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Anti-metabolites
Sapacitabine/decitabine (Part 1 - completed) for Myelodysplastic Syndrome
Phase 1 & 2
Waitlist Available
Research Sponsored by Cyclacel Pharmaceuticals, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2 years
Awards & highlights
Study Summary
This is a combination study to evaluate sapacitabine administered in alternating cycles with decitabine in previously untreated Acute Myeloid Leukemia (AML) or concomitantly with venetoclax in previously treated AML or MDS
Eligible Conditions
- Myelodysplastic Syndrome
- Acute Myeloid Leukemia
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of patients who achieve a clinical benefit response including CR, CRp, PR and major HI
Secondary outcome measures
hospitalized days
overall survival
response duration
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: sapacitabine/venetoclax (Part 2 - recruiting)Experimental Treatment1 Intervention
sapacitabine will be administered concomitantly with venetoclax
Group II: Sapacitabine/decitabine (Part 1 - completed)Experimental Treatment1 Intervention
decitabine will be administered in alternating cycles with sapacitabine
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Who is running the clinical trial?
Cyclacel Pharmaceuticals, Inc.Lead Sponsor
19 Previous Clinical Trials
2,414 Total Patients Enrolled
M.D. Anderson Cancer CenterOTHER
2,973 Previous Clinical Trials
1,789,256 Total Patients Enrolled
Hagop M Kantarjian, MDStudy ChairM.D. Anderson Cancer Center
4 Previous Clinical Trials
668 Total Patients Enrolled
Frequently Asked Questions
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