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Looking for participantsPhase1/Phase2

A Study of Oral Nuvisertib (TP-3654) in Patients With Myelofibrosis

Sponsor: Sumitomo Pharma America, Inc.

NCT ID: NCT04176198

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Access to the study treatment being tested
Type of study
Interventional (receives a drug or procedure)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Nusivertib (drug), Ruxolitinib (drug), Momelotinib (drug)
How long the study runs
Study runs about 124 months (dates as stated)
About the drug or intervention
Nusivertib — drug: Oral PIM Inhibitor · Ruxolitinib — drug: Oral JAK inhibitor · Momelotinib — drug: Oral JAK inhibitor
Patient visit burden
Not specified by the sponsor
Type of study
Testing a treatment
Ages
18 Years and over
Who
All
Number of participants
240
Started
2019-12-16
Last checked
2026-09

Plain English Summary

What is this study?

  • • Testing a new treatment for myelofibrosis
  • • Phase1/Phase2 - 240 participants
  • • This study is a Phase 1/2, multicenter, dose-escalation, open-label trial to assess safety, tolerability, pharmacokinetics and pharmacodynamics of nuvisertib (TP-3654) in patients with intermediate or high-risk primary or secondary MF

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with myelofibrosis

Where?

  • • Lincoln - Lincoln County Hospital
  • • Lincoln - United Lincolnshire Hospitals NHS Trust - Pilgrim Hospital
  • • London - University College London Hospital's NHS foundation Trust
  • • Oxford - Oxford University Hospitals NHS Foundation

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

This study is a Phase 1/2, multicenter, dose-escalation, open-label trial to assess safety, tolerability, pharmacokinetics and pharmacodynamics of nuvisertib (TP-3654) in patients with intermediate or high-risk primary or secondary MF.

More detail

Arm 1 will enroll patients who have been previously treated and failed on a JAK inhibitor or ineligible to receive treatment with a JAK inhibitor. Arm 2 will enroll patients who are on a stable dose of ruxolitinib, but who have either lost response or had a suboptimal or plateau in response. Arm 3 will enroll patients who have been previously treated with a JAK inhibitor (except momelotinib)

Myelofibrosis

How this trial compares with your answers

Answer 2 more questions to improve match

What we know so far

Condition· Matched your search
Age· Tell us your age for better matching
Gender· Tell us your sex for better matching

Still need:

  • • Tell us your age for better matching
  • • Tell us your sex for better matching

Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders
  • How fit you need to be: ECOG 1 or better

Treatment history

Treatments you must have had:

  • ✓ nuvisertib is not allowed
  • ✓ additional testing, as needed)
  • ✓ (stable Grade 2 conditions may be permitted in consultation with the Spons
  • ✓ momelotinib

