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Study of Elenestinib (BLU-263) in Advanced Systemic Mastocytosis (AdvSM) and and Other KIT Altered Hematologic Malignancies

Recruiting
18 years of age
Both
Phase 1/2

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Overview

The goal of this clinical trial is to evaluate elenestinib (BLU-263) in participants with Advanced Systemic Mastocytosis (AdvSM), SM with an associated hematologic neoplasm (SM-AHN), and other hematologic malignancies. The main questions it aims to answer are:

  • Determine Recommended Dose of elenestinib (BLU-263) monotherapy for participants with AdvSM
  • Safety and tolerability of elenestinib (BLU-263) monotherapy
  • Efficacy of elenestinib (BLU-263) monotherapy in participants with AdvSM
  • Determine Recommended Dose of elenestinib (BLU-263) in combination with azacitidine in participants with AdvSM
  • Safety and tolerability of elenestinib (BLU-263) in combination with azacitidine
  • Efficacy of elenestinib (BLU-263) in combination with azacitidine in participants with AdvSM

The estimated study duration for each participant will be approximately 4 years: 2 years of treatment followed by 2 years of follow-up. Participants may be required to attend monthly visits for the first six months, followed by quarterly visits for the remainder of the study.

Description

Systemic mastocytosis includes five major subtypes: Indolent SM (ISM), SM with an associated hematologic neoplasm (SM-AHN), aggressive SM (ASM), and MC leukemia (MCL). In 2016, the smoldering subtype of SM, a former provisional ISM subvariant, was designated as a distinct variant of SM by the World Health Organization (WHO). Aggressive SM, SM-AHN, and MCL together are referred to as Advanced SM (AdvSM).

Eligibility

Key Inclusion Criteria :

  • Participant has Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0-2
  • Participant must have a new Bone Marrow (BM) biopsy or may use archival tissue if taken within 56 days prior to C1D1 and participant must be willing to have follow-up BM Biopsies.
  • Participants receiving antineoplastic therapy within the preceding 12 weeks must have discontinued therapy due to disease progression, refractory disease, lack of efficacy, or intolerance.
  • Participants treated with 1 prior selective KIT inhibitor (such as avapritinib or CGT9486) will be permitted on study after confirmation of KIT D816V mutation and with written approval of the study Sponsor. Participants who discontinued treatment with a prior selective KIT inhibitor due to a severe AE that was thought to be related to prior treatment will not be eligible to participate in the study.
        Arm 1 (Monotherapy): Participants must have one of the following AdvSM diagnoses, based on
        World Health Organization (WHO) diagnostic criteria.
        Before enrollment, diagnosis of AdvSM must be confirmed based on Central Pathology
        Laboratory assessment of BM:
          1. Aggressive SM (ASM).
          2. SM-AHN that in the opinion of the Investigator is not considered to be a candidate for
             Hypomethylating agent (HMA) monotherapy. Incidental indolent, low-grade lymphoid AHNs
             (eg, chronic lymphocytic leukemia) not requiring treatment are eligible.
          3. Mast cell leukemia (MCL), including diagnoses with an AHN component, that does not
             require a C-finding.
          4. Upon discussion with the Sponsor, other relapsed or refractory hematologic neoplasms
             with evidence of aberrant KIT or PDGFR may be considered for enrollment. (eg,
             participants with chronic myeloid neoplasms, such as subvariants of MDS/MPN that
             harbor activating KIT exon 17 mutations but do not fulfill the diagnostic criteria of
             SM-AHN, and participants with myeloid/lymphoid neoplasms with PDGFRa/b fusion genes
             and mutations conferring resistance to imatinib, such as T674I or D842V).
        Key Exclusion Criteria:
          -  Diagnosis of a Philadelphia chromosome positive malignancy
          -  Acute myeloid leukemia.
          -  If the participant is receiving corticosteroids, and the dose has not been stable for
             ≥7 days.
          -  Within the 14 days prior to enrollment, participant has received any antineoplastic
             therapy (including midostaurin, avapritinib and other tyrosine kinase inhibitors
             [TKIs]) or an investigational agent.
          -  Participant has received hydroxyurea within 7 days prior to the first dose of
             elenestinib (BLU-263).
          -  Participant received prior HMA therapy (e.g., azacitidine, decitabine) for the current
             diagnosis.
          -  Participant must not be eligible for allogenic hematopoietic stem cell
             transplantation.
          -  Participant received prior radiotherapy within 14 days of screening BM biopsy.
          -  Participant received any hematopoietic growth factor (except erythropoietin) within 14
             days of screening BM biopsy, or requiring growth factors to maintain adequate
             neutrophil or platelet levels.
        Those participants maintained on a chronic dose of erythropoietin, whose hemoglobin is
        stable, and dose of erythropoietin has not been changed in the prior 28 days are allowed on
        study.
          -  Participant received >1 prior selective KIT inhibitor (eg: avapritinib or
             bezuclastinib).
          -  Participant have any of the following laboratory abnormalities on last laboratory
             assessment within 14 days prior to the first dose of initiation of study drug: a.
             Alanine aminotransferase and aspartate aminotransferase > 3 × ULN; > 5 × ULN if
             associated with clinically suspected liver infiltration by mastocytosis or another
             disease for which the patient enrolled into the study b. Total bilirubin > 1.5 × ULN;
             > 3 × ULN if associated with liver infiltration by the disease being treated or in the
             presence of Gilbert's Disease. (In the case of Gilbert's disease, a direct bilirubin >
             2.0 ULN would be an exclusion) c. Estimated (Cockcroft-Gault formula) or measured
             creatinine clearance < 40 mL/min d. Absolute neutrophil count < 0.5 × 10^9/L
          -  Participant has had a major surgical procedure within 14 days of the first dose of
             study drug.
          -  History of another primary malignancy that has been diagnosed or required therapy
             within 1 year prior to the first dose of study drug. The following are exempt from the
             1-year limit: completely resected basal cell and squamous cell skin cancer, curatively
             treated localized prostate cancer, GI stromal tumor, and completely resected carcinoma
             in situ of any site.
          -  Mean resting QTcF > 480 msec, a history of prolonged QT syndrome or Torsades de
             pointes, or a familial history of prolonged QT syndrome.
          -  Clinically significant, uncontrolled, cardiovascular disease.
        Arm 1 (Monotherapy):
          -  Myelodysplastic Syndrome (MDS) that is very high- or high-risk as defined by the
             International Prognostic Scoring System for Myelodysplastic Syndromes-Revised
             (IPSS-R).
          -  A myeloid AHN with ≥10% BM or peripheral blood blasts.
          -  Platelet count <50 x 10^9/L (within 4 weeks prior to the first dose of study drug) or
             receiving platelet transfusions or thrombopoietin receptor agonists (TPO-RA) within
             the prior 14 days.

Study details

Advanced Systemic Mastocytosis

NCT05609942

Blueprint Medicines Corporation

12 April 2024

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