[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hsil-high-grade-squamous-intraepithelial-lesion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hsil-high-grade-squamous-intraepithelial-lesion":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100589083","phase-2-cascade-2002-protect-study-probiotics-to-treat-anal-precancer-trial-100589083",false,"NCT06949800","CASCADE 2002: PROTECT Study, \"PRObiotics to TrEat Anal preCancer Trial","Probiotics to Treat HSIL and Reduce Persistent High Risk HPV Infection in Women and Men Living With HIV","Inclusion Criteria:\n\n1. Signed informed consent\n2. Participant in ULACNet-101 or participant screened specifically for ULACNet-102.\n3. Biopsy-proven anal HSIL (men or women) shown as part of participation in the ULACNet-101 study or at a screening visit for ULACNet-102.\n4. At least one focus of anal HSIL must be large enough to be monitored for response, i.e.,not completely removed after the screening biopsy.\n5. Total volume of HSIL is less than 50% of the anal canal or perianal region.\n6. Must be actively on treatment with effective antiretroviral therapy (ART) regimen for at least three months preceding enrollment (Visit 1, Day 1) in ULACNet-101 or at screening for ULACNet-102.\n7. HIV RNA \\\u003C200 copies\u002Fml at baseline.\n8. Cluster of differentiation 4 (CD4) nadir above 200 cells per microliter (uL)\n9. Eastern Cooperative Oncology Group (ECOG) performance status \\\u003C=1 (Karnofsky \\>= 70%).\n10. Participants must meet the following laboratory parameters within 3 months before enrollment:\n\n    1. Leukocytes: ≥3,000\u002Fmm\\^3.\n    2. Absolute neutrophil count: ≥1,500\u002Fmm\\^3.\n    3. Platelets: ≥100,000\u002Fmm\\^3.\n    4. Elevation of aspartate aminotransferase (AST), alanine aminotransferase (ALT), or bilirubin \\\u003C2 times the upper limit of normal.\n11. Not pregnant or breast feeding and one of the following:\n\n    1. Of non-childbearing potential (i.e. persons aged 60 years or older or who have had a hysterectomy or tubal ligation or are postmenopausal, as defined by no menses for at least 12 months and without an alternative medical cause).\n    2. Persons aged less than 60 years of childbearing potential and agree to practice highly effective contraception from initiation of taking EXE-346 or placebo through 14 days after taking the last dose of EXE-346 or placebo. Highly effective methods of contraception include one or more of the following:\n\n    i.Male partner who is sterile (medically effective vasectomy) prior to the female participant's entry into the study and is the sole sexual partner for the female participant.\n\nii.Hormonal (oral, intravaginal, transdermal, implantable or injectable); Progestogen-only hormonal contraceptives without inhibition of ovulation are not considered to be highly effective.\n\niii. An intrauterine hormone-releasing system. iv. An intrauterine device. v. Bilateral tubal occlusion or removal. vi. Sexual abstinence, only if the participant refrains from heterosexual intercourse from initiation taking EXE-346 or placebo through 14 days after taking the last dose of EXE-346 or placebo and it is the usual lifestyle of the participant.\n\nExclusion Criteria:\n\n1. History of any anogenital cancer.\n2. Presence of untreated cervical HSIL or cervical cancer.\n3. Anal HSIL on clinical examination or biopsy that clinicians are concerned for cancer.\n4. Receipt of chemotherapy, radiotherapy or immunosuppressive medication in three months preceding enrollment in ULACNet-101 or at the screening visit for ULACNet-102.\n5. Immunosuppression as a result of underlying illness or treatment including:\n\n   1. Use of high dose corticosteroids (\\>10 mg\u002Fday prednisone or equivalent) for \\>=7 days (inhaled, otic, topical and ophthalmic corticosteroids are permitted).\n   2. Primary immune deficiency disease.\n   3. Use of synthetic or biologic disease-modifying anti-rheumatic drugs.\n   4. History of bone marrow or solid organ transplant.\n   5. History of any other clinically significant autoimmune or immunosuppressive disease.\n6. Participant initiated a new treatment with antibiotics within the 2 weeks prior to screening or plans to start antibiotic therapy during the study period.\n7. Participant is taking NSAIDs as a long-term treatment (ie, consistent use for at least 4 days\u002Fweek each month). Acute use of NSAIDs is allowed.