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临床试验/EUCTR2022-002356-39-SE
EUCTR2022-002356-39-SE进行中(未招募)1 期

DiaPrecise, A Phase II Open Label Study to evaluate the safety andfeasibility of intralymphatic administration of Diamyd® inindividuals at risk for Type 1 diabetes carrying the HLA DR3-DQ2haplotype - DiaPrecise

Diamyd Medical AB0 个研究点目标入组 16 人开始时间: 2022年10月13日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
16

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
All

入选标准

  • 1. Written informed consent/assent from the individual and the individual’s parents or caretaker(s)
  • according to local regulations.
  • 2. Males and females aged =8 and <18 years old at the time of Screening.
  • 3. Possess the HLA DR3-DQ2 haplotype.
  • 4. Seropositive for GADA and at least one additional T1D-associated autoantibody (IA-2A,
  • ZnT8A or IAA).
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 16
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 1. Diagnosis of T1D (stage 3 T1D, according to the American Diabetes Association
  • [ADA] classification).
  • 2. Fasting glucose > 7 mmol/L (126 mg/dl), 2-hour-OGTT plasma glucose > 11.1 mmol/L (200
  • mg/dL) or HbA1c > 6.5% (48 mmol/mol) at the screening Visit.
  • 3. Treatment with any anti-diabetic medication, including the use of external insulin.
  • 4. Participation in any other clinical trial testing pharmaceutical treatments.
  • 5. Recent (past 12 months) or current treatment with immunosuppressant therapy, including
  • chronic use of glucocorticoid therapy. Inhaled, topical, and intranasal steroid use is acceptable.
  • Short courses (e.g., =5 days) of oral or intra-articular injections of steroids will be permitted on
  • 6. History of hyperparathyroidism, hypercalcemia and/or nephrolithiasis, unless appropriately
  • treated, or any other contraindication to use of Vitamin D.
  • 7. History of epilepsy, serious head trauma or cerebrovascular accident, or clinical features of
  • continuous motor unit activity in proximal muscles
  • 8. Any clinically significant history of an acute reaction to a vaccine or its constituents (e.g.,
  • Alhydrogel) or lidocaine (local anesthetic)
  • 9. Any acute or chronic skin infection or condition that would preclude intralymphatic injection.
  • 10. Treatment with any (live or inactive) vaccine, including influenza vaccine and Coronavirus
  • Disease 2019 (COVID-19) vaccine, within 4 weeks prior to planned first dose of study drug; or
  • planned treatment with any vaccine up to 4 weeks after the last injection with study drug.
  • 11. Ongoing diagnosed post-COVID19 syndrome.
  • 12. Known diagnosis of human immunodeficiency virus (HIV), hepatitis B or hepatitis C infection.
  • Individuals with previous hepatitis C infection that is now cured may be eligible.
  • 13. Any clinically significant concomitant medical condition, including but not limited to other
  • autoimmune diseases, cardiovascular, gastrointestinal, hematological, immune, renal including a
  • history of renal transplantation or neurological that in the opinion of the investigator would
  • interfere with trial participation or procedures. Celiac disease with adequate diet as well as
  • stable autoimmune thyroiditis will be permitted.
  • 14. Any clinically significant abnormal findings detected during Screening that might jeopardize the
  • individual’s safety or ability to complete the trial.
  • 15. Females who are lactating or pregnant (for females who have started menstruating the
  • possibility of pregnancy must be excluded by urine ßHCG onsite prior to the study drug
  • administration).
  • 16. Males or females not willing to use adequate contraception, if sexually active, until 90 days
  • after the last Diamyd administration. Adequate contraception is as follows:
  • For females of childbearing potential (FOCBP)
  • a. oral (except low-dose gestagen (lynestrenol and norestisteron)), injectable, or implanted
  • hormonal contraceptives
  • b. intrauterine device
  • c. intrauterine system (for example, progestin-releasing coil)
  • d. refraining from heterosexual intercourse if that is the preferred and usual lifestyle of the
  • For sexually active males
  • b. Abstinence from heterosexual intercourse if that is the preferred and usual lifestyle of the
  • c. Vasectomy

研究者

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