What the study is looking for

  • ✓Patients must meet all of the following inclusion criteria to be eligible:
  • ✓Nuvisertib (TP-3654) Monotherapy Arm:
  • ✓Confirmed pathological diagnosis of primary myelofibrosis (PMF) or post-PV-MF/post-ET- MF and intermediate or...
  • ✓Previously treated with JAK inhibitor(s) and is intolerant, resistant, refractory or has lost response to the JAK...
  • ✓Fulfill the following clinical laboratory parameters:
See the full criteria
Patients must meet all of the following inclusion criteria to be eligible: Nuvisertib (TP-3654) Monotherapy Arm: * Confirmed pathological diagnosis of primary myelofibrosis (PMF) or post-PV-MF/post-ET- MF and intermediate or high-risk primary or secondary MF * Previously treated with JAK inhibitor(s) and is intolerant, resistant, refractory or has lost response to the JAK inhibitor(s) or is ineligible to be treated with JAK inhibitor * Fulfill the following clinical laboratory parameters: * Platelet count ≥ 25 x 10\^9 /L, without assistance of growth factors or platelet transfusions * ANC ≥ 1 x 10\^9/L without assistance of granulocyte growth factors * Peripheral blood blast count \< 5% * ECOG performance status ≤ 1 * Life expectancy ≥ 6 months * Adequate renal function * Adequate hepatic function * Adequate coagulation function * Splenomegaly (spleen volume of ≥ 450 cm3 by MRI or CT scan) within 2 weeks prior to Cycle 1 Day 1. * Dose escalation: At least 2 symptoms measurable (score ≥ 1) using the MF-SAF * Dose expansion: At least 2 symptoms measurable with each score of ≥ 3 or a total average score of ≥ 10 per MFSAF Nuvisertib (TP-3654) + Ruxolitinib Arm: * Confirmed pathological diagnosis of PMF or post-PV-MF/post ET- MF and intermediate or high-risk primary or secondary MF * On ruxolitinib treatment for ≥ 6 months, and on a stable dose of ruxolitinib (5 to 25 mg BID) for ≥ 8 weeks prior to the first dose of nuvisertib, but has either lost response or had a suboptimal or plateau in response * Fulfills the following clinical laboratory parameters: * Platelet count ≥ 50 × 10\^9/L (without assistance of growth factors or platelet transfusions) * ANC ≥ 1 × 109/L without assistance of granulocyte growth factors * Peripheral blood blast count \< 5% at screening * Adequate renal function * Adequate hepatic function * Adequate coagulation function * Splenomegaly (spleen volume of ≥ 450 cm3 by MRI/CT scan) within 2 weeks prior to Cycle 1 Day 1 * At least 2 symptoms measurable with each score ≥ 3 or a total average score of ≥ 10 per MFSAF v4.0 * ECOG performance status ≤ 1 * Life expectancy ≥ 6 months Nuvisertib (TP-3654) + Momelotinib Arm * Confirmed pathological diagnosis of PMF or post-PV-MF/post ET-MF and intermediate or high-risk primary or secondary MF * Previously treated with an approved JAK inhibitor (except momelotinib) for PMF or Post-PV/ET MF for ≥ 12 weeks, or ≥ 4 weeks if JAK inhibitor therapy was complicated by a transfusion requirement of ≥ 4 units of red blood cells in 8 weeks, or Grade 3/4 AEs of thrombocytopenia, anemia, or hematoma * Fulfills the following clinical laboratory parameters: * Anemic, defined as Hb \<10 g/dL or requiring RBC transfusion at baseline * Platelet count ≥ 50 × 109/L (without assistance of growth factors or platelet transfusions) * ANC ≥ 1 × 109/L without assistance of granulocyte growth factors * Peripheral blood blast count \< 5% at screening * Adequate renal function * Adequate hepatic function * Adequate coagulation function * Splenomegaly (spleen volume of ≥ 450 cm3 by MRI/CT scan) within 2 weeks prior to Cycle 1 Day 1 * At least 2 symptoms measurable with each score of ≥ 3 or a total average score of ≥ 10 per MFSAF v4.0 * ECOG performance status ≤ 1 * Life expectancy ≥ 6 months Patients meeting any one of these exclusion criteria will be prohibited from participating in this study: Nuvisertib (TP-3654) Monotherapy Arm: * Received previous systemic antineoplastic therapy or any experimental therapy within 2 weeks or 5 half-lives, whichever is longer, prior to Cycle 1 Day 1. Hydroxyurea or anagrelide are allowed up to 24 hours prior to Cycle 1 Day 1). * Major surgery within 4 weeks prior to Cycle 1 Day 1 and/or not recovered adequately from from surgery prior to first dose. * Splenic irradiation within 6 months prior to Screening or prior splenectomy. * Prior allogeneic stem cell transplant within the last 6 months. * Eligible for allogeneic bone marrow or stem cell transplantation. * Unresolved Grade ≥ 2 non-hematological toxicity related to prior treatment * History of symptomatic congestive heart failure, or myocardial infarction, or uncontrolled arrhythmia within 6 months prior to Cycle 1 Day 1; left ventricular ejection fraction (LVEF) \< 45% by echocardiogram within 4 weeks prior to Cycle 1 Day 1. * Corrected QT interval \> 480msec. * Prior or concurrent malignancy that could interfere with the investigational regime. * Known history of chronic liver disease, e.g. portal hypertension or any of its complications, cirrhosis, Child-Pugh C, auto-immune hepatitis, alpha-1 anti-trypsin deficiency, Wilson's disease, etc. * Active, uncontrolled bacterial, viral, or fungal infections, requiring systemic antimicrobial within 1 week prior to Cycle 1 Day 1. * Chronic active or acute viral hepatitis A, B, or C infection (testing for hepatitis B and C are required) * Exhibited allergic reactions or sensitivity to nuvisertib, or similar compound. * Medical condition or GI tract surgery that could impair absorption or result in short bowel syndrome with diarrhea. * Systemic steroid therapy (\>10 mg daily prednisone or equivalent) within 1 week prior to the first dose of study treatment (note: topical, inhaled, nasal, and ophthalmic steroids are not prohibited). * Known clinically significant anemia due to iron, vitamin B12, or folate deficiencies, or autoimmune or hereditary hemolytic anemia, or thalassemia, or severe GI bleeding. * Pregnant or breastfeeding * Currently receiving any other investigational agent. Nuvisertib (TP-3654) + Ruxolitinib Arm: * Received previous systemic antineoplastic therapy (other than ruxolitinib) or any other experimental therapy within 2 weeks or 5 half-lives, whichever is longer, prior to Cycle 1 Day 1 (Note: Prior treatment with nuvisertib is not allowed. Hydroxyurea or anagrelide are allowed up to 24 hours prior to Cycle 1 Day 1). * Received systemic steroid therapy (\>10 mg daily prednisone or equivalent) within 1 week prior to Cycle 1 Day 1 (Note: Topical, inhaled, nasal, and ophthalmic steroids are not prohibited) * Known allergic reactions or sensitivity to nuvisertib, or similar compound. * Splenic irradiation within 6 months prior to Screening or prior splenectomy * Prior allogeneic stem cell transplant within the last 6 months (Note: Patients who have relapsed after 6 months post-transplant and do not have active GVHD are eligible). * Eligible for allogeneic bone marrow or stem cell transplantation (Note: Patients who are not willing to undergo transplantation or for whom a suitable donor is not available are considered as transplant ineligible.) * Major surgery within 4 weeks prior to Cycle 1 Day 1 and/or have not recovered adequately prior to first dose. * Active, uncontrolled bacterial, viral, or fungal infections, requiring parenteral antimicrobial within 1 week prior to Cycle 1 Day 1 * Chronic active or acute viral hepatitis A, B, or C infection (testing for hepatitis B and C are required) * Known history of chronic liver disease (eg, portal hypertension or any of its complications, cirrhosis, Child-Pugh C, auto-immune hepatitis, alpha-1 anti-trypsin deficiency, Wilson's disease, etc) (Note: Abnormal liver morphology at baseline imaging may require additional testing, as needed). * Unresolved Grade ≥ 2 non-hematological adverse events related to prior treatment (stable Grade 2 conditions may be permitted in consultation with the Sponsor) * History of myocardial infarction or symptomatic congestive heart failure or uncontrolled arrhythmia within 6 months prior to Cycle 1 Day 1; LVEF \<45% by echocardiogram within 4 weeks prior to Cycle 1 Day 1 * Corrected QTcF of \> 480 msec * Prior or concurrent malignancy that could interfere with the safety or efficacy assessment of the study intervention * History of a medical condition or GI tract surgery that could impair absorption or could result in short bowel syndrome with diarrhea * Known