NCT04307953进行中（未招募）2 期
Saracatinib Trial TO Prevent FOP
Amsterdam UMC, location VUmc6 个研究点 分布在 3 个国家目标入组 20 人开始时间: 2020年8月5日最近更新:
适应症
干预措施
相关药物
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 20
- 试验地点
- 6
- 主要终点
- The objective change between the two arms measured in heterotopic bone volume measured by low-dose whole body CT over the initial 6 month RCT
研究概览
简要总结
This is a phase 2 study, designed as a European multicentre 6-month double blind random-ized controlled trial (RCT) of AZD0530 versus matched placebo, followed by a 12 month trial comparing open-label extended AZD0530 treatment with historical control data.
Study population: Male and female adult patients aged 18 years and older with a diagnosis of FOP who meet the inclusion (active disease) and exclusion criteria will be eligible for participation in this study. The total number of enrolled patients will be 20.
Intervention: Patients will be randomized to receive either AZD0530 100mg once daily or matched placebo, taken orally for the first 6 months, immediately followed by an open-label extension in which all patients will receive AZD0530 100mg once daily oral dose for a further 12 months.
Endpoints: Endpoints include change in number of active heterotopic bone lesions measured by low-dose whole-body computer tomography (CT)/ [18F] NaF Positron Emission Tomography (PET) activity
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Male or female aged 18-65 with a clinical diagnosis of FOP at screening, including congenital malformation of the great toes and a history of spontaneous or injury-induced heterotopic ossification (HO), and have a confirmed classic FOP phenotype by the documentation of an ACVR1R206H/+ or variant genomic sequence.
- •Female participants who are women of child-bearing potential will be required to use a highly effective method of contraception as defined in section 5.4, in combination with a condom or diaphragm or cervical/vault caps with spermicidal foam/gel/film/suppository), from the time of enrolment until 4 weeks after final dose of study drug, unless practicing true sexual abstinence as defined in section 5.
- •Male participants will be required to avoid procreative sexual intercourse with women of child-bearing potential from time of enrollment until 4 weeks after final dose of study drug through use of highly effective contraceptive methods. Male participants with a pregnant female partner will be required to use a condom for the duration of the study and for 4 weeks final dose of study drug. Male study participants will not be permitted to donate sperm for from the time of enrolment and until 4 weeks after final dose of study drug.
- •Participants will have to be able to understand and complete study and willing to sign informed consent (IC). They have to be able to attend and comply with the study visits and related activities, adhere to all study-related restrictions, and able to undergo procedures such as PET and CT imaging.
排除标准
- •Not willing to strictly adhere to the reproductive restrictions as defined in section 5.4
- •Women who are pregnant or breast-feeding (from the time 3 months prior to 4 weeks after completion of participation in the study)
- •The presence of significant concomitant illness or history of significant illness such as cardiac, respiratory, renal, rheumatologic, neurologic, psychiatric, endocrine, metabolic, lymphatic disease, or infectious disease, that might confound the results of the study or pose additional risk to the patient;
- •Evidence of active bleeding (including hematuria or hematochezia,) acute or chronic gastrointestinal illness, inflammatory bowel disease, or mucositis
- •Malignant disease / cancer requiring treatment in the past 3 years (except some primary non melanoma skin cancer);
- •Severely impaired renal function defined as estimated glomerular filtration rate <30 mL/min/1.73 m2 calculated by the Modification of Diet in Renal Disease equation;
- •Showing uncontrolled diabetes mellitus with an HbA1C > 9%;
- •Significant viral illness or active infections at screening or randomisation; Subjects should not have subacute or acute fevers of >101 degrees F at time of screening or randomisation
- •Evidence of prolonged QT interval at screening or randomization (defined as QTc of >450 ms) .or known congenital long-QT syndrome.
- •Neutropenia defined as an absolute neutrophil count of <1,500/µl,
- •Thrombocytopenia defined as platelet count <100 × 103/µl,
- •Current blood clotting or bleeding disorder, or significantly abnormal INR-prothrombin time or partial thromboplastin time at screening, or clinically significant abnormalities in other screening laboratories, including significant abnormalities in vitamin B12 or thyroid function tests would be cause for exclusion.-
- •Abnormal liver function test results defined as aspartate aminotransferase (AST) >2.0 x upper limit of normal (ULN); alanine aminotransferase (ALT) >2.0 x ULN; and / or total bilirubin >1.5 x ULN;
- •Known allergy or intolerance to AZD0530 or any excipients used in the investigational medicinal products.
