Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D008268', 'term': 'Macular Degeneration'}], 'ancestors': [{'id': 'D012162', 'term': 'Retinal Degeneration'}, {'id': 'D012164', 'term': 'Retinal Diseases'}, {'id': 'D005128', 'term': 'Eye Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000069579', 'term': 'Ranibizumab'}], 'ancestors': [{'id': 'D061067', 'term': 'Antibodies, Monoclonal, Humanized'}, {'id': 'D000911', 'term': 'Antibodies, Monoclonal'}, {'id': 'D000906', 'term': 'Antibodies'}, {'id': 'D007136', 'term': 'Immunoglobulins'}, {'id': 'D007162', 'term': 'Immunoproteins'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D012712', 'term': 'Serum Globulins'}, {'id': 'D005916', 'term': 'Globulins'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE'}, 'primaryPurpose': 'TREATMENT'}, 'enrollmentInfo': {'count': 426}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2003-05'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2014-03', 'completionDateStruct': {'date': '2006-09', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2014-03-18', 'studyFirstSubmitDate': '2003-05-29', 'studyFirstSubmitQcDate': '2003-05-29', 'lastUpdatePostDateStruct': {'date': '2014-03-19', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2003-05-30', 'type': 'ESTIMATED'}}, 'conditionsModule': {'keywords': ['Neovascular age-related macular degeneration'], 'conditions': ['Macular Degeneration']}, 'referencesModule': {'references': [{'pmid': '17021319', 'type': 'RESULT', 'citation': 'Brown DM, Kaiser PK, Michels M, Soubrane G, Heier JS, Kim RY, Sy JP, Schneider S; ANCHOR Study Group. Ranibizumab versus verteporfin for neovascular age-related macular degeneration. N Engl J Med. 2006 Oct 5;355(14):1432-44. doi: 10.1056/NEJMoa062655.'}, {'pmid': '17949673', 'type': 'RESULT', 'citation': 'Kaiser PK, Brown DM, Zhang K, Hudson HL, Holz FG, Shapiro H, Schneider S, Acharya NR. Ranibizumab for predominantly classic neovascular age-related macular degeneration: subgroup analysis of first-year ANCHOR results. Am J Ophthalmol. 2007 Dec;144(6):850-857. doi: 10.1016/j.ajo.2007.08.012. Epub 2007 Oct 22.'}, {'pmid': '19118696', 'type': 'RESULT', 'citation': 'Brown DM, Michels M, Kaiser PK, Heier JS, Sy JP, Ianchulev T; ANCHOR Study Group. Ranibizumab versus verteporfin photodynamic therapy for neovascular age-related macular degeneration: Two-year results of the ANCHOR study. Ophthalmology. 2009 Jan;116(1):57-65.e5. doi: 10.1016/j.ophtha.2008.10.018.'}, {'pmid': '19255158', 'type': 'RESULT', 'citation': 'Suner IJ, Kokame GT, Yu E, Ward J, Dolan C, Bressler NM. Responsiveness of NEI VFQ-25 to changes in visual acuity in neovascular AMD: validation studies from two phase 3 clinical trials. Invest Ophthalmol Vis Sci. 2009 Aug;50(8):3629-35. doi: 10.1167/iovs.08-3225. Epub 2009 Feb 28.'}, {'pmid': '19139332', 'type': 'RESULT', 'citation': 'Bressler NM, Chang TS, Fine JT, Dolan CM, Ward J; Anti-VEGF Antibody for the Treatment of Predominantly Classic Choroidal Neovascularization in Age-Related Macular Degeneration (ANCHOR) Research Group. Improved vision-related function after ranibizumab vs photodynamic therapy: a randomized clinical trial. Arch Ophthalmol. 2009 Jan;127(1):13-21. doi: 10.1001/archophthalmol.2008.562.'}, {'pmid': '24424249', 'type': 'DERIVED', 'citation': 'Thach AB, Yau L, Hoang C, Tuomi L. Time to clinically significant visual acuity gains after ranibizumab treatment for retinal vein occlusion: BRAVO and CRUISE trials. Ophthalmology. 2014 May;121(5):1059-66. doi: 10.1016/j.ophtha.2013.11.022. Epub 2014 Jan 11.'}, {'pmid': '23453513', 'type': 'DERIVED', 'citation': 'Weinberg DV, Shapiro H, Ehrlich JS. Ranibizumab treatment outcomes in phakic versus pseudophakic eyes: an individual patient data analysis of 2 phase 3 trials. Ophthalmology. 2013 Jun;120(6):1278-82. doi: 10.1016/j.ophtha.2012.11.042. Epub 2013 Feb 28.'}, {'pmid': '23009891', 'type': 'DERIVED', 'citation': 'Bressler NM, Chang TS, Varma R, Suner I, Lee P, Dolan CM, Ward J, Ianchulev T, Fine J. Driving ability reported by neovascular age-related macular degeneration patients after treatment with ranibizumab. Ophthalmology. 2013 Jan;120(1):160-8. doi: 10.1016/j.ophtha.2012.07.027. Epub 2012 Sep 23.'}, {'pmid': '21794843', 'type': 'DERIVED', 'citation': 'Rosenfeld PJ, Shapiro H, Ehrlich JS, Wong P; MARINA and ANCHOR Study Groups. Cataract surgery in ranibizumab-treated patients with neovascular age-related macular degeneration from the phase 3 ANCHOR and MARINA trials. Am J Ophthalmol. 2011 Nov;152(5):793-8. doi: 10.1016/j.ajo.2011.04.025. Epub 2011 Jul 26.'}, {'pmid': '20920825', 'type': 'DERIVED', 'citation': 'Rosenfeld PJ, Shapiro H, Tuomi L, Webster M, Elledge J, Blodi B; MARINA and ANCHOR Study Groups. Characteristics of patients losing vision after 2 years of monthly dosing in the phase III ranibizumab clinical trials. Ophthalmology. 2011 Mar;118(3):523-30. doi: 10.1016/j.ophtha.2010.07.011.'}, {'pmid': '20378094', 'type': 'DERIVED', 'citation': 'Barbazetto IA, Saroj N, Shapiro H, Wong P, Ho AC, Freund KB. Incidence of new choroidal neovascularization in fellow eyes of patients treated in the MARINA and ANCHOR trials. Am J Ophthalmol. 2010 Jun;149(6):939-946.e1. doi: 10.1016/j.ajo.2010.01.007. Epub 2010 Apr 8.'