[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"low-grade-upper-tract-urothelial-carcinoma\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:low-grade-upper-tract-urothelial-carcinoma":64},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,50],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100613389","phase-2-phase-2ab-efficacy-and-safety-of-dabogratinib-in-participants-with-low-grade-upper-tract-urothelial-carcinoma-100613389",false,"NCT07265947","Phase 2A\u002FB Efficacy and Safety of Dabogratinib in Participants With Low Grade Upper Tract Urothelial Carcinoma","A Phase 2A\u002FB, Multi-center, Open-Label Study Evaluating the Efficacy and Safety of Dabogratinib (TYRA-300) in Participants With Low Grade Upper Tract Urothelial Carcinoma (SURF303)","SURF303","1. Participants ≥ 18 years of age at the time of informed consent and willing and able to comply with all required study procedures\n2. Confirmed LOW RISK LG UTUC (both favorable and unfavorable) per AUA\n3. At least 5mm of marker lesion left behind\n4. Participants must have previous genomic report or archival\u002Ffresh tissue in addition to urine sample for retrospective genomic testing\n5. Identification of marker lesion(s) within 8 weeks prior to randomization (refer to Inclusion Criterion #2)\n6. If synchronous NMIBC, NMIBC must be fully resected and low-grade Ta or T1\n7. No prior BCG administration within 1 year of date of consent.\n8. No intravesical chemotherapy within 8 weeks prior to C1D1 (including UGN-101).\n9. No systemic chemotherapy within 3 months prior to C1D1\n10. ECOG 0-2\n11. Pathology consists of pure urothelial carcinoma\n12. Adequate bone marrow, liver, and renal function:\n\n    1. i. Absolute neutrophil count (ANC) ≥1,500\u002Fmm3 ii. Platelet count ≥75,000\u002Fmm3 iii. Hemoglobin ≥10.0 g\u002FdL\n    2. i. Total bilirubin ≤ ULN ii. Alanine aminotransferase (ALT) ≤ ULN iii. Aspartate aminotransferase (AST) ≤ ULN\n    3. Estimated glomerular filtration rate \\>60 mL\u002Fmin\n    4. Serum Phosphate level ≤ ULN prior to starting treatment\n    5. International normalized ratio (INR) ≤1.5 × ULN\n\nExclusion Criteria:\n\n1. Evidence or any features of high grade (HG) UTUC\n2. History of carcinoma in situ (CIS)\n3. History of prostatic urethral involvement\n4. Current or previous history of muscle invasive bladder cancer\n5. Current or previous history of lymph node positive and\u002For metastatic bladder cancer\n6. Evidence of squamous cell carcinoma, adenocarcinoma or undifferentiated carcinoma or small cell of the bladder\n7. Currently receiving systemic cancer therapy (cytotoxic or immunotherapy)\n8. Current or prior history of pelvic external beam radiotherapy for bladder cancer\n9. Current or history of receiving a prior FGFR inhibitor\n10. Systemic immunotherapy within 6 months prior to randomization\n11. Treatment with an investigational agent within 30 days or 5 half-lives from randomization, whichever is shorter; compounds with an unknown half-life will be default to 30 days.\n12. Prior treatment with an intravesical or intracavitary agent within 8 weeks of C1D1.\n13. Current evidence of central serous retinopathy or retinal pigmented epithelial detachment of any grade at time of baseline examination.\n14. Requiring use of medications that are potential inhibitors or inducers of CYP3A (prohibited list of medications)","ALL","18 Years",{"count":20,"type":21},230,"ESTIMATED","INTERVENTIONAL",[24],"PHASE2","A Phase 2A\u002FB study of Dabogratinib (TYRA-300) in Low Grade Upper Tract Urothelial Carcinoma",[27],"Low Grade Upper Tract Urothelial Carcinoma",[29,30,27,31,32,33,34,35,36],"Low-grade UTUC","Upper Tract Urothelial Carcinoma","FGFR Gene Amplification","FGFR Gene Alteration","FGFR Gene Alterations","FGFR3 Mutation","FGFR3 Mutations","FGFR3 Gene Fusions","RECRUITING","2026-06-30",{"date":40,"type":41},"2026-07-02","ACTUAL",{"date":43,"type":41},"2025-12-22",{"date":45,"type":21},"2030-11",{"name":47,"class":48},"Tyra Biosciences, Inc","INDUSTRY",12,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":56,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":62,"conditions":63,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100567461","phase-1-low-grade-utuc-treated-with-nadofaragene-firadenovec-administered-to-renal-pelvis-100567461","NCT06668493","Low-grade UTUC Treated With Nadofaragene Firadenovec Administered to Renal Pelvis","A Phase 1\u002F2, Single-arm, Open-Label Trial to Evaluate the Safety and Efficacy of Nadofaragene Firadenovec Instilled to the Renal Pelvis in Adult Subjects With Low-grade Upper Tract Urothelial Carcinoma (LG-UTUC)","LUNAR","Inclusion Criteria:\n\n1. Aged ≥18 years at the time of signing informed consent.\n2. Able to give written informed consent.\n3. Have biopsy-proven low-grade upper tract urothelial cancer (LG-UTUC) confirmed by a pathology report ≤2 months prior to enrolment.\n4. Have ≥1 measurable papillary low-grade tumour (5-15 mm in maximum diameter), evaluated visually above the ureteropelvic junction before enrolment.\n\n   * Subjects with low-grade tumour larger than 15 mm will be eligible if endoscopic downsizing of the tumour to 5-15 mm in maximum diameter has been performed before enrolment.\n5. Willing to be available for at least 18 months after first dosing.\n6. Have life expectancy \\>2 years, in the opinion of the investigator.\n7. Have an Eastern Cooperative Oncology Group (ECOG) status of 2 or less.