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NCT04854096TerminatedPhase 2

Study to Assess Efficacy and Safety of NS-018 Compared to BAT in Patients With Myelofibrosis

A Phase 2b, Open-label, Multicenter, Randomized, Controlled, 2-Arm Study to Assess the Efficacy and Safety of Orally Administered NS-018 Versus Best Available Therapy in Subjects With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis With Severe Thrombocytopenia (Platelet Count <50,000/μL)

Source: ClinicalTrials.gov · Last updated 23 May 2025

Reason given: The study was stopped due to a business decision.

Brief summary (registry, in English)

This study will enroll male and female subjects who are 18 years of age or older with Primary Myelofibrosis, post-polycythemia Vera Myelofibrosis, or post-essential Thrombocythemia Myelofibrosis with severe thrombocytopenia (platelet count <50,000/µL) including subjects with intermediate-2 or high-risk MF according to the Dynamic International Prognostic Scoring System (DIPSS).

Status (registry)
Terminated
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
7 (actual)
First submitted
9 Apr 2021
Start date
31 Jan 2023
Primary completion date
16 May 2024
Lead sponsor
NS Pharma, Inc.
NCT number
NCT04854096

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Any prior treatment with more than two JAK inhibitors.
  • Previous treatment with NS-018.
  • Subjects actively receiving a concurrent investigational agent.
  • Subjects with any unresolved AE greater than Grade 1 other than hematological AEs from previous anticancer therapy.
  • Currently taking medication that is substantially metabolized by cytochrome P450 (CYP) 1A2 or CYP3A4 (see Appendix 5) or taking medication known to be strong inhibitors or inducers of CYP3A4 (see Appendix 5).
  • Radiation therapy for splenomegaly within 6 months prior to study entry (screening).
  • Subjects diagnosed with another malignancy within 2 years prior to an enrollment.
  • Subjects who have had surgery (other than placement of vascular access and bone marrow biopsy) within 4 weeks of study entry (screening), or subjects with incomplete recovery from any prior surgical procedures.

Other illness

  • Active, uncontrolled systemic infection.
  • History of splenectomy or planning to undergo splenectomy.
  • Subjects with a serious cardiac condition within the past 6 months such as uncontrolled arrhythmias, myocardial infarction, angina or heart disease

Who the study is looking for

  • Primary MF, post-PVMF or post-ETMF according to the DIPSS risk categories of intermediate-2 or high-risk MF
  • Average platelet count of <50,000/µL at Screening based on 2 measurements taken on different days; both measurements must be <50,000/µL.
  • ECOG performance status ≤2.
  • Life expectancy >6 months.
  • Spleen volume of at least 450 cm3 measured by MRI (or by CT for applicable subjects).
  • Total Symptom Score (TSS) ≥10 on the Myelofibrosis Symptom Assessment Form (MFSAF) version 4.0.
  • Peripheral blast count <10%.
  • No MF-directed treatment for at least 2 weeks prior to initiation of NS-018, including JAK inhibitor, erythropoietic, thrombopoietic agent, or any use of corticosteroids for MF symptom or blood count management. Low dose corticosteroids <10 mg/day prednisone or equivalent is allowed for non-MF purposes.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (51)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Hamatologisch-onkologische Praxis Heinric/Bangerter Ausgsburg GbRAugsburgGermanyUnknown status
Universitaetsklinikum Halle - SaaleHalleGermanyUnknown status
Universitaetsklinikum JenaJenaGermanyUnknown status
Universitätsmedizin RostockRostockGermanyUnknown status
Royal United Hospitals BathBathUnited KingdomUnknown status
Western General HospitalEdinburghUnited KingdomUnknown status
University College London HospitalsLondonUnited KingdomUnknown status
Guys HospitalLondonUnited KingdomUnknown status
The Christie NHS Foundation TrustManchesterUnited KingdomUnknown status
Derriford HospitalPlymouthUnited KingdomUnknown status
Sandwell & West Birmingham HospitalWest BromwichUnited KingdomUnknown status
AO SS AntonioAlessandriaItalyUnknown status
Azienda Ospedaliera SS. AntonioAlessandriaItalyUnknown status
ASST Spedali Civili di BresciaBresciaItalyUnknown status
Azienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaBresciaItalyUnknown status
AOU Policlinico-San MarcoCataniaItalyUnknown status
ASST Fatebenefratelli SaccoMilanItalyUnknown status
Fondazione IRCCS Cà Granda Ospedale Maggiore PoliclinicoMilanItalyUnknown status
AO di Rilievo Ntl A CardarelliNaplesItalyUnknown status
Azienda Ospedaliera di Rilievo NazionaleNaplesItalyUnknown status
AO di Rilievo NazionaleNaplesItalyUnknown status
Azienda Ospedaliera di PadovaPadovaItalyUnknown status
Azienda Ospedaliero Universitaria Policlinico Paolo GiacconePalermoItalyUnknown status
Istituto Nazionale Tumori Regina Elena IRCCSRomaItalyUnknown status
Azienda Ospedaliera Universitaria Policlinico Umberto IRomaItalyUnknown status
AO Uni Policlinico Umberto IRomeItalyUnknown status
The Catholic University of Korea, Seoul St. Mary's HospitalBanpo-dongSouth KoreaUnknown status
Gachon University Gil Medical CenterIncheonSouth KoreaUnknown status
Gyeongsang National University HospitalJinjuSouth KoreaUnknown status
CHA Bundang Medical Center, CHA UniversitySeongnamSouth KoreaUnknown status
Soon Chun Hyang Central Medical CenterSeoulSouth KoreaUnknown status
Hospital AmpangAmpangMalaysiaUnknown status
Hospital Raja Permaisuri BainunIpohMalaysiaUnknown status
Hospital Sultanah AminahJohor BahruMalaysiaUnknown status
Hospital Raja Perempuan Zainab IIKota BharuMalaysiaUnknown status
Hospital Queen ElizabethKota KinabaluMalaysiaUnknown status
University Malaya Medical CentreKuala LumpurMalaysiaUnknown status
Sunway Medical CentrePetaling JayaMalaysiaUnknown status
Hospital Pulau PinangPulau PinangMalaysiaUnknown status
Szpital Uniwersytecki nr 2 im.dr J. BizielaBydgoszczPolandUnknown status
Pratia Onkologia KatowiceKatowicePolandUnknown status
Dolnośląskie Centrum Onkologii we Wrocławiu, Oddział HematologicznyWroclawPolandUnknown status
Srinagarind HospitalKhon KaenThailandUnknown status
Songklanagarind HospitalSongkhlaThailandUnknown status
Istanbul Medipol UniversityBağcılarTürkiyeUnknown status
Ege Universitesi Tip Fak,IzmirTürkiyeUnknown status
Namik Kemal University Medicine SchoolTekirdağTürkiyeUnknown status
Karadeniz Teknik Universitesi Tip Fak,TrabzonTürkiyeUnknown status
Houston Methodist HospitalHoustonUnited StatesUnknown status
MD Anderson Cancer CenterHoustonUnited StatesUnknown status
University of Massachusetts Chan Medical SchoolWorcesterUnited StatesUnknown status

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