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
調査の概要
詳細な説明
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.
研究の種類
介入
入学 (推定)
80
段階
- フェーズ2
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究連絡先
- 名前:Pedro Gutiérrez Castrellón, MD, PhD
- 電話番号:+525554198746
- メール:pedro.gutierrez@elemental.org.mx
研究連絡先のバックアップ
- 名前:Diana M Andrade Platas, MD
- 電話番号:+525535209755
- メール:diana.andrade@elemental.org.mx
研究場所
-
-
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Mexico City、メキシコ、14340
- 募集
- Innovacion y Desarrollo de Estrategias en Salud
-
コンタクト:
- Diana M Andrade Platas, MD, MSc
- 電話番号:+525535209755
- メール:diana.andrade@elemental.org.mx
-
コンタクト:
- Tom Jilmer Castillo, MD
- 電話番号:+523324120245
- メール:tom.castillo@idecsa.com.mx
-
主任研究者:
- Miguel Gonzalez Thompson, MD
-
-
参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
いいえ
説明
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.
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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
|
|
プラセボコンパレーター: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
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Frequency of oxycodone use
時間枠:28 days
|
Number of oxycodone tablets required to controlled the moderate to severe pain management after hip or knee replacement.
|
28 days
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Oxycodone total requirements
時間枠:28 days
|
Number of days where the use of oxycodone is required
|
28 days
|
|
Changes on Quality of Life
時間枠: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
時間枠: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
時間枠: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
時間枠:28 days
|
Changes on inflamatory cytokines between baseline and end of treatment (day 28)
|
28 days
|
協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
スポンサー
捜査官
- 主任研究者:Jorge González Thompson, MD、Innovacion y Desarrollo de Estrategias en Salud SA de CV
出版物と役立つリンク
研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。
一般刊行物
- 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.
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始 (実際)
2026年5月8日
一次修了 (推定)
2026年6月30日
研究の完了 (推定)
2026年9月30日
試験登録日
最初に提出
2026年6月25日
QC基準を満たした最初の提出物
2026年7月2日
最初の投稿 (実際)
2026年7月7日
学習記録の更新
投稿された最後の更新 (実際)
2026年7月7日
QC基準を満たした最後の更新が送信されました
2026年7月2日
最終確認日
2026年7月1日
詳しくは
本研究に関する用語
その他の研究ID番号
- CBP0276-PillRed2026
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
いいえ
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
いいえ
米国FDA規制機器製品の研究
いいえ
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