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Study of SX-682 Alone and in Combination with Oral or Intravenous Decitabine in Subjects with Myelodysplastic Syndrome

Exploring SX-682 with Decitabine for Myelodysplastic Syndrome.

Recruiting
18 years and older
All
Phase 1

This study looks at how safe the drug SX-682 is for people with Myelodysplastic Syndrome (MDS), a condition where bone marrow doesn’t make enough healthy blood cells. Participants will take SX-682 by mouth twice a day for six cycles, each lasting 28 days. The dose of SX-682 will start at 25 mg and may increase to find the safest dose. If you respond well, treatment may continue. Some patients will also receive another drug, Decitabine.

People with different risks of MDS will be grouped based on their condition and previous treatments. Those who have tried other treatments like Hypomethylating Agents (HMA) or lenalidomide without success are eligible. To join, you must have a specific performance status, lab results, and life expectancy. Women and men must agree to use birth control. You cannot participate if you have used certain medications recently, have serious heart or other health issues, or have had recent surgeries.

  • Expect to attend multiple visits over 6 months for the study.
  • Participants must not have recent severe illnesses or treatments.
  • No concurrent MDS treatments are allowed during this study.
Study details
    Myelodysplastic Syndromes

NCT04245397

Syntrix Biosystems, Inc.

13 December 2024

Step 1 Get in touch with the nearest study center
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  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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