jRCT2051240208招募中不适用
Efficacy, Safety, and Pharmacokinetics of Orforglipron Once Daily Oral Versus Placebo in Adolescent Participants Who Have Obesity, or Overweight With Weight-Related Comorbidities: A Randomized, Double-Blind Trial (ADVANCE-ATTAIN-ADOLESCENTS) (J4M-MC-PW01)
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 125
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Double Blind
入排标准
- 年龄范围
- 12age old over 至 17age old under(—)
- 性别
- All
入选标准
- •J4M-MC-PWMP
- •Have a history of at least 1 unsuccessful effort to lose sufficient body weight after participation in a structured lifestyle modification program (diet and exercise counseling for at least 3 months) prior to screening.
- •Obesity as defined by BMI equal to or above the 95th percentile for age and sex (on age- and gender-specific growth chart [CDC-NCHS, 2022]); OR
- •Overweight as defined by BMI equal to or above the 85th percentile but less than the 95th percentile for age and sex, on age- and sex-specific growth chart (CDC-NCHS, 2022), and at least 1 weight-related comorbidity,
- •hypertension
- •type 2 diabetes (T2D)
- •prediabetes
- •dyslipidemia
- •obstructive sleep apnea
- •metabolic dysfunction-associated steatohepatitis (MASH) or metabolic dysfunction-associated steatotic liver disease (MASLD)
排除标准
- •J4M-MC-PW01
- •Prepubertal (Tanner stage 1)
- •Have a self-reported, or by parent or legal guardian where applicable, decrease in body weight greater than 5 kilograms (kg) (11 pounds) within 90 days before screening
- •J4M-MC-PWMP
- •Have undergone or plan to undergo weight reduction procedure during the study, such as, but not limited to:
- •gastric bypass
- •sleeve gastrectomy
- •restrictive bariatric surgery, such as Lap-BandR gastric banding, or
- •any other procedure intended to result in weight reduction.
- •Have a diagnosis that is a secondary cause of obesity or have a history of abrupt onset of obesity suggesting a secondary cause, such as hypothalamic, monogenetic, syndromic, or endocrine causes.
- •Have type 1 diabetes or history of ketoacidosis, or hyperosmolar state.
- •Have HbA1c >9.0% (75 mmol/mol) as measured by central laboratory at screening.
- •Have a family or personal history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia Syndrome Type 2.
结局指标
主要结局
-
Percent Change from Baseline in Body Mass Index (BMI) [ Time Frame: Baseline, Week 72
次要结局
未报告次要终点
研究者
相似试验
尚未招募
不适用
A Study of Orforglipron (LY3502970) in Participants With Obesity or Overweight and Type 2 Diabetes
(J2A-MC-GZP2)jRCT2051250035Eli Lilly Japan K.K.600
尚未招募
不适用
A Study of Orforglipron (LY3502970) in Participants With Obesity or Overweight and at Least One Weight-Related Comorbidity
(J2A-MC-GZP1)jRCT2051250032Eli Lilly Japan K.K.600
招募中
2 期
efficacy evaluation of livergol in children with attention deficit hyperactivity disorderattention deficit hyperactivity disorder.Attention-deficit hyperactivity disordersIRCT20160813029327N22Islamic Azad University40
已完成
3 期
A Study of Daily Oral Orforglipron (LY3502970) Compared With Insulin Glargine in Participants With Type 2 Diabetes and Obesity or Overweight at Increased Cardiovascular RiskOverweight or ObesityOverweightCardiovascular DiseasesType 2 DiabetesChronic Kidney DiseaseObesityNCT05803421Eli Lilly and Company2,749
进行中(未招募)
3 期
A Study of Orforglipron (LY3502970) in Adult Participants With Obesity or Overweight With Weight-Related ComorbiditiesOverweightOverweight or ObesityObesityNCT05869903Eli Lilly and Company3,127
