[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"myeloproliferative-neoplasms-mpn\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:myeloproliferative-neoplasms-mpn":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,69,110],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100640159","phase-1-phase-1-phase-2-study-to-assess-safety-and-efficacy-of-orally-administered-jbi-802-in-subjects-with-myeloproliferative-neoplasms-mpn-and-myelodysplasticmyeloproliferative-neoplasms-mdsmpn-with-thrombocytosis-100640159",false,"NCT07612280","Phase 1\u002F Phase 2 Study to Assess Safety and Efficacy of Orally Administered JBI-802 in Subjects With Myeloproliferative Neoplasms (MPN) and Myelodysplastic\u002FMyeloproliferative Neoplasms (MDS\u002FMPN) With Thrombocytosis","Study to Assess Safety and Preliminary Efficacy of Orally Administered JBI-802 in Subjects With Myeloproliferative Neoplasms (MPN) and Myelodysplastic\u002FMyeloproliferative Neoplasms (MDS\u002FMPN) With Thrombocytosis","Inclusion Criteria:\n\n\\- Male or female subjects aged ≥18 years at the time of screening visit.\n\nFor Dose Escalation Phase:\n\nSubjects diagnosed with any one of the following:\n\n* Subject with diagnosis of Essential Thrombocythemia (ET) per World Health Organization (WHO) diagnostic criteria for myeloproliferative neoplasms .\n* Subject requires treatment in order to lower platelet count based on subject age over 60 or history of thrombosis.\n* Subject with Morphologically confirmed diagnosis of MDS\u002FMPN neoplasms, excluding Juvenile Myelomonocytic Leukaemia (JMML), CMML and aCML (Atypical Chronic Myeloid Leukaemia), in accordance with WHO 2016 revised criteria, that is relapsed and\u002For refractory or intolerant to standard of care and that, in the opinion of the Investigator, subjects who have no available therapies known to provide clinical benefits.\n* Subject with Myelodysplastic\u002Fmyeloproliferative neoplasm, (unclassifiable (MDS\u002FMPN-UC) and MDS\u002FMPN-RS-T).\n\nFor Dose Expansion Phase\n\nSubjects diagnosed with any one of the following:\n\n* Subject with diagnosis of Essential Thrombocythemia (ET) per WHO diagnostic criteria for myeloproliferative neoplasms which requires treatment in order to lower platelet count based on subject age over 60 or history of thrombosis.\n* Subject with diagnosis of Polycythemia Vera (PV) per WHO diagnostic criteria that is relapsed and\u002For refractory or intolerant to standard of care and that, in the opinion of the Investigator, subjects who have no available therapies known to provide clinical benefits Subject with morphologically confirmed diagnosis of pre-fibrotic myelofibrosis (MF) subject in accordance with the WHO 2016 revised criteria, that is relapsed, intolerant, and\u002For refractory and that, in the opinion of the Investigator, subjects who have no available therapies known to provide clinical benefits. (Refer Appendix II)\n* MDS\u002FMPN (MDS\u002FMPN-RS-T, MDS\u002FMPN unclassifiable and CMML subjects providing the marrow blast count is ≤5%.). 2. Subject must have disease that failed at least one standard therapy or being intolerant to standard of care. 3. Subject must have discontinued immediate prior therapy at least 1 week (4 weeks for interferon) prior to study drug administration. 4. Subject with screening laboratory values:\n* Hb ≥ 9 g\u002FdL, if subject is transfused to meet this criterion, transfusion must be completed ≥ 14 days prior to first dose.\n* Absolute neutrophil count ≥ 1500 × 109\u002FL\n* Absolute neutrophil count ≥ 1000 × 109\u002FL, if significant marrow infiltration\n* Platelet count ≥ 450 × 109\u002FL for dose finding\n* Platelet count ≥ 100 × 109\u002FL for expansion cohort at RP2D, if subject is transfused to meet this criterion, transfusion must be completed ≥14 days prior to first dose\n* Total bilirubin ≤ 1.5 × ULN. Subjects with Gilbert's syndrome may be enrolled with up to 3.0 × ULN\n* Aspartate transaminase (AST) and Alanine transaminase (ALT) ≤ 2.5 × ULN (unless liver metastases are present then up to 5 × ULN is allowed)\n* Calculated creatinine clearance (CrCL) ≥ 30 mL\u002Fmin (Cockcroft- Gault formula) (Refer Appendix IV)\n* Prothrombin Time (PT) or Activated Partial Thromboplastin Time (aPTT) ≤ 1.5 × ULN, if subject is not anticoagulated (Note: If subject is on anticoagulants, the subject must be on a stable dose for at least 2 weeks prior to screening) 5. Subject with resolution of any clinically significant toxic effects of prior therapy to Grade 0 or 1 according to the NCI CTCAE, Version 5.0 (exception of alopecia and Grade 2 peripheral neuropathy, chronic Grade 2 endocrinopathies as a result of prior immunotherapy). (Refer Appendix VII) 6. Subject with Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 2. (Refer Appendix III) 7. Subject able to swallow oral medication. 