[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100655701":3},{"organization":4,"outcomesModule":7,"designInfo":26,"detailedDescription":24,"studyPopulation":24,"armGroups":32,"interventions":43,"overallOfficials":24,"centralContacts":24,"locations":24,"responsibleParty":51,"collaborators":24,"id":53,"slug":54,"hasResults":55,"nctId":56,"briefTitle":57,"officialTitle":58,"acronym":24,"eligibilityCriteria":59,"healthyVolunteers":55,"sex":60,"minAge":61,"maxAge":24,"enrollmentInfo":62,"targetDuration":24,"studyType":65,"phases":66,"briefSummary":68,"conditions":69,"keywords":24,"overallStatus":71,"whyStopped":24,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":24},{"fullName":5,"class":6},"Guangzhou JOYO Pharma Co., Ltd","INDUSTRY",{"primaryOutcomes":8,"secondaryOutcomes":13,"otherOutcomes":24},[9],{"measure":10,"description":11,"timeFrame":12},"Progression-Free Survival (PFS) assessed by Blinded Independent Central Review (BICR\u002FBIRC) per RECIST v1.1","PFS is defined as the time from randomization to the first occurrence of radiographic disease progression determined by blinded independent central review (BIRC) according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1), or death due to any cause within 12 weeks after last tumor assessment (to avoid censoring death as non-event if no progression documented). Patients alive and without progression at data cutoff are censored at the date of last adequate tumor assessment.","From randomization to the date of first documented radiographic disease progression or death from any cause, whichever occurs first, assessed up to approximately 24 months",[14,18,22],{"measure":15,"description":16,"timeFrame":17},"Investigator-assessed Progression-Free Survival (PFS) per RECIST v1.1","PFS assessed by the local investigator using the same RECIST v1.1 criteria and scan schedule as the BIRC pathway, but without blinding to treatment assignment. Defined as time from randomization to first investigator-determined radiographic disease progression, or death from any cause (if no prior progression). No central adjudication. Used for sensitivity analysis against the primary BIRC-based PFS.","From randomization to first documented radiographic progression by investigator or death from any cause, whichever occurs first, assessed up to ~24 months",{"measure":19,"description":20,"timeFrame":21},"Overall Survival (OS)","OS is defined as the time from randomization to the date of death due to any cause. Patients alive at the time of data cutoff will be censored at the last known alive date. OS will be estimated using the Kaplan-Meier method and compared between arms by log-rank test; hazard ratio and 95% CI from Cox proportional hazards model reported.","From randomization to date of death from any cause, assessed up to approximately 36 months (or final analysis cut-off)",{"measure":23,"description":24,"timeFrame":25},"Incidence, severity, and relationship of Adverse Events (AEs) and Serious Adverse Events (SAEs)",null,"From first dose of study drug to 30 days after last dose (or 90 days for SAEs \u002F death), assessed up to ~24 months",{"allocation":27,"interventionModel":28,"interventionModelDescription":24,"primaryPurpose":29,"observationalModel":24,"timePerspective":24,"maskingInfo":30},"RANDOMIZED","PARALLEL","TREATMENT",{"masking":31,"maskingDescription":24,"whoMasked":24},"NONE",[33,38],{"label":34,"type":35,"description":24,"interventionNames":36},"JYP0322 Tablets","EXPERIMENTAL",[37],"Drug: JYP0322 Tablets",{"label":39,"type":40,"description":24,"interventionNames":41},"Crizotinib Capsules","ACTIVE_COMPARATOR",[42],"Drug: Crizotinib Capsules",[44,48],{"type":45,"name":34,"description":46,"armGroupLabels":47,"otherNames":24},"DRUG","Oral administration, 150 mg each dose, three times daily (TID), continuous dosing.",[34],{"type":45,"name":39,"description":49,"armGroupLabels":50,"otherNames":24},"Oral administration, 250 mg twice daily (BID), continuous dosing.",[39],{"type":52,"investigatorFullName":24,"investigatorTitle":24,"investigatorAffiliation":24,"oldNameTitle":24,"oldOrganization":24},"SPONSOR","100655701","phase-3-a-phase-iii-study-to-evaluate-the-efficacy-and-safety-of-jyp0322-versus-crizotinib-in-previously-untreated-ros1-positive-locally-advanced-or-metastatic-non-small-cell-lung-cancer-100655701",false,"NCT07816380","A Phase III Study to Evaluate the Efficacy and Safety of JYP0322 in Previously Untreated ROS1-Positive Locally Advanced or Metastatic Non-Small Cell Lung Cancer","A Randomized, Open-Label, Multicenter, Phase III Study to Evaluate the Efficacy and Safety of JYP0322 Versus Crizotinib in Previously Untreated ROS1-Positive Locally Advanced or Metastatic Non-Small Cell Lung Cancer","Inclusion Criteria:\n\n* Voluntary participation and signed written informed consent (ICF) before any study-specific procedure.\n\nAge ≥ 18 years at screening. Histologically or cytologically confirmed, unresectable locally advanced (AJCC 9th edition stage IIIB or IIIC not amenable to multimodality therapy) or metastatic (stage IV) ROS1-positive non-small cell lung cancer (NSCLC).\n\nROS1 gene rearrangement\u002Ffusion positivity confirmed by a qualified local laboratory using PCR, NGS, or FISH. IHC alone is not acceptable. A written report of the ROS1 test must be provided.\n\nSufficient and adequate archival tumor tissue must be available for central laboratory ROS1 retesting per the Central Lab Manual; if no archival tissue is available, a fresh tumor biopsy is required.\n\nNo prior ROS1 TKI therapy. Prior systemic therapy limited to ≤1 line of standard chemotherapy:\n\nA prior chemotherapy-based regimen administered for ≥1 cycle counts as one line.\n\nDisease recurrence within 6 months after completion of adjuvant chemotherapy counts that adjuvant regimen as one prior line.\n\nAsymptomatic central nervous system (CNS) metastases allowed (leptomeningeal carcinomatosis excluded). Previously treated and controlled\u002Fstabilized CNS metastases permitted if:\n\nOn non-enzyme-inducing antiepileptic drugs (non-EIAED) for seizure prophylaxis; or EIAED discontinued ≥14 days before randomization.\n\nIf corticosteroids needed, stable or tapering dose ≤10 mg\u002Fday prednisone (or equivalent) for ≥14 days before randomization.\n\nPrior local therapy (WBRT, SRS\u002FSRT) completed ≥14 days before randomization; treatment-related toxicities (except alopecia) resolved to ≤ Grade 1 (CTCAE v5.0).\n\nAt least one measurable lesion per RECIST v1.1. ECOG performance status 0-1. Expected survival ≥ 3 months.\n\nAdequate organ function within 14 days before randomization (no blood products, growth factors, or platelet\u002F WBC boosters within 14 days):\n\n1. ANC ≥ 1.5 × 10\\^9\u002FL\n2. Platelets ≥ 100 × 10\\^9\u002FL\n3. Hemoglobin ≥ 90 g\u002FL (stable erythropoietin ≥3 months allowed)\n4. CrCl \\> 45 mL\u002Fmin (Cockcroft-Gault)\n5. Total bilirubin \\\u003C 1.5 × ULN (Gilbert syndrome ≤ 3.0 × ULN)\n6. AST and ALT \\\u003C 2.5 × ULN (\\\u003C 5 × ULN if liver metastasis)\n7. APTT and INR \\\u003C 1.5 × ULN Women of childbearing potential: negative serum pregnancy test within 7 days before randomization. All participants with reproductive potential (male and female) must agree to use highly effective contraception (hormonal, barrier, or abstinence) during treatment and for 6 months after last dose. Willing and able to comply with scheduled visits, treatment, labs, and procedures.