RecruitingPhase 1

Onvansertib for the Treatment of Recurrent or Refractory Chronic Myelomonocytic Leukemia and Myelodysplastic Syndrome/MPN Overlap Neoplasms

Phase 1 Study to Determine the Safety and Efficacy of Onvansertib, A Novel, Oral, PLK1 Inhibitor in Patients With Proliferative Chronic Myelomonocytic Leukemia (CMML) and Myelodysplastic Syndrome/MPN Overlap Neoplasms Relapsed/Refractory or Intolerant to Available Therapies

Who can join

As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.

Age
18 Years and older
Sex
All sexes
Healthy volunteers
Not accepted
Compensation
Not stated

Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.

What to expect

No one can promise a trial will help you personally — that is what the research is trying to find out.

What participation involves

  • Procedures mentioned: Ultrasound, Blood draws, Biopsies

Only what the study's summary and detailed description on ClinicalTrials.gov say. Time periods may describe the whole study or a part of it — ask the study team what applies to you.

Show the study's own words
  • "Volumetric spleen response rate, as determined by ultrasound scan (US)."
  • "Patients also undergo bone marrow aspiration and biopsy, collection of blood samples, and ultrasound imaging during screening and throughout the trial."
Compensation
Not stated
  • Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
  • Participants are monitored closely by the research team throughout the study.
  • Some participants may receive access to an investigational treatment, which is still being studied.
  • Your participation helps researchers learn whether this approach could help future patients.

About this study

In plain language

This study tests the safety, effects, and best dose of onvansertib, a drug that blocks a protein cancer cells need to grow. It is for adults with chronic myelomonocytic leukemia (CMML) or certain related blood cancers called MDS/MPN overlap cancers that have come back or have not responded to treatment.

This phase I trial evaluates the safety, effectiveness, and best dose of onvansertib for the treatment of patients with chronic myelomonocytic leukemia and Myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) overlap neoplasms that has come back (recurrent) or that does not respond to treatment (refractory). Onvansertib is a drug that binds to and inhibits an enzyme called PLK1, preventing cancer cell proliferation and causing cell death.

Compensation is read from the study's own description and may be missing — always confirm with the study team.

Eligibility

Who can join

  • Be age 18 or older.
  • Have confirmed CMML, atypical chronic myeloid leukemia, or MDS/MPN not otherwise specified. Your white blood cell count must have been at least 13,000 at diagnosis; lower counts caused by treatment may be allowed.
  • Have cancer that returned or did not respond after hydroxyurea or at least 4 cycles of hypomethylating drugs, or be unable to tolerate either treatment.
  • Be able to care for yourself and be out of bed for at least half the day. Side effects from past treatment must be mild, back to your usual level, or lasting effects; hair loss is allowed.
  • Meet liver and kidney test limits. Have at least 20,000 platelets, the blood cells that help stop bleeding; transfusions may help meet this limit in some cases.
  • Be willing and able to give written consent, return for follow-up visits, and complete surveys with or without help.
  • Agree to give blood and bone marrow samples for research.
  • If you or your partner could become pregnant, agree to prevent pregnancy during treatment and for 180 days after the last dose. Those who could become pregnant must have a negative pregnancy test.

Who can't join

  • Past treatment with another experimental PLK1-blocking drug, or any past bone marrow test showing that the cancer changed into acute leukemia.
  • A donor stem cell transplant 100 days ago or less, certain active graft-versus-host disease (when donor cells attack your body), or use of certain drugs that weaken the immune system.
  • Active disease in the brain or spinal cord, or another active cancer. Some treated skin cancers and cancers cured more than 2 years ago are allowed.
  • Severe heart failure, active chest pain linked to heart disease, or other uncontrolled illness that could make study participation unsafe or difficult.
  • Recent cancer drug treatment, another experimental treatment for this cancer, or major surgery within 6 weeks. Hydroxyurea is allowed under study rules.
  • A stomach or bowel problem that would greatly limit how much medicine your body absorbs.
  • Being unable or unwilling to swallow the study drug.
  • Active HIV or hepatitis C with virus detected in the blood, or a positive hepatitis B surface antigen test.

Simplified for readability. The official criteria below are what the study team uses.