8. Subject who has willing and able to give informed consent and comply with protocol requirements for the duration of the study. 9. Subject who is willing to undergo bone marrow biopsy with aspiration and tissue collection for disease assessment and correlative studies during screening and periodically throughout the study. 10. Subject with willingness to use contraception by a method that is deemed effective by the Investigator by both males and female of childbearing potential (post-menopausal women must have been amenorrhoeal for at least 12 months to be considered of non-childbearing potential (i.e., surgically sterilised \\[hysterectomy, bilateral salpingectomy, bilateral oophorectomy at least 6 weeks before the screening visit\\] or postmenopausal \\[where postmenopausal is defined as no menses for 12 months without an alternative medical cause and a follicle-stimulating hormone \\[FSH\\] level consistent with postmenopausal status, per local laboratory guidelines\\]) and their partners throughout the treatment period and for at least 3 months following the last dose of study drug.\n\nExclusion Criteria:\n\n* 1\\. Subject who is treated with systemic anticancer therapy or biological therapy or an investigational agent within 2 weeks or 5 half-lives, whichever is shorter, prior to start of study drug treatment.\n\n  * For MF subject who come off JAK2 antagonists or hydroxyurea, shorter washout is permitted as these subject progress quickly after treatment discontinuation and remain eligible (steroids must be stop at least 7 day before start of study drug treatment)\n  * Subject who is in need of immediate cytoreduction should be excluded 2. Subject who has undergone autologous\u002Fallogeneic Haematopoietic Stem Cell Transplantation (HSCT) therapy within 60 days of the first dose of study drug, or subject on immunosuppressive therapy post-HSCT at the time of screening, or currently with clinically significant Graft-Versus- Host Disease (GVHD) as per treating physician (subjects in relapse after allogeneic transplantation must be off treatment with systemic immunosuppressive agents for at least 4 weeks prior to screening.\n\n    3\\. Subject with major surgery less than or equal to 21 days prior to starting study drug or has not recovered from adverse effects of such procedure.\n\n    4\\. Subject who underwent surgery (e.g., stomach bypass) or medical condition that might significantly affect absorption of medicines.\n\n    5\\. Subject who underwent radiotherapy within 2 weeks prior to start of study drug treatment (palliative radiation or stereotactic radiosurgery within 7 days prior to start of study treatment). Subjects must have recovered from all radiotherapy-related toxicities.\n\n    6\\. Subject with known malignant central nervous system disease other than neurologically stable, treated brain metastases- defined as metastasis having no evidence of progression or hemorrhage for at least 4 weeks after treatment (including brain radiotherapy). Must be off any systemic corticosteroids for the treatment of symptomatic brain metastases for at least 14 days prior to enrollment.\n\n    7\\. Subject with severe or unstable medical condition, such as congestive heart failure ischemic heart disease, uncontrolled hypertension, uncontrolled diabetes mellitus, psychiatric condition, as well as an uncontrolled cardiac arrhythmia requiring medication ( less than or equal to Grade 2, according to NCI CTCAE Version 5), myocardial infarction within 6 months prior to starting study treatment, or any other significant or unstable concurrent cardiac illness.\n\n    8\\. Subject with congenital long QT syndrome or corrected QT interval by Fridericia (QTcF interval) greater than 450 msec for males and greater than 470 msec for females at screening.\n\n    9\\. Subject with history of other previous or concurrent cancer that would interfere with the determination of safety or efficacy assessments with the exception:\n    * Patient with previous cancers can be included to the study provided they are in remission at the time of screening and enrolment.\n    * Patient with localized skin cancer can also be included for screening and enrollment.\n\n      10\\. Subject with live vaccines within 30 days prior to the first dose of JBI-802.