Study of ponatinib and azacitidine combination treatment in patients with accelerated phase or blast crisis chronic myelogenous leukemia

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What is this study about?

This study focuses on treating patients with Chronic Myelogenous Leukemia that has progressed to an advanced stage called accelerated phase or myeloid blast crisis. The study evaluates a combination treatment using two medications: ponatinib (taken as tablets by mouth) and azacitidine (given as an injection under the skin).

The purpose of this research is to determine how long patients survive when treated with this drug combination over a two-year period. The treatment plan involves taking ponatinib tablets daily and receiving azacitidine injections for 7 days during each treatment cycle. The maximum daily dose of ponatinib is 45 mg, while azacitidine is given at 75 mg per square meter of body surface.

During the study, patients will be monitored for their response to treatment and any side effects they may experience. Doctors will regularly check blood samples and perform other medical tests to evaluate how well the treatment is working. The study will track various measures of treatment success, including changes in blood cell counts and the presence of cancer cells.

1 Initial medical assessment

A doctor will perform medical tests to confirm your eligibility for the study, including blood tests to check your liver and kidney function

You will need to undergo an electrocardiogram (ECG) test to check your heart rhythm

If you are a woman who can become pregnant, you will need to take a pregnancy test

2 Starting treatment

You will receive two medications as part of your treatment:

Azacitidine will be given as an injection under your skin

Ponatinib will be given as tablets (15 mg or 30 mg) that you take by mouth

3 Regular monitoring

Your doctor will regularly check your blood counts and monitor your response to treatment

You will have tests to check your liver and kidney function throughout the study

The medical team will monitor you for any side effects

Your bone marrow may be examined to check how well the treatment is working

4 Long-term follow-up

The study will continue for up to 2 years

Your overall survival and response to treatment will be tracked during this period

The medical team will document any changes in your condition

If your disease improves, you may be evaluated for a possible bone marrow transplant

Who Can Join the Study?

  • Must be at least 18 years old
  • Must agree to use effective contraception throughout the study if able to have children
  • Must have recovered from previous cancer treatments (side effects must be mild or gone)
  • Must have signed informed consent form
  • Must have Philadelphia chromosome positive CML in blast crisis with at least 20% blast cells in bone marrow or blood (blast cells are immature blood cells)
  • Must have an ECOG performance status of 0-3 (a measure of daily living abilities)
  • Must have adequate kidney function (serum creatinine no more than 1.5 times the normal limit)
  • Must have adequate liver function, measured by:
    • Bilirubin levels no more than 1.5 times normal
    • Liver enzymes (ALT and AST) no more than 2.5 times normal, or 5 times if related to disease
  • Must have normal pancreas function (normal lipase and amylase levels)
  • Must have normal heart rhythm on ECG (QTcF interval no more than 450ms for males or 470ms for females)
  • Women who can become pregnant must have a negative pregnancy test before starting

Who Cannot Join the Study?

  • Age under 18 years old
  • Pregnant or breastfeeding women
  • Previous participation in another clinical trial within the last 30 days
  • Known allergy or hypersensitivity to ponatinib or 5-azacitidine (the study medications)
  • Severe liver problems (liver failure)
  • Severe kidney problems (kidney failure)
  • Uncontrolled heart conditions
  • Active, uncontrolled infections
  • Other types of cancer that require treatment
  • Mental conditions that could interfere with following study procedures
  • Unable to give informed consent
  • History of non-compliance with medical treatments
  • Life expectancy less than 3 months
  • Any condition that, in the opinion of the study doctor, would make participation unsafe

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Institut Gustave Roussy Villejuif France
University Hospital Of Clermont-Ferrand Clermont Ferrand France
Centre Hospitalier Universitaire De Lille Lille France
Oncopole Claudius Regaud Toulouse France
CHU Grenoble Alpes La Tronche France

Other Sites

Site Name City Country Status
Centre Hospitalier De Versailles Le Chesnay-Rocquencourt France
Hopital Saint Antoine Paris France
Hopitaux Universitaires Pitie Salpetriere Paris France
Hôpital Avicenne Bobigny France
Centre Hospitalier De Perpignan Perpignan France
Hopital D’Instruction Des Armees Percy Clamart France
Centre Hospitalier D Avignon Avignon France
Institut De Cancerologie Strasbourg Europe STRASBOURG, Alsace France
Centre Hospitalier Le Mans Le Mans France
Centre Hospitalier De La Cote Basque Bayonne France
Centre Hospitalier Metropole Savoie Chambery France
Centre Hospitalier Universitaire De Nantes Nantes France
Centre Hospitalier Universitaire De Rennes Rennes France
Centre Hospitalier Lyon Sud Pierre Benite France
Centre Hospitalier Universitaire De Caen Normandie Caen France
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Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
France France
Not recruiting
19.06.2019

Trial locations

Investigated drugs:

Ponatinib is a targeted therapy medication used to treat certain types of leukemia. It works by blocking specific proteins that cause cancer cells to grow and multiply. This medication is taken orally and helps control the growth of cancer cells in patients with chronic myelogenous leukemia.

5-Azacitidine is a chemotherapy medication that affects how cells grow and divide. It is commonly used to treat blood disorders and certain types of blood cancers. This medication works by helping bone marrow produce normal blood cells and by killing abnormal cells in the blood. It is typically given as an injection under the skin or through an intravenous line.

The combination of these two medications is being studied to treat patients with chronic myelogenous leukemia that has progressed to more advanced stages (accelerated phase or blast crisis).

Investigated diseases:

Chronic Myelogenous Leukemia – A type of blood cancer that begins in the bone marrow and affects blood cell production. The disease develops when bone marrow cells that produce white blood cells begin to grow and function abnormally. It typically progresses through three phases: chronic phase, accelerated phase, and blast crisis phase. In the accelerated phase, there is an increase in abnormal blood cells, and the disease becomes more aggressive. The blast crisis phase is the most advanced stage, where immature blood cells (blasts) multiply rapidly in the bone marrow and blood. During these advanced phases, the bone marrow produces excessive amounts of abnormal white blood cells that don’t mature properly.

Trial ID:
2024-516048-24-00
Protocol code:
PONAZA_P16/23
NCT ID:
NCT03895671
Trial Phase:
Therapeutic exploratory (Phase II)

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