- •Simultaneous participation in another interventional clinical study or a non-interventional study with imaging measures or invasive procedures (eg. collection of blood or tissue samples); Participation in the FOP Connection Registry (www.fopconnection.org) or other studies in which patients completed study questionnaires are possible.
- •Treatment with another investigational or drug that might interfere with HO formation and the interpretation of the study drug in the last 90 days
- •Current use or history of regular alcohol consumption exceeding 14 units/week (6 glasses of 13.0% wine (175ml), 6 pints of 4.0% lager or ale (568ml), 5 pints of 4.5% cider (568 ml) or 14 glasses of 10.0% spirits (25ml)) within 6 months of screening.
- •Currently active metabolic bone disease, other than FOP.
研究组 & 干预措施
AZD0530
Experimental
干预措施: AZD0530 Difumarate (Drug)
Placebo/AZD0530
Experimental
干预措施: Matching placebo (Drug)
结局指标
主要结局
The objective change between the two arms measured in heterotopic bone volume measured by low-dose whole body CT over the initial 6 month RCT
时间窗: Baseline, month 6
Number of new active HO lesions on [18F] NaF PET/ CT
时间窗: Baseline, month 6
The change between the two arms in development of new active heterotopic bone lesions measured by \[18F\] NaF PET/low-dose whole body CT during the initial 6-month RCT
次要结局
- Safety and tolerability assessments are the incidence and severity of adverse events (AE) during the RCT at the end of week 28.(Baseline, month 6 (+overall duration study))
- The change in heterotopic bone volume measured by low-dose whole body CT over six-months treatment during open-label extension of AZD0530 compared to the previous placebo arm of the RCT(Baseline, month 6, month 12)
- The change in heterotopic bone volume measured by low-dose whole body CT over twelve-months treatment during open-label extension of AZD0530 compared to the historical data of Clementia (NCT02322255)(Baseline, month 6, month 12, month 18)
- Change in the volume of individual HO lesions(Baseline, month 6, month 12, month 18)
- Change in number of HO lesions measured by CT over the initial 6 month RCT and in addition the change over twelve-months during open-label extension of AZD0530 compared to the historical data of Clementia and compared to the 6 months placebo-arm.(Baseline, month 6, month 12, month 18)
- In patients with at least 1 active lesion at baseline: Change (and Area Under the Curve (AUC) analysis) of lesion activity(Baseline, month 6, month 12)
- In patients with at least 1 active lesion at baseline: Change in number of active lesion on 18F-NaF PET from baseline to 6 and 12months(Baseline, month 6, month 12)
- Change and percent change from baseline in biomarkers of bone formation levels in serum over time.(Baseline, week 3 through month 18)
- Joint function assessment by physician at baseline and week 3, month 3,6,9,12,and18 by the cumulative analog joint involvement scale (CAJIS) and the quantitative detailed multi-joint assessment at baseline and month 6, 12 and 18(baseline, week 3, month 3,6,9,12,and 18)
- Patient-reported global health status the 36-item Short Form Health Survey (SF-36) at baseline and week 3, month 3,6,9,12,and 18(baseline, week 3, month 3,6,9,12,and 18)
- FOP disease activity assessed by movement disabilities and quality of life using FOP Independent Activity of Daily Living (FOP I-ADL)(baseline, week 3, month 3,6,9,12,and 18)
- Number of reported flare-ups by the patient(Each day (day 0-month18))
- Pharmacokinetic measurements: blood for determination of plasma concentrations of AZD0530 (pre-dose)on the day of the study visits at 6, 12 and 18months(6,12 and 18months)
- Safety and tolerability assessments are the incidence and severity of adverse events (AE) during the RCT at the end of week 26.(Baseline, month 6 (+overall duration study))
- New active HO lesions of the placebo arm during 26 weeks RCT compared to its roll over to 26-week open label treatment(Baseline, month 6, month 12)
- In patients follow-up of lesion activity(Baseline, month 6, month 12)
- Follow-up of HO growth(Baseline, month 6, month 12)
- Joint function assessment by physician at baseline and week 3, month 3,6,9,12,and18 by the cumulative analog joint involvement scale (CAJIS) and the quantitative detailed multi-joint assessment and mounth at baseline and month 6, 12 and 18(baseline, week 3, month 3,6,9,12,and 18)
- Number of patient reported and investigator confirmed flare-ups(Each day (day 0-month18))
研究者
Elisabeth MW Eekhoff
Coordinating Principal Investigator
Amsterdam UMC, location VUmc
研究点 (6)
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