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A Phase 1 first-in-human dose-escalation and dose-expansion study of BMF-500, an oral FLT3 inhibitor, in adult patients with acute leukemia.
A Phase 1 first-in-human dose-escalation and dose-expansion study of BMF-500, an oral covalent FLT3 inhibitor, in adult patients with acute myeloid leukemia (AML), who may or may not be on Antifungals.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Arm A: Escalation Phase | Experimental | BMF-500 taken twice daily by participants who are not receiving drugs that inhibit CYP3A4 activity. |
|
| Arm B: Escalation Phase | Experimental | BMF-500 taken twice daily by participants who are receiving necessary azole antifungals that are Strong CYP3A4 inhibitors. |
|
| Arm C: Escalation Phase | Experimental | BMF-500 taken twice daily by participants who are receiving necessary azole antifungals that are moderate CYP3A4 inhibitors. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| BMF-500 | Drug | Investigational Product |
|
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate the safety and tolerability of BMF-500 by incidence of Treatment Emergent Adverse Events (TEAEs). | Assessed by the NCI CTCAE version 5.0. | At the end of each 28 Day cycle for a maximum of 32 cycles |
| Evaluate the safety and tolerability of BMF-500 by incidence of Serious Adverse Events (SAEs). | Assessed by the NCI CTCAE version 5.0. | At the end of each 28 Day cycle for a maximum of 32 cycles |
| Determine the recommended Phase 2 Dose (RP2D) of BMF-500. | Safety, as determined by Dose-Limiting Toxicities (clinically significant Adverse Event) within each dose level assessed NCI CTCAE version 5.0. | At the end of 28 day Dose-Limiting Toxicities (DLT) observation Period |
| Determine the recommended Phase 2 Dose (RP2D) of BMF-500. | Efficacy within each dose level as determined by composite complete remission (CRc). | At the end of 28 day Dose-Limiting Toxicities (DLT) observation Period |
| Determine the recommended Phase 2 Dose (RP2D) of BMF-500. | Pharmacovigilance (PK) at each dose level as determined by the maximum plasma concentration (Cmax). | At the end of 28 day Dose-Limiting Toxicities (DLT) observation Period |
| Determine the recommended Phase 2 Dose (RP2D) of BMF-500. | Pharmacovigilance (PK) at each dose level as determined by area under the curve plasma concentration from time 0 to last quantifiable concentration (AUClast). | At the end of 28 day Dose-Limiting Toxicities (DLT) observation Period |
| Measure | Description | Time Frame |
|---|---|---|
| Determine the pharmacokinetics of BMF-500. | Maximum plasma concentration (Cmax). | At the end of each cycle (each cycle is 28 days in duration) for 7 cycles |
| Determine the pharmacokinetics of BMF-500. |
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Key Inclusion Criteria:
Key Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mayo Clinic | Phoenix | Arizona | 85054 | United States | ||
| City of Hope National Medical Center |
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Accelerated Titration Design, Followed by Modified 3+3
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Area under the curve plasma concentration from time 0 to last quantifiable concentration (AUClast).
| At the end of Cycle 1 and 2 (each cycle is 28 days in duration) |
| Evaluate the efficacy of BMF-500 | Composite Complete Remission (CRc). | At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles |
| Assess additional evidence of antitumor activity per investigator assessment as per corresponding response criteria. | Duration of Response (DOR). | At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles |
| Evaluate the efficacy of BMF-500 | Overall Reasons Rate (ORR). | At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles |
| Assess additional evidence of antitumor activity per investigator assessment as per corresponding response criteria. | Relapse free survival (RFS). | At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles |
| Assess additional evidence of antitumor activity per investigator assessment as per corresponding response criteria. | Overall Survival (OS). | At the end of each cycle (each cycle is 28 days in duration) for a maximum of 32 cycles |
| Duarte |
| California |
| 91010 |
| United States |
| University of California, San Francisco | San Francisco | California | 94143 | United States |
| Colorado Blood Cancer Institute | Denver | Colorado | 80218 | United States |
| Mayo Clinic | Jacksonville | Florida | 32224 | United States |
| Winship Cancer Institute, Emory University | Atlanta | Georgia | 30322 | United States |
| Northwestern Memorial Hospital | Chicago | Illinois | 60611 | United States |
| University of Kentucky - Markey Cancer Center | Lexington | Kentucky | 40536 | United States |
| Mayo Clinic | Rochester | Minnesota | 55902 | United States |
| Roswell Park Comprehensive Cancer Center | Buffalo | New York | 14203 | United States |
| Texas Oncology-PA USOR | Dallas | Texas | 75251 | United States |
| MD Anderson Cancer Center | Houston | Texas | 77030 | United States |
| Virginia Cancer Specialists | Gainesville | Virginia | 20155 | United States |
| Fred Hutchinson Cancer Center | Seattle | Washington | 98109 | United States |
| ID | Term |
|---|---|
| D015470 | Leukemia, Myeloid, Acute |
| ID | Term |
|---|---|
| D007951 | Leukemia, Myeloid |
| D007938 | Leukemia |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
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