A Study of BH-30236 in Relapsed/ Refractory Acute Myelogenous Leukemia and Higher Risk Myelodysplastic Syndrome

Phase 1RecruitingNCT06501196

BlossomHill Therapeutics170 enrolled

Overview

Study BH-30236-01 is a first-in-human (FIH), Phase 1/1b, open-label, dose escalation and expansion study in participants with relapsed/refractory acute myelogenous leukemia (R/R AML) or higher-risk myelodysplastic syndrome (HR-MDS). Phase 1, Part 1 Dose Escalation - Monotherapy will evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of BH-30236 administered orally. Approximately 50 participants may be enrolled in Phase 1, Part 1 Dose Escalation - Monotherapy. Phase 1, Part 2 Dose Escalation - Combination with Venetoclax will evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary efficacy of BH-30236 administered as a combination therapy with venetoclax. Approximately 48 participants may be enrolled in Phase 1, Part 2 Dose Escalation - Combination with Venetoclax. Phase 1b (Dose Expansion) will follow Phase 1 to further understand the relationships among dose, exposure, toxicity, tolerability, and clinical activity. Up to 72 participants may be enrolled in Phase 1b of the study as a monotherapy or in combination with venetoclax.

This is a Phase 1/1b, multi-center, open-label, dose escalation, first-in-human study to evaluate the safety, tolerability, PK, PD, and preliminary anti-leukemic activity of the CLK inhibitor, BH-30236 as a monotherapy or in combination with venetoclax, in adult participants with R/R AML or HR-MDS. The study consists of three parts: Phase 1, Part 1 Dose Escalation - Monotherapy, Phase 1, Part 2 Dose Escalation - Combination with Venetoclax, and Phase 1b Dose Expansion. Phase 1, Part 1 Dose Escalation - Monotherapy is anticipated to enroll approximately 50 participants to evaluate the safety, tolerability, PK, PD, and preliminary anti-leukemic activity of BH-30236, as well as determine the MTD and/or the preliminary recommended dose(s) for expansion (RDEs). Phase 1, Part 2 Dose Escalation - Combination with Venetoclax is anticipated to enroll approximately 48 participants to evaluate the safety, tolerability, PK, PD, and preliminary anti-leukemic activity of BH-30236, as well as determine the MTD and/or the preliminary recommended dose(s) for expansion (RDEs). Phase 1 will follow a Bayesian optimal interval (BOIN) design dose escalation, where participants will receive ascending doses of BH-30236 to determine the recommended RDEs. Phase 1b Dose Expansion will enroll approximately 72 participants to evaluate the safety, tolerability, and preliminary anti-leukemic activity of BH-30236 as a monotherapy or in combination with venetoclax at selected RDEs determined in Phase 1 Dose Escalation.

Study Type

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion criteria: * ≥18 years. * Diagnosis of relapsed/refractory acute myelogenous leukemia (R/R) AML or higher-risk myelodysplastic syndrome (HR-MDS) with ≥5% bone marrow blast at time of inclusion. * Prior treatment history must include 1-5 prior lines of therapy. * ECOG performance status ≤2. * Adequate organ function evidenced by the following laboratory values: * Hepatic: Transaminase levels aspartate aminotransferase \[AST\]/ alanine transaminase \[ALT\] ≤ 2.5 × upper limit of normal (ULN). In cases of liver involvement by AML or MDS, AST and ALT \< 5.0 × ULN is acceptable. Total bilirubin ≤ 1.5 × ULN in the absence of documented Gilbert's disease. * Renal: Measured or calculated creatinine clearance ≥ 60 mL/min (Cockcroft-Gault formula) The above are a summary, other inclusion criteria details may apply. Exclusion Criteria: * Diagnosis of acute promyelocytic leukemia or chronic myeloid leukemia with blast crisis. * Prior allogeneic HSCT within 3 months or donor lymphocyte infusion within 30 days of start of therapy; * Active and uncontrolled infections. * Unresolved AEs greater than Grade from prior therapies. * History of other active malignancy (with certain exceptions) * Prior treatment with a CLK inhibitor. * Any acute or chronic graft versus host disease requiring systemic therapy within 4 weeks prior to study drug administration with the exception of topical steroids or the equivalent of 20 mg of prednisone or less. The above is a summary, other exclusion criteria details may apply.

