe in most older or unfit patients with acute myeloid leukaemia.

Testing Oral Decitabine and Cedazuridine (ASTX727) in ...

Giving ASTX727 in combination with venetoclax may help in the treatment of patients with higher-risk acute myeloid leukemia. Detailed Description. PRIMARY ...

astx727 improves aml mds outcomes post-hsct

ASTX727, oral decitabine and cedazuridine, boosts AML and MDS survival post-HSCT by 70.4% in a phase 2 study.