[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100551050":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":28,"centralContacts":32,"locations":42,"responsibleParty":58,"collaborators":60,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":36,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":36,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":36,"overallStatus":44,"whyStopped":36,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Fujian Cancer Hospital","OTHER_GOV",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"AK104 Combined With Chemotherapy and Recombinant Human Adenovirus 5 Injection","EXPERIMENTAL","The Combined Treatment Stage consists of AK104 at a dosage of 10 mg\u002Fkg, Pemetrexed at a dosage of 500mg\u002Fm2, Cisplatin with an AUC of 4-6 mg\u002FmL\u002Fmin, and Human Adenovirus 5 Injection. This treatment is administered every 3 weeks for a total of 4 cycles. Upon enrollment, the drugs are given in the following sequence on the first day of each combined treatment cycle: local injection of Human Adenovirus 5 Injection (d1-d5), intravenous infusion of AK104 (d1), intravenous infusion of Pemetrexed (d2), and intravenous infusion of Cisplatin (d2). The Maintenance Treatment Stage involves single-drug AK104 at a dose of 10 mg\u002Fkg every 3 weeks for a duration lasting up to two years.",[13,14],"Drug: AK104","Drug: Recombinant Human Adenovirus 5 Injection",[16,23],{"type":17,"name":18,"description":19,"armGroupLabels":20,"otherNames":21},"DRUG","AK104","PD-1\u002FCTLA-4 bispecific antibody",[9],[22],"Cadonilimab",{"type":17,"name":24,"description":24,"armGroupLabels":25,"otherNames":26},"Recombinant Human Adenovirus 5 Injection",[9],[27],"Recombinant Human Adenovirus Type 5 Injection",[29],{"name":30,"affiliation":5,"role":31},"Qin Xu","PRINCIPAL_INVESTIGATOR",[33,38],{"name":30,"role":34,"phone":35,"phoneExt":36,"email":37},"CONTACT","+8613950419396",null,"1379423879@qq.com",{"name":39,"role":34,"phone":40,"phoneExt":36,"email":41},"Li Li","+8615259835038","15259835038@163.com",[43],{"facility":5,"status":44,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"RECRUITING","Fuzhou","Fujian","350011","China","CN",{"type":51,"coordinates":52},"Point",[53,54],119.30611,26.06139,{"lat":54,"lon":53},[57],{"name":30,"role":34,"phone":35,"phoneExt":36,"email":37},{"type":59,"investigatorFullName":36,"investigatorTitle":36,"investigatorAffiliation":36,"oldNameTitle":36,"oldOrganization":36},"SPONSOR",[61],{"name":62,"class":63},"Zhangzhou Municipal Hospital of Fujian Province","OTHER","100551050","phase-2-efficacy-and-safety-of-ak104-combined-with-chemotherapy-and-recombinant-human-adenovirus-5-injection-in-cervical-cancer-100551050",false,"NCT06455046","Efficacy and Safety of AK104 Combined With Chemotherapy and Recombinant Human Adenovirus 5 Injection in Cervical Cancer","Efficacy and Safety of AK104 Combined With Pemetrexed, Carboplatin and Recombinant Human Adenovirus 5 Injection in Advanced Recurrent Cervical Cancer: a Multicenter, Single-arm, Prospective Phase II Clinical Study","Inclusion Criteria:\n\n\\- 1）Enrollees in this study will be voluntary participants who sign a written informed consent form and are capable of adhering to scheduled visits and related procedures.2) Ages between 18 and 75 years old.3) Histologically or cytologically confirmed cases of persistent, recurrent, or metastatic cervical squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma. Note: A pathological report is necessary for confirmation of the original primary tumor histology.4) Must have experienced failure with at least one standard systemic treatment and documented disease progression: Failure is defined as progression or recurrence within six months after at least one cycle of standard systemic treatment. Patients who have developed immune acquired resistance may also be included if they experienced PD after achieving CR or PR with anti-PD-1\u002FPD-L1 antibody treatment, or PD after experiencing SD≥6 months with anti-PD-1\u002FPD-L1 antibody treatment.\n\n5\\) Not suitable for local treatments such as unresectable surgery and\u002For definitive concurrent radiotherapy and chemotherapy.6) The interval between the end of previous systemic treatment and the first dose of the study drug must be ≥2 weeks. Additionally, any treatment-related adverse events must have recovered to a grade ≤1 according to Common Terminology Criteria for Adverse Events (CTCAE) V5.0 (excluding hair loss and fatigue).7) At least one measurable target lesion must be present according to RECIST V1.1 criteria.8）At least one lesion that can receive local injection therapy using recombinant human adenovirus type 5 should also meet RECIST V1.1 criteria as a measurable lesion.9) ECOG PS 0 or 1.10) The anticipated survival time should be ≥12 weeks.11) Female subjects of reproductive age are required to use effective contraception throughout the treatment period and for at least 5 months after their final dose of the investigational drug.12) Participants must consent to providing an adequate amount of tumor tissue samples for PD-L1 expression detection, which may include archived tumor samples such as paraffin blocks or a sufficient number of unstained slides meeting the study's detection requirements. If no archived tumor tissue samples are available, participants agree to undergo biopsy of the tumor lesion.13）With good organ and hematopoietic function.\n\nExclusion Criteria:\n\n\\- 1) Diagnosed with other malignancies within the 5 years preceding initial dosing, excluding surgically cured basal cell carcinoma or squamous cell carcinoma of the skin, in situ carcinoma that has been surgically resected, and\u002For papillary thyroid carcinoma. Subjects with histologically confirmed small cell (neuroendocrine) cervical cancer, cervical sarcoma, and gastric-type cervical adenocarcinoma.2) Infection at the injection site.3) Presence of ascites, pleural effusion, or pericardial effusion accompanied by clinical symptoms or necessitating drainage. Subjects without clinical symptoms or requiring drainage who have ceased drainage for a minimum of 3 days and show no significant increase in fluid accumulation may be included.4) Individuals scheduled for or having undergone organ or bone marrow transplantation previously.5) Acute or chronic active hepatitis B or C infection with HBV DNA \\>200IU\u002Fml or 103 copies\u002Fml; positive anti-HCV antibody and HCV-RNA level above detection limit. Those treated with nucleoside analog antiviral agents resulting in HBV DNA\u002FHCV-RNA levels below specified standards can be included.\n\n6\\) Central nervous system (CNS) metastasis involving meningeal metastasis or symptomatic CNS metastasis. Asymptomatic brain metastases patients showing stable symptoms after treatment for at least 2 weeks may participate if they meet specific criteria: measurable lesions outside the CNS; absence of meningeal\u002Fmidbrain\u002Fpons\u002Fcerebellum\u002Fmedulla oblongata\u002Fspinal cord metastases; no history of intracranial hemorrhage; cessation of hormone therapy 14 days before first dose.7）Any life-threatening bleeding event within the past three months including need for blood transfusion，surgery，local treatment，or ongoing medication therapy.8）Arterial thrombosis，embolism，or ischemia within six months prior to enrollment including myocardial infarction，unstable angina pectoris ，cerebrovascular accident etc。A history of deep vein thrombosis（DVT）or any other serious thromboembolic events within three months prior to enrollment are not considered \"serious\" thromboembolic events.9）Hepatic vein thrombosis involving both hepatic portal trunk \\& left\u002Fright branches；hepatic portal trunk \\& mesenteric superior\u002Finferior veins；superior vena cava thrombosis\u002Fsuperior vena cava syndrome.10）Tumor invasion into important surrounding organs\u002Fblood vessels such as great mediastinal vessels\u002Fsuperior vena cava\u002Finferior vena cava\u002Fabdominal aorta\u002Filiac vessels\u002Ftrachea\u002Fesophagus；risk of tracheoesophageal fistula \u002Fmediastinal pleural fistula development.11）Uncontrollable hypertension defined as systolic blood pressure ≥150mmHg\u002Fdiastolic blood pressure ≥100mmHg\u002Fhistory hypertension crisis\u002Fhypertensive encephalopathy.12）Symptomatic congestive