Official eligibility criteria

Inclusion Criteria: PRE-REGISTRATION - INCLUSION CRITERIA: * Age \>= 18 years * History of World Health Organization (WHO)-defined diagnosis of proliferative CMML (WBC count \>= 13,000/mm\^3 at time of diagnosis), or MDS/MPN overlap neoplasm with WBC count \>= 13,000/mm3 at time of diagnosis (atypical CML and MDS/MPN-NOS). * NOTE: Hydroxyurea or hypomethylating induced leukopenia does not preclude inclusion. Discussion of WBC \< 13,000/mm\^3 due to treatment at the time of preregistration must be discussed with the Sponsor/Principal Investigator * Relapsed/refractory following treatment with hydroxyurea; or at least 4 cycles of treatment with hypomethylating agents; or who are intolerant of treatment with either therapy. Note: Prior exposure to erythropoiesis stimulating agents is allowed. Hydroxyurea may continue for the first 28 days on study. Continuation of hydroxyurea beyond the first cycle must be discussed with the Sponsor/Principal Investigator * Willing and able to review, understand, and provide written consent before starting any study-specific procedures or therapy * Willing to return to enrolling institution for follow-up (during the active monitoring phase of the study) * Willingness to provide mandatory bone marrow specimens for correlative research * Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1 or 2 * Recovered to grade 1 or baseline or established as sequelae from all toxic effects of previous therapy except alopecia * Platelet count \>= 20,000/mm\^3 (obtained =\< 14 days prior to pre-registration) * NOTE: For platelet count \< 20,000/mm3 and in situations where the primary investigator deems the thrombocytopenia to be attributable to the underlying CMML, patients can be enrolled as long as they are able to achieve a platelet count of 20,000/mm3 with transfusional support * Total bilirubin =\< 1.5 x upper limit of normal (ULN) (=\< 3 x ULN for patients with Gilbert's syndrome) (obtained =\< 14 days prior to pre-registration) * Alanine aminotransferase (ALT) and aspartate transaminase (AST) =\< 3 x ULN (obtained =\< 14 days prior to pre-registration) * Estimated glomerular filtration rate (eGFR) \>= 50 mL/min/m\^2 using one of the following methods (obtained =\< 14 days prior to pre-registration): * Chronic Kidney Disease-Epidemiology Collaboration (CKDEPI) 2021 formula * Corrected creatinine clearance via serum and 24-hour urine creatinine assessment * Iothalamate/Iohexol glomerular filtrate rate via plasma/urine assessment * Ability to complete questionnaire(s) by themselves or with assistance * Willingness to provide mandatory blood specimens for correlative research REGISTRATION - INCLUSION CRITERIA: * Histological confirmation of WHO-defined diagnosis of a myelodysplastic/myeloproliferative neoplasm (MDS/MPN) including one of the following (NOTE: to confirm patient is still eligible and has not progressed to AML): * Proliferative CMML * Atypical chronic myeoloid leukemia (aCML) * MDS/MPN not otherwise specified (MDS/MPN, NOS) * NOTE: Hydroxyurea or hypomethylating agent induced leukopenia does not preclude inclusion. Discussion of WBC \< 13,000/mm\^3 due to treatment at the time of registration must be discussed with the Sponsor/Principal Investigator. * For a man or a woman of child-bearing potential (WOCBP): Must agree to use contraception or take measures to avoid pregnancy during the study and for 180 days after the final dose of any study drug. Adequate contraception is defined as follows: * Complete true abstinence * Consistent and correct use of one of the following methods of birth control: * Male partner who is sterile prior to the female patient's entry into the study and is the sole sexual partner for that female patient * Implants of levonorgestrel * Injectable progestogen * Intrauterine device (IUD) with a documented failure rate of less than 1% per year * Oral contraceptive pill (either combined or progesterone only) * Barrier method, for example: diaphragm with spermicide or condom with spermicide in combination with either implants of levonorgestrel or injectable progestogen * WOCBP must have a negative serum or urine pregnancy test =\< 7 days prior to registration * NOTE: WOCBP include any female who has experienced menarche and who has not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or is not postmenopausal (defined as amenorrhea \> 12 consecutive months); or women on hormone replacement therapy with documented serum follicle stimulating hormone (FSH) level \> 35 mIU/mL. Even women who are using oral, implanted or injectable contraceptive hormones or mechanical products such as an IUD or barrier methods (diaphragm, condoms, spermicides) to prevent pregnancy or practicing abstinence or where partner is sterile (eg, vasectomy), must be considered to be of child-bearing