CBP-0276 to Reduce Opioid Use in Adults Undergoing Major Orthopedic Surgery (CBP0276-Opd)
2026年7月2日 更新者:Clarent Biopharma, Inc.
Proof-of-concept, Double-blind, Randomized Clinical Study to Evaluate the Safety and Efficacy of CBP-0276 at Doses of 600 mg/Day vs Placebo in Reducing Opioid Use in Pain Management in Adult Patients Undergoing Major Orthopedic Surgery
Randomized, double-blind, clinical study to evaluate the safety and efficacy of CBP-0276 at doses of 600 mg/day in reducing opioid use in pain management in adult patients undergoing major orthopedic surgery.
Subjects will be allocated in 2 groups.
One group will receive oxycodone (standard of care) + CBP-0276 at a dose of 600 mg, orally once daily for 28 days.
A second group will receive oxycodone (standard of care) + placebo for CBP-0276, orally once daily for 28 days
研究概览
详细说明
Randomized, Phase 2, Proof-of-concept, double-blind, parallel-group, placebo controlled clinical study to evaluate the safety and efficacy of CBP-0276 at doses of 600 mg/day in reducing opioid use in pain management in adult patients undergoing major orthopedic surgery.
Subjects will be allocated in 2 groups.
One group (n=40) will receive oxycodone (standard of care) + CBP-0276 at a dose of 600 mg, orally once daily for 28 days.
A second group (n=40) will receive oxycodone (standard of care) + placebo for CBP-0276, orally once daily for 28 days.
Primary outcome is the reduction on the number of oxycodone tablets required to controlled the moderate to severe pain management during the 28 days post-major orthopaedic surgery.
Secondary and Exploratory outcomes are: A) Number of days where the use of oxycodone is required; B) Changes in quality of life according to the WHOQOL-BREF score, from baseline and at 28 days post-surgery; C) The number of oxycodone tablets required for pain management at day 15 post-surgical; D) Frequency and intensity of pain at day 28 post-surgery and at 3 months of post-surgical follow-up; E) Changes on inflamatory cytokines between baseline and end of treatment (day 28) Characteristics of the subject to be enrolled included age between 40 and 75y, male or female, BMI 18.5 to 35, under surgery of hip or knee replacement.
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
- 姓名:Pedro Gutiérrez Castrellón, MD, PhD
- 电话号码:+525554198746
- 邮箱:pedro.gutierrez@elemental.org.mx
研究联系人备份
- 姓名:Diana M Andrade Platas, MD
- 电话号码:+525535209755
- 邮箱:diana.andrade@elemental.org.mx
学习地点
-
-
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Mexico City、墨西哥、14340
- 招聘中
- Innovacion y Desarrollo de Estrategias en Salud
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接触:
- Diana M Andrade Platas, MD, MSc
- 电话号码:+525535209755
- 邮箱:diana.andrade@elemental.org.mx
-
接触:
- Tom Jilmer Castillo, MD
- 电话号码:+523324120245
- 邮箱:tom.castillo@idecsa.com.mx
-
首席研究员:
- Miguel Gonzalez Thompson, MD
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-
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
- 年长者
接受健康志愿者
不
描述
Inclusion criteria:
- Men or women
- Age between 40 and 75 years (inclusive)
- Body weight between 50 and 90 Kg
- Post-surgical patient of major orthopedic surgery, with opioid treatment (oxycodone) at discharge by treating physician
- Physical status of ASA I to III
- Be able and willing to read, understand, sign, and date the Informed
- Consent Form prior to entering the study.
- Woman of childbearing age with effective contraception, not pregnant, not on breastfeeding, not pregnancy plans during the development of the study, postmenopausal, defined by cessation of menstruation for at least 12 consecutive months and confirmed by serum FSH levels > 40 mIU/mL and estradiol < 20 pg/mL or surgically sterile (with hysterectomy, bilateral salpingectomy, or bilateral oophorectomy) and not undergoing in vitro fertilization or other fertility treatments)
- Men agreed to use contraception or remain abstinent (when this is the subject's usual and preferred lifestyle)Be willing to complete all study visits and procedures.
Exclusion criteria:
- History of respiratory depression, severe bronchial asthma, chronic obstructive pulmonary disease, or acute and/or severe hypercepnia and cor pulmonale.
- History of gastrointestinal motility disorders (e.g., severe reflux esophagitis, gastroparesis, severe irritable bowel syndrome, active inflammatory bowel disease, and paralytic ileus).
- History of depression, seizures, and epilepsy.
- Uncontrolled hypertension: systolic BP ≥160 mmHg or diastolic BP ≥100 mmHg confirmed by at least two measurements.
- History of allergic reactions, anaphylactic reactions, severe systemic hypersensitivity, or any allergic reaction that, in the opinion of the Principal Investigator or his /her delegate, is likely to be exacerbated by the study drug (RAP-103 and oxycodone).
- History of human immunodeficiency virus or positive HIV test result (HIV 1-2 antibodies).
- History of hepatitis C infection or positive hepatitis C virus (HCVAb) antibody screening result.
- Current hepatitis B (HBV) infection (defined as positive for HepBsAg and/or HepBcAb). Subjects with immunity to hepatitis B from prior natural infection (defined as HepBsAg negative, HepBcAb positive, and HepBsAb positive) or vaccination (defined as HepBsAg negative, HepBCAb negative, and HepBSAb positive) are eligible to participate in the study.
- Transcutaneous oxygen saturation (SpO₂) <90%.
- Patients with severe liver or kidney disease.
- Patients with immunosuppression, neoplasms, or HIV infection.
- Active substance use disorder (SUD) or within the previous 12 months, including opioid, alcohol, benzodiazepines, or any other substance with potential for abuse.
