Phase 1 Study on the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults
Phase 1, Randomized, Double-blind, Placebo-controlled, Single Ascending Dose Study to Assess the Safety, Tolerability, and Pharmacokinetics of JST-018 in Healthy Adults
The goal of this clinical trial is to learn if a single dose of the study drug, JST-018, is safe and tolerable when administered by injection into the arm or thigh muscle of healthy men and women aged 18 to 55. The main questions it aims to answer are:
- Is a single administration of JST-018 safe?
- What is the concentration of the JST-018 in the blood over time?
- Do antibodies to JST-018 develop following a dose of JST-018? Researchers will compare JST-018 to Placebo to see if there are any differences in the safety and tolerability of a single dose at different dose levels.
Participants will be confined to the clinic for the first 3 days. They will receive an injection on the second day, and then return for 9 more visits over the period of 1 year for:
- Physical exam with vital signs
- Electro-cardiogram (ECG)
- Bood collection for clinical labs and research samples
- Urine sample
- Assessment of potential adverse effects and medications taken
調査の概要
状態
状態
条件
条件
介入・治療
介入・治療
詳細な説明
This is a Phase 1, first-in-human (FIH), randomized, double-blind, placebo-controlled, single ascending dose (SAD) study to assess the safety, tolerability, and PK of a single dose of JST-018 administered IM to healthy participants.
The study will be comprised of a minimum of 3 cohorts (Cohorts A, B, and C, with 12 participants per cohort), each evaluating a single dose of JST-018 administered IM. In each cohort, 2 sentinel participants will be randomized 1:1 such that one participant receives JST-018 and 1 participant receives placebo. Following a favorable blinded safety review committee (SRC) review of sentinel safety data collected through Day 8, the remainder of the cohort (10 non-sentinel participants) will be randomized 4:1 to JST-018 or placebo, and will be dosed.
All safety data for all participants in the current cohort through Day 8 will be reviewed by the SRC in a blinded fashion for each dose cohort before escalating to the next dose cohort (for escalation from Cohort A to Cohort B and escalation from Cohort B to Cohort C); A recommendation on whether to implement Cohort D (along with a recommended dose of JST-018 to be evaluated in Cohort D) may be provided by the SRC following review of blinded safety data from Cohorts A, B, and C.
研究の種類
研究の種類
入学 (推定)
入学
段階
段階
- フェーズ 1
連絡先と場所
研究連絡先
研究連絡先
- 名前:Nels Royer
- 電話番号:(206)651-5094
- メール:jeb.clinicaltrials@evotec.com
研究場所
-
-
Nevada
-
Las Vegas、Nevada、アメリカ、89113
- 募集
- PPD Las Vegas Clinical Research Unit
-
コンタクト:
- 電話番号:(877) 362-2608
-
-
参加基準
適格基準
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:
- Healthy men or women 18 to 55 years of age
- BMI between 18 and 32 kg/m2
- Negative serum pregnancy test
- Use of highly effective birth control method(s) for a minimum of 60 days prior to consent and is willing to continue use for at least 12 months, or abstinence
- In good general health as determined by medical history, exams and tests
Exclusion Criteria:
- Acute illness or fever (≥100.4°F) within 7 days prior to dosing
- Any history of receiving treatment, vaccine, or monoclonal antibodies (mAbs) against smallpox, monkeypox, or other orthopox viruses.
- Receipt of any vaccine within 30 days prior to Screening, planned receipt of any vaccine prior to Day 1, or planned receipt of any vaccines before 45 days post-injection.
- Any medical condition for which IM injections would be contraindicated in the opinion of the investigator (eg, bleeding disorders, anticoagulant therapy, and severe thrombocytopenia)
- History of congenital or acquired immunodeficiency syndrome, , including positive human immunodeficiency virus (HIV-1/-2) antibody result
- Prior solid organ or bone marrow transplant
Clinically significant corneal or lens abnormality as determined by history, clinical examination, or diagnostic imaging. Including, but not limited to:
- Corrected vision of less (worse) than 20/40
- History of any clinically significant history of eye trauma, in the opinion of the investigator
- History of cataracts or current cataracts
- Lens opacity greater than NC2, C2, or P0 as determined by the Lens Opacities Classification System (LOCS) III
- History of uveitis (including acute)
- Use of ocular or inhaled prescription steroids within 1 year prior to Screening nasal steroids are permissible). A single short course (ie, less than 14 days) of systemic steroid therapy is allowed provided it is concluded more than 6 months prior to Screening.
- History of diabetes
- Use of immunosuppressive agents, anticoagulants, or antiarrhythmics within 1 year prior to Screening. Nasal steroid use is permissible.
