A Study to Test the Safety and Blood Levels of PMG1016 in Healthy Adults
A Phase 1a, First-in-human, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of PMG1016 in Healthy Volunteers
This study is a first-in-human (FIH), randomized, double-blind, placebo-controlled study of PMG1016 in healthy adult participants. It aims to investigate the safety, tolerability, PK, and immunogenicity of PMG1016 administered via IV infusion.
Cohort 1: Healthy participants receiving single doses of PMG1016 Dose 1 or placebo.
Cohort 2: Healthy participants receiving single doses of PMG1016 Dose 2 or placebo.
Cohort 3: Healthy participants receiving single doses of PMG1016 Dose 3 or placebo.
Cohort 4: Healthy participants receiving single doses of PMG1016 Dose 4 or placebo.
調査の概要
詳細な説明
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Yaohui Wang
- 電話番号:+86 13810669548
- メール:yaohui_wang@pulmongene.com
研究場所
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Queensland
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Brisbane、Queensland、オーストラリア、4006
- Nucleus Network (Brisbane)
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コンタクト:
- Richard Friend, Dr
- 電話番号:(07) 3707 2720
- メール:r.friend@nucleusnetwork.com.au
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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
説明
Inclusion Criteria:
- Participants must be in good health based on medical history, physical exam, vital signs, ECG, and lab results at screening, as judged by the PI.
- BMI 17.5-32.0 kg/m² and body weight 50-100 kg for males or 45-100 kg for females
- No clinically significant lab abnormalities (hematology, coagulation, biochemistry, urinalysis) per PI discretion
- Females: Must be non-pregnant, non-lactating, and use double contraception (condom + hormonal method/vaginal ring/IUD) through study completion, unless surgically sterile, postmenopausal, or in same-sex relationships. Negative pregnancy tests required. No oocyte donation for 90 days post dose.
- Males: Must be surgically sterile, abstinent, or use condoms plus a highly effective method for female partners. Vasectomized males without proof of azoospermia must use condoms with WOCBP partners. No sperm donation for 90 days post dose.
Exclusion Criteria:
- History or evidence of any clinically significant medical condition (e.g., cardiovascular, gastrointestinal, endocrine, hematologic, psychiatric, renal, musculoskeletal, infectious, neurological, or other major disease) as determined by the PI.
- A PR <40 or >100 bpm or mean SBP >140 mmHg or DBP >95 mmHg (based on triplicate supine measurements after 5 minutes' rest).
- Mean QTcF >450 ms (males) or >470 ms (females) at Screening; one repeat triplicate ECG allowed at PI discretion
- Any clinically significant ECG abnormalities (rhythm, conduction, morphology) that may affect QTc interpretation, per PI judgment
- ALT, AST, or creatinine >1.5 × ULN, or total bilirubin or lymphocytes > ULN.
- Hemoglobin (HGB) below the lower limit of the normal range (ULN) prior to enrollment.
- Participants with a positive toxicology screening panel or positive alcohol breath test at Screening and on Day -1.
- Regular alcohol consumption defined as > 21 alcohol units per week. Participant is unwilling to abstain from alcohol beginning 48 hours prior to admission to the CRU and while residing at the CRU.
- Blood donation or significant blood loss (≥500 mL) within 60 days prior to the first IP administration.
- Plasma donation within 7 days prior to the first IP administration.
- Use of any investigational product/device within 30 days or 5 half-lives (whichever is longer), or participation in >4 investigational drug studies in the past year.
- Pregnant or lactating at Screening or planning pregnancy (self or partner) during the study or follow-up.
- Fever >37.5°C or symptomatic infection within 2 weeks before Screening; any infection requiring systemic antibiotics within 3 months; history of recurrent infections; or a positive SARS-CoV-2 PCR before CRU admission.
- Active malignancy, history of malignancy, or untreated precancerous lesions. Adequately treated or fully excised precancerous lesions are allowed.
- Participants with a known history of retinal diseases, including conditions such as prior retinal detachment.
- Participants with a history of recurrent epistaxis or gingival bleeding.
- Use of prescription medications (except hormonal contraception) within 2 weeks before dosing; mAb products within 5 half-lives; or OTC drugs, supplements, or herbal products within 7 days before dosing.
