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.
- Diseases
- Myeloproliferative neoplasms
- 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
Sites (51)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hamatologisch-onkologische Praxis Heinric/Bangerter Ausgsburg GbR | Augsburg | Germany | Unknown status |
| Universitaetsklinikum Halle - Saale | Halle | Germany | Unknown status |
| Universitaetsklinikum Jena | Jena | Germany | Unknown status |
| Universitätsmedizin Rostock | Rostock | Germany | Unknown status |
| Royal United Hospitals Bath | Bath | United Kingdom | Unknown status |
| Western General Hospital | Edinburgh | United Kingdom | Unknown status |
| University College London Hospitals | London | United Kingdom | Unknown status |
| Guys Hospital | London | United Kingdom | Unknown status |
| The Christie NHS Foundation Trust | Manchester | United Kingdom | Unknown status |
| Derriford Hospital | Plymouth | United Kingdom | Unknown status |
| Sandwell & West Birmingham Hospital | West Bromwich | United Kingdom | Unknown status |
| AO SS Antonio | Alessandria | Italy | Unknown status |
| Azienda Ospedaliera SS. Antonio | Alessandria | Italy | Unknown status |
| ASST Spedali Civili di Brescia | Brescia | Italy | Unknown status |
| Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia | Brescia | Italy | Unknown status |
| AOU Policlinico-San Marco | Catania | Italy | Unknown status |
| ASST Fatebenefratelli Sacco | Milan | Italy | Unknown status |
| Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico | Milan | Italy | Unknown status |
| AO di Rilievo Ntl A Cardarelli | Naples | Italy | Unknown status |
| Azienda Ospedaliera di Rilievo Nazionale | Naples | Italy | Unknown status |
| AO di Rilievo Nazionale | Naples | Italy | Unknown status |
| Azienda Ospedaliera di Padova | Padova | Italy | Unknown status |
| Azienda Ospedaliero Universitaria Policlinico Paolo Giaccone | Palermo | Italy | Unknown status |
| Istituto Nazionale Tumori Regina Elena IRCCS | Roma | Italy | Unknown status |
| Azienda Ospedaliera Universitaria Policlinico Umberto I | Roma | Italy | Unknown status |
| AO Uni Policlinico Umberto I | Rome | Italy | Unknown status |
| The Catholic University of Korea, Seoul St. Mary's Hospital | Banpo-dong | South Korea | Unknown status |
| Gachon University Gil Medical Center | Incheon | South Korea | Unknown status |
| Gyeongsang National University Hospital | Jinju | South Korea | Unknown status |
| CHA Bundang Medical Center, CHA University | Seongnam | South Korea | Unknown status |
| Soon Chun Hyang Central Medical Center | Seoul | South Korea | Unknown status |
| Hospital Ampang | Ampang | Malaysia | Unknown status |
| Hospital Raja Permaisuri Bainun | Ipoh | Malaysia | Unknown status |
| Hospital Sultanah Aminah | Johor Bahru | Malaysia | Unknown status |
| Hospital Raja Perempuan Zainab II | Kota Bharu | Malaysia | Unknown status |
| Hospital Queen Elizabeth | Kota Kinabalu | Malaysia | Unknown status |
| University Malaya Medical Centre | Kuala Lumpur | Malaysia | Unknown status |
| Sunway Medical Centre | Petaling Jaya | Malaysia | Unknown status |
| Hospital Pulau Pinang | Pulau Pinang | Malaysia | Unknown status |
| Szpital Uniwersytecki nr 2 im.dr J. Biziela | Bydgoszcz | Poland | Unknown status |
| Pratia Onkologia Katowice | Katowice | Poland | Unknown status |
| Dolnośląskie Centrum Onkologii we Wrocławiu, Oddział Hematologiczny | Wroclaw | Poland | Unknown status |
| Srinagarind Hospital | Khon Kaen | Thailand | Unknown status |
| Songklanagarind Hospital | Songkhla | Thailand | Unknown status |
| Istanbul Medipol University | Bağcılar | Türkiye | Unknown status |
| Ege Universitesi Tip Fak, | Izmir | Türkiye | Unknown status |
| Namik Kemal University Medicine School | Tekirdağ | Türkiye | Unknown status |
| Karadeniz Teknik Universitesi Tip Fak, | Trabzon | Türkiye | Unknown status |
| Houston Methodist Hospital | Houston | United States | Unknown status |
| MD Anderson Cancer Center | Houston | United States | Unknown status |
| University of Massachusetts Chan Medical School | Worcester | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.