NCT07280936RecruitingPhase 1
A Randomized, Double-blind, Placebo-controlled, Dose-escalation Phase I Study on the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SHR-2906 Injection in Healthy Subjects With a Single Dose and in Obese Patients With Multiple Doses
Beijing Suncadia Pharmaceuticals Co., Ltd1 site in 1 country124 target enrollmentStarted: January 5, 2026Last updated:
Conditions
Interventions
Drugs
Trial Snapshot
- Phase
- Phase 1
- Status
- Recruiting
- Sponsor
- Enrollment
- 124
- Locations
- 1
- Primary Endpoint
- Incidence of adverse events (AEs).
Study Overview
Brief Summary
This study is a randomized, double-blind, placebo-controlled, dose-escalation phase I clinical trial. This study consists of two parts: the single-dose escalation study (SAD) in healthy subjects and the multiple-dose escalation study (MAD) in obese patients.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to 55 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Voluntarily sign the informed consent form prior to any study-related activities, understand the procedures and methods of the study, and agree to complete this study in strict accordance with the clinical study protocol;
- •Males or females aged 18-55 years (inclusive);
- •Subjects who are generally healthy as judged by the investigator based on medical history, vital signs, physical examination, laboratory tests, and electrocardiogram (ECG);
- •At screening, 19.0 ≤ BMI ≤ 23.9 kg/m2 (inclusive) for Part I or 28.0 ≤ BMI ≤ 35.0 kg/m2 (inclusive) for Part II.
Exclusion Criteria
- •During screening, electrocardiogram (ECG) indicated that QTcF>450 ms in males and QTcF> 470 ms in females, as well as other abnormal ECG and vital signs that were judged by the researchers to have clinical significance;
- •There are endocrine diseases or medical histories that may significantly affect body weight during screening (such as Cushing's syndrome, diabetes, hypothyroidism or hyperthyroidism, etc.);
- •There is a history or family history of medullary thyroid carcinoma, multiple endocrine adenomatosis type 2, or a history of pancreatitis or symptomatic gallbladder disease;
- •Other clinical findings within 12 months prior to screening that show clinical significance in the following diseases (including but not limited to gastrointestinal, kidney, liver, nervous, blood, endocrine, tumor, lung, immune, mental or cardiovascular and cerebrovascular diseases);
- •Use of prescription drugs (excluding topical eye/nasal drops and creams without systemic exposure risk), over-the-counter drugs, food supplements, vitamins and Chinese herbal medicines (excluding conventional vitamins) within two weeks prior to screening;
- •Having undergone gastrointestinal surgery that may cause malabsorption before screening, or having taken drugs that directly affect gastrointestinal peristalsis for a long time. For example: having undergone bariatric surgery or procedures (such as gastric banding), or having used weight-reducing drugs (including but not limited to orlistat) within 3 months before administration, or having a weight change of more than 10% within 3 months before administration;
- •Those who have a history of drug abuse in the past five years or have used drugs in the three months prior to the trial; Or the urine drug screening is positive;
- •Blood donation of ≥200 mL within one month prior to screening; Or those who have donated ≥400 mL of blood or lost ≥400 mL of blood within 3 months prior to screening due to trauma or major surgical operations;
- •Inability to tolerate venipuncture for blood collection or fainting at the sight of needles and blood;
- •There are special dietary requirements and they cannot follow the uniform diet;
- •Subjects who the researchers consider to have other factors that make them unsuitable for participating in this trial.
Arms & Interventions
SHR-2906 Injection Group
Experimental
Intervention: SHR-2906 Injection (Drug)
SHR-2906 Injection Placebo Group
Placebo Comparator
Intervention: SHR-2906 Injection Placebo (Drug)
Outcomes
Primary Outcomes
Incidence of adverse events (AEs).
Time Frame: Part1: 57 days; Part2: 113 days.
Incidence of serious adverse events (SAEs).
Time Frame: Part1: 57 days; Part2: 113 days.
Secondary Outcomes
- Area under the concentration-time curve from time zero to the end of the dosing interval tau (AUC0-tau).(Part1: 57 days; Part2: 113 days.)
- Maximum concentration (Cmax).(Part1: 57 days; Part2: 113 days.)
- Time of maximum concentration (Tmax).(Part1: 57 days; Part2: 113 days.)
- Area under the concentration-time curve from time zero to the time of the last quantifiable concentration (AUC0-last).(Part1: 57 days; Part2: 113 days.)
- Area under the concentration-time curve from time zero to infinity (AUC0-inf).(Part1: 57 days; Part2: 113 days.)
- Apparent clearance (CL/F).(Part1: 57 days; Part2: 113 days.)
- Apparent volume of distribution (Vz/F).(Part1: 57 days; Part2: 113 days.)
- Elimination half-life (t1/2).(Part1: 57 days; Part2: 113 days.)
Investigators
Study Sites (1)
Loading locations...
Similar Trials
Recruiting
Phase 1
A Study to Evaluate the Safety, Tolerability and PK of SK-09FSGSNCT07267026Consun Pharmaceutical Group84
Recruiting
Phase 1
TCR-engineered T Cells (NW-101C) in Patients With Solid Malignant TumorsNCT07266298Neowise Biotechnology24
Recruiting
Phase 2
Topical Ketotifen 0.25% for Secondary VestibulodyniaNCT07257029Center for Vulvovaginal Disorders54
Not yet recruiting
Phase 3
A Phase III Study to Evaluate the Efficacy and Safety of MDR-001 in Adult Participants With Overweight or Obesity (MOBILE）NCT07274137MindRank AI Ltd738
Recruiting
Phase 2
Study Evaluating ISM5411 Administered Orally to Subjects With Active Ulcerative Colitis (BETHESDA)Ulcerative ColitisNCT07265570InSilico Medicine Hong Kong Limited80