potential * NOTE: If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required Exclusion Criteria: PRE-REGISTRATION - EXCLUSION CRITERIA: * Previous exposure to an alternative (investigational) PLK1 inhibitor * Demonstration of transformation to acute leukemia on any prior bone marrow biopsy * Prior allogeneic hematopoietic stem cell transplantation with active grade 2-4 graft-versus-host disease (GVHD) or with moderate to severe chronic GVHD * NOTE: The patient should not have received calcineurin inhibitors ≤28 days prior to pre-registration and should not be actively receiving immunosuppressive therapy for acute or chronic GVHD. * NOTE: CMML or MDS/MPN overlap neoplasms relapse after allogeneic stem cell transplant is allowed as long as they are \>100 days after transplant and do not have the aforementioned GVHD criteria. * Active central nervous system disease * Concurrent active malignancy, except adequately treated nonmelanoma skin cancer. History of curatively treated in situ cancer of the cervix, curatively treated in situ cancer of the breast, or other solid tumors curatively treated is allowed as long as there is no evidence of disease for \> 2 years * NOTE: Precursor states such as monoclonal gammopathy of undetermined significance (MGUS), monoclonal B-cell lymphocytosis (MBL), and indolent lymphoproliferative disorders must be discussed with the Sponsor/Principal Investigator. * New York Heart Association (NYHA) class III/IV heart failure or active angina/angina equivalents * Anticancer chemotherapy (exception: hydroxyurea) or biologic therapy administered within 2 weeks (and at least 4 elimination half-lives for clinical trial agents) prior to pre-registration. NOTE: Hydroxyurea is allowed for the first 28 days on study. Continuation of hydroxyurea beyond the first cycle must be discussed with the Sponsor/Principal Investigator * Receiving any other investigational agent which would be considered as a treatment for the primary neoplasm * Major surgery =\< 6 weeks prior to pre-registration * Gastrointestinal (GI) disorder(s) that, in the opinion of the Investigator, would significantly impede the absorption of an oral agent (eg, intestinal occlusion, active Crohn's disease, ulcerative colitis, extensive gastric and small intestine resection) * Unable or unwilling to swallow study drug * Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, clinically significant nonhealing or healing wounds, clinically significant cardiac arrhythmia, significant pulmonary disease (shortness of breath at rest or mild exertion), uncontrolled infection, or psychiatric illness/social situations that would limit compliance with study requirements * Known active infection with human immunodeficiency virus (HIV) with measurable viral titer, hepatitis B surface antigen positivity, or hepatitis C with measurable viral titer. NOTE: Patients with antibody to hepatitis B core antibody are eligible if they have no measurable viral titer. Patients who have had a hepatitis B virus (HBV) immunization are eligible * Patient is receiving any live vaccine (eg, varicella, pneumococcus) =\< 28 days prior to pre-registration. NOTE: messenger ribonucleic acid (mRNA)-based (eg, Pfizer or Moderna) or replication-deficient virus (eg, Oxford/AstraZeneca) COVID19 vaccines are permitted * Disease requiring systemic treatment with systemic immunosuppression with steroid steroids at a dose of \>= 20 mg/day prednisone (or equivalent). Exceptions: Intermittent use of bronchodilators or inhaled steroids, local steroid injections, topical steroids * Any active disease condition that would render the protocol treatment dangerous or impair the ability of the patient to receive study drug * Strong CYP3A4 inhibitors/inducers as identified per institutional guidelines * QT interval with Fridericia's correction (QTcF) \> 470 milliseconds. In the case of potentially correctible causes of QT prolongation, (eg, medications, hypokalemia), the electrocardiogram (ECG) may be repeated once during screening and that result may be used to determine eligibility REGISTRATION - EXCLUSION CRITERIA: * Any of the following because this study involves an investigational agent whose genotoxic, mutagenic and teratogenic effects on the developing fetus and newborn are unknown: * Pregnant persons * Nursing persons * Persons of childbearing potential who are unwilling to employ adequate contraception * Increased risk of Torsade des Pointes (TdP) defined as follows: * A marked baseline prolongation of QT/QTc interval (eg, repeated demonstration of a QTc interval \> 480 msec \[CTCAE Grade \>= 2\] using Fredericia's QT correction formula) * A history of additional risk factors for TdP (eg. heart failure, family history of long QT syndrome) * Transformation to acute leukemia on registration bone marrow biopsy

Study sites (1)

MN