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A Phase 2A Clinical Trial to Assess the Safety and Tolerability of ERX1000 in Men and Women for the Treatment of Obesity.

2026年6月18日 更新者:ERX Pharmaceuticals

A Phase 2A, Randomized, Double-Blind, Placebo-Controlled, Clinical Study to Assess Efficacy, Safety and Tolerability of Orally Administered ERX1000 in Subjects With Obesity

The primary objective is to assess the safety and tolerability of oral dose ERX1000 in obese subjects.

研究概览

地位

招聘中

研究类型

介入性

注册 (估计的)

80

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Kentucky
      • Louisville、Kentucky、美国、40213
        • 招聘中
        • Monroe Biomedical Research
        • 首席研究员:
          • Harold Bays, MD
    • North Carolina
      • Monroe、North Carolina、美国、28112
        • 招聘中
        • Monroe Biomedical Research
        • 首席研究员:
          • Awawu Igbinadolor, MD
    • South Carolina
      • North Charleston、South Carolina、美国、29406
        • 招聘中
        • Monroe Biomedical Research
        • 首席研究员:
          • Gregory J Feldman, MD

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Able to comprehend and willing to sign an ICF and to abide by the study requirements.
  2. Male and female subjects ages 18-60 years, inclusive.
  3. BMI >30 to <50 kg/m2
  4. Stable body weight for 3 months (self-reported loss/gain <5%).
  5. Stable diet and/or nutritional lifestyle for 3 months prior to randomization.
  6. If a subject has current diagnosis of prediabetes, the following criteria must be met:

    1. Hemoglobin A1c (HbA1c) ≤6.4%
    2. Fasting glucose ≤125 mg/dL (≤6.94 mmol/L)
    3. No history of ketoacidosis or hyperosmolar coma
  7. Female subjects must not be pregnant or lactating. Nonpregnancy will be confirmed for all females by a urine pregnancy test conducted at Screening and at the Baseline Visit prior to enrollment into the study.

If of childbearing potential, the subject agrees to the use two of the following accepted contraceptive regimens from Screening to the first administration of the study drug, during the study, and for at least 30 days after the last dose of the study drug. Acceptable methods of contraception includes one of the following:

  1. Hormonal contraceptives (birth control pills, injectable/implant/insertable hormonal birth control products, transdermal patch), OR
  2. Intrauterine device (with or without hormones), AND
  3. Agrees to use a barrier method (e.g., male or female condom) during the study and for at least 30 days after the last dose of the study drug.

Exclusion Criteria:

  1. Poorly controlled severe psychiatric disorders (e.g., bipolar disorder, or major depressive disorder), recent (within 6 months) psychotic episodes, history of suicide attempts or suicidal ideation, or any other psychiatric disorders that the Investigator believes will interfere significantly with study compliance.
  2. Lifetime history of DSM-5 diagnosis of schizophrenia or schizoaffective disorder. Diagnosis of bipolar 1 disorder within the previous 2 years.
  3. History of any bleeding disorders, deep vein thrombosis (DVT), or thromboembolic disease.
  4. Current liver, renal, pulmonary, cardiac, oncologic, or gastrointestinal (GI) disease including:

    1. Significant cardiovascular disease including history of congestive heart failure (CHF), coronary artery disease, myocardial infarction (MI), second degree or greater heart block, prolonged time from electrocardiogram Q wave to the end of the T wave corresponding to electrical systole (QT) syndrome, or clinically significant arrhythmias.
    2. Fridericia-corrected QT interval (QTcF) >460 msec for males and QTcF >480 msec for females pre-dose on Day 1.
    3. Liver disease or liver function tests, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) >1.5 upper limit of normal (ULN), alkaline phosphatase (ALP) or serum bilirubin > ULN, or history of underlying liver disease including, hepatic cirrhosis, alcoholic hepatitis, or confirmed diagnosis of NASH; nonalcoholic fatty liver disease with qualifying LFTs will be allowed.
    4. History or presence of impaired renal function as indicated by clinically significant abnormal creatinine, blood urea nitrogen (BUN), or urinary constituents or moderate to severe renal dysfunction as defined by the Chronic Kidney Disease-Epidemiology Collaboration (CKD-EPI) equation (<60 mL/min/1.73m2).
  5. Type 1 diabetes mellitus or Type 2 diabetes mellitus or current or recent use of insulin (more than 1 week within 3 months prior to screening).
  6. Obesity induced by other endocrine disorders (e.g., Prader-Willi syndrome, Cushing's syndrome).
  7. Active autoimmune disease who are currently using or will likely require systemic glucocorticoid therapy in the next 6 months.
  8. Any previous surgical treatment or procedures with medical devices (such as insertion of lap band or gastric balloons) for obesity (excluding liposuction if performed > 1 year prior to screening).
  9. History of stomach or intestinal surgery or resection that would potentially alter absorption and/or excretion of orally administered drugs (uncomplicated appendectomy, cholecystectomy, and hernia repair > 6 months prior to Screening will be allowed).
  10. Uncontrolled endocrine disorders (e.g., Cushing syndrome, Addison's, Hashimoto's, hypothyroidism, hypogonadism).
  11. Clinically significant and abnormal screening hematology lab results or recurring infections, or if any of the following are observed regardless of the Investigator's assessment of clinical significance (laboratory tests may be repeated once for confirmation of out-of-range values):

