SAD Study of CGB3002 in Healthy Participants
2026年6月16日 更新者:ChainGen Biopharma Ltd
A Randomized, Double-blind, Placebo-controlled, Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenicity of Single Ascending Doses of CGB3002 in Healthy Participants
This is a randomized, double-blind, placebo-controlled phase I clinical study to evaluate the safety, tolerability, pharmacokinetics and immunogenicity of single ascending IV doses of CGB3002 in healthy participants.
CGB3002 is being developed to treat Alzheimer's Disease.
調査の概要
状態
まだ募集していません
条件
詳細な説明
This study includes 5 planned sequential cohorts.
Participants will be randomized to receive a single IV dose of CGB3002, active comparator or placebo, with doses administered in ascending order.
Based on the emerging data, there will be options to adjust the number of participants on active or placebo per subsequent dose level, and doses may be repeated or adjusted based on safety, tolerability and plasma pharmacokinetic data.
Optional cohorts may be added to evaluate an intermediate dose level or to expand the dose level by SRC.
研究の種類
介入
入学 (推定)
46
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。
研究連絡先
- 名前:Ofer Gonen, M.D.
- 電話番号:(03) 8593 9801
- メール:o.gonen@nucleusnetwork.com.au
研究場所
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Victoria
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Melbourne、Victoria、オーストラリア、3004
- Nucleus Network
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コンタクト:
- Nucleus Network Melbourne
- 電話番号:1800 243 733
- メール:melbourne@nucleusnetwork.com
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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
- 大人
健康ボランティアの受け入れ
はい
説明
Inclusion Criteria:
- Must have signed written informed consent before any study-related activities are carried out and must be able to understand the full nature and purpose of the trial, including possible risks and adverse effects. Be willing and able to comply with all study assessments and adhere to the protocol schedule and restrictions.
- Age≥18 years and<55 years at the time of consent, healthy participants, male or female.
- A body mass index (BMI) of 18 to 32 kg/m2 (cutoff inclusive), with male participants weighing no less than 50 kg, female participants weighing no less than 40 kg.
- Males and females of childbearing potential agree to have no plans for childbearing, use reliable contraceptive measures and not to donate sperm or ova from 30 days prior to dosing until 120 days after dosing. For females of childbearing potential, hormonal contraceptives should begin at least 1 month prior to screening to ensure contraceptive is in full effect.
Exclusion Criteria:
- A known history of clinically significant drug allergy or atopic allergic disease (asthma, urticaria, eczematous dermatitis) or a known history of allergy to biologics or any excipients in biologics, fully resolved childhood asthma can be enrolled.
- Any disease that may affect the safety evaluation of the participants or the in vivo process of the investigational product, including the central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, hematopoietic system, metabolic endocrine system, etc.
- Use of prescription drugs within 14 days or five half-lives (whichever is longer) prior study drug administration, unless determined by the Investigator and Sponsor to be non-interfering (e.g., hormonal contraceptives).
- Use of over-the-counter (OTC) or Chinese herbal medicine within 7 days or 5 half-lives (whichever is longer) prior to study drug administration, unless determined by the Investigator and Sponsor to be non-interfering.
- With a history of drug abuse within 12 months prior to dosing.
- Cannot tolerate punction, have a history of needle fainting or blood fainting.
- Have participated in clinical trials, whether for drugs or medical devices, within 30 days prior to administration or within 7 times the known elimination half-life, whichever is longer.
- Blood donation or significant blood loss (> 300 mL) within 30 days prior to dosing, and planning to blood donate during the study.
- Any vaccinations with a live vaccine (excluding influenza vaccine) within 60 days prior to dosing.
- Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≥1.5×ULN at screening or Day -2. Total bilirubin (TBIL) > ULN at screening or Day -2(except in those due to findings consistent with Gilbert's disease).
- Estimated creatinine clearance < 80 mL/ min (Cockroft-Gault equation) at screening or Day-2.
- Test positive for syphilis, hepatitis B virus surface antigen (HbsAg), hepatitis B core antibody (HBcAb), hepatitis C virus antibody (HCV-Ab) or HIV antibody at screening.
