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An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 in Combination With TL-895 for the Treatment of Relapsed or Refractory Myelofibrosis and KRT-232 for the Treatment of JAK Inhibitor Intolerant Myelofibrosis.


Description

This study evaluates KRT-232 in Combination With TL-895 for the Treatment of Relapsed or Refractory Myelofibrosis and KRT-232 for the Treatment of JAK Inhibitor Intolerant Myelofibrosis.Cohorts 1 and 2 will undergo dose finding and dose expansion. Eligible patients will be randomly assigned to an open cohort, either Cohort 1 or Cohort 2. Cohort 3 will be conducted as a dose expansion, independent of Cohorts 1 and 2. Cohort 1 will follow a 3+3 dose escalation design to determine the maximum tolerated dose (MTD)/maximum administered dose (MAD) and recommended Phase 2 dose (RP2D) of TL-895 administered QD in combination with KRT-232. A Safety Review Committee (SRC) will review the safety data during the dose escalation to decide on dose escalation and/or exploration of intermediate doses. Cohort 2 will follow a 3+3 dose escalation design to determine the MTD/MAD and recommended RP2D of TL-895 administered BID in combination with KRT-232. An SRC will review the safety data during the dos

Trial Eligibility

Inclusion Criteria: * Confirmed diagnosis of primary MF, post-PV MF, or post-ET MF, (WHO 2016) * ECOG ≤ 2 * Cohort 1 and Cohort 2: R/R following JAK inhibitor treatment * Cohort 3: patients who are intolerant to JAK inhibitor treatment Exclusion Criteria: * Prior treatment with MDM2 inhibitors or p53-directed therapies * Prior treatment with a BCR-ABL, phosphoinositide 3-kinase (PI3k), mammalian target of rapamycin (mTOR), bromodomain and extraterminal domain (BET), histone deacetylase (HDAC), or spleen tyrosine kinase (Syk) inhibitor * Prior splenectomy * Splenic irradiation within 3 months prior to the first dose of study treatment * Clinically significant thrombosis within 3 months of screening * Grade 2 or higher QTc prolongation

Study Info

Organization

Kartos Therapeutics, Inc.


Primary Outcome

Phase 1b - The MTD/MAD and RP2D of TL-895 in combination with KRT-232 in patients with R/R MF (Cohort 1 and Cohort 2)


Outcome Timeframe 56 Days

NCTID NCT04640532

Phases PHASE1,PHASE2

Primary Purpose TREATMENT

Start Date 2020-11-17

Completion Date 2022-05-11

Enrollment Target 116

Interventions

DRUG KRT-232

DRUG TL-895

Locations Recruiting

University of Alabama at Birmingham School of Medicine, Division of Hematology and Oncology

United States, Alabama, Birmingham


The Oncology Institute of Hope

United States, California, Whittier


Lake City Cancer Center

United States, Florida, Lake City


Carle Cancer Center

United States, Illinois, Urbana


Columbia University Medical Center

United States, New Jersey, Fort Lee


Interested in joining this trial?

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