- History of anaphylaxis or severe allergy per PI judgment; mild untreated hay fever may be allowed.
- History of allergic reaction or hypersensitivity to any of the excipients in the IP.
- Positive screening test for HIV-1/2, HBsAg, HCV antibody, or syphilis.
- Any condition that, in the PI's judgment, may pose a risk to the participant or the study.
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:順次割り当て
- 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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実験的:コホート1
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Participants will be administered PMG1016 Dose 1 or placebo in a 100 mL IV infusion volume
他の名前:
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実験的:コホート 2
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Participants will be administered PMG1016 Dose 2 or placebo in a 100 mL IV infusion volume
他の名前:
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実験的:コホート3
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Participants will be administered PMG1016 dose 3 or placebo in a 100 mL IV infusion volume
他の名前:
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実験的:コホート4
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Participants will be administered PMG1016 dose 4 or placebo in a 100 mL IV infusion volume
他の名前:
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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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Treatment-emergent adverse events (TEAEs)
時間枠:Day 1 to Day 57
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The incidence and severity occurred
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Day 1 to Day 57
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Serious adverse events (SAEs)
時間枠:From Day 1 to Day 57
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The incidence and severity occurred
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From Day 1 to Day 57
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Number of participants with abnormal pulse rate
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of participants with abnormal blood pressure
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of participants with abnormal respiratory rate
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of participants with abnormal tympanic temperature
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal PR Interval
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal QRS Duration
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal QT interval
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal RR interval
時間枠:From Day 1 to Day 57
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From Day 1 to Day 57
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Number of Participants with Clinically Significant Valvular Abnormalities
時間枠:Day 1 to Day 29
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The number of participants with clinically significant valvular abnormalities identified by transthoracic echocardiography (TTE)
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Day 1 to Day 29
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Number of Participants with Clinically Significant Abnormal Left Ventricular Ejection Fraction
時間枠:Day 1 to Day 29
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The number of participants with clinically significant abnormalities in left ventricular ejection fraction (LVEF) assessed by transthoracic echocardiography (TTE)
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Day 1 to Day 29
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Number of Participants with Clinically Significant Abnormal Hematology Results
時間枠:Day 1 to Day 57
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Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal Clinical Chemistry Results
時間枠:Day 1 to Day 57
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Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal Urinalysis Results
時間枠:Day 1 to Day 57
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Day 1 to Day 57
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Number of Participants with Clinically Significant Abnormal Physical Examination Findings
時間枠:Day 1 to Day 57
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assessment of general appearance; head; ears; eyes; nose; throat; dentition; thyroid; chest (heart and lungs); abdomen; skin; neurological system; extremities; back; neck; musculoskeletal system; and lymph nodes
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Day 1 to Day 57
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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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Incidence of anti-drug antibodies (ADA)
時間枠:From Day 1 to Day 57
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Percentage of PMG1016-induced ADA positive participants and percentage of PMG1016-boosted ADA positive participants
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From Day 1 to Day 57
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Maximum serum PMG1016 concentration (Cmax)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Cmax in Serum
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Varying timepoints through end of treatment, up to Day 57
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Time to maximum concentration (Tmax)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Tmax in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Area under the serum drug concentration-time curve (AUC) from time zero to the last time point with measurable concentration (AUC0-t)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC and AUC0-t in Serum.
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Varying timepoints through end of treatment, up to Day 57
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AUC from time zero to infinity (AUC0-∞)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 AUC0-∞ in Serum.
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Varying timepoints through end of treatment, up to Day 57
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The extrapolated portion of AUC0-∞ from Tlast to infinity (%AUCextrap)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 %AUCextrap in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Terminal elimination half-life (t1/2)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 t1/2 in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent total body clearance (CL)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 CL in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent volume of distribution during the terminal phase (Vz)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 Vz in Serum.
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Varying timepoints through end of treatment, up to Day 57
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Apparent terminal elimination rate constant (λz)
時間枠:Varying timepoints through end of treatment, up to Day 57
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Determine PMG1016 λz in Serum.
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Varying timepoints through end of treatment, up to Day 57
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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
追加の関連 MeSH 用語
その他の研究ID番号
- PMG1016-1031
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
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