\n8. Participant has known hypersensitivity to EXE-346 or any product components.\n9. Current known infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).\n10. Warts so extensive that they preclude the clinician from determining the extent and location of HSIL.\n11. Sustained, manually confirmed, sitting systolic blood pressure \\>150 mm Hg or \\\u003C90 mm Hg or a diastolic blood pressure \\>95 mm Hg as measured by 3 readings taken 15 minutes apart at screening or Visit 1.\n12. History of significant thrombocytopenia, history of thrombosis with thrombocytopenia (TTS) syndrome or heparin-induced thrombocytopenia.\n13. Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, cardiac arrhythmia, or psychiatric illness\u002Fsocial situations that, in the opinion of the investigator, would limit compliance with study requirements.\n14. Participant has participated in any clinical study of an approved or unapproved investigational medicinal product within the 30 days prior to screening.\n15. Any other finding that, in the opinion of the Investigator deems the participant unsuitable for the study","ALL","21 Years",{"count":19,"type":20},90,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","This study is focused on treatment of anal high-grade squamous intraepithelial lesions (HSIL) in persons with HIV (PWH), with the ultimate goal of applying the approach toward prevention of anal cancer in this population",[26,27,28],"HSIL, High Grade Squamous Intraepithelial Lesion","HPV-Related Squamous Cell Carcinoma","Anal HSIL",[30,31,32],"HIV","Anal intraepithelial neoplasia (AIN) 3","p16+ AIN 2","NOT_YET_RECRUITING","2026-04-29",{"date":36,"type":37},"2026-05-01","ACTUAL",{"date":39,"type":20},"2026-06-01",{"date":41,"type":20},"2027-05-31",{"name":43,"class":44},"University of California, San Francisco","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":53,"minAge":54,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":21,"phases":58,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100616488","multicenter-prospective-non-randomized-controlled-study-of-ella-photodynamic-therapy-for-cervical-hsilcin2-100616488","NCT07306260","Multicenter Prospective Non-randomized Controlled Study of Ella Photodynamic Therapy for Cervical HSIL\u002FCIN2","PDT for CIN2","Inclusion Criteria:\n\n1. Female, 25-60 years, understands study procedures and consents to participate;\n2. Colposcopy-guided cervical biopsy within 3 months showing HSIL\u002FCIN2;\n3. Provides written informed consent.\n\nExclusion Criteria:\n\n1. Cytology showing ASC-H, HSIL, AGC, or AIS; or evidence of malignant cells on cytology\u002Fhistology, or suspicion of malignancy or invasive cancer;\n2. Colposcopy findings suggestive of invasive cancer or lesion extension to the vaginal wall;\n3. Severe pelvic, cervical, or other gynecological inflammatory conditions identified clinically;\n4. Undiagnosed vaginal bleeding;\n5. Active allergic disease, porphyria, or history of allergy to the study drug or structurally similar agents;\n6. Severe cardiovascular, neurological, psychiatric, endocrine, hepatic, or hematologic disorders; known immunodeficiency; long-term glucocorticoid or immunosuppressant use; active autoimmune disease; or other malignancies;\n7. Pregnant or breastfeeding women;\n8. History of hysterectomy, cervical cancer treatment, or cervical excision\u002Fablation within 6 months (e.g., conization, LEEP, laser);\n9. Use of interferon or antiviral therapy within 3 months;\n10. Any other condition deemed unsuitable for participation by the investigator.",true,"FEMALE","25 Years","65 Years",{"count":57,"type":20},560,[59],"NA","This study evaluates the efficacy and safety of ALA-PDT versus LEEP in treating cervical HSIL\u002FCIN2, aiming to demonstrate non-inferiority in clinical efficacy.",[26,62,63,64],"CIN 2","HPV (Human Papillomavirus)-Associated","Photodynamic Therapy (PDT)",[66,67,68,69,70],"photodynamic therapy","High Grade Squamous Intraepithelial Lesion","human papillomavirus","loop electrosurgical excision procedure","efficacy","2025-12-14",{"date":73,"type":37},"2025-12-29",{"date":75,"type":20},"2026-01",{"date":77,"type":20},"2027-12",{"name":79,"class":44},"Second Affiliated Hospital, School of Medicine, Zhejiang University",5]