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Adult Healthy Volunteers Study to Evaluate ALPN-101 Safety

2019年12月4日 更新者:Alpine Immune Sciences, Inc.

A Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ALPN-101 in Adult Healthy Volunteers

This study is testing the safety, tolerability, pharmacokinetics (PK--the amount of study drug in the blood), pharmacodynamics (PD), how the study drug affects the body) and immunogenicity (how the study drug affects the immune system) of single and multiple doses and dose levels of an investigational drug called ALPN-101.

研究概览

地位

完全的

详细说明

AIS-A01 is a phase 1, randomized, placebo-controlled, double-blinded study in healthy volunteers. It will be conducted at a single center and will enroll approximately 104 participants. The study will have 2 parts:

  • In Part A, participants will receive a single dose of study drug or placebo. Multiple dose levels of ALPN-101 will be evaluated.
  • In Part B, participants will receive 4 doses of ALPN-101 or placebo--1 dose each week for 4 weeks. Multiple dose levels of ALPN-101 will be evaluated.

In each Part, safety assessments will be performed throughout the dosing and follow-up periods, and multiple PK and PD samples will be collected.

研究类型

介入性

注册 (实际的)

96

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Victoria
      • Melbourne、Victoria、澳大利亚、3004
        • Nucleus Network- Centre for Clinical Studies

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 65年 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Able to participate and willing to give written informed consent.
  2. Healthy adult participant 18 to 65 years of age, inclusive, at the time of informed consent.
  3. BMI between 18 and 30 kg/m2, inclusive.
  4. Male participants must agree to use a highly effective method of contraception consistently and correctly during the treatment period and for at least 30 days after the last dose of study intervention and to refrain from donating sperm during this period.
  5. Female participants must not be pregnant or breastfeeding

    Exclusion Criteria:

    General Health Exclusions

  6. Any concomitant disease, condition or treatment that could interfere with the conduct of the study or that would, in the opinion of the Investigator or Sponsor, pose an unacceptable risk to the participant in the study or interfere with the interpretation of study data.
  7. History or symptoms of significant psychiatric disease in the opinion of the Principal Investigator, including but not limited to depression and schizophrenia.
  8. History of immunological disorders, auto-immune disorders, acquired or congenital immune deficiency.
  9. History of significant hepatic or renal disease or impairment.
  10. Evidence of an active or suspected cancer or a history of malignancy within the previous 3 years, except for the following, which did not require systemic therapy and are considered cured: nonmelanoma skin cancer, curatively treated localised prostate cancer or other in situ cancer.
  11. History of major organ transplantation with an existing functional graft. Therapeutic and Intervention-Related Exclusions
  12. Use of prescription medications or herbal remedies within 14 days or 5 elimination half-lives (whichever is longer) of study intervention administration or use of over-the-counter medications (OTC) within 7 days of study intervention administration (apart from recommended doses of vitamin/mineral supplements, OTC analgesics, etc., approved by the Investigator and Sponsor). Participants who have been on hormone replacement therapy (HOURST) for a period of at least 2 months will not be excluded from the study, provided the HOURST regimen remains unchanged during the conduct of the study.
  13. Any concomitant medications that prolong QT/QTc interval.
  14. Dosed with an investigational drug within 30 days or 5 elimination half-lives (whichever is longer) prior to study drug administration.
  15. Received any systemic steroid within 1 month or systemic immunosuppressant agent within 6 months prior to study drug administration.
  16. Received any antibody therapy or biologic products within 6 months prior to study drug administration.
  17. Significant loss of blood including blood donation over 500 mL or transfusion of any blood product within 3 months before the Screening Visit.
  18. Unwilling to refrain alcohol use 48 hours prior to your admission into the clinical research unit.
  19. Known hypersensitivity, allergy or intolerance to the study drug or any of the excipient contained in the intervention formulation.
  20. Immunisation with any vaccine within 6 weeks prior to study drug administration.
  21. For participants enrolled in cohorts in which KLH will be administered: known administration of KLH within 6 months prior to study drug administration; known seafood or shellfish allergy, or known hypersensitivity or allergy to KLH Laboratory Exclusions
  22. Any clinically significant (at the discretion of the Investigator) abnormalities in laboratory test results, including complete blood count, chemistry panels and urinalysis. If out of range at the Screening Visit and/or admission to the CRU and deemed clinically significant by investigator, the tests may be repeated once on a separate day.
  23. Estimated creatinine CL < 90 mL/minute at the Screening Visit
  24. Positive test at the Screening Visit and/or at baseline for drugs of abuse (e.g., phencyclidine, opiates, benzodiazepines, barbiturates, amphetamines, methamphetamines, cocaine and THC). The repeat test is permitted once for a suspected false positive test.
  25. Positive alcohol breath test at the Screening Visit and/or at baseline.
  26. Positive result on tests for HIV-1 and/or HIV-2 antibody, anti-hepatitis B virus antibodies (core antibody [HBcAb], surface antigen [HBsAg]) or anti-hepatitis C virus antibody.
  27. Positive serum pregnancy test at the Screening Visit or admission to the CRU. Infection-related Exclusions.
  28. Acute infection including viral infections in the preceding 6 weeks
  29. History or presence of any chronic infectious condition, including but not limited to tuberculosis or parasitic infections. Evidence of tuberculosis may include either a positive tuberculosis blood test (by a positive QuantiFERON® TB-Gold test or a positive tuberculin skin test) or chest X-ray radiographic findings consistent with active or latent tuberculosis.

