RecruitingPhase 2

(Apex) Bezuclastinib in Patients With Advanced Systemic Mastocytosis

A Phase 2 Open-Label, Multicenter Clinical Study of the Safety, Efficacy, Pharmacokinetic, and Pharmacodynamic Profiles of CGT9486 as a Single Agent in Patients With Advanced Systemic Mastocytosis

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

Not stated in the study description — ask the study team about visits and procedures.

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 Phase 2 study tests bezuclastinib (CGT9486) for advanced systemic mastocytosis, a disease involving mast cells, a type of immune cell. It includes people with aggressive disease, a related blood cancer, or mast cell leukemia. Everyone knows which treatment they receive.

This is an open-label, two-part Phase 2 study investigating CGT9486 for the treatment of patients with Advanced Systemic Mastocytosis (AdvSM), including patients with Aggressive SM (ASM), SM with Associated Hematologic Neoplasm (SM-AHN), and Mast Cell Leukemia (MCL).

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

Eligibility

Who can join

  • Main study: A study committee must confirm aggressive systemic mastocytosis, systemic mastocytosis with a related blood cancer, or mast cell leukemia.
  • Main study: Disease must be measurable using study rules. Some people whose disease cannot be measured this way may also join.
  • Main study: Have a daily activity score of 0 to 3. This ranges from fully active to needing help with self-care and spending much of the day in bed or a chair.
  • All groups: Blood counts and other blood tests must be within the study’s allowed limits.
  • Rollover group: Bezuclastinib has helped you, but your related blood cancer has worsened during treatment and needs treatment right away.
  • High-risk group: Be receiving or need treatment for a related blood cancer. You must have one of the listed high-risk blood cancers: high- or very high-risk MDS, accelerated-phase MPN, MDS with too many immature blood cells, or CMML-2.

Who can't join

  • Main study: Lasting side effects from past treatment that are more than mild, a related blood cancer needing treatment right away, or serious heart disease.
  • Main study: A positive test for the FIP1L1-PDGFRA gene change, HIV-1 or HIV-2, hepatitis B surface antigen, or hepatitis C antibodies. Some people with high eosinophils, a type of white blood cell, need extra gene testing.
  • Main study: Serious bleeding in the past 30 days, a need for blood thinners to treat clots during the study, or another cancer diagnosed or treated in the past 3 years.
  • Main study: Recent use of treatments that lower blood cell counts, experimental drugs, blood cell growth medicines, or certain drugs that affect how the body breaks down medicines. Required waiting times vary by drug. Needing high-dose steroids also rules you out.
  • Substudy: Acute myeloid leukemia (AML), a cancer with the Philadelphia chromosome gene change, or being suited for a stem cell transplant from a donor.
  • Substudy: A medical reason you cannot safely take the chosen treatment given with bezuclastinib. Rollover group: Past bezuclastinib side effects were not acceptable under study rules.
  • High-risk group: Past experimental treatment for advanced systemic mastocytosis, or stopping a treatment that lowers blood cell counts because of side effects.
  • High-risk group: Treatment that lowers blood cell counts or an experimental drug within 14 days before the bone marrow sample used for screening. The wait is 28 days for cladribine, interferon alpha, pegylated interferon, or antibody treatment.

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

Official eligibility criteria

Key Inclusion Criteria for Main Study: 1. Diagnosed with one of the following advanced mastocytosis diagnoses by Eligibility Committee 1. Aggressive Systemic Mastocytosis (ASM) 2. Systemic Mastocytosis with an Associated Hematologic Neoplasm (SM-AHN) 3. Mast Cell Leukemia (MCL) 2. Measurable disease according to modified IWG-MRT-ECNM criteria. (A subset of patients inevaluble per mIWG-MRT-ECNM will be included in the study). 3. ECOG (0 to 3) 4. Have clinically acceptable local laboratory screening results (clinical chemistry, hematology) within certain limits Key Exclusion Criteria for Main Study: 1. Persistent toxicity from previous therapy for AdvSM that has not resolved to ≤ Grade 1 2. Associated hematologic neoplasm requiring immediate antineoplastic therapy 3. Clinically significant cardiac disease 4. Known positivity for the FIP1L1 PDGFRA fusion. Patients with eosinophilia without detectable KIT D816V mutation must demonstrate lack of PDGFRA fusion mutation prior to enrollment 5. Seropositive for human immunodeficiency virus (HIV) 1 or 2, or positive for hepatitis B surface antigen or hepatitis C virus (HCV) antibody 6. History of clinically significant bleeding event within 30 days before the first dose of study drug or need for therapeutic anticoagulation on study 7. Diagnosed with or treated for malignancy other than the disease under study within the prior 3 years before enrollment 8. Received any cytoreductive therapy or any investigational agent less than 14 days, and for cladribine, interferon alpha, pegylated interferon, and any antibody therapy less than 28 days, before screening bone marrow biopsy 9. Received hematopoietic growth factor support within 14 days before the first dose of study drug 10. Received strong CYP3A4 inhibitors or inducers within 14 days or 5 drug half-lives, whichever is longer, before the first dose of study drug 11. Need for treatment with high dose steroids Key Inclusion Criteria for Substudy Population: Rollover Cohort 1. Demonstrate AHN progression requiring immediate AHN-directed therapy while receiving bezuclastinib 2. Demonstrated clinical benefit from bezuclastinib therapy 3. Have clinically acceptable local laboratory screening results (clinical chemistry, hematology) within certain limits High-Risk Cohort 1. Receiving or indicated for AHN-directed therapy. 2. Diagnosed with one of the following pathologic diagnoses of SM-AHN: 1. Myelodysplastic syndrome (MDS) that is high- or very high-risk 2. Accelerated phase myeloproliferative neoplasm (MPN) 3. MDS with excessive blasts in bone marrow or peripheral blood 4. Chronic myelomonocytic leukemia-2 (CMML-2) 3. Have clinically acceptable local laboratory screening results (clinical chemistry, hematology) within certain limits. Key Exclusion Criteria for Substudy Population: 1. Diagnosis of Philadelphia chromosome-positive malignancy 2. Diagnosis of acute myeloid leukemia (AML) 3. Appropriate for allogenic hematopoietic stem cell transplantation 4. Any contraindication to selected concomitant therapy 5. Rollover Cohort: Have not demonstrated acceptable tolerability of previous bezuclastinib therapy 6. High-Risk Cohort: Previously treated with investigational therapy for AdvSM 7. High-Risk Cohort: Previously treated with cytoreductive therapy and discontinued due to treatment-related toxicity 8. High-Risk Cohort: Received any cytoreductive therapy or any investigational agent less than 14 days, and for cladribine, interferon alpha, pegylated interferon, and any antibody therapy less than 28 days, before screening or archival bone marrow biopsy

Study sites (14)

AL

AZ

CA

FL

GA

IL

MA

NY

OH

SC

TX

UT