\n\n      11\\. Subjects who receive Glucocorticoids for any purpose other than to modulate symptoms from an event of clinical interest or for use as a premedication in participants with a known history of an IV contrast allergy administered as part of CT radiography.\n\n      12\\. Bisphosphonates and\u002For receptor activator of nuclear factor kappa-B ligand inhibitor therapies cannot be initiated after the Informed Consent Document(s) has been signed. These therapies may be continued if treatment with an agent from 1 of these 2 classes was initiated prior to signing the Informed Consent Document(s).\n\n      13\\. Subject with prophylactic antidiarrheals and antiemetics before the first dose of on Day 1.\n\n      14\\. Subject with prophylactic anti-inflammatory or antipyretic drugs (e.g., nonsteroidal anti-inflammatory drugs, acetaminophen, corticosteroids)before the first dose of on Day 1.\n\nIf a patient is taking low dose steroids for therapeutic purposes (less than or equal to 10 mg prednisone or its equivalent), they are eligible to participate in the study provided they meet all other pertinent criteria.\n\n15\\. Subject with Prophylactic use of colony-stimulating factors (including G-CSF, pegylated G-CSF, or granulocyte-macrophage colony-stimulating factor) before the first dose of on Day 1.\n\n16\\. Subject with use of strong inhibitors of cytochrome P450 3A (CYP3A) within 14 days or 5 half-lives (whichever is longer) or grapefruit juice or grapefruit containing products within 7 days prior to Cycle 1 Day 1.\n\n17\\. Subject with use of strong inducers of CYP3A within 14 days or 5 halflives prior to Cycle 1 Day 1.\n\n18\\. Subject with use of strong inhibitors of CYP2D6 within 14 days or 5 halflives prior to Cycle 1 Day 1 19. Subject with use of strong inducers of CYP2D6 within 14 days or 5 halflives prior to Cycle 1 Day 1.\n\n20\\. Subject with known active Human Immunodeficiency Viruses (HIV)infection or active infection with hepatitis B or C.\n\n21\\. Subject with active gastrointestinal disease (e.g., Crohn's disease,ulcerative colitis, or short gut syndrome) or other malabsorption syndromes that would reasonably impact drug absorption 22. Subject with acute illness within 14 days prior to first dose of study treatment unless mild in severity and approved by the Investigator and Sponsor's medical representative.\n\n23\\. Subject with presence of active infection requiring systemic antibiotics. 24. Pregnant, breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the screening visit through 90 days after the last dose of trial treatment.\n\n25\\. Subject with current participation in another clinical study of an investigational agent. Simultaneous participation in observational studies is acceptable after Sponsor approval.\n\n26\\. Subject with COVID vaccine within 7 days prior to Cycle 1 Day 1. 27. Subject with previously received JBI-802. 28. Subject with any other condition that in the opinion of the Investigator would place the participant at an unacceptable risk or cause the participant to be unlikely to fully participate or comply with study procedures.","ALL","18 Years",{"count":19,"type":20},30,"ESTIMATED","INTERVENTIONAL",[23,24],"PHASE1","PHASE2","This study aims to assess the safety and efficacy of orally administered JBI-802 in subjects with Myeloproliferative Neoplasms (MPN) and Myelodysplastic\u002F Myeloproliferative Neoplasms (MDS\u002FMPN) with Thrombocytosis.\n\nWho is it for? You may be eligible to join this study if you are aged 18 years and over have been diagnosed with Essential Thrombocythemia and either a Morphologically confirmed diagnosis of Myeloproliferative Neoplasms (MPN) or Myelodysplastic\u002FMyeloproliferative Neoplasms (MDS\u002FMPN).\n\nStudy details:\n\nParticipants in this study will receive JBI-802 administered orally daily for a 28 day treatment cycle for up to 2-years as long as the participant experiences clinical benefit in the opinion of the Investigator and shows no signs or symptoms of unequivocal progression of disease, unacceptable toxicity, or other reasons for study discontinuation. The starting dose of the study drug is 5 mg\u002Fday, a total dose of 35 mg. Dose escalation will occur as per the 3+3 design after an internal Safety Review Committee (SRC) review of each dose stage. Dose expansion to other subtypes of MPN and MDS\u002FMPN will occur after Recommended Phase 2 Dose is determined from the dose escalation phase. Eligibility\u002FScreening for this study will occur within 21 days