minimat-trial Search Results


90
Thomas RECORDING five-channel multielectrode recording minimatrix
Five Channel Multielectrode Recording Minimatrix, supplied by Thomas RECORDING, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc06622013-57-26-30?v=Thomas+RECORDING
Average 90 stars, based on 1 article reviews
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90
Thomas RECORDING computer controlled micro drive (minimatrix)
Computer Controlled Micro Drive (Minimatrix), supplied by Thomas RECORDING, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc04454453-96-18-23?v=Thomas+RECORDING
Average 90 stars, based on 1 article reviews
computer controlled micro drive (minimatrix) - by Bioz Stars, 2026-07
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90
Acera Surgical m-sefm
Results of USP <51> Antimicrobial Effectiveness Testing for <t> micronized </t> SEFM The limit of detection for this assay was 50 CFU/mL. Values observed below this limit are presented as <5.00E+01 in the table above. USP = United States Pharmacopeia; SEFM = synthetic electrospun fiber matrix; m-SEFM = <t> micronized </t> synthetic electrospun fiber matrix; CFU = colony forming units.
M Sefm, supplied by Acera Surgical, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc10768939-47-18-22?v=Acera+Surgical
Average 90 stars, based on 1 article reviews
m-sefm - by Bioz Stars, 2026-07
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90
Genentech inc anti-vegf antibody ranibizumab
Table of study acronyms
Anti Vegf Antibody Ranibizumab, supplied by Genentech inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc06419319-406-10-27?v=Genentech+inc
Average 90 stars, based on 1 article reviews
anti-vegf antibody ranibizumab - by Bioz Stars, 2026-07
90/100 stars
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90
Thomas RECORDING 5-channel multielectrode recording system minimatrix
Table of study acronyms
5 Channel Multielectrode Recording System Minimatrix, supplied by Thomas RECORDING, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc08751855-61-7-12?v=Thomas+RECORDING
Average 90 stars, based on 1 article reviews
5-channel multielectrode recording system minimatrix - by Bioz Stars, 2026-07
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90
MiniMed Inc hybrid closed-loop system
Table of study acronyms
Hybrid Closed Loop System, supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc12017971__mmc1-45-128-128?v=MiniMed+Inc
Average 90 stars, based on 1 article reviews
hybrid closed-loop system - by Bioz Stars, 2026-07
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90
ChangePoint Inc spike in oddball probability
Table of study acronyms
Spike In Oddball Probability, supplied by ChangePoint Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc06716947-44-23-38?v=ChangePoint+Inc
Average 90 stars, based on 1 article reviews
spike in oddball probability - by Bioz Stars, 2026-07
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90
Comedicus Inc pericardial access device perducer
Table of study acronyms
Pericardial Access Device Perducer, supplied by Comedicus Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
pericardial access device perducer - by Bioz Stars, 2026-07
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99
ATCC eagle s minimum essential medium
Table of study acronyms
Eagle S Minimum Essential Medium, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc07018538-38-5-9?v=ATCC
Average 99 stars, based on 1 article reviews
eagle s minimum essential medium - by Bioz Stars, 2026-07
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90
MiniMed Inc medtronic
Table of study acronyms
Medtronic, supplied by MiniMed Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc06647052-399-17-18?v=MiniMed+Inc
Average 90 stars, based on 1 article reviews
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99
Qiagen proteinase k
Table of study acronyms
Proteinase K, supplied by Qiagen, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pmc05812437-86-3-8?v=Qiagen
Average 99 stars, based on 1 article reviews
proteinase k - by Bioz Stars, 2026-07
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90
NSABP Foundation nsabp p1 trial
Table of study acronyms
Nsabp P1 Trial, supplied by NSABP Foundation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/minimat-trial/pm08007704-90-30-18?v=NSABP+Foundation
Average 90 stars, based on 1 article reviews
nsabp p1 trial - by Bioz Stars, 2026-07
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Image Search Results


Results of USP <51> Antimicrobial Effectiveness Testing for  micronized  SEFM The limit of detection for this assay was 50 CFU/mL. Values observed below this limit are presented as <5.00E+01 in the table above. USP = United States Pharmacopeia; SEFM = synthetic electrospun fiber matrix; m-SEFM =  micronized  synthetic electrospun fiber matrix; CFU = colony forming units.

Journal: Cureus

Article Title: Antimicrobial Effectiveness Testing of Resorbable Electrospun Fiber Matrix per United States Pharmacopeia (USP) <51>

doi: 10.7759/cureus.50055

Figure Lