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NCT05365035 · ClinicalTrials.gov registry record · Phase 2

A Phase II Study of Cladribine and Low Dose Cytarabine in Combination With Venetoclax, Alternating With Azacitidine and Venetoclax, in Patients With Higher-risk Myeloproliferative Chronic Myelomonocytic Leukemia or Higher-risk Myelodysplastic Syndromes With Excess Blasts

A Phase 2 study of Myelodysplastic Syndromes and Myeloproliferative Chronic Myelomonocytic Leukemia, sponsored by M.D. Anderson Cancer Center.

Recruiting
Registry status
Phase 2
Development phase
60
Enrollment target
1
Study location

NCT05365035 is a Phase 2 study of Myelodysplastic Syndromes and Myeloproliferative Chronic Myelomonocytic Leukemia that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 60 participants, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05365035, a Phase 2 study of Myelodysplastic Syndromes and Myeloproliferative Chronic Myelomonocytic Leukemia, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.

RECRUITING
Registry status
Phase 2
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

To learn if the combination of cladribine, cytarabine, venetoclax, and azacitidine can help to control higher-risk myelodysplastic syndrome (MDS) with excess blasts and/or higher-risk chronic myelomonocytic leukemia (CMML).

Interventions

  • DRUG Venetoclax
  • DRUG Cladribine
  • DRUG Azacitidine
  • DRUG Cytarabine

Study Locations (1)

Texas

  • M D Anderson Cancer Center - Houston

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2022-09-23
Est. Completion 2027-12-31
Phase Phase 2

Sponsor

M.D. Anderson Cancer Center

2,692 total trials

What the Registry Record Tells You About NCT05365035

The ClinicalTrials.gov registry entry for NCT05365035 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 285-participant average among 173 other Myelodysplastic Syndromes trials with a reported enrollment target (79% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Myelodysplastic Syndromes appearing as the primary indexed condition, and to 4 interventions - of which Venetoclax is the first listed.

NCT05365035 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT05365035 about?

NCT05365035 is a clinical study titled "A Phase II Study of Cladribine and Low Dose Cytarabine in Combination With Venetoclax, Alternating With Azacitidine and Venetoclax, in Patients With Higher-risk Myeloproliferative Chronic Myelomonocytic Leukemia or Higher-risk Myelodysplastic Syndromes With Excess Blasts". To learn if the combination of cladribine, cytarabine, venetoclax, and azacitidine can help to control higher-risk myelodysplastic syndrome (MDS) with excess blasts and/or higher-risk chronic myelomonocytic leukemia (CMML).

What is the current status of trial NCT05365035?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 60 participants. The study started on 2022-09-23. Estimated completion is 2027-12-31.

What conditions does trial NCT05365035 study?

This clinical trial studies the following conditions: Myelodysplastic Syndromes, Myeloproliferative Chronic Myelomonocytic Leukemia.

What interventions are being tested in trial NCT05365035?

The interventions under investigation include: Venetoclax (DRUG), Cladribine (DRUG), Azacitidine (DRUG), Cytarabine (DRUG).

Who is sponsoring clinical trial NCT05365035?

This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05365035 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

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