A Phase 1/2A, Randomized, Double-Blind Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of HT31-1 (hCitH3-mAb) in Healthy Volunteers and in Patients With Mild-to-Moderate ARDS: Part A (Healthy Volunteers)
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 24
- 试验地点
- 2
- 主要终点
- Incidence of Adverse Events (AEs) and Serious Adverse Events (SAEs)
研究概览
简要总结
This Phase 1/2A, randomized, double-blind study will evaluate the safety, tolerability, and pharmacokinetics (PK) of HT31-1 (hCitH3-mAb) in healthy adult volunteers and in patients with mild-to-moderate acute respiratory distress syndrome (ARDS) due to an infectious source.
The current trial (Part A) focuses on single ascending doses (SAD) in healthy volunteers to characterize the safety profile, PK parameters, and immunogenicity of HT31-1. Emerging data from this phase will inform dose selection for the subsequent Part B study in ARDS patients and help establish the recommended Phase 2 dose (RP2D). Additionally, exploratory pharmacodynamic and biomarker assessments will be performed to evaluate target engagement and potential early biological activity.
详细描述
HT31-1 injection is a first-in-class humanized monoclonal antibody that neutralizes citrullinated histone H3 (CitH3), a critical damage-associated molecular pattern (DAMP) driving neutrophil extracellular trap (NETosis-induced endothelial injury, microvascular thrombosis, and hyper-inflammation in sepsis and ARDS. HT31-1 addresses the underlying pathophysiology of sepsis/ARDS without impacting the innate immune defense function, thus provide a potentially safe and effective means to treat ARDS.
Design: Randomized, double-blind, placebo-controlled, single ascending dose (SAD) study.
Cohort size: 8 participants per cohort (6 assigned to HT31-1 and 2 assigned to placebo).
Randomization: 3:1 ratio (HT31-1: placebo). Blinding: HT31-1 and placebo will be provided as identical, indistinguishable investigational products supplied by the Investigational Pharmacy. Both participants and all study site personnel (including investigators, study staff, and safety assessors) will remain blinded to treatment allocation. Randomization codes will be maintained by an independent statistician or designated unblinded party and will not be disclosed until database lock unless required for subject safety.
Population: Approximately 24 healthy adult volunteers.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Sequential
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
入排标准
- 年龄范围
- 18 Years 至 65 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Participants must meet all of the following criteria:
- •Age 18 to 65 years old, inclusive, at the time of consent.
- •Able and willing to provide written informed consent and to comply with all study procedures and requirements.
- •Healthy as determined by medical history, physical examination, and baseline investigations. No clinically significant abnormalities on physical exam.
- •Body Mass Index (BMI) between 18.0 and 32.0 kg/m², inclusive.
- •Vital signs and 12-lead ECG without clinically significant abnormalities, in the investigator's judgment, at screening (e.g., resting blood pressure and heart rate within normal limits).
- •Screening clinical laboratory tests (hematology, chemistry, liver and kidney function, etc.) within normal ranges or not clinically significant as judged by the investigator.
- •Female volunteers must be of non-childbearing potential (either surgically sterile by tubal ligation, bilateral oophorectomy or hysterectomy at least 6 months prior, or postmenopausal for ≥1 year) OR if of childbearing potential must agree to use 2 approved effective contraceptions from screening through at least 90 days after the last dose. Acceptable methods include hormonal contraception, intrauterine device, or barrier methods with spermicide.
- •Male volunteers with partners of childbearing potential must agree to use 2 approved effective contraception (e.g., condom plus spermicide) from screening through 90 days after their dose of study drug.
- •Able to communicate well with the investigator and comply with study requirements (e.g., availability for all follow-up visits).
排除标准
- •Participants will be excluded if they meet any of the following criteria:
- •History of any severe allergy or hypersensitivity to drugs, or known hypersensitivity to any monoclonal antibody (including prior biologic therapy reactions).
- •Known autoimmune disease or immunodeficiency condition, including a positive test for HIV at screening.
- •Active or chronic viral hepatitis infection: positive screening test for hepatitis B surface antigen (HBsAg) or hepatitis C antibody.
- •History of tetanus infection, or receipt of tetanus toxoid vaccine within 6 months prior to first dose of study drug. (Rationale: CitH3 is associated with NETs, and recent tetanus immunization may confound immune status or antibody responses).
