[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650817":3},{"organization":4,"armGroups":7,"interventions":35,"overallOfficials":41,"centralContacts":46,"locations":41,"responsibleParty":52,"collaborators":56,"id":62,"slug":63,"hasResults":64,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":41,"eligibilityCriteria":68,"healthyVolunteers":69,"sex":70,"minAge":71,"maxAge":72,"enrollmentInfo":73,"targetDuration":41,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":82,"overallStatus":88,"whyStopped":41,"lastUpdateSubmitDate":89,"lastUpdatePostDateStruct":90,"startDateStruct":93,"completionDateStruct":95,"leadSponsor":97,"locationsCount":41},{"fullName":5,"class":6},"The Third Xiangya Hospital of Central South University","OTHER",[8,15,19,23,27,31],{"label":9,"type":10,"description":11,"interventionNames":12},"1.Alfentanil 5 µg\u002Fkg + KL0011034 0.3 mg\u002Fkg","EXPERIMENTAL","Part 1: Participants receive a single dose of Alfentanil Hydrochloride Injection 5 μg\u002Fkg combined with KL0011034 Injection 0.3 mg\u002Fkg on Day 1. Safety, tolerability, and pharmacodynamic evaluations are conducted.",[13,14],"Drug: KL0011034 injection","Drug: Alfentanil Hydrochloride Injection",{"label":16,"type":10,"description":17,"interventionNames":18},"2.Alfentanil 5 µg\u002Fkg + KL0011034 0.35 mg\u002Fkg","Part 1: Participants receive a single dose of Alfentanil Hydrochloride Injection 5 μg\u002Fkg combined with KL0011034 Injection 0.35 mg\u002Fkg on Day 1. Safety, tolerability, and pharmacodynamic evaluations are conducted.",[13,14],{"label":20,"type":10,"description":21,"interventionNames":22},"3.Alfentanil 5 µg\u002Fkg + KL0011034 0.4 mg\u002Fkg","Part 1: Participants receive a single dose of Alfentanil Hydrochloride Injection 5 μg\u002Fkg combined with KL0011034 Injection 0.4 mg\u002Fkg on Day 1. Safety, tolerability, and pharmacodynamic evaluations are conducted.",[13,14],{"label":24,"type":10,"description":25,"interventionNames":26},"4.Sequence A: KL0011034 → Alfentanil → Alfentanil + KL0011034","Part 2, Sequence A: Participants receive three interventions across three periods (Day 1, Day 4, Day 7) with a 3-day washout between periods: Period 1: KL0011034 Injection (selected dose from Part 1); Period 2: Alfentanil Hydrochloride Injection 5 μg\u002Fkg; Period 3: Alfentanil Hydrochloride Injection 5 μg\u002Fkg + KL0011034 Injection (selected dose from Part 1). Pharmacokinetic, pharmacodynamic, and safety evaluations are conducted.",[13,14],{"label":28,"type":10,"description":29,"interventionNames":30},"5. Sequence B: Alfentanil → Alfentanil + KL0011034 → KL0011034","Part 2, Sequence B: Participants receive three interventions across three periods (Day 1, Day 4, Day 7) with a 3-day washout between periods: Period 1: Alfentanil Hydrochloride Injection 5 μg\u002Fkg; Period 2: Alfentanil Hydrochloride Injection 5 μg\u002Fkg + KL0011034 Injection (selected dose from Part 1); Period 3: KL0011034 Injection (selected dose from Part 1). Pharmacokinetic, pharmacodynamic, and safety evaluations are conducted.",[13,14],{"label":32,"type":10,"description":33,"interventionNames":34},"6. Sequence C: Alfentanil + KL0011034 → KL0011034 → Alfentanil","Part 2, Sequence C: Participants receive three interventions across three periods (Day 1, Day 4, Day 7) with a 3-day washout between periods: Period 1: Alfentanil Hydrochloride Injection 5 μg\u002Fkg + KL0011034 Injection (selected dose from Part 1); Period 2: KL0011034 Injection (selected dose from Part 1); Period 3: Alfentanil Hydrochloride Injection 5 μg\u002Fkg. Pharmacokinetic, pharmacodynamic, and safety evaluations are conducted.",[13,14],[36,42],{"type":37,"name":38,"description":39,"armGroupLabels":40,"otherNames":41},"DRUG","KL0011034 injection","KL0011034 Injection is an investigational drug being studied for its analgesic properties in combination with alfentanil. It is administered via intravenous infusion. The dose levels evaluated are 0.3 mg\u002Fkg, 0.35 mg\u002Fkg, and 0.4 mg\u002Fkg in Part 1; the selected dose from Part 1 is used in Part 2.",[9,16,20,24,28,32],null,{"type":37,"name":43,"description":44,"armGroupLabels":45,"otherNames":41},"Alfentanil Hydrochloride Injection","Alfentanil Hydrochloride Injection is an opioid analgesic administered via intravenous bolus at a fixed dose of 5 μg\u002Fkg. It is used alone and in combination with KL0011034 Injection to evaluate drug-drug interaction.",[9,16,20,24,28,32],[47],{"name":48,"role":49,"phone":50,"phoneExt":41,"email":51},"Huang Jie","CONTACT","+86 731 8991 8665","cellahuang1988@163.com",{"type":53,"investigatorFullName":54,"investigatorTitle":55,"investigatorAffiliation":5,"oldNameTitle":41,"oldOrganization":41},"PRINCIPAL_INVESTIGATOR","Guoping Yang","Professor of Clinical Pharmacology",[57,60],{"name":58,"class":59},"Hunan Kelun Pharmaceutical Co., Ltd.","INDUSTRY",{"name":61,"class":59},"Sichuan Kelun Pharmaceutical