- Patients with the use of antipsychotic medications.
- Any clinical condition that makes it difficult to self-assess pain.
- Recent opioid use (14 days prior recruitment).
- Previous exposure to RAP-103 or DAPTA (T-Peptide) at any time in your life.
- Abnormal and clinically significant results at the discretion of the Principal investigator (or his/her delegate) in the laboratory tests and electrocardiogram of visit 0. Laboratory values out of range and determined to be not clinically significant at the discretion of the Principal Investigator or his/her delegate may be repeated on one occasion, the subject may be enrolled if the repeated value is within the normal range.
- Participation in any other investigational study with drugs, biologics, medical devices, or treatment with an investigational product or therapy approved for investigational use within 30 days or 5 halflives at visit 0.
- Any other condition that, in the judgment of the PI or Sponsor, determines that the subject is not suitable to participate in the study.
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 |
|---|---|
|
实验性的:CBP-0276 600mg QD
First group (n=40) will receive oxycodone (standard of care) + CBP-0276 at a dose of 600 mg, orally once daily for 28 days.
|
Oxycodone CBP-0276 orally 600mg QD, orally once a day for 30 days
|
|
安慰剂比较:Placebo for CBP-0276
Second group (n=40) will receive oxycodone (standard of care) + placebo for CBP-0276, orally once daily for 28 days
|
Oxycodone (standard of care) + placebo for CBP-0276, orally once daily for 30 days
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Frequency of oxycodone use
大体时间:28 days
|
Number of oxycodone tablets required to controlled the moderate to severe pain management after hip or knee replacement.
|
28 days
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Oxycodone total requirements
大体时间:28 days
|
Number of days where the use of oxycodone is required
|
28 days
|
|
Changes on Quality of Life
大体时间:28 days
|
Changes in quality of life according to the WHOQOL-BREF score, from baseline and at 28 days post-surgery.
This is a 26-item self-report questionnaire that assesses an individual's subjective perception of their well-being and quality of life over the previous two weeks.
The raw item scores are converted into transformed domain scores on a standardized scale from 0 to 100.
0 represents the lowest possible perceived quality of life, meanwhile 100 represents the highest.
|
28 days
|
|
Number of oxycodone tablets required
大体时间:28 days
|
The number of oxycodone tablets required for pain management at day 15 post-surgical
|
28 days
|
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Changes on Pain Intensity
大体时间:28 days
|
Frequency and intensity of pain evaluated by visual analoge scale (VAS) at day 28 post-surgery and at 3 months of post-surgical follow-up, where 0 is no pain and 10 is the most severy level of pain
|
28 days
|
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Chnages on inflamatory cytokines
大体时间:28 days
|
Changes on inflamatory cytokines between baseline and end of treatment (day 28)
|
28 days
|
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。
调查人员
- 首席研究员:Jorge González Thompson, MD、Innovacion y Desarrollo de Estrategias en Salud SA de CV
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Apfelbaum JL, Chen C, Mehta SS, Gan TJ. Postoperative pain experience: results from a national survey suggest postoperative pain continues to be undermanaged. Anesth Analg. 2003 Aug;97(2):534-540. doi: 10.1213/01.ANE.0000068822.10113.9E.
- Glare P, Aubrey KR, Myles PS. Transition from acute to chronic pain after surgery. Lancet. 2019 Apr 13;393(10180):1537-1546. doi: 10.1016/S0140-6736(19)30352-6.
- DeWire SM, Yamashita DS, Rominger DH, Liu G, Cowan CL, Graczyk TM, Chen XT, Pitis PM, Gotchev D, Yuan C, Koblish M, Lark MW, Violin JD. A G protein-biased ligand at the mu-opioid receptor is potently analgesic with reduced gastrointestinal and respiratory dysfunction compared with morphine. J Pharmacol Exp Ther. 2013 Mar;344(3):708-17. doi: 10.1124/jpet.112.201616. Epub 2013 Jan 8.
- Mattia C, Coluzzi F, Sonnino D, Anker-Moller E. Efficacy and safety of fentanyl HCl iontophoretic transdermal system compared with morphine intravenous patient-controlled analgesia for postoperative pain management for patient subgroups. Eur J Anaesthesiol. 2010 May;27(5):433-40. doi: 10.1097/EJA.0b013e3283349d82.
- Padi SSV, Shi XQ, Zhao YQ, Ruff MR, Baichoo N, Pert CB, Zhang J. Attenuation of rodent neuropathic pain by an orally active peptide, RAP-103, which potently blocks CCR2- and CCR5-mediated monocyte chemotaxis and inflammation. Pain. 2012 Jan;153(1):95-106. doi: 10.1016/j.pain.2011.09.022. Epub 2011 Oct 26.
- Noda M, Tomonaga D, Kitazono K, Yoshioka Y, Liu J, Rousseau JP, Kinkead R, Ruff MR, Pert CB. Neuropathic pain inhibitor, RAP-103, is a potent inhibitor of microglial CCL1/CCR8. Neurochem Int. 2018 Oct;119:184-189. doi: 10.1016/j.neuint.2017.12.005. Epub 2017 Dec 14.
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8日
初级完成 (估计的)
2026年6月30日
研究完成 (估计的)
2026年9月30日
研究注册日期
首次提交
2026年6月25日
首先提交符合 QC 标准的
2026年7月2日
首次发布 (实际的)
2026年7月7日
研究记录更新
最后更新发布 (实际的)
2026年7月7日
上次提交的符合 QC 标准的更新
2026年7月2日
最后验证
2026年7月1日
更多信息
与本研究相关的术语
其他研究编号
- CBP0276-PillRed2026
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
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.