- •Receipt of any live attenuated vaccine within 4 weeks prior to first dose, or any inactivated vaccine within 2 weeks prior to first dose. (This is to avoid confounding immune activation or risk to the volunteer's health).
- •History of any significant acute or chronic illness that, in the investigator's opinion, could interfere with the trial or pose additional risk in administering the investigational drug. Examples include significant cardiovascular, hepatic, renal, gastrointestinal, hematologic, neurologic, psychiatric, or respiratory conditions that are not well-controlled.
- •Recent major surgery (within 3 months prior to screening) or planned elective surgery during the study period. (Minor outpatient procedures are allowed at the investigator's discretion.)
- •Difficulty with venous access or an inability to tolerate blood draws, such that required PK sampling would be compromised.
- •History of drug or alcohol abuse: positive urine drug screen at screening for illicit substances, or a history of significant drug abuse in the past 5 years. Regular use of cannabis is also exclusionary unless stopped prior to study.
- •Positive screening alcohol breath test, or history of excessive alcohol intake (more than ~14 units per week; 1 unit = 360 mL beer, 150 mL wine, or 45 mL of 40% spirit) within 6 months. Any indication of alcoholism or inability to refrain from alcohol during study participation.
- •Use of any prescription or over-the-counter medications, herbal remedies, or supplements within 14 days prior to first dose, except hormonal contraceptives or occasional acetaminophen. (Any necessary medications may be reviewed by the investigator for approval if unlikely to interfere with study outcomes).
- •Participation in another clinical trial of an investigational drug or device within 4 weeks (or 5 half-lives of that investigational product, whichever is longer) prior to dosing.
- •Donation of >400 mL of blood (or significant blood loss of similar volume) within 3 months prior to screening, or donation of >200 mL within 1 month prior. (This is to avoid anemia or confounding volume loss).
- •Receipt of any blood products or immunoglobulin therapy within 90 days before dosing.
- •Chronic use of immunosuppressive medications (systemic corticosteroids, immunomodulators) within 45 days before dosing (inhaled/topical steroids for mild conditions may be permitted).
- •Regular use of nicotine products (smoking more than 5 cigarettes per day or equivalent) within 3 months prior to screening, or inability to refrain from tobacco/nicotine during the study.
- •Pregnant or breastfeeding women. (Female volunteers must have a negative pregnancy test and not be nursing.)
- •Any other condition that, in the opinion of the investigator, makes the volunteer unsuitable for study participation (e.g. inability to comply with protocol, or any factor that would jeopardize the volunteer's safety or the validity of the data).
研究组 & 干预措施
Cohort 1: 1 mg/kg
HT31-1 1mg/kg single intravenous dosing
干预措施: HT31-1 (Drug)
Cohort 2: Placebo
Saline single intravenous dosing
干预措施: Saline (0.9%, sterile, for infusion) (Other)
Cohort 3: Placebo
Saline single intravenous dosing
干预措施: Saline (0.9%, sterile, for infusion) (Other)
Cohort 3: 20 mg/kg
HT31-1 20mg/kg single intravenous dosing
干预措施: HT31-1 (Drug)
Cohort 1: Placebo
Saline single intravenous dosing
干预措施: Saline (0.9%, sterile, for infusion) (Other)
Cohort 2: 5 mg/kg
HT31-1 5mg/kg single intravenous dosing
干预措施: HT31-1 (Drug)
结局指标
主要结局
Incidence of Adverse Events (AEs) and Serious Adverse Events (SAEs)
时间窗: 0-28 days
The number and percentage of participants experiencing treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) following administration of HT31-1.
Assess dose-limiting toxicities (DLTs)
时间窗: 0-28 days
Number and percentage of participants experiencing DLTs at each dose level.
次要结局
- Clearance (CL)(From pre-dose through Day 28 post-dose)
- Volume of distribution (Vd)(From pre-dose through Day 28 post-dose)
- Maximum observed concentration (Cmax)(From pre-dose through Day 28 post-dose)
- Time to maximum concentration (Tmax)(From pre-dose through Day 28 post-dose)
- Area under the curve (AUC)(From pre-dose through Day 28 post-dose)
- Half-life (t1/2)(From pre-dose through Day 28 post-dose)
- Assess preliminary pharmacodynamic (PD) effects(From pre-dose through Day 28 post-dose)