- Urine drug screening positive at screening or Day-2.
- Have a head MRI demonstrating either cerebral microhemorrhages, or superficial siderosis, or prior evidence of microhemorrhage, or any other major intracranial pathology.
- Still needed or planned to engage in vigorous physical activity or exercise during study participation.
- Other conditions deemed inappropriate by the investigator to participate in the clinical trial.
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:並列代入
- マスキング:ダブル
武器と介入
参加者グループ / アーム |
介入・治療 |
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プラセボコンパレーター:Placebo
Cohorts 1-5 each has 2 participants who will receive placebo, 10 in total.
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Healthy participants will be administered a single intravenous dose of matching placebo.
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アクティブコンパレータ:Active Comparator
Cohorts 1-5 each has 2 participants will receive active comparator, 10 in total.
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Healthy participants will receive a single intravenous dose of the comparator drug at the same dose level as CGB3002.
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実験的:CGB3002 0.08 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (0.08 mg/kg).
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Cohorts 1: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 0.08 mg/kg.
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実験的:CGB3002 0.4 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (0.4 mg/kg).
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Cohorts 2: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 0.4 mg/kg.
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実験的:CGB3002 1.2 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (1.2 mg/kg).
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Cohorts 3: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 1.2 mg/kg.
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実験的:CGB3002 3.6 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (3.6 mg/kg).
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Cohorts 4: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 3.6 mg/kg.
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実験的:CGB3002 7.2 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (7.2 mg/kg).
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Cohorts 5: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 7.2 mg/kg.
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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 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Percentage of Participants with Adverse Events as a Measure of Safety and Tolerability
時間枠:up to Day 15 weeks.
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Safety assessment variables will include all adverse events (AEs) including AEs, physical examinations, neurological examinations, vital sign measurements, electrocardiograms, laboratory parameters.
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up to Day 15 weeks.
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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PK of CGB3002: Maximum Concentration (Cmax)
時間枠:up to 8 weeks
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Cmax after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: time attain to Cmax (Tmax)
時間枠:up to 8 weeks
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Tmax after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: Apparent terminal half-life (T1/2)
時間枠:up to 8 weeks
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T1/2 after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: Area under the plasma concentration versus time curve from zero to t h post-dose (AUC0-t)
時間枠:up to 8 weeks
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AUC0-t after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: Area under the plasma concentration versus time curve extrapolated to infinity (AUC0-inf)
時間枠:up to 8 weeks
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AUC0-inf after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: the total body clearance (CL)
時間枠:up to 8 weeks
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CL after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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PK of CGB3002: Volume of distribution during the terminal phase (Vz)
時間枠:up to 8 weeks
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Vz after single intravenous infusion of CGB3002 based on non-compartmental analysis.
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up to 8 weeks
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Concentration ratio of CSF to plasma
時間枠:Day 3
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CSF concentrations were measured by a specific and validated method.
Concentration ratio of CSF to plasma on Day 3 post dose will be calculated.
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Day 3
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Incidence of anti-CGB3002 antibodies (ADAs)
時間枠:up to 8 weeks
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For each dose group, the numbers and proportions of participants who were positive or negative for anti-drug antibodies (ADA) at baseline (baseline prevalence) and after study drug administration (post-baseline incidence during the treatment and follow-up periods) were summarized.
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up to 8 weeks
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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。
スポンサー
捜査官
- スタディディレクター:Zhizheng Zhang, M.D.、ChainGen Biopharma Ltd
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 (推定)
2026年6月30日
一次修了 (推定)
2027年4月30日
研究の完了 (推定)
2027年4月30日
試験登録日
最初に提出
2026年6月16日
QC基準を満たした最初の提出物
2026年6月16日
最初の投稿 (実際)
2026年6月22日
学習記録の更新
投稿された最後の更新 (実際)
2026年6月22日
QC基準を満たした最後の更新が送信されました
2026年6月16日
最終確認日
2026年6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。
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