Locations (13)

City of Hope Medical Center

Duarte, California, United States

RECRUITING

University of California Los Angeles

Los Angeles, California, United States

RECRUITING

Stanford Cancer Center

Palo Alto, California, United States

RECRUITING

Sylvester Comprehensive Cancer Center

Miami, Florida, United States

RECRUITING

Moffitt Cancer Center

Tampa, Florida, United States

RECRUITING

Northwestern Medicine - Northwestern Memorial Hospital Galter Pavilion

Chicago, Illinois, United States

RECRUITING

Roswell Park Cancer Institute

Buffalo, New York, United States

RECRUITING

Memorial Sloan Kettering Cancer Center

New York, New York, United States

RECRUITING

The Ohio State University Wexner Medical Center - James Cancer Hosp

Columbus, Ohio, United States

RECRUITING

Sarah Cannon Research Institute

Nashville, Tennessee, United States

RECRUITING

...and 3 more locations

Outcomes

Primary Outcomes

Dose Escalation: Frequency of dose limiting toxicities (DLTs)

DLTs are dose-limiting toxicities as defined in the study protocol.

Time frame: Dose-limiting toxicities are collected during the first treatment cycle (28 days)

Dose Escalation and Expansion: Safety evaluation of BH-30236: Number of participants with treatment-related adverse events as assessed by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) v5.0

Frequency, severity and relationship to study drug of AEs and SAEs

Time frame: From first dose until 28 days after last dose of BH-30236

Dose Expansion: Composite Complete Remission (CR) Rate

Composite CR rate disease assessment in accordance with the following guidelines: European Leukemia Network (ELN) 2022 for acute myelogenous leukemia (AML) and International Working Group (IWG) 2023 for myelodysplastic syndrome (MDS).

Time frame: From first dose of BH-30236 until disease progression (up to approximately 1 year)

Secondary Outcomes

Dose Escalation and Expansion: Maximum observed blood concentration (Cmax) of BH-30236.

Blood samples for PK analyses will be collected at predetermined time points and analyzed.

Time frame: Evaluation performed in Cycle 1 (cycle duration is 28 days).

Dose Escalation: Area under the blood concentration time curve (AUC) of BH-30236.

Blood samples for PK analyses will be collected at predetermined time points and analyzed.

Time frame: Evaluation performed in Cycle 1 (cycle duration is 28 days).

Dose Escalation and Expansion: Concentration before dose at steady state (Ctrough).

Blood samples for PK analyses will be collected at predetermined time points and analyzed.

Time frame: Evaluation performed in all treatment cycles up to one year (cycle duration is 28 days).

Dose Escalation and Expansion: Objective Response Rate (ORR)

Objective response rate disease assessments in accordance with the following guidelines: ELN 2022 recommendations for AML and IWG 2023 for MDS (CR, CR with partial hematologic recovery \[CRh\], CR with incomplete count recovery \[CRi\], CR with limited count recovery \[CRL\], morphologic leukemia-free state \[MLFS\], or partial response \[PR\]).

Time frame: From first dose of BH-30236 until disease progression (up to approximately 1 year)

Dose Escalation and Expansion: Duration of Response (DoR)

Time from first documented response until the date of relapse or death.

Time frame: Time from first documented response until disease progression or death (approximately 1 year).

Dose Escalation and Expansion: Time to remission (TTR)

Time from first dose to the achievement of first remission Disease assessments will follow the following guidelines: ELN 2022 for AML and IWG 2023 for MDS.

Time frame: From first dose of BH-30236 until complete remission, disease progression or death (approximately 1 year).

Dose Escalation and Expansion: Relapse-free Survival (RFS)

The time from the start of treatment date to disease progression, death, or initiation of a new anti-leukemic therapy.

Time frame: From first dose of BH-30236 until disease progression, death, or initiation of a new anti-leukemic therapy (approximately 1 year).

Dose Escalation and Expansion: Measurable Residual Disease (MRD)

For AML, using ELN 2022 criteria for disease assessment from Screening, then at the beginning of Cycle 2 and 3, and then every second cycle thereafter.

Time frame: From time of first dose until discontinuation of BH-30236 (approximately 1 year).

Dose Escalation and Expansion: Measurement of the change in RNA alternative splicing markers on BH-30236 treatment

Peripheral blood samples for pharmacodynamic (PD) analyses will be collected at predetermined time points and analyzed.

Time frame: From time of first dose until discontinuation of BH-30236 (approximately 1 year).

Dose Escalation and Expansion: Complete remission (CR) / complete remission with partial hematologic recovery (CRh) rate for AML and complete remission/partial remission (CR/PR) rate for HR-MDS

In accordance with the following guidelines: ELN 2022 recommendations for AML and IWG 2023 for MDS (CR, CR with partial hematologic recovery \[CRh\], CR with incomplete count recovery \[CRi\], CR with limited count recovery CRL, morphologic leukemia-free state \[MLFS\], or partial response \[PR\])

Time frame: Time from first documented response until disease progression or death (approximately 1 year)

A Study of BH-30236 in Relapsed/ Refractory Acute Myelogenous Leukemia and Higher Risk Myelodysplastic Syndrome

Overview

Conditions

Interventions

Eligibility

Locations (13)

Outcomes

Primary Outcomes

Secondary Outcomes

Central Contacts