- Upper arms and thighs are with insufficient muscular tissue for IM injections or is obscured by tattoos or rash
Use of any medications started within 30 days prior to Day -1, including prescription medications, nutritional supplements, and over-the-counter medications
- Vitamin supplements are allowed
- Recommended doses of acetaminophen are allowed, except for 24 hours prior to dosing
- Recommended doses of non-steroidal anti-inflammatory drugs (NSAIDs) (eg, aspirin, ibuprofen) are also allowed, except for 7 days prior to dosing
- Positive hepatitis B surface antigen, hepatitis B core antigen, or hepatitis C antibody
- Positive urine drug test or cotinine (indicating active current smoking) at Screening or Day -1, positive alcohol breath test at Screening or on Day -1, or suspected/known drug abuse and/or alcohol use disorder
- Smoking or has used nicotine or nicotine-containing products (eg, snuff, nicotine patch, nicotine chewing gum, mock cigarettes, or inhalers) within 3 months before study drug dosing
- Dosing in any clinical research study evaluating another investigational drug or therapy within 30 days or at least 5 half-lives (whichever is longer) of receiving the investigational drug prior to Screening
- Progressive, unstable, or uncontrolled medical conditions that have required medical attention or changes to medication for medical reasons within 90 days prior to consent
- History of allergic reactions or hypersensitivity reactions to other therapeutic antibodies or immunoglobulins
- Receipt of any mAbs in the 12 months prior to Screening
- High blood pressure
- Women who are either pregnant or breast-feeding
- Vulnerable individuals (eg, military recruits, persons in compulsory detention, those with limited legal capacity)
- Receipt of immunoglobulins or any blood products within 90 days prior to consent or planned receipt during the study period
- Donation or loss of >500 mL of blood within 30 days or plasma within 7 days of Day 1; any planned donation of blood or plasma during the study period
- History of any malignant neoplasm within the last 5 years, with the exception of adequately treated localized or in situ non-melanoma carcinoma of the skin or the cervix
- Strenuous activity or contact sports within 48 hours before study drug dosing and through Day 8
26. History of relevant drug and/or food allergies
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:防止
- 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
アーム数
武器と介入
参加者グループ / アーム参加者グループ / アーム |
介入・治療介入・治療 |
|---|---|
|
アクティブコンパレータ:JST-018 Investigational Product
|
Monoclonal antibodies
|
|
プラセボコンパレーター:JST-017 Placebo
|
プラセボコンパレーター
|
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety and tolerability of of JST-018 administered intramuscularly (IM)
時間枠:From injection to Day 7
|
Incidence of solicited local (injection site) and systemic AEs post-injection through Day 7 (with the inpatient and outpatient participant diaries being collected on Day 3 and Day 8, respectively)
|
From injection to Day 7
|
|
Safety and tolerability of of JST-018 administered IM
時間枠:From injection to final visit at Week 48
|
Incidence of unsolicited AEs through end of study (EOS)
|
From injection to final visit at Week 48
|
|
Safety and tolerability of of JST-018 administered IM
時間枠:From injection to final visit at Week 48
|
Incidence of SAEs, medically attended AEs (MAAEs), and AEs of special interest (AESIs)
|
From injection to final visit at Week 48
|
|
Safety and tolerability of of JST-018 administered IM
時間枠:From injection to final visit at Week 48
|
Incidence of Clinically Significant Changes in Laboratory Values
|
From injection to final visit at Week 48
|
|
Safety and tolerability of JST-018 administered as IM
時間枠:From injection to final visit at Week 48
|
Incidence of Clinically Significant Changes in Vital Sign Measurements
|
From injection to final visit at Week 48
|
|
Safety and tolerability of JST-018 administered as IM
時間枠:From injection to final visit at Week 48
|
Incidence of Clinically Significant Changes in ECG results
|
From injection to final visit at Week 48
|
二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Pharmacokinetic Cmax of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Maximum observed concentration (Cmax)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic Tmax of JST-018
時間枠:Time Frame: From enrollment to the end of study at 48 weeks
|
Time to reach maximum observed concentration (Tmax)
|
Time Frame: From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic Tlast of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
The timepoint with the last quantifiable concentration (Tlast)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic AUC0-t of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Area under the concentration versus time curve (AUC) from time 0 to the timepoint with the last quantifiable concentration (AUC0-t)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic AUC0-inf of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
AUC from time 0 extrapolated to infinity (AUC0-inf)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic t1/2 of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Terminal elimination half-life (t1/2)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic CL/F of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Apparent clearance after IM administration (CL/F)
|
From enrollment to the end of study at 48 weeks
|
|
Pharmacokinetic Vz/F of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Apparent volume of distribution after IM administration (Vz/F)
|
From enrollment to the end of study at 48 weeks
|
|
Evaluation the effect of anti-drug antibodies (ADA)
時間枠:From enrollment to the end of study at 48 weeks
|
Effect of ADAs on pharmacokinetics of JST-018
|
From enrollment to the end of study at 48 weeks
|
|
Evaluate if and to what extent ADAs develop following a single dose of JST-018
時間枠:From enrollment to the end of study at 48 weeks
|
Proportion of participants with pre-existing ADAs and those who develop ADAs (treatment boosted and treatment induced) to JST-018
|
From enrollment to the end of study at 48 weeks
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
研究開始
一次修了 (推定)
一次修了
研究の完了 (推定)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (実際)
最初の投稿
学習記録の更新
投稿された最後の更新 (実際)
投稿された最後の更新
QC基準を満たした最後の更新が送信されました
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
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
その他の研究ID番号
- DDF4-CL101
- MCDC No. W15QKN-16-9-1002 (その他の識別子:US Department of War)
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?
IPD プランの説明
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
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