Recruiting PHASE1 Healthy Subjects

Tests treatment safety and results for Healthy Subjects

Official title A Study to Evaluate the Safety, Tolerability, PK/PD of HEC-007 Injection in Healthy and Overweight/Obese Subjects

ClinicalTrials.gov ID: NCT07102251

What this study is testing

What is HEC-007 injection?

HEC-007 injection is an investigational medicine, given as an injectable medicine, being studied as a potential treatment for healthy subjects.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
This trial adopts a single-center, randomized, double-blind, placebo-controlled, dose-escalation design to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of HEC-007 Injection after single-dose administration in healthy subjects and multiple-dose administration in overweight or obese subjects. The trial consists of two parts: Part A is a single ascending dose (SAD) study, planning to enroll 54 Chinese healthy subjects; Part B is a multiple ascending dose (MAD) study, planning to enroll 72 Chinese overweight or obese subjects.
  • Phase 1: an early, usually small safety study
  • You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance. You may not know which one you got.

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 to 65. Healthy volunteers may be eligible.

You may be able to join if

  • people understand and comply with the study procedures, voluntarily participate, and sign the informed consent form.
  • Healthy adult people (including borderline values) aged 18 to 45 years, regardless of sex.
  • Male people weigh no less than 50 kg, and female people weigh no less than 45 kg. BMI =Body weight (kg)/height2 (m2), with a body mass index ranging...
  • Normal results or abnormalities deemed clinically insignificant by the investigator in vital signs, physical examination, laboratory tests...
  • Female people of childbearing potential or male people must agree to use effective contraception from signing the informed consent until 6 months...