Co.,Ltd.","100650817","phase-1-a-study-to-evaluate-the-drug-drug-interaction-between-kl0011034-injection-and-alfentanil-hydrochloride-injection-in-participants-with-moderate-to-severe-non-cancer-chronic-pain-100650817",false,"NCT07751094","A Study to Evaluate the Drug-Drug Interaction Between KL0011034 Injection and Alfentanil Hydrochloride Injection in Participants With Moderate-to-Severe Non-Cancer Chronic Pain","A Single-Center, Randomized, Open-Label, Three-Sequence, Three-Period Crossover Study to Evaluate the Drug-Drug Interaction Between KL0011034 Injection and Alfentanil Hydrochloride Injection in Trial Participants With Moderate-to-Severe Non-Cancer Chronic Pain","Inclusion Criteria:\n\n1. Those who fully understand the purpose, content, process and possible risks of the trial, and voluntarily participate and sign the informed consent form;\n2. Male and female patients with moderate to severe non-cancerous chronic pain (such as patients with shoulder inflammation, chronic back pain, myofascial pain syndrome) aged between 18 and 55 years (inclusive of the boundary values), with a NRS score of \\>= 4;\n3. Male weight not less than 50.0 kg, female weight not less than 45.0 kg; Body Mass Index (BMI) within the range of 19.0 to 26.0 kg\u002Fm2 (including the critical value);\n4. From the date of signing the informed consent form to the last administration of the trial medication within 3 months, the trial participants (and their partners) have no plans for conception, and the trial participants have no plans for sperm donation\u002Fegg donation; From the date of signing the informed consent form to the completion of the exit examination, the participants voluntarily adopt non-pharmacological contraceptive measures; After the exit examination to the last 3 months after the last administration of the trial medication, the participants voluntarily adopt effective contraceptive measures;\n5. Able to communicate well with the researchers, willing and able to comply with the lifestyle restrictions stipulated in the protocol, and cooperate to complete the trial process.\n\nExclusion Criteria:\n\n1. Known to be allergic to alfentanil or other opioid analgesics, etomidate or other anesthetic drugs, or to be of allergic constitution (such as allergy to two or more drugs, food or pollen), or prone to develop rashes, urticaria, etc., or having a history of allergic diseases, or known to be allergic to the excipients or raw materials of this product;\n2. Having a history of head trauma, possible intracranial hypertension, cerebral aneurysm, cerebrovascular accident, or mental illness such as schizophrenia, mania, bipolar disorder, mental confusion, long-term use of psychotropic drugs or cognitive dysfunction;\n3. Having a history of serious cardiovascular diseases (such as hypertension, heart failure, severe arrhythmia, etc.) and\u002For heart diseases, family history of heart disease and\u002For unstable angina pectoris, or having had a myocardial infarction in the past 6 months;\n4. Having a history of other cardiovascular, endocrine, respiratory, digestive, urinary, nervous, hematological and\u002For lymphatic system diseases, and the investigator considers that it still has clinical significance during the screening;\n5. Having a history of anesthesia accidents, severe adverse reactions during anesthesia or family history of anesthesia accidents, or having contraindications for general anesthesia;\n6. Having difficulty breathing or suspected difficult airway or estimated difficulty in tracheal intubation (such as modified Mallampati score grade III-IV, congenital small tongue, maldevelopment of mandible, etc.);\n7. Having a history of airway diseases such as bronchial asthma, chronic obstructive pulmonary disease, sleep apnea syndrome, etc.;\n8. Having a history of adrenal insufficiency, adrenal tumor or hereditary hemoglobin biosynthesis disorder or hereditary acute porphyria;\n9. Having a surgical history within 3 months before screening, or not recovering from surgery, or having planned surgery during the trial;\n10. Having conditions, surgical history, diseases related to the use of the test drug, or any other special circumstances that may significantly affect drug absorption, distribution, metabolism and excretion;\n11. Abnormal results of physical examination, vital signs, full thoracic radiograph, abdominal B-ultrasound, laboratory tests (blood routine, urine routine, blood biochemistry, coagulation function) have clinical significance;\n12. Having clinically significant electrocardiogram abnormalities found during screening, such as QTcF \\>=450 ms (male) or \\>=460 ms (female), etc.;\n13. Positive for hepatitis B surface antigen (HBsAg), hepatitis C antibody (HCV-Ab), human immunodeficiency virus antibody (HIV-Ab), and syphilis spirochete antibody (TP-Ab);\n14. Having unprotected sexual behavior within 2 weeks before the first administration of the