Apheresis Collection for New Drug Development and Evaluation Research
調査の概要
研究の種類
入学 (推定)
連絡先と場所
研究連絡先
- 名前:WeiChi Zhou
- 電話番号:+86 17368691876
- メール:ksh-clinicalt@tcrximmune.com
研究場所
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Anhui
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Bengbu、Anhui、中国、233000
- 一時停止
- The First Affiliated Hospital of Bengbu Medical University
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Hefei、Anhui、中国、230001
- 募集
- The First Affiliated Hospital of Anhui Medical University
-
コンタクト:
- WeiChi Zhou
- 電話番号:+86 17368691876
- メール:ksh-clinicalt@tcrximmune.com
-
-
参加基準
適格基準
就学可能な年齢
- 大人
健康ボランティアの受け入れ
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Aged between 18 and 40 (inclusive), male or non-pregnant female, regardless of nationality.
Weight: Male ≥ 50kg; Female ≥ 45kg, and 19kg/m2 ≤ BMI ≤ 30kg/m2 (BMI, Body Mass Index = weight (kg) ÷ height (m)2).
Blood pressure: Measurement results are either normal or abnormal, but without clinical significance.
Pulse rate: Measurement of normal or abnormal pulse rate has no clinical significance.
Temperature (ear temperature): 35.4-37.2℃. The patient's general condition is good: there is no damage to vital organs such as the heart, lungs, liver, and kidneys, no severe or uncontrolled infections, and no history of severe mental disorders.
Clinical examination must meet the following criteria: • Hemoglobin (Hb) measurement is normal or abnormal without clinical significance • White blood cell count (WBC) measurement is normal or abnormal without clinical significance • Platelet count (PLT) measurement is normal or abnormal without clinical significance • Neutrophil count (NEU) measurement is normal or abnormal without clinical significance • Liver function test indicators <1.5ULN • Coagulation function is normal or abnormal without clinical significance • 12-lead electrocardiogram results are normal or abnormal without clinical significance • Hepatitis A virus antibody (HAV) is negative.
Hepatitis B virus surface antigen (HBsAg) negative Hepatitis C virus antibody (HCV antibody) negative.
Human immunodeficiency virus antibody (HIV-1 and HIV-2 antibody) negative. Treponema pallidum antibody test is negative. The test result for CMV IgM antibody is negative.
Exclusion Criteria:
- Previously had adverse reactions to blood donation. The following diseases are considered clinically significant by researchers: autoimmune diseases, severe endocrine and metabolic diseases, malignant tumors, neuropsychiatric diseases; Creutzfeldt-Jakob disease and those with a family history, or those who have received treatment with tissues or tissue derivatives that may have been infected with the Creutzfeldt-Jakob pathogen; chronic skin diseases, especially infectious, allergic, or inflammatory systemic skin diseases; those with allergic diseases or recurrent allergies; those who have undergone surgical operations in the past three months.
Women who are in their menstrual period, pregnancy, less than 6 months after abortion, or less than 1 year since the end of childbirth and lactation period.
Individuals who have recovered from an upper respiratory infection within the past week, or those who have recovered from pneumonia within the past three months.
Individuals with urinary system infections less than 3 months old, or those experiencing an acute episode of urinary system stones.
Equipment contaminated by blood or tissue fluid causing injury or contaminating wounds, or individuals who have undergone tattooing less than one year ago.
Long-term uninterrupted use of hormone drugs or immunosuppressants exceeding physiological replacement doses is required, including but not limited to glucocorticoids and steroids, hydroxyurea, and immunomodulatory drugs (such as alpha or gamma interferon, GM-CSF, mTOR inhibitors, cyclosporine, thymosin, etc.) in doses exceeding physiological replacement levels.
Those who have received whole blood and blood component transfusions within 1 year.
Those who have received their last dose of antitoxin or immune serum within 1 year, or those who have received their last dose of hepatitis B immunoglobulin injection within 1 year.
Individuals who have received the last dose of live attenuated vaccines such as measles, mumps, or polio vaccines within 2 weeks, or the last dose of live rubella vaccines or live attenuated Japanese encephalitis vaccines within 4 weeks.
Individuals who have received the final immunization dose of rabies vaccine within one year after being bitten by an animal.
Poor conditions for vascular puncture, unable to tolerate venipuncture, or history of fainting at the sight or touch of blood. Upon inquiry, individuals with a history of drug use, drug abuse, or positive drug abuse screening (morphine, methamphetamine, ketamine, tetrahydrocannabinolic acid, MDMA) within the previous 12 months prior to screening. Healthy volunteers who have participated in intervention drug clinical studies and have used study drugs within 7 days prior to screening.
Other situations where the researcher believes participation in this study is not appropriate.
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
コホートと介入
グループ/コホート |
介入・治療 |
|---|---|
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DCX-001
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No intervention measures
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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 |
|---|---|
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Research on the in vitro isolation, cell expansion, and function of mononuclear cells;
時間枠:Baseline and 6 months
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Baseline and 6 months
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協力者と研究者
スポンサー
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
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 (実際)
学習記録の更新
投稿された最後の更新 (実際)
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
- DCX-001
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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。