prior to starting treatment. If the study is suitable for you, you will enter the treatment period. The dose level selected for evaluation in Phase 2 will only be selected if it was safe and well tolerated during Phase 1. The treatment cycles will continue until you wish to stop, or you do not tolerate JBI-802 treatment,\n\nSome of the study procedures that include during your treatment period are :Medical, surgical, and cancer history, Height and weight, Physical examination, Vital signs, Eastern Cooperative Oncology Group (ECOG) evaluation, Electrocardiogram, Myeloproliferative neoplasm symptom assessment questionnaire,CT\u002FMRI scan, Bone marrow biopsy, medication usage, Side effects assessment, blood and urine Sampling , liver and thyroid function tests, haematology and coagulation tests, Participants will be followed-up at the start and end of each 28-day cycle to assess safety and tolerability Blood samples will be collected to assess safety and tolerability during the study.\n\nAfter the end of study, subjects will be treated in accordance with local practice. Compassionate use of JBI-802 may be allowed in subjects after study completion, based on the Investigator's judgment in consultation with the Sponsor and on a case-by-case basis. Compassionate use will be controlled by a separate protocol or process as defined by the local regulatory authorities. Continuation of study therapy beyond 2 years may be approved by the Sponsor based on the safety profile and will be contingent on the continued availability of product.",[27,28,29],"Essential Thrombocythemia (ET)","Myelodysplastic\u002FMyeloproliferative Neoplasms (MDS\u002FMPN)","Myeloproliferative Neoplasms (MPN)","RECRUITING","2026-06-01",{"date":33,"type":34},"2026-06-03","ACTUAL",{"date":36,"type":34},"2024-10-21",{"date":38,"type":20},"2028-09-15",{"name":40,"class":41},"Jubilant Therapeutics Inc.","INDUSTRY",7,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":51,"targetDuration":4,"studyType":21,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":68},"100622470","exercise-training-in-patients-with-myeloproliferative-neoplasms-100622470","NCT07384039","Exercise Training in Patients With Myeloproliferative Neoplasms","Effects of Individually Tailored Exercise on Quality of Life and Physical Performance in Patients With Myeloproliferative Neoplasms-a Randomized Controlled Study","MPN-Exercise","Inclusion Criteria:\n\n* age ≥ 18 years\n* diagnosis of myeloproliferative neoplasia according to WHO\u002FICC 2022.\n\nExclusion Criteria:\n\n* current participation in another intervention study\n* the presence of any diseases or functional impairments that, in the opinion of the examining physician, exclude participation in a physical training intervention.",{"count":52,"type":20},80,[54],"NA","The investigators will investigate the response of an individualized exercise training program on quality of life, cardiorespiratory fitness and disease-specific markers in patients with myeloproliferative neoplasms (MPN). To this end, the investigators will randomly assign patients with MPN to a training group and a waiting control group.\n\nThe training group will undergo an individually tailored exercise training program for three months, while the control group will maintain their usual lifestyle for three months and then has the opportunity to undergo the three-month intervention program. At the beginning and at the end of the three-month intervention phase, the investigators will evaluate physical performance, daily physical activity, muscular strength, and self-reported outcomes and compare them between the training and the control group, in order to assess potential benefits of the exercise training program.",[29],"NOT_YET_RECRUITING","2026-02-03",{"date":60,"type":34},"2026-02-05",{"date":62,"type":20},"2026-02-04",{"date":64,"type":20},"2027-02-28",{"name":66,"class":67},"Hannover Medical School","OTHER",1,{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":75,"eligibilityCriteria":76,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":77,"enrollmentInfo":78,"targetDuration":4,"studyType":80,"phases":4,"briefSummary":81,"conditions":82,"keywords":90,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":104,"completionDateStruct":106,"leadSponsor":108,"locationsCount":4},"100601248","hematological-disorders-in-ehpvo-patients-100601248","NCT07108023","Hematological Disorders in EHPVO Patients","A Prospective Study of the Spectrum of Haematological Disorders in Patients With Extrahepatic Portal Vein Obstruction","EHPVO-HEM","Inclusion Criteria:\n\n* Age 18 years or older . Diagnosis of extra hepatic portal vein obstruction based on imaging ( Doppler, CT , MRI ) preserved liver function . Available complete medical records including CBC , LFTs and coagulation profile .