    Cardiovascular Exclusions

  30. Supine sustained (i.e. 3 independent measurements within 30 min) systolic blood pressure greater than 140 or less than 90 mmHg.
  31. Supine sustained (i.e. 3 independent measurements within 30 min) diastolic blood pressure greater than 90 or less than 40 mmHg.
  32. Sustained (i.e. 3 independent measurements within 30 min) heart rate (pulse) greater than 100 or less than 40 beats per minute (bpm).
  33. QTcF < 300 msec or ≥ 450 msec.
  34. Personal and/or family history of congenital long QT syndrome or sudden cardiac death

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
安慰剂比较:单剂量安慰剂
Single or multiple doses of placebo delivered via intravenous or subcutaneous injection, matched to ALPN-101 cohorts.
有源比较器:Single Ascending Dose ALPN-101
Single or multiple doses of ALPN-101 delivered via intravenous or subcutaneous injection. Ascending dose levels will be evaluated.
有源比较器:Multiple Ascending Dose ALPN-101
Single or multiple doses of ALPN-101 delivered via intravenous or subcutaneous injection. Ascending dose levels will be evaluated.
安慰剂比较:Multiple Dose Placebo
Single or multiple doses of placebo delivered via intravenous or subcutaneous injection, matched to ALPN-101 cohorts.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Safety, as assessed by adverse events according to CTCAE v5.0
大体时间:From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4-8 weeks)
The rate of adverse events will be compared between the 2 treatment groups.
From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4-8 weeks)

次要结果测量

结果测量
措施说明
大体时间
Pharmacokinetics of ALPN-101 as assessed by time of maximum ALPN-101 concentration.
大体时间:From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
Plasma levels of ALPN-101 will be serially evaluated following dosing of study drug, and the time of maximum plasma concentration (Tmax) will be identified.
From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
Pharmacokinetics of ALPN-101 as assessed by the maximum concentration of ALPN-101.
大体时间:From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
Plasma levels of ALPN-101 will be serially evaluated following dosing of study drug, and the maximum plasma concentration (Cmax) will be calculated.
From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
Pharmacokinetics of ALPN-101 as assessed by AUC on all subjects.
大体时间:From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
Plasma levels of ALPN-101 will be serially evaluated following dosing of study drug, and the area under the curve (AUC) will be calculated.
From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
The incidence of ADA against ALPN-101 will be assessed and summarized.
大体时间:From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)
The incidence of ADA against ALPN-101 will be assessed by the percentage of patients with a positive ADA result of all the treated patients.
From study Day 1 (dosing of ALPN-101 or placebo) until the End of Study visit (approx. 4 weeks for Part A of the study, and approx 6 weeks for Part B)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2019年1月29日

初级完成 (实际的)

2019年11月18日

研究完成 (实际的)

2019年11月18日

研究注册日期

首次提交

2018年11月5日

首先提交符合 QC 标准的

2018年11月19日

首次发布 (实际的)

2018年11月21日

研究记录更新

最后更新发布 (实际的)

2019年12月5日

上次提交的符合 QC 标准的更新

2019年12月4日

最后验证

2019年10月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • AIS-A01

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

是的

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