\n\nExclusion Criteria:\n\n* History of severe cardiovascular or cerebrovascular disease, including but not limited to: clinically significant cardiac rhythm or conduction abnormality (e.g., ventricular arrhythmia requiring intervention, 2nd-3rd degree AV block); acute coronary syndrome, congestive heart failure, aortic dissection, severe stable\u002Funstable angina, coronary\u002Fperipheral vascular intervention, stroke or other ≥Grade 3 cerebrovascular event (including TIA), pulmonary embolism, DVT or other clinically significant thrombosis within 6 months before randomization; NYHA \\> Class II heart failure or LVEF \\\u003C 50%; any uncontrolled atrial fibrillation; QTcF \\> 470 ms or symptomatic bradycardia \\\u003C 45 bpm; known congenital long QT syndrome or history of QT prolongation.\n\nActive infection requiring IV antibiotics or hospitalization at randomization. Acute flare of dysphagia or GI disease affecting absorption (Crohn's, UC, short bowel syndrome, or other malabsorption).\n\nFailure to recover from prior antitumor therapy toxicity to baseline or ≤Grade 1 (CTCAE v5.0), except alopecia, Grade 2 peripheral neuropathy, or hypothyroidism controlled by replacement judged safe by investigator.\n\nMajor surgical procedure (other than dx\u002Fbiopsy\u002Fdrainage) within 4 weeks before randomization, or anticipated major surgery during study; vascular access placement and minor procedures (catheter, core needle biopsy) allowed.\n\nOther primary malignancy except: adequately treated melanoma\u002Fskin carcinoma\u002Fcervical carcinoma in situ; treated non-metastatic prostate cancer; or other primary malignancy with no relapse ≥3 years.\n\nUntreated spinal cord compression by tumor. Participated in another interventional trial within 4 weeks before first dose (screen failures exempt).\n\nInterstitial fibrosis, ILD, or drug-induced pneumonitis within 6 months before first dose not recovered to Grade 1 (asymptomatic radiation pneumonitis exempt).\n\nSystemic anticancer therapy (chemo-based or other) within 14 days or 5 half-lives (whichever shorter, minimum 14 days) before randomization.\n\nClinically uncontrolled serous effusion needing drainage \\> once\u002Fmonth (pericardial\u002Fpleural\u002Fascites), or \\\u003C 2 weeks observation after last drainage before randomization.\n\nHistory of severe allergy or hypersensitivity to JYP0322 or crizotinib excipients.\n\nActive HBV (HBsAg+ and HBV DNA ≥1000 IU\u002FmL or 5000 copies\u002FmL), active HCV (RNA+), syphilis requiring treatment (RPR ≤1:2 with TPHA+ allowed), or HIV infection.\n\nPregnant or lactating. Use of strong CYP3A4 inhibitors\u002Finducers or narrow-therapeutic-index CYP3A4 substrates within 14 days or 5 half-lives (shorter) before randomization, or inability to discontinue during study.\n\nActive or recurrent autoimmune disease, depression\u002Faffective disorder or suicidal risk, prior bone marrow\u002Forgan transplant, or any condition investigator judges unsafe.\n\nUncontrolled hyperthyroidism or hypothyroidism with prior severe comorbidity. Moderate-to-severe hepatic impairment history: prior ≥Grade 3 hepatotoxicity, or serious liver baseline (cirrhosis etc.).\n\nTumor invasion of great vessels (aorta, pulmonary artery\u002Fvein, vena cava) on imaging; OR any prior TKI therapy including ROS1-TKI.","ALL","18 Years",{"count":63,"type":64},216,"ESTIMATED","INTERVENTIONAL",[67],"PHASE3","This is a randomized, open-label, multicenter phase III study to evaluate the efficacy and safety of JYP0322 compared with crizotinib in previously untreated ROS1-positive locally advanced or metastatic non-small cell lung cancer.",[70],"NSCLC (Advanced Non-small Cell Lung Cancer)","NOT_YET_RECRUITING","2026-09-20",{"date":74,"type":75},"2026-09-22","ACTUAL",{"date":77,"type":64},"2026-10-30",{"date":79,"type":64},"2029-12-30",{"name":5,"class":6}]