heart failure(NYHA class II-IV)\u002Fsymptomatic\u002Fpoorly controlled arrhythmias\u002Fprolonged QT interval(QTcF\\>470ms).13）Severe bleeding tendency\u002Fcoagulation dysfunction\u002Fcurrently receiving thrombolytic therapy.14）History gastrointestinal perforation\u002Ffistula last six months\u002Fbowel obstruction(including incomplete bowel obstruction requiring parenteral nutrition)\u002Finflammatory bowel disease\u002Fextensive bowel resection(Crohn's disease\u002Fulcerative colitis\u002Fchronic diarrhea).15 ) History interstitial pneumonitis\u002Fdrug-induced pneumonitis\u002Fradiation pneumonitis\u002Fidopathic pneumonitis \u002Factive pneumonitis.16 ) Active tuberculosis(TB)，currently receiving anti-TB therapy\u002For received study drug previous year.17 ) Human immunodeficiency virus(HIV)(HIV1\u002FHIV2 antibody positive), known active syphilis infection.18 ) Active\u002Fseverely uncontrolled infections hospitalization severe infections(infections\u002Fsepsis\u002Fsevere pneumonia complications etc.)within four weeks prior to first dose.19 ) Oral\u002Fintravenous therapeutic antibiotics one week before starting study treatment.20 ) Systemic autoimmune diseases\u002Frequiring systemic treatment\u002Ftwo-year history(white vitiligo、psoriasis、alopecia、Graves' disease not requiring systemic treatment\u002Fhypothyroidism only needing thyroid hormone replacement\u002Ftype1 diabetes only needing insulin replacement). Known primary immunodeficiency history Only patients with positive autoimmune antibodies need confirmation by investigator presence autoimmune disease.21 ) Immunosuppressive drugs use four weeks except nasal inhalant local corticosteroids\u002Fsystemic corticosteroids physiological doses(no more than prednisone equivalent daily doses other cortico steroids temporary use relief breathing difficulties due asthma\u002FCOPD).22 ) Live attenuated vaccine four weeks planned during study period.23 ) System immune stimulant treatments four weeks.24)Major surgery(craniotomy\u002Fthoracotomy\u002Flaparotomy)prior four weeks\u002Funhealed wound ulcer fracture.25)Uncontrolled\u002Fmetabolic disorder\u002Fnon-malignant organ\u002Fsystemic diseases\u002Fcancer-related complications\u002Fhigher medical risk uncertainty survival period evaluation.26) Other acute chronic conditions psychiatric disorders laboratory test abnormalities increasing risk participating study\u002Freceiving study drug interfering interpretation results determined investigator patient eligible participate thisstudy.27) Received oncolytic virus therapy past received anti-CTLA-4 antibodytherapy past.28) Known allergic AK104,pemetrexed,cisplatin,and Recombinant Human Adenovirus 5 Injection components\u002Fsevere allergic reaction monoclonal antibodies past.29) Received investigational drug treatment previousfourweeks starting studytreatment.30) No anticancer therapies received previousfourweeks startingstudyoral chemotherapy(two-week washout oral fluoropyrimidine-based drugs), endocrine targeted therapies(small molecule targeted therapies two-week half-life longer),immunotherapy,tumor embolization Chinese herbal medicine indications.31) Pregnant breastfeeding femalepatients","FEMALE","18 Years","75 Years",{"count":75,"type":76},37,"ESTIMATED","INTERVENTIONAL",[79],"PHASE2","In order to improve the clinical effect and find a new safe and effective treatment model for advanced recurrent cervical cancer, this study explored the efficacy level safety of pemetrexed, carboplatin, recombinant human adenovirus type 5, and AK104 regimen in recurrent and refractory advanced cervical cancer. For some patients with immune-resistant cervical cancer, combination chemotherapy and oncolytic virus therapy can promote the transformation of cold tumors into hot tumors, eliminate and then reverse the suppressor factors of immune resistance, and break the dilemma of immunotherapy drug resistance, which is a new method and strategy under immunotherapy drug resistance.",[82],"Cervical Cancer Recurrent","2024-06-06",{"date":85,"type":86},"2024-06-12","ACTUAL",{"date":88,"type":86},"2023-10-11",{"date":90,"type":76},"2025-10-10",{"name":5,"class":6},1]