\n8. Females of reproductive potential must have a negative highly sensitive urine or serum pregnancy test upon entry into this trial and be willing to use highly effective contraception during treatment with the investigational medicinal product (IMP) and for 6 months following the last dose. Otherwise, female subjects must be postmenopausal (no menstrual period for a minimum of 12 months) or surgically sterile. Highly effective methods of contraception include: combined (oestrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal or transdermal), progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable or implantable), intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomised partner, and sexual abstinence.\n9. Male subjects with female partners of reproductive potential must be surgically sterile or willing to use a condom in addition to effective contraception in their female partner during treatment with the IMP and for 3 months following the last dose.\n10. Adequate laboratory values:\n\n    * haemoglobin ≥10 g\u002FdL\n    * white blood cells (WBC) ≥4000\u002FμL\n    * absolute neutrophil count (ANC) ≥2000\u002FμL\n    * platelet count ≥100,000\u002FμL\n    * international normalized ratio (INR)\\* below institutional upper limit of normal (ULN)\n    * activated partial thromboplastin time (aPTT)\\* below institutional ULN\n    * aspartate aminotransferase (AST) ≤1.5 x ULN\n    * alanine aminotransferase (ALT) ≤1.5 x ULN\n    * total bilirubin ≤1.5 x ULN\n    * sodium \\>135 mmol\u002FL\n    * potassium between 3.6 and 5.0 mmol\u002FL\n11. Have an estimated glomerular filtration rate (eGFR) ≥45 mL\u002Fmin\u002F1.73 m2 (for inclusion in the safety lead-in the eGFR must be ≥60 mL\u002Fmin\u002F1.73 m2 \\[see exclusion criteria #20\\]).\n\nExclusion Criteria:\n\n1. UTUC characterised by one or more of the following:\n\n   * High-grade cytology or high-grade histology\n   * Multi-focal UTUC\n\n     * Exception: Subjects with low-grade multi-focal tumours will be eligible if any ureteral tumours can be ablated before enrolment and if the total diameter of the multifocal tumours above the ureteropelvic junction is not exceeding 15 mm in diameter.\n   * Bilateral disease\n\n     * Exception: Subjects who have had bilateral disease are eligible (not in the safety lead-in) if one renal unit is removed or rendered disease-free by endoscopic ablation before enrolment.\n2. Current or previous evidence of carcinoma in situ, of muscle invasive (muscularis propria) urothelial cancer in the urogenital tract presented at the screening visit.\n3. Concomitant lower tract urothelial carcinoma and\u002For concomitant or prior urothelial carcinoma within the prostatic urethra.\n4. History of high grade papillary urothelial cancer within 2 years prior to screening.\n5. Current or prior treatment with mitomycin gel and\u002For any investigational drug for the treatment of UTUC.\n6. Current systemic chemo- or immunotherapy for bladder cancer or any other malignancy.\n7. Current or prior investigational treatment for Bacillus Calmette-Guerin (BCG) unresponsive non-muscle invasive bladder cancer (NMIBC) or any other investigational drug within 1 month prior to screening.\n8. Current or prior retroperitoneal external beam radiotherapy within 5 years of screening.\n9. Prior treatment with adenovirus-based drugs including use of other adenovirus vector medications, including COVID-19 vaccines, within 2 weeks before instillation.\n10. Suspected and\u002For a medical history of hypersensitivity to nadofaragene firadenovec, interferon-α2b (IFN-α2b) and\u002For adenovector medications.\n11. Urinary tract infection or bacterial cystitis (once satisfactorily treated, subjects can enter the trial).\n12. Clinically significant and unexplained elevated liver or renal function tests at screening.\n13. Women who are pregnant (highly sensitive urine or serum pregnancy test at screening) or breastfeeding.\n14. Any other significant disease or other clinical findings which in the opinion of the investigator would prevent trial entry.\n15. History of malignancy in any other organ system than the upper urinary tract within the past 5 years prior to screening. However, subjects with the following exceptions will be allowed inclusion in the trial:\n\n    * Treated basal cell carcinoma or squamous cell carcinoma of the skin.\n    * History of ≤pT2 upper tract urothelial carcinoma, at least 24 months after radical nephroureterectomy (RNU).\n    * Cervical intraepithelial carcinoma (CIN) without evidence of invasive carcinoma.\n    * Prostate cancer that is under active surveillance or urothelial cancer. All other genitourinary cancers are excluded.\n16. Inability to deliver IMP to the pyelocaliceal system.\n17. Previous BCG treatment during 6 months before the initiation of treatment.\n18. Any immunosuppressive therapy within 3 months prior to screening.\n19. Subjects who are immunocompromised or immunodeficient at screening.\n20. Subjects with solitary kidney and\u002For an eGFR \\\u003C60 mL\u002Fmin\u002F1.73 m2 (only applicable for subjects in the safety lead-in period).",{"count":59,"type":21},20,[61,24],"PHASE1","The primary purpose of this trial is to evaluate the safety \\& tolerability of Nadofaragene Firadenovec in subjects with LG-UTUC. To help with this evaluation, a safety lead-in period will be conducted for the first 6 subjects. Complete response is at 3 or 6 months defined as absence of any UTUC in the renal pelvis.",[64],"Low-grade Upper Tract Urothelial Carcinoma","2026-05-06",{"date":67,"type":41},"2026-05-08",{"date":69,"type":41},"2025-06-12",{"date":71,"type":21},"2029-11-30",{"name":73,"class":48},"Ferring Pharmaceuticals",9]