A Study of Oral TP-3654 in Patients With Myelofibrosis
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This study is a Phase 1, multicenter, dose-escalation, open-label trial to assess safety, tolerability, pharmacokinetics and pharmacodynamics of TP-3654 in patients with intermediate-2 and high-risk primary or secondary MF.
Determine the incidence of dose-limiting toxicities (DLTs) at escalated doses of TP-3654 [ Time Frame: 28 days ]
Determine the incidence of treatment emergent adverse events [ Time Frame: 28 days ]
Secondary Outcome Measures :
Determine the incidence of QT interval changes and morphology as assessed by intensive electrocardiogram (ECG) monitoring [ Time Frame: 25 hours ]
Establish the pharmacokinetic (PK) parameters of TP-3654 by assessing Half-life (t½) [ Time Frame: 24 hours ]
Establish the pharmacokinetic (PK) parameters of TP-3654 by assessing Peak Plasma Concentration (Cmax) [ Time Frame: 24 hours ]
Establish the pharmacokinetic (PK) parameters of TP-3654 by assessing Time of Maximum concentration observed (tmax) [ Time Frame: 24 hours ]
Establish the pharmacokinetic (PK) parameters of TP-3654 by assessing Area under the plasma concentration versus time curve (AUC) [ Time Frame: 24 hours ]
Assess patients for any evidence of Preliminary activity by proportion of patients with responses in complete remission, partial remission, clinical improvement, progressive disease and stable disease [ Time Frame: 12 months ]
Other Outcome Measures:
Study potential pharmacodynamic (PD) markers of TP-3654 [ Time Frame: 12 months ]
Evaluate exploratory biomarkers in peripheral blood samples and bone marrow biopsy samples
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Layout table for eligibility information
Ages Eligible for Study:
18 Years and older (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Patients must meet all of the following inclusion criteria to be eligible:
Confirmed pathological diagnosis of primary myelofibrosis (PMF) or post-PV-MF/post-ET- MF as per WHO diagnostic criteria and intermediate-2 or high-risk primary or secondary MF based on the Dynamic International Prognostic Scoring System (DIPSS)
Previously treated with a JAKi and failed on a JAK inhibitor or are ineligible to be treated with Ruxolitinib or Fedratinib at the discretion of the investigator
Grade ≥ 2 MF23, as confirmed by bone marrow biopsy within 12 weeks prior to Screening
Fulfill the following laboratory parameters:
Platelet count > 50 X 109 /L, without the assistance of growth factors or platelet transfusions
Absolute Neutrophil Count (ANC) ≥ 1 x 109/L without the assistance of granulocyte growth factors
Hemoglobin ≥ 8 g/dL
Peripheral blood blast count < 10%
Eastern Cooperative Oncology Group (ECOG) performance status ≤2
Life expectancy ≥ 3 months
Adequate renal function, as determined by clinical laboratory tests (serum creatinine < 1.5 x upper limit of normal (ULN), and calculated creatinine clearance ≥60 mL/min) (Cockcroft-Gault)
Adequate hepatic function (ALT/AST < 2.5 x ULN, bilirubin < 1.5 x ULN), and coagulation ([PT and PTT] < 1.5 x ULN)
Agree to provide 3 bone marrow biopsies during the study: at baseline or within 12 weeks prior to enrollment, and every 6 months post-treatment.
Splenomegaly during the screening period as demonstrated by splenic length ≥ 5 cm by palpation or spleen volume of ≥ 450 cm3 by Magnetic Resonance Imaging (MRI) or Computerized Tomography (CT) scan
Show at least 2 symptoms measurable (score ≥ 1) using the MFSAF, v4.0.
Patients meeting any one of these exclusion criteria will be prohibited from participating in this study:
Received previous systemic antineoplastic therapy (including unconjugated therapeutic antibodies, toxin immunoconjugates, and alpha-interferon) or any experimental therapy within 14 days or 5 half-lives, whichever is shorter, before the first dose of study treatment.
Major surgery within 2 weeks before the first dose of either study drug.
Splenic irradiation within 6 months prior to Screening or prior splenectomy.
AML, MDS, or peripheral blasts ≥ 10%.
Prior autologous or allogeneic stem cell transplant at any time.
Eligible for allogeneic bone marrow or stem cell transplantation. Experiencing electrolyte abnormalities of NCI CTCAE Grade ≥ 2 unless they can be corrected during screening and are deemed not clinically significant by the Investigator.
History of congestive heart failure, myocardial infarction within the past 6 months prior to Cycle 1/Day 1; left ventricular ejection fraction < 45% by echocardiogram or MUGA, unstable arrhythmia, or evidence of ischemia on electrocardiogram (ECG) within 14 days prior to Cycle 1/Day 1.
Corrected QT interval (using Fridericia's correction formula) of > 450 msec in men and > 470 msec in women.
Central nervous system (CNS) cancer or metastases, meningeal carcinomatosis, malignant seizures, or a disease that either causes or threatens neurologic compromise (eg, unstable vertebral metastases).
Other invasive malignancies within the last 3 years, except non-melanoma skin cancer, and localized cured prostate and cervical cancer
Experienced portal hypertension or any of its complications.
Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic therapy.
Known bleeding diathesis or signs of uncontrolled active bleeding (hematuria, GI bleeding) other than self-limited causes of benign etiology that have been adequately investigated at the discretion of the Investigator.
Requiring anticoagulation with aspirin > 81mg daily, unfractionated heparin, low molecular weight heparin (LMWH), direct anti-thrombin inhibitors, or vitamin K antagonists (eg, warfarin).
Severe chronic obstructive pulmonary disease with hypoxemia (defined as resting O2 saturation of < 90% breathing room air).
Medical condition or have undergone significant surgery to the gastrointestinal tract that could impair absorption or that could result in short bowel syndrome with diarrhea due to malabsorption.