Combination therapy aims to boost blood cells in Hard-to-Treat MDS
NCT ID NCT06020833
First seen Jul 07, 2026 · Last updated Jul 08, 2026 · Updated 1 time
Summary
This trial tests whether combining roxadustat with retinoic acid can help people with low-risk myelodysplastic syndromes (MDS) whose disease hasn't responded to initial treatment. The goal is to improve blood cell counts and reduce the need for transfusions. Participants will take both drugs orally for 8 weeks, and researchers will measure how many achieve complete or partial remission.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- roxadustat combined with retinoic acid
- What this could lead to
- If it works, this combination could offer a new treatment option for people with low-risk MDS who haven't responded to standard therapy, potentially reducing or eliminating the need for blood transfusions.
- What could go wrong
- This is an early-phase, single-arm trial with no control group, so results are preliminary. The combination may cause side effects or prove no more effective than existing options.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Expected to start
-
Aug 2023
An estimate. Start dates often move.
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Low-risk MDS unresponsive to first-line therapy Exclusion Criteria: * myelofibrosis * Severe heart and kidney function bu'quan
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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