Essential Thrombocythemia
Conditions
Interventions
Experimental group:Subcutaneous injection of drug P1101
Control group:Take anaglyl orally
Sponsors
Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: 1. Male or female subjects >=18 years old; 2. Subjects diagnosed with high-risk ET (either older than 60 years and JAK2V617-positive at screening, or having disease-related thrombosis or hemorrhage in the past), diagnosed according to the World Health Organization (WHO) 2016 criteria; 3. Subjects have received prior HU for ET, while the washout between the last dose of HU and the screening visit should not be shorter than 14 days; 4. Interferon treatment-nave; 5. Documented resistance/intolerance to prior HU for ET, as defined by ELN criteria (Barosi, et al, 2007), whereby at least one of the following criteria is met: Platelet count > 600 x 10^9/L at >=2 g/day (or >=2.5 g/day if subject body weight >80 kg) or maximally tolerated dose if 400 x 10^9/L and WBC count 400 x 10^9/L and hemoglobin (HGB) 450 x 10^9/L at screening; 7. WBC > 10 x 10^9/L at screening; 8. HGB >= 11 g/dL at screening for males and 10 g/dL at screening for females 9. Neutrophil count >= 1.0 x 10^9/L at screening; 10. Adequate hepatic function defined as bilirubin 3.5 g/dL, alanine aminotransferase =40 mL/min (by Cockcroft-Gault equation); 12. Males and females of childbearing potential, as well as all women < 2 years after the onset of menopause, must agree to use an acceptable form of birth control until 28 days following the last dose of the study drug, and females must agree to not breastfeed during the study; 13. Written informed consent obtained from the subjectand ability for the subject to comply with the requirements of the study.
Exclusion criteria
Exclusion criteria: 1. Any subject requiring a legally authorized representative; 2. Any contraindications or hypersensitivity to IFN-a or ANA and their excipients; 3. Known risk factors for QT-prolongation (e.g., congenital long QT, known history of acquired QT-prolongations); 4. Co-morbidity with severe or serious condition that, in the Investigators opinion, would jeopardize the safety of the subject or their compliance with the protocol, including significant cardiac disease (including New York Heart Association Class III-IV congestive heart failure and clinically significant arrhythmias) and pulmonary hypertension; 5. History of major organ transplantation; 6. Pregnant or lactating females; 7. Subjects with any other significant medical conditions that, in the opinion of the Investigator, would compromise the results of the study or may impair compliance with the requirements of the protocol, including but not limited to: a) Documented autoimmune disease at screening or in the history (e.g., thyroid dysfunction, hepatitis, idiopathic thrombocytopenic purpura, scleroderma, psoriasis, or any arthritis of autoimmune origin); b) Clinically relevant pulmonary infiltrates, pneumonia, and pneumonitis at screening that, in the Investigators opinion, would jeopardize the safety of the subject or their compliance with the protocol; c) Infections with systemic manifestations (e.g., bacterial, fungal, or human immunodeficiency virus [HIV], except hepatitis B [HBV] and/or hepatitis C [HCV], at screening); d) Evidence of severe retinopathy (e.g., cytomegalovirus retinitis, macular degeneration) or clinically relevant ophthalmological disorder (due to diabetes mellitus or hypertension); e) History or presence of clinically relevant depression; f) Previous suicide attempts or at any risk of suicide at screening, in the judgement of the Investigator; g) History or presence of clinically significant neurologic diseases; h) History of any malignancy within 5 years (except Stage 0 chronic lymphocytic leukemia, basal cell, squamous cell, and superficial melanoma) i) History of alcohol or drug abuse within the last year; j) History or evidence of any other (than ET) MPN; 8. Use of any investigational drug <4 weeks prior to the first dose of study drug or not recovered from effects of prior administration of any investigational agent; 9. Subjects with documented ANA resistance or intolerance.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Peripheral blood cell count; | — |
Secondary
| Measure | Time frame |
|---|---|
| Genetic Assessment of CALR, JAK-2, and MPL;Spleen Size Assessment;Quality of Life (EQ-5D-3L) Assessment;Myeloproliferative Neoplasm-SAF (MPN-SAF TSS) Assessment; | — |
Countries
American
Contacts
Public ContactPan Ling
West China Hospital of Sichuan University
Outcome results
None listed