A Study to Evaluate the Safety of ASP2408 After Subcutaneous Administration to Healthy Male Subjects
Phase I Study of ASP2408 -Subcutaneous Single-dose, Placebo-controlled Study in Non-elderly Healthy Adult Male Subjects
調査の概要
詳細な説明
This clinical study will be conducted as a double-blind, placebo-controlled, single ascending subcutaneous dose study. As shown in the table below, the study will be conducted using 3 cohorts, to which a total of 24 subjects will be randomly assigned (18 subjects receiving ASP2408 and 6 subjects receiving placebo). Each cohort will consist of 8 subjects, who will be randomly assigned to either the ASP2408 group or the placebo group at the ratio of 3 to 1.
Each subject will need to be hospitalized until Day 8 (start date of study drug administration will be regarded as Day 1) and will be observed until Day 90. The investigator or subinvestigator will carefully observe each subject for any sign or symptom of adverse events.
研究の種類
入学 (実際)
段階
- フェーズ 1
連絡先と場所
研究場所
-
-
-
Kyushu、日本
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- BMI (at screening): ≥ 17.6 kg/m2, < 26.4 kg/m2
- Healthy, as judged by the investigator or subinvestigator based on the results of medical examination (subjective symptoms and objective findings) and all tests obtained at screening and during the period from hospitalization (Day -2) to immediately before study drug administration
- Subjects who agree to use effective contraception until 90 days after study drug administration
Exclusion Criteria:
- Received any investigational drugs in other clinical or post-marketing studies within 120 days before the study or is scheduled to receive any investigational drugs
- Donated 400 mL of whole blood within 90 days before the study or during the period from the screening, 200 mL of whole blood within 30 days, or blood components within 14 days before the study, or is scheduled to donate 400 mL of whole blood or blood components
- Received medication within 7 days before hospitalization (Day -2) or is scheduled to receive medication
- Received systemic medications influencing immune functions (e.g., steroids, tacrolimus hydrate, anticancer drugs, and biological products) within 365 days before study drug administration
- Received a live virus vaccine (e.g., BCG, polio, measles, and rubella) within 180 days before study drug administration, or cannot agree not to receive these vaccines for 180 days after study drug administration
- Received a live virus vaccine (e.g., BCG, polio, measles, and rubella) within 180 days before study drug administration, or cannot agree not to receive these vaccines for 180 days after study drug administration
- A deviation from the normal range of blood pressure, pulse rate, body temperature, or standard 12-lead ECG (see Table 3.3-1) at screening or the day before study drug administration (Day -1)
- Any deviation of the normal ranges in laboratory tests before study drug administration
- Failure to meet any criteria for standard 12-lead ECG for QT assessment at screening
- A positive result for tuberculosis test
- Concurrent or history of drug allergies, anaphylaxis, or severe allergic reaction
- Upper GI disease
- Concurrent or previous hepatic disease (e.g., viral hepatitis and drug-induced liver injury)
- Concurrent or previous heart disease (e.g., congestive heart failure, angina pectoris, and arrhythmia requiring treatment)
- Concurrent or previous respiratory disease (e.g., bronchial asthma and chronic bronchitis; except for a history of childhood asthma)
- Previous operation of gut excision
- Concurrent or previous renal disease (e.g., acute renal failure, glomerulonephritis, and interstitial nephritis; except for a history of calculus)
- Concurrent or previous endocrine disease (e.g., hyperthyroid, abnormality of growth hormone)
- Concurrent or previous cerebrovascular disorder (e.g., cerebral infarction)
- Concurrent or previous malignant tumor
- Concurrent or previous serious infection (e.g., sepsis, pneumonia requiring hospitalization, and pyelonephritis)
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
プラセボコンパレーター:プラセボ群
|
皮下投与
|
|
実験的:ASP2408 low dose group
|
subcutaneous administration
|
|
実験的:ASP2408 middle dose group
|
subcutaneous administration
|
|
実験的:ASP2408 high dose group
|
subcutaneous administration
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
Safety assessed by the incidence of adverse events, vital signs, lab tests, and 12-lead ECG
時間枠:Up to 90 days after administration
|
Up to 90 days after administration
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Pharmacokinetics of serum ASP2408
時間枠:On day-1, day-2, day-3, day-4, day-5, day-6, day-7, day-8, day-9, day-11, day-13, day-15, day-22, day-29 day-43, day-60 and day-90
|
The pharmacokinetic analysis employed non-compartmental methods using serum concentrations of ASP2408.
The following pharmacokinetic parameters were estimated: AUCinf, AUClast, Cmax, CL/F, tmax, t1/2, and Vz/F.
|
On day-1, day-2, day-3, day-4, day-5, day-6, day-7, day-8, day-9, day-11, day-13, day-15, day-22, day-29 day-43, day-60 and day-90
|
|
CD80/CD86 receptor occupancy
時間枠:On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
|
|
Total lymphocyte count
時間枠:On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
|
|
Peripheral blood lymphocyte subset
時間枠:On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
On day-1, day-2, day-3, day-5, day-8, day 15, day-22, day-29 and day-90
|
協力者と研究者
スポンサー
出版物と役立つリンク
便利なリンク
研究記録日
主要日程の研究
研究開始
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (見積もり)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
キーワード
その他の研究ID番号
- 2408-CL-9101
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。