An Open-Label Study in Adolescent and Adult Severe (Coagulation Factor Activity <1%) Hemophilia A or B Patients With or Without Inhibitors Comparing Standard Treatment to PF-06741086 Prophylaxis

Pfizer Inc., 235 East 42nd Street, New York, NY 100170 个研究点目标入组 106 人开始时间: 2019年11月21日最近更新: 2021年4月5日

试验速览

阶段: 1 期
状态: 进行中（未招募）
发起方: Pfizer Inc., 235 East 42nd Street, New York, NY 10017
入组人数: 106

研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型: Interventional clinical trial of medicinal product

入排标准

性别: Male

入选标准

•Participants are eligible to be included in the study only if all of the following criteria apply:
•1.Participant must be male and 12 to <75 years of age with a minimum body weight of 30 kg at the time of signing the informed consent.
•Type of Participant and Disease Characteristics
•2.Participants with a diagnosis of severe hemophilia A or B (FVIII or FIX activity <1%, respectively).
•3.Participants who are enrolled into the Non-Inhibitor Cohort must also meet the following criteria:
•No detectable or documented history of inhibitors (=0.6 BU/mL or greater than the upper limit of normal [ULN] for the testing laboratory) against FVIII or FIX prior to enrollment (Baseline of Observational Phase).
•Participants receiving routine prophylaxis (defined as treatment by IV injection of factor concentrate to prevent bleeding) treatment with FVIII/FIX replacement, have demonstrated at least 80% compliance with scheduled prophylaxis regimen during 6 months prior to enrollment, and willing to continue to receive routine prophylaxis treatment with FVIII/FIX replacement during the Observational Phase.
•Participants with on-demand treatment regimen with =6 acute bleeding episodes (spontaneous or traumatic) that required coagulation factor infusion during the 6 months period prior to Enrollment into Observational Phase and willing to continue to receive on demand treatment during the Observational Phase. Surgical bleeding episodes do not apply to this criterion.
•4.Participants who are enrolled into the Inhibitor Cohort must also meet the following criteria:
•Documentation of current high titer inhibitor (=5 BU/mL); or current low titer inhibitor (<5 BU/mL) refractory to FVIII or FIX replacement and with FVIII or FIX recovery <60% of expected within previous 6 months prior to Enrollment into Observational Phase.
•Participants who have documented inhibitors while on factor-replacement therapy but who do not meet the quantitative inhibitor criteria described in the prior bullet at the time of Screening (eg, participant with a previously documented high-titer inhibitor (=5 BU/mL) and whose condition precludes re-challenge with FVIII or FIX replacement) may be considered for eligibility on a case-by-case basis with prior approval from the Pfizer Medical Monitor.
•Participants with on-demand treatment regimen with =6 bleeding episodes (spontaneous or traumatic) necessitating treatment with bypass factor during the 6 months prior to Enrollment into Observational Phase and willing to continue to receive on-demand treatment during the Observational Phase. Surgical bleeding episodes do not apply to this criterion.
•Informed Consent
•6.Participant or legally authorized representative, or participant’s caregiver capable of giving signed informed consent (or minor assent, when applicable) as described in Appendix 1 which includes compliance with the requirements and restrictions listed in the informed consent document (ICD) and in this protocol.
•Are the trial subjects under 18? yes
•Number of subjects for this age range: 29
•F.1.2 Adults (18-64 years) yes
•F.1.2.1 Number of subjects for this age range 104
•F.1.3 Elderly (>=65 years) yes
•F.1.3.1 Number of subjects for this age range 12

排除标准

•Participants are excluded from the study if any of the following criteria apply:
•Medical Conditions
•1.Previous or current treatment for or history of coronary artery diseases, venous or arterial thrombosis (Common Terminology Criteria for Adverse Events [CTCAE] Grade >1), or ischemic disease (except treatment for catheter associated thrombosis).
•2.Known planned surgical procedure during the planned study period.
•3.Known hemostatic defect other than hemophilia A or B.
•4.Abnormal renal or hepatic function as defined by the following laboratory results at Screening:
•a.Alanine transaminase (ALT) >2 × upper limit of normal (ULN)
•b.Bilirubin >1.5 × ULN (isolated bilirubin >1.5 × ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%)
•c.Current unstable liver or biliary disease per investigator assessment defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminaemia, oesophageal or gastric varices, persistent jaundice, or cirrhosis. NOTE: Stable chronic liver disease (including Gilbert’s syndrome, asymptomatic gallstones, and chronic stable hepatitis B or C -eg, presence of hepatitis B surface antigen [HBsAg] or positive hepatitis C antibody test result at screening or within 3 months prior to starting study intervention) is acceptable if the participant otherwise meets entry criteria
•d.Serum albumin less than the lower limit of normal (LLN).
•e.Estimated glomerular filtration rate (eGFR) <30 mL/min/1.73 m2 (see Appendix 10.2.1 for formulas used in eGFR calculation).
•5.Abnormal hematology values as defined by the following laboratory tests at Screening:
•a.Platelet count <100,000/uL
•b.Hemoglobin level <10 g/dL
•6.Other acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the participant inappropriate for entry into this study.
•7.QTc >450 msec for male participants or QTc >480 msec in participants with bundle branch block.
•8.Individuals with hypersensitivity or an allergic reaction to hamster protein or other components of the study intervention.
•Prior/Concomitant Therapy
•9.Current routine prophylaxis with bypassing agent (eg, aPCC, BYCLOT, Prothrombin Complex Concentrates [PCC], or rFVIIa) or non-coagulation non-factor replacement therapy (eg, emicizumab).
•10.Regular, concomitant therapy with immunomodulatory drugs (eg, IV immunoglobulin [IVIG], and routine systemic corticosteroids, rituximab).
•11.Ongoing or planned use of immune tolerance induction during the Observational Phase or Active Treatment Phase, or prophylaxis with FVIII or FIX replacement during the Active Treatment Phase.
•Prior/Concurrent Clinical Study Experience
•12.Participation in other studies involving investigational drug(s) within 30 days (or as determined by local requirements) or 5 half-lives prior to study entry or during study participation.
•13.Previous exposure to PF 06741086 during to participation in studies B7841002 and B7841003.
•Diagnostic assessments
•14.CD4 cell count =200/uL if human immunodeficiency virus (HIV)-positive
•15.Screening 12-lead ECG that demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study result

研究者

发起方

Pfizer Inc., 235 East 42nd Street, New York, NY 10017

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