    1. Hemoglobin <10 g/dL (<100 g/L)
    2. Absolute neutrophil count (ANC) <2000/mm3
    3. Platelets <135 x 109/L
    4. ALT or AST > 1.5 ULN
    5. GGT, ALP, total bilirubin, or INR > ULN
  12. Results of screening clinical laboratory tests (complete blood count [CBC] with differential and platelets, chemistry, and urinalysis profile) and electrocardiogram (ECG) outside normal range and considered to be clinically significant by the Investigator.
  13. Body weight of > 350 pounds (158.8 kilograms) due to weight limits of the DEXA scanner.
  14. Current use, or within the 30 days prior to screening, of the following atypical antipsychotic medications:

    1. Olanzapine
    2. Clozapine
    3. Quetiapine
  15. Subjects on the following systemic concomitant medications who have not been on stable dose (or stable weight-based dose), defined as no more than ±25% variation in dose, for at least 3 months prior to study entry:

    1. Vasopressin
    2. Thyroid hormone
    3. Testosterone
    4. Other hormone or hormone replacement therapies
    5. Anti-diabetes medications other than metformin (e.g., glucagon-like peptide-1 [GLP-1] receptor agonists, sodium-glucose linked transporter 2 (SGLT2) inhibitors, sulfonylureas)
    6. Modafinil
    7. Atypical anti-psychotics, other than those noted above
    8. Anti-depressives
    9. Attention deficit hyperactivity disorder (ADHD) medications
  16. Subjects on any prescription or over-the-counter anti-obesity agents in the 3 months prior to screening (e.g., Saxenda, Wegovy, Zepbound, Xenical, Acutrim, Qsymia, Adipex, compounded peptides).
  17. Chronic (>2 weeks) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled preparations) within 1 month prior to study screening.
  18. Vital signs unstable, or with the following values:

    1. Systolic blood pressure >160 mm Hg
    2. Diastolic blood pressure >100 mm Hg
    3. Pulse rate >100 beats per minute (bpm)
  19. Recent (within the last year) and/or recurrent history of autonomic dysfunction (e.g., unexplained syncope or palpitations).
  20. Current or anticipated chronic use (more than 2 days) of narcotics or opiates.
  21. Significant history of abuse of drugs or solvents in the year before screening, or history of alcohol abuse in the past year before screening or currently drinks in excess of 21 units or servings per week.
  22. Participation in any clinical study with an investigational drug/device within 3 months.
  23. Positive result for human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV) prior to initiation of dosing with study drug.
  24. Serious adverse reaction or hypersensitivity to any drug which the Investigator believes is clinically significant and relevant to study participation.
  25. Significant blood loss or blood donation >500 mL within 3 months.
  26. Females who are pregnant, nursing, or intend to become pregnant during the study.
  27. Subjects who are planning or likely to undergo surgery during the course of the study.
  28. Subject is, in the opinion of the Investigator, not suitable to participate in the study (e.g., clinically significant illness in the 8 weeks before screening; unable to commit to study visits, etc.).

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
有源比较器:Treatment Arm
This arm will receive oral doses of ERX1000.
2mg tablet administered orally twice weekly.
安慰剂比较:Placebo Arm
This arm will receive placebo doses.
2mg Placebo tablet identical in appearance to 2mg ERX1000 tablet

研究衡量的是什么?

主要结果指标

结果测量
大体时间
Change in Body Weight of Participants from Baseline to Weeks 12 and 24
大体时间:From enrollment to the end of treatment at Week 24.
From enrollment to the end of treatment at Week 24.

次要结果测量

结果测量
措施说明
大体时间
Number of subjects with Adverse Safety Parameters
大体时间:From enrollment to the end of study participation at Week 28.
The number of participants with (1) treatment related adverse events; (2) adverse changes in vital signs; (3) adverse changes in 12-lead ECG results; (4) adverse changs in safety laboratory results; (5) adverse changes as observed though physical examinations
From enrollment to the end of study participation at Week 28.
Change in Body Composition in Participants
大体时间:From enrollment to the end of treatment at Week 24.
(1) Change in % body fat by DEXA) from baseline to Weeks 12 and 24; (2) Change in BMI from baseline to Weeks 12 and 24; (3) Change in waist circumference from baseline to Weeks 12 and 24.
From enrollment to the end of treatment at Week 24.
Change in Metabolic Biomarkers
大体时间:From enrollment to the end of treatment at Week 24.
  1. Change in fasting lipid profile from baseline to Weeks 12 and 24: total cholesterol, low density lipoprotein (LDL), high density lipoprotein (HDL), and triglycerides;
  2. Change in plasma biomarkers from baseline to Weeks 12 and 24: leptin, insulin, glucose, and HbA1c
From enrollment to the end of treatment at Week 24.
Relationship Between Peak Drug Exposure and LFT Elevations
大体时间:From enrollment to Week 20.
Number of participants with elevated LFT results concurrent with peak concentration of ERX1000.
From enrollment to Week 20.

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年5月28日

初级完成 (估计的)

2027年5月1日

研究完成 (估计的)

2027年5月1日

研究注册日期

首次提交

2026年4月30日

首先提交符合 QC 标准的

2026年4月30日

首次发布 (实际的)

2026年5月6日

研究记录更新

最后更新发布 (实际的)

2026年6月22日

上次提交的符合 QC 标准的更新

2026年6月18日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • ERX1000-O-100

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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