Vitamin c boost: could high doses help fight bone marrow cancer?
NCT ID NCT07283900
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether adding high-dose vitamin C to a standard chemotherapy drug (azacitidine) can improve outcomes for adults with myelodysplastic syndrome (MDS), a bone marrow disorder. About 38 people with higher-risk MDS who haven't had much prior treatment will receive the combination intravenously. The goal is to see if the combo is safe and leads to remission or better survival.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- high-dose vitamin C (ascorbate) and azacitidine (Vidaza)
- What this could lead to
- If it works, this could point toward a more effective treatment for myelodysplastic syndrome, potentially improving remission rates and survival.
- What could go wrong
- This is a small, early-phase trial with only 38 participants, so results may not apply to everyone. High-dose vitamin C can cause side effects like kidney stones or infusion reactions.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 38 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2026
- Expected to finish
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May 2029
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
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18 to 99 years
- Sex
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Anyone
- Healthy volunteers
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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 * Age ≥ 18 years. * Diagnosis of myelodysplastic syndrome (MDS) requiring treatment with a hypomethylating agent (HMA). * Higher-risk MDS per the Molecular International Prognostic Scoring System (IPSS-M) - Moderate High, High, or Very High risk categories. * No prior MDS-directed therapy, except: ≤ 1 prior cycle of azacitidine, decitabine, or oral decitabine-cedazuridine; or prior use of ESA, luspatercept, or imetelstat. Prior hydroxyurea use is allowed but continuation beyond Cycle 1 requires PI approval. * ECOG performance status 0-2. * Adequate organ function: Creatinine clearance \>45 mL/min; total bilirubin ≤1.5 × ULN; ALT and AST ≤3 × ULN. * Ability to provide written informed consent. * Willingness to comply with study visits, treatment, and contraception requirements. * Negative pregnancy test for women of childbearing potential at screening. Exclusion Criteria * MDS with isolated del(5q) eligible for lenalidomide therapy. * MDS/MPN overlap syndromes other than MDS. * Known hypersensitivity or allergy to ascorbate or azacitidine. * Pregnant or nursing individuals. * Inability or unwillingness to use adequate contraception. * Uncontrolled intercurrent illness including active infection, recent myocardial infarction (≤6 months), uncontrolled heart failure or arrhythmia, pulmonary edema, unstable angina, or significant psychiatric illness. * Renal disease requiring dialysis, diabetic nephropathy, renal transplant recipients, or history of oxalate nephropathy. * Paroxysmal nocturnal hemoglobinuria. * Uncontrolled HIV infection (patients on effective antiretroviral therapy with undetectable viral load within 6 months are eligible). * G6PD deficiency. * Use of warfarin (due to potential interaction with high-dose ascorbate). * Diabetic patients using fingerstick or continuous glucose monitors to adjust insulin doses (ascorbate can cause false readings). * Concurrent active malignancy, except adequately treated nonmelanoma skin cancer or curatively treated in situ cancers with \>2 years disease-free. * Systemic immunosuppressive therapy with prednisone ≥20 mg/day (or equivalent), except for inhaled or topical steroids. * Primary hemochromatosis or transfusion-related iron overload (ferritin \>1000 ng/mL).
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University of Iowa
RECRUITINGIowa City, Iowa, 52242, United States
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