Status:
RECRUITING
A Phase 2 Study Evaluating Olutasidenib in Combination With Hypomethylating Agents in Patients With IDH1-mutated Higher-risk Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia, or Advanced Myeloproliferative Neoplasm
Lead Sponsor:
M.D. Anderson Cancer Center
Collaborating Sponsors:
Rigel Pharmaceuticals
Conditions:
Chronic Myelomonocytic Leukemia
Advanced Myeloproliferative Neoplasms
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
To learn if olutasidenib, when combined with a drug called a hypomethylating agent (HMA) can help to control MDS, CMML, and/or MPN. The safety of the drug combination will also be studied.
Detailed Description
Primary Objectives To determine the overall response rate of olutasidenib in combination with investigator's choice of HMA in patients with IDH1-mutated higher-risk MDS/CMML or advanced MPN Secondary ...
Eligibility Criteria
Inclusion
- Pathologically proven higher-risk MDS/CMML or advanced MPN
- MDS participants must have International Prognostic Scoring System (IPSS) intermediate-2- or high-risk disease or Revised IPSS (IPSS-R) score \>= 3.5 or Molecular IPSS (IPSS-M) moderate high-, high-, or very high-risk disease or bone marrow blast percentage.
- CMML patients must have CPSS-Mol int-1, int-2, or high-ris disease (Elena C et al, Blood 2016)
- Advanced MPN is defined as bone marrow blast percentage \>=/=10%.
- Participants on the treatment-naive arm must not have received a prior HMA. Agents such as growth factors (e.g. erythropoietin stimulating agents, luspatercept, eltrombopag, granulocyte colony stimulating factors), cyclosporine, and/or hydroxyurea are allowed.
- Patients on the previously-treated arm must have received a prior HMA and/or ivosidenib. Prior stem cell transplantation in allowed\>
- Participants must have a documented IDH1 mutation
- Patients with previously-treated MDS must be ineligible to receive treatment with ivosidenib or have progressed on treatment with ivosidenib.
- Participants \>=/= 18 years old
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 2 (Appendix A)
- Acceptable liver function
- Bilirubin \</= 2 times upper limit of normal (ULN) or \<;/= 3 times ULN in participants with Gilbert Syndrome
- Aspartate transaminase (AST), alanine transaminase (ALT), and alkaline phosphatase \</= 3 times ULN
- Acceptable renal function calculated creatinine clearance \>/= 50 mL/min (as assessed by Cockcroft-Gault, MDRD, or CKD-Epi validated measures)
- Negative serum or urine pregnancy test if female of childbearing potential c. For fertile men and women, agreement to use highly effective contraceptive methods for the duration of study participation and 90 days after the last dose of study medication d. Agreement for male participants not to donate sperm and for female participants of childbearing potential not to donate ova during the study and for 90 days after the final dose of study drug
- Ability and willingness to sign informed consent prior to beginning study and undergoing procedures
Exclusion
- Participants unable to swallow oral medications, or participants with gastrointestinal conditions (e.g., malabsorption, resection, etc.) deemed by the Investigator to jeopardize intestinal absorption
- Participants with any concurrent uncontrolled clinically significant medical condition, including life-threatening severe infection or psychiatric illness, which could place the participant at unacceptable risk of study treatment
- Patients must have discontinued prior chemotherapy at least 1 week prior to the start of study treatment. Patients with MPN must be off JAK inhibitors at the start of study treatment
- Patients with active graft-versus-host-disease (GVHD) status post stem cell transplantation, including active chronic GVHD requiring topical therapy. Patients must have discontinued calcineurin inhibitors at least 4 weeks prior to the start of study treatment
- Known active hepatitis B (HBV) or hepatitis C (HCV) or HIV infection
- Pregnant or nursing women or women of childbearing potential not using highly effective contraception; male participants not using highly effective contraception
- Participants with white blood cell count \> 25 x109/L Note: hydroxyurea use is permitted to meet this criterion
- Unwillingness or inability to comply with procedures either required in this protocol or considered standard of care
Key Trial Info
Start Date :
January 28 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
August 31 2029
Estimated Enrollment :
45 Patients enrolled
Trial Details
Trial ID
NCT06597734
Start Date
January 28 2025
End Date
August 31 2029
Last Update
October 9 2025
Active Locations (1)
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1
MD Anderson Cancer Center
Houston, Texas, United States, 77030