test drug;\n15. Female subjects during the screening period are in pregnancy or lactation, or have a positive pregnancy result;\n16. Having a history of drug abuse or drug dependence within the past 1 year, or having a positive urine drug screening at the time of screening;\n17. Having a history of alcohol abuse within 6 months before screening \\[that is, consuming more than 14 standard units of alcohol per week (1 unit = 360 ml of beer or 45 ml of 40% alcohol liquor or 150 ml of wine)\\], or being unwilling to stop drinking alcohol or any alcoholic products during the trial, or having a positive alcohol breath test at the time of screening;\n18. Having a history of smoking within 3 months before screening (daily smoking quantity \\>= 5 cigarettes), or being unwilling to stop using any tobacco products during the trial, or having a positive smoke test result at the time of screening;\n19. Having consumed excessive (8 cups or more, 1 cup = 250 ml) tea, coffee or caffeine-containing beverages (such as milk tea, cola, etc.) every day within 14 days before screening, or being unwilling to stop drinking these beverages during the trial;\n20. Individuals who consumed grapefruit\u002Fgrapefruit juice, foods or beverages rich in xanthine components (such as shiitake mushrooms, white carp, black carp, whelk, white bream, oysters, white snapper, sea eel, duck liver, chicken liver, pork intestines, pork liver, beef liver, etc.) within 48 hours before the first administration of the test drug, or those who had any special diet that could affect the absorption, distribution, metabolism, or excretion of the drug;\n21. Individuals who had used any medication within 14 days before the first administration of the test drug, including prescription drugs, over-the-counter drugs, traditional Chinese medicines, health supplements, and vitamins;\n22. Individuals who had used inhibitors or inducers of CYP3A4 or CYP2C19 (such as CYP3A4 inhibitors: sirivatinib, atalenti, edalizumab, telifast, clarithromycin, itraconazole, ketoconazole, posaconazole, voriconazole, indinavir, nelfinavir, ritonavir, sapparin, tipranavir, lopinavir, nafamoxin, cobizumet; CYP3A4 inducers: apalutamide, enzalutamide, rumactat, mitotane, evolizumab, phenytoin, carbamazepine, rifampicin, St. John's wort; CYP2C19 inhibitors: fluvoxamine, fluconazole, fluoxetine, ticlopidine, phenabarbital, nalfurafine, voriconazole; CYP2C19 inducers: rifampicin, apalutamide, efavirenz, enzalutamide, phenytoin) within 1 month before the first administration of the test drug;\n23. Individuals who had been using sedative drugs and\u002For opioid analgesics for more than 3 months before screening;\n24. Individuals who had participated in any clinical trials and used the test drug\u002Fmedical device within 3 months before the first administration of the test drug, or were still in the follow-up period of other trials;\n25. Individuals who had received inactivated vaccines within 1 month before screening, or received live\u002Fdeleted vaccines within 3 months before screening, or planned to receive inactivated\u002Flive\u002Fdeleted vaccines during the trial;\n26. Individuals who had undergone blood loss or blood donation or transfusion or received a total amount of blood products exceeding 400 ml within 3 months before screening, or planned to donate blood or undergo surgery within 1 month after the trial or after the trial ends;\n27. Individuals with difficulty in blood collection, or those who cannot tolerate venipuncture, or those with a history of fainting or needle shock;\n28. Individuals with poor compliance, or other situations that the researcher deems unsuitable for participation in the study.",true,"ALL","18 Years","55 Years",{"count":74,"type":75},27,"ESTIMATED","INTERVENTIONAL",[78],"PHASE1","This study will evaluate the drug-drug interaction between KL0011034 Injection and Alfentanil Hydrochloride Injection in participants with moderate-to-severe non-cancer chronic pain. The study consists of two parts. Part 1 is a single-center, randomized, open-label, parallel-design study to evaluate the safety, tolerability, and pharmacodynamics of the combination. Approximately 9 participants will be enrolled and randomized to one of three dose groups (n=3 per group). Part 2 is a single-center, randomized, open-label, three-sequence, three-period crossover study to evaluate the pharmacokinetic interaction, safety, tolerability, and pharmacodynamic effects. Approximately 18 participants will be enrolled and randomized to one of three sequences (n=6 per sequence), with a 3-day washout period between each period.",[81],"Chronic Pain",[83,84,85,86,87],"Drug-Drug Interaction","KL0011034","Alfentanil","Pharmacokinetics","Non-Cancer Chronic Pain","NOT_YET_RECRUITING","2026-08-03",{"date":91,"type":92},"2026-08-07","ACTUAL",{"date":94,"type":75},"2026-07-30",{"date":96,"type":75},"2027-07-31",{"name":5,"class":6}]