\n\nExclusion Criteria:\n\n* Patients with cirrhosis or intrahepatic portal hypertension • Incomplete or missing medical records • Patients with known hematologic malignancies or undergoing chemotherapy","75 Years",{"count":79,"type":20},115,"OBSERVATIONAL","This study focuses on patients who have a condition called extrahepatic portal vein obstruction (EHPVO), where a blood clot blocks the portal vein outside the liver. This blockage can cause problems like an enlarged spleen, bleeding from swollen veins in the digestive system, and low blood cell counts. Many of these patients may have hidden blood disorders that increase the risk of clotting, such as myeloproliferative neoplasms (MPNs), antiphospholipid syndrome (APS), or paroxysmal nocturnal hemoglobinuria (PNH). This study will collect and analyze blood test results-such as complete blood count (CBC), liver function tests (LFTs), and clotting tests-from patients with EHPVO. The aim is to find patterns that may suggest an underlying blood disorder, even if the patient doesn't show obvious symptoms.By understanding these patterns early, doctors may be able to diagnose and treat the root causes of clotting in these patients more accurately, helping prevent complications and improve outcomes.",[83,84,29,85,86,87,88,89],"Extrahepatic Portal Vein Obstruction (EHPVO)","Thrombophilia","Antiphospholipid Syndrome (APS)","Paroxysmal Nocturnal Hemoglobinuria (PNH)","Thrombocytopenia","Anemia","Leukopenia",[91,92,93,94,95,96,97,98,99,100],"Portal vein thrombosis","EHPVO","Hypersplenism","Hematological disorders","Coagulation profile","Liver function tests","CBC","JAK2 mutation","Thrombosis in MPN","Cross-sectional study","2025-07-31",{"date":103,"type":34},"2025-08-06",{"date":105,"type":20},"2025-08",{"date":107,"type":20},"2025-12",{"name":109,"class":67},"Rahab Nady",{"id":111,"slug":112,"hasResults":11,"nctId":113,"briefTitle":114,"officialTitle":115,"acronym":4,"eligibilityCriteria":116,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":117,"targetDuration":4,"studyType":21,"phases":119,"briefSummary":121,"conditions":122,"keywords":123,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":126,"lastUpdatePostDateStruct":127,"startDateStruct":129,"completionDateStruct":131,"leadSponsor":133,"locationsCount":68},"100573026","phase-3-long-term-efficacy-of-once-daily-versus-twice-daily-aspirin-in-high-risk-mpn-patients-with-aspirin-resistance-100573026","NCT06740916","Long-term Efficacy of Once Daily Versus Twice Daily Aspirin in High-risk MPN Patients With Aspirin Resistance","Long-term Efficacy of Once Daily Versus Twice Daily Aspirin in High-risk Myeloproliferative Neoplasms Patients With Aspirin Resistance","Inclusion Criteria:\n\n* Philadelphia negative Myeloproliferative neoplasms aged at least 18 years old\n\nExclusion Criteria:\n\n* Concomitant other active malignancy or cured less than 6 months\n* Platelet count less than 50,000\u002FmicroL\n* Receiving anticoagulant\n* Active peptic ulcer\n* Active bleeding or Planning to undergo procedure\u002Foperation with bleeding risk\n* No laboratory aspirin resistance with LTA method",{"count":118,"type":20},240,[120],"PHASE3","Patients with myeloproliferative neoplasm (MPN) could have laboratory aspirin resistance and then increasing dose of aspirin from once daily to twice daily regimen is suggested. However, it is not routinely recommended to perform platelet function testing to determine aspirin resistance in MPN patients. Moreover, it is not known whether increasing dose of aspirin would always correct aspirin resistance and significantly prevent the thrombotic events in MPN patients. Therefore, this study aims to compare the efficacy of once daily versus twice daily aspirin in high-risk MPN patients with aspirin resistance. MPN patients with laboratory aspirin resistance will be included in this prospective randomized study and platelet function testing will be repeated at one and six months later. Clinical thrombosis and side effect from aspirin will be recorded for at least 2 years after intervention.",[29],[124,125],"myeloproliferative neoplasm","aspirin resistance","2024-12-23",{"date":128,"type":34},"2024-12-27",{"date":130,"type":34},"2024-12-12",{"date":132,"type":20},"2030-12-31",{"name":134,"class":67},"Siriraj Hospital"]