A Clinical Trial to Investigate the Pharmacokinetics and Safety/Tolerability of CKD-386 in Healthy Adult Volunteers
2020年1月8日 更新者:Chong Kun Dang Pharmaceutical
Phase I Clinical Trial to Compare the Pharmacokinetics and Tolerability of CKD-386 With Co-administration of D012, D326, and D337 in Healthy Adult Volunteers
The purpose of this study is to evaluate the pharmacokinetics and Safety/Tolerability of CKD-386
調査の概要
詳細な説明
Phase I clinical trial to compare the pharmacokinetics and tolerability of CKD-386 with co-administration of D012, D326, and D337 in healthy adult volunteers
研究の種類
介入
入学 (予想される)
30
段階
- フェーズ 1
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
19年歳以上 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Those who are over 19 years old at the screening visit
- Those who weigh more than 50kg (45kg or more for women) at the screening visit and have a body mass index (BMI) within the range of 18-30kg/m^2
Those who meet the following conditions of blood pressure measured in a sitting position after sufficient rest at the screening visit
- Systolic blood pressure: 90mmHg or more and 139mmHg or less
- Diastolic blood pressure: 60mmHg or more and 89mmHg or less
- Those who no congenital or chronic disease based on screening and no pathological symptoms or findings in medical examination results (e.g. EEG, ECG, chest and gastroscopy or gastrointestinal radiographs, if necessary)
- The person in charge of the examination (or authorized test physician) who has determined that the test subject is suitable for the diagnostic test and electrocardiogram test such as hematology test, blood chemistry test, serology test and urine test performed according to the characteristics of the investigational drug product
- Persons agreeing to exclude the possibility of pregnancy using appropriate contraceptive methods and not providing sperm or eggs from the date of first administration of the investigational drug to the 14th day after the last administration of the investigational drug
Exclusion Criteria:
- Those who participated in other clinical trials (including bioequivalence studies) within 6 months before the first dose and received the investigational drug
- Those who used drugs that induce and inhibit metabolic enzymes, such as barbital drugs, within one month before the first dose, or who used drugs that may interfere with this test within 10 days before the first dose
- Those who have donated whole blood within 2 months before the first dose or component donation within 1 month, or have transfused within 1 month
- Those who have had a history of gastrointestinal resection that may affect the absorption of the investigational drug (except appendectomy and hernia surgery)
A person who meets the following conditions within one month before the first administration date
Excess alcohol: 21 cups / week for men and 14 cups / week for women.
[1 glass = 50 mL of shochu or 30 mL of liquor or 250 mL of beer]
- Smokers exceeding 20 cigarettes per day
Patients with the following diseases
- Patients with hypersensitivity to the main constituents or components of the investigational drug
- Severe hepatic impairment, biliary atresia or cholestasis
- Patients with hereditary angioedema or with a history of angioedema in the treatment of ACE inhibitors or angiotensin II receptor antagonists
- Diabetes mellitus
- Patients with moderate to severe renal impairment [glomerular filtration rate (eGFR) <60 mL / min / 1.73m^2]
- Renal vascular hypertension patients
- Patients with active liver disease, including unexplained persistent serum transaminase elevations or elevated serum transaminase elevations greater than three times the normal upper limit
- Patients with myopathy or have a history of family or genetic history of myopathy
- Hypothyroidism
- If you have a history of muscle toxicity for other HMG-CoA converting enzymes or fibrate class drugs
- Genetic problems such as galactose intolerance, Lapp lactose deficiency, or glucose-galactose malabsorption
- person who is considered to be unsuitable for participation in this clinical trial for reasons other than the above selection / exclusion criteria.
- In the case of female volunteers, the suspected or lactating woman
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
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:クロスオーバー割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Group 1
Period 1: D012, D326, D337(3 tabs, once) / Period 2: CKD-386 F1(1 tab, once)/ Period 3: CKD-386 F2(1 tab, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
|
実験的:Group 2
Period 1: D012, D326, D337(3 tabs, once) / Period 2: CKD-386 F2(1 tab, once)/ Period 3: CKD-386 F1(1 tab, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
|
実験的:Group 3
Period 1: CKD-386 F1(1 tab, once) / Period 2: D012, D326, D337(3 tabs, once) Period 3: CKD-386 F2(1 tab, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
|
実験的:Group 4
Period 1: CKD-386 F1(1 tab, once) / Period 2: CKD-386 F2(1 tab, once) / Period 3: D012, D326, D337(3 tabs, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
|
実験的:Group 5
Period 1: CKD-386 F2(1 tab, once) / Period 2: D012, D326, D337(3 tabs, once)/ Period 3: CKD-386 F1(1 tab, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
|
実験的:Group 6
Period 1: CKD-386 F2(1 tab, once) / Period 2: CKD-386 F1(1 tab, once) / Period 3: D012, D326, D337(3 tabs, once)
|
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 1 tablet under fasting conditions for each period
他の名前:
A single oral dose of 3 tablets(D012, D326 and D337) under fasting conditions for each period
|
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
AUCt: Area under the concentration-time curve
|
0(predose)~72 hours
|
|
Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
Cmax: Maximum plasma concentration of the drug
|
0(predose)~72 hours
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
AUCinf: Area under the concentration-time curve from zero up to ∞
|
0(predose)~72 hours
|
|
tmax each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
tmax: Time to maximum plasma concentration
|
0(predose)~72 hours
|
|
AUCt/AUCinf each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
AUCt/AUCinf: AUCt/AUCinf Ratio
|
0(predose)~72 hours
|
|
t1/2 each main component or the metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D012, D326, D337
時間枠:0(predose)~72 hours
|
t1/2: Terminal elimination half-life
|
0(predose)~72 hours
|
|
AUCt of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337
時間枠:0(predose)~72 hours
|
AUCt: Area under the concentration-time curve
|
0(predose)~72 hours
|
|
Cmax of each main component or metabolite of the component after single dose of CKD-386 F1, CKD-386 F2 and D326, D337
時間枠:0(predose)~72 hours
|
Cmax: Maximum plasma concentration of the drug
|
0(predose)~72 hours
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
捜査官
- 主任研究者:70-4665-9174 70-4665-9174、H Plus Yangji Hospital
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (予想される)
2020年2月1日
一次修了 (予想される)
2020年3月4日
研究の完了 (予想される)
2020年6月15日
試験登録日
最初に提出
2020年1月8日
QC基準を満たした最初の提出物
2020年1月8日
最初の投稿 (実際)
2020年1月10日
学習記録の更新
投稿された最後の更新 (実際)
2020年1月10日
QC基準を満たした最後の更新が送信されました
2020年1月8日
最終確認日
2020年1月1日
詳しくは
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。