}, {'pmid': '20189654', 'type': 'DERIVED', 'citation': 'Bressler NM, Chang TS, Suner IJ, Fine JT, Dolan CM, Ward J, Ianchulev T; MARINA and ANCHOR Research Groups. Vision-related function after ranibizumab treatment by better- or worse-seeing eye: clinical trial results from MARINA and ANCHOR. Ophthalmology. 2010 Apr;117(4):747-56.e4. doi: 10.1016/j.ophtha.2009.09.002. Epub 2010 Mar 2.'}]}, 'descriptionModule': {'briefSummary': 'This is a phase III, multicenter, randomized, double-masked, active treatment-controlled study of intravitreally administered ranibizumab compared with verteporfin (Visudyne) photodynamic therapy (PDT) in treating subfoveal neovascular mascular degeneration.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '50 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Signed informed consent\n* Age \\>=50 years\n* Eligibility for treatment with PDT using verteporfin in the study eye according to the Visudyne product labeling\n* Future treatment with PDT using verteporfin anticipated or expected in the study eye\n* Primary or recurrent subfoveal choroidal neovascularization (CNV) lesions secondary to age-related macular degeneration (AMD) in the study eye\n* A classic CNV component (well-demarcated hyperfluorescence boundaries in the early phase of the fluorescein angiogram) that is \\>=50% of the total lesion size\n* Total lesion size of less than or equal to 5400 um in greatest linear dimension (GLD)\n* Best corrected visual acuity, using Early Treatment of Diabetic Retinopathy Study (ETDRS) charts, of 20/40 to 20/320 (Snellen equivalent) in the study eye\n\nExclusion Criteria:\n\n* Prior treatment with verteporfin, external-beam radiation therapy, or transpupillary thermotherapy (TTT) in the study eye\n* Treatment with verteporfin in the non-study eye less than 7 days preceding Day 0\n* Previous participation in a clinical trial (for either eye) involving anti angiogenic drugs (pegaptanib, ranibizumab, anecortave acetate, protein kinase C inhibitors, etc.)\n* Previous intravitreal drug delivery (e.g., intravitreal corticosteroid injection or device implantation) in the study eye\n* Previous subfoveal focal laser photocoagulation in the study eye\n* Laser photocoagulation (juxtafoveal or extrafoveal) in the study eye within 1 month preceding Day 0\n* History of vitrectomy surgery in the study eye\n* History of submacular surgery or other surgical intervention for AMD in the study eye\n* Previous participation in any studies of investigational drugs within 1 month preceding Day 0 (excluding vitamins and minerals)\n* Subretinal hemorrhage in the study eye that involves the center of the fovea, if the size of the hemorrhage is either \\>=50% of the total lesion area or \\>=1 disc area (DA) in size\n* Subfoveal fibrosis or atrophy in the study eye\n* CNV in either eye due to other causes, such as ocular histoplasmosis, trauma, or pathologic myopia\n* Retinal pigment epithelial tear involving the macula in the study eye\n* Any concurrent intraocular condition in the study eye (e.g., cataract or diabetic retinopathy) that, in the opinion of the Investigator could either: (1) Require medical or surgical intervention during the 24-month study period to prevent or treat visual loss that might result from that condition, or (2) If allowed to progress untreated, could likely contribute to loss of at least 2 Snellen equivalent lines of best corrected visual acuity over the 24-month study period\n* Active intraocular inflammation (grade trace or above) in the study eye\n* Current vitreous hemorrhage in the study eye\n* History of rhegmatogenous retinal detachment or macular hole (Stage 3 or 4) in the study eye\n* History of idiopathic or autoimmune-associated uveitis in either eye\n* Infectious conjunctivitis, keratitis, scleritis, or endophthalmitis in either eye\n* Aphakia or absence of the posterior capsule in the study eye\n* Spherical equivalent of the refractive error in the study eye demonstrating more than -8 diopters of myopia\n* Intraocular surgery (including cataract surgery) in the study eye within 2 months preceding Day 0\n* Uncontrolled glaucoma in the study eye (defined as intraocular pressure \\>=30 mmHg despite treatment with anti-glaucoma medication)\n* History of glaucoma filtering surgery in the study eye\n* History of corneal transplant in the study eye\n* Premenopausal women not using adequate contraception\n* History of other disease, metabolic dysfunction, physical examination finding, or clinical laboratory finding giving reasonable suspicion of a disease or condition that contraindicates the use of an investigational drug or that might affect interpretation of the results of the study or render the subject at high risk for treatment complications\n* Current treatment for active systemic infection\n* History of allergy to fluorescein, not amenable to treatment\n* Inability to obtain fundus photographs or fluorescein angiograms of sufficient quality to be analyzed and graded by the central reading center\n* Inability to comply with study or follow up procedures'}, 'identificationModule': {'nctId': 'NCT00061594', 'briefTitle': 'A Study to Compare rhuFab V2 With Verteporfin Photodynamic in Treating Subfoveal Neovascular Macular Degeneration', 'organization': 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