clinically significant anemia due to iron, vitamin B12, or folate deficiencies, or autoimmune or hereditary hemolytic anemia, or thalassemia, or severe GI bleeding * Pregnant or breastfeeding Nuvisertib (TP-3654) + Momelotinib Arm: * Received previous systemic antineoplastic therapy or any experimental therapy within 2 weeks or 5 half-lives, whichever is longer, prior to Cycle 1 Day 1 (Notes: Prior treatment with momelotinib or nuvisertib is not allowed; in patients with ongoing JAK inhibitor therapy, ie, ruxolitinib, at screening, JAK inhibitor therapy must be tapered over a period of at least 1 week. Patients on a low dose of ruxolitinib (eg, 5 mg QD) may have a reduced taper period or no taper; hydroxyurea or anagrelide are allowed up to 24 hours prior to Cycle 1 Day 1). * Received systemic steroid therapy (\>10 mg daily prednisone or equivalent) within 1 week prior to Cycle 1 Day 1 (Note: Topical, inhaled, nasal, and ophthalmic steroids are not prohibited). * Known allergic reactions or sensitivity to nuvisertib, momelotinib, or any structurally similar drug, or to any component of the formulations of either study intervention * Splenic irradiation within 6 months prior to screening or prior splenectomy * Prior allogenic stem cell transplant within the last 6 months (Note: Patients who have relapsed after 6 months post-transplant and do not have active GVHD are eligible). * Eligible for allogeneic bone marrow or stem cell transplantation (Note: Patients who are not willing to undergo transplantation or for whom a suitable donor is not available are considered as transplant ineligible). * Major surgery within 4 weeks prior to Cycle 1 Day 1 and/or have not recovered adequately from surgery prior to first dose. * Active, uncontrolled bacterial, viral, or fungal infections, requiring parenteral antimicrobial within 1 week prior to Cycle 1 Day 1 * Chronic active or acute viral hepatitis A, B, or C infection (testing for hepatitis B and C are required) * Known history of chronic liver disease (eg, portal hypertension or any of its complications, cirrhosis, Child-Pugh C, auto-immune hepatitis, alpha-1 anti-trypsin deficiency, Wilson's disease, etc) (Note: Abnormal liver morphology at baseline imaging may require additional testing, as needed) * Unresolved Grade ≥ 2 non-hematological adverse events related to prior treatment (stable Grade 2 conditions may be permitted in consultation with the Sponsor) * Presence of Grade ≥ 2 peripheral neuropathy * History of myocardial infarction or symptomatic congestive heart failure or uncontrolled arrhythmia within 6 months prior to Cycle 1 Day 1; LVEF \< 45% by echocardiogram within 4 weeks prior to Cycle 1 Day 1 * Corrected QTcF of \> 480 msec * Prior or concurrent malignancy that could interfere with the safety or efficacy assessment of the study intervention * History of a medical condition or GI tract surgery that could impair absorption or could result in short bowel syndrome with diarrhea * Known clinically significant anemia due to iron, vitamin B12, or folate deficiencies, or autoimmune or hereditary hemolytic anemia, or thalassemia, or severe GI bleeding * Pregnant or breastfeeding

Where Is This Study? (4 UK sites)

Lincoln County Hospital

Lincoln, United Kingdom

Recruiting
Hospital R&D contact (matched)

Ms Hannah Finch

hannah.finch9@nhs.net01522 573941 ext 582059-

United Lincolnshire Hospitals NHS Trust - Pilgrim Hospital

Lincoln, United Kingdom

Recruiting
Hospital R&D contact (matched)

Ms Hannah Finch

hannah.finch9@nhs.net01522 573941 ext 582059-

University College London Hospital's NHS foundation Trust

London, United Kingdom

Recruiting
Hospital R&D contact (matched)

Rajinder Sidhu - Associate Director, Research Governance and Operations

uclh.jro-communications@nhs.net020 3447 9825

Oxford University Hospitals NHS Foundation

Oxford, United Kingdom

Recruiting
Hospital R&D contact (matched)

Shahista Hussain

ouhtma@ouh.nhs.uk---

How to Get in Touch

Reyna Bishop

Sponsor contact

CONTACT

617-674-6800 reyna.bishop@us.sumitomo-pharma.com

Jordan Simpson

Sponsor contact

CONTACT

jordan.simpson@us.sumitomo-pharma.com
Data sourced from ClinicalTrials.gov · Last verified: 2026-09