You likely can't join if

  • Those diagnosed with type 1, type 2, or other types of diabetes before screening;
  • History or family history of medullary thyroid carcinoma (MTC), thyroid C-cell hyperplasia, or multiple endocrine neoplasia syndrome type 2 (MEN2)...
  • Acute, chronic, or suspected pancreatitis during screening, or prior pancreatectomy;
  • Those diagnosed with any malignancy within 5 years before screening (except for basal cell carcinoma treated curatively and considered cured);
  • Presence of clinically significant diseases (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine...
  • Diseases or conditions affecting gastric emptying or gastrointestinal nutrient absorption during screening;
See the full eligibility criteria
Who can join
  • people understand and comply with the study procedures, voluntarily participate, and sign the informed consent form.
  • Healthy adult people (including borderline values) aged 18 to 45 years, regardless of sex.
  • Male people weigh no less than 50 kg, and female people weigh no less than 45 kg. BMI =Body weight (kg)/height2 (m2), with a body mass index ranging from 19.0 to 35.0 kg/m2 (including boundary values).
  • Normal results or abnormalities deemed clinically insignificant by the investigator in vital signs, physical examination, laboratory tests, electrocardiogram, chest CT, abdominal ultrasound (liver, gallbladder, spleen...
  • Female people of childbearing potential or male people must agree to use effective contraception from signing the informed consent until 6 months after the last administration of the investigational product to avoid...
  • Glycated hemoglobin (HbA1c) \<5.7% during the screening period. MAD 1\. people understand and comply with the study procedures, voluntarily participate, and sign the informed consent form. 2\. Age between 18 to 65 years...
What rules you out
  • Those diagnosed with type 1, type 2, or other types of diabetes before screening;
  • History or family history of medullary thyroid carcinoma (MTC), thyroid C-cell hyperplasia, or multiple endocrine neoplasia syndrome type 2 (MEN2) during screening, or genetic predisposition to MTC;
  • Acute, chronic, or suspected pancreatitis during screening, or prior pancreatectomy;
  • Those diagnosed with any malignancy within 5 years before screening (except for basal cell carcinoma treated curatively and considered cured);
  • Presence of clinically significant diseases (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine, oncological, pulmonary, immunological, psychiatric, or cardiovascular...
  • Diseases or conditions affecting gastric emptying or gastrointestinal nutrient absorption during screening;
  • Major surgery within 3 months before screening or planned surgery during the study;
  • History of hypersensitivity to the investigational product or any of its components, or allergic constitution (allergy to two or more drugs or foods).
  • Use of medications (including prescription drugs, over-the-counter drugs, herbal medicines, health supplements, etc.) within 3 months prior to screening that, in the investigator's judgment, significantly affect weight...
  • Individuals who have undergone bariatric surgery prior to screening;
  • Those with a history of recurrent skin disorders (e.g., urticaria) or skin lesions at the administration site;
  • Those who received chronic (lasting more than 2 weeks) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled formulations) within 3 months prior to screening, or...
  • Female people with HbA1c \<110 g/L or male people with HbA1c \<120 g/L at screening, or any other known condition that interferes with HbA1c measurement;
  • Those with suicidal behaviors or ideation within 6 months prior to screening;
  • Use of GLP-1R, GLP-1R/GIPR, GLP-1R/GCGR, or GLP-1R/GIPR/GCGR agonists within 6 months prior to screening;
  • Those with regular alcohol consumption within 3 months prior to screening, defined as more than 14 units of alcohol per week (1 unit = 360 mL beer, 45 mL spirits with 40% alcohol, or 150 mL wine); or those with a...
  • Those with a history of drug abuse or illicit drug use within 2 years prior to screening, or those with a positive urine drug screen before administration;
  • Smoking more than 5 cigarettes per day within 3 months prior to screening or inability to abstain from smoking during intensive PK blood sampling;
  • Those with a history of needle or blood phobia, intolerance to venipuncture, or difficulty in blood collection;
  • Those with positive results for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody, or Treponema pallidum-specific antibody;
  • Alanine aminotransferase \>1.5 × upper limit of normal (ULN), aspartate aminotransferase \>1.5 × ULN, alkaline phosphatase \>1.5 × ULN, or total bilirubin \>1.5 × ULN at screening;
  • Those with blood amylase or lipase \> ULN at screening;
  • Those with serum calcitonin ≥20 ng/L at screening;
  • Those with fasting blood glucose ≥6.1 mmol/L or \<3.9 mmol/L at screening;
  • Those with glomerular filtration rate (GFR) \<90 mL/min/1.73m2 at screening;
  • Fridericia-corrected QT interval (QTcF=QT/RR0.33) \>450 ms (for male) or \>470 ms (for female) on 12-lead ECG at screening;
  • Use of strong inhibitors or inducers of hepatic metabolic enzymes (CYP1A2, 2A6, 2C8, 2C19, 3A4, and 3A5) within 4 weeks prior to the first dose, including strong inhibitors such as ciprofloxacin, clopidogrel...
  • Use of any prescription drugs, over-the-counter medications, vitamin products, or Chinese herbal medicines within 2 weeks prior to the first dose;
  • Consumption of any foods or beverages affecting CYP3A4, CYP2E1, or CYP2D6 metabolic enzymes, such as grapefruit or grapefruit-containing beverages, within 48 hours prior to the first dose;
  • Ingestion of chocolate, any caffeine-containing or xanthine-rich food or beverage within 48 hours prior to the first dose;
  • Blood donation ≥200 mL, any component blood donation, or total blood loss ≥200 mL due to any reason within 3 months prior to screening, or a history of blood transfusion or blood product use;
  • Participation in other clinical trials within 3 months prior to screening (people who withdrew from the study before treatment, i.e., were not assigned by chance or did not receive treatment, may be enrolled in this...
  • Occurrence of acute illness or concomitant medication use from the signing of the informed consent form until the first dose;
  • Female people who are currently breastfeeding or have a positive pregnancy test result at screening;
  • people deemed by the investigator to have other factors unsuitable for participation in this trial. MAD
  • Those diagnosed with type 1, type 2, or other types of diabetes before screening;
  • Those diagnosed with overweight or obesity caused by other diseases or medications, such as Cushing's syndrome;
  • History or family history of medullary thyroid carcinoma (MTC), thyroid C-cell hyperplasia, or multiple endocrine neoplasia syndrome type 2 (MEN2) during screening, or genetic predisposition to MTC;
  • Acute, chronic, or suspected pancreatitis during screening, or prior pancreatectomy;
  • Those diagnosed with any malignancy within 5 years before screening (except for basal cell carcinoma treated curatively and considered cured);
  • Presence of clinically significant diseases at screening, including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine, oncological, pulmonary, immunological, psychiatric, or...
  • Any of the following diseases or medical histories within 6 months prior to screening or before randomization: cardiac insufficiency (New York Heart Association [NYHA] Class III or IV), myocardial infarction, unstable...
  • Diseases or conditions affecting gastric emptying or gastrointestinal nutrient absorption during screening;
  • Major surgery within 3 months before screening or planned surgery during the study;
  • History of hypersensitivity to the investigational product or any of its components, or to acetaminophen and its excipients, or allergic constitution (allergy to two or more drugs or foods);
  • Use of medications (including prescription drugs, over-the-counter medications, Chinese herbal medicines, health supplements, etc.) within 3 months prior to screening that, in the investigator's judgment, significantly...
  • people taking lipid-lowering or antihypertensive medications with unstable doses within 30 days prior to screening;
  • Individuals who have undergone bariatric surgery prior to screening;
  • Those with a history of recurrent skin disorders (e.g., urticaria) or skin lesions at the administration site;
  • Those who received chronic (lasting more than 2 weeks) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled formulations) within 3 months prior to screening, or...
  • Female people with HbA1c \<110 g/L or male people with HbA1c \<120 g/L at screening, or any other known condition that interferes with HbA1c measurement;
  • Those with suicidal behaviors or ideation within 6 months prior to screening;
  • History of depression or other psychiatric disorders within 6 months prior to screening;
  • Use of GLP-1R, GLP-1R/GIPR, GLP-1R/GCGR, or GLP-1R/GIPR/GCGR agonists within 6 months prior to screening;
  • Those with regular alcohol consumption within 3 months prior to screening, defined as more than 14 units of alcohol per week (1 unit = 360 mL beer, 45 mL spirits with 40% alcohol, or 150 mL wine); or those with a...
  • Those with a history of drug abuse or illicit drug use within 2 years prior to screening, or those with a positive urine drug screen before the first dose;
  • Smoking more than 5 cigarettes per day within 3 months prior to screening or inability to abstain from smoking during intensive PK blood sampling;
  • Those with a history of needle or blood phobia, intolerance to venipuncture, or difficulty in blood collection;
  • Resting seated blood pressure at screening: systolic blood pressure \>160 mmHg or \ 100 mmHg or \<55 mmHg;
  • Heart rate at screening \>100 beats per minute or \<50 beats per minute;
  • Those with positive results for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody, or Treponema pallidum-specific antibody;
  • Alanine aminotransferase \>2 × ULN, aspartate aminotransferase \>2 × ULN, alkaline phosphatase \>1.5 × ULN, or total bilirubin \>1.5 × ULN at screening;
  • Blood amylase or lipase \> ULN at screening;
  • Those with serum calcitonin ≥20 ng/L at screening;
  • Fasting triglyceride levels ≥5.6 mmol/L at screening;
  • Fasting blood glucose ≥7.0 mmol/L or \<3.9 mmol/L at screening; or OGTT 2-hour ≥11.1 mmol/L;
  • Those with glomerular filtration rate (GFR) \<90 mL/min/1.73m2 at screening;
  • Fridericia-corrected QT interval (QTcF=QT/RR0.33) \>450 ms (for male) or \>470 ms (for female) on 12-lead ECG at screening; or severe arrhythmia (second-degree or higher atrioventricular block, ventricular tachycardia...
  • Use of strong inhibitors or inducers of hepatic metabolic enzymes (CYP1A2, 2A6, 2C8, 2C19, 3A4, and 3A5) within 4 weeks prior to the first dose, including strong inhibitors such as ciprofloxacin, clopidogrel...
  • Consumption of any foods or beverages affecting CYP3A4, CYP2E1, or CYP2D6 metabolic enzymes, such as grapefruit or grapefruit-containing beverages, within 48 hours prior to the first dose;
  • Ingestion of chocolate, any caffeine-containing or xanthine-rich food or beverage within 48 hours prior to the first dose;
  • Blood donation ≥200 mL, any component blood donation, or total blood loss ≥200 mL due to any reason within 3 months prior to screening, or a history of blood transfusion or blood product use;
  • Participation in other clinical trials within 3 months prior to screening (people who withdrew from the study before treatment, i.e., were not assigned by chance or did not receive treatment, may be enrolled in this...
  • Occurrence of acute illness or concomitant medication use from the signing of the informed consent form until the first dose;
  • Female people who are currently breastfeeding or have a positive pregnancy test result at screening;
  • people deemed by the investigator to have other factors unsuitable for participation in this trial.

The study team makes the final eligibility decision.

Where it's taking place

  • Hefei, Anhui, China

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years to 65 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Hefei, Anhui, China. Enter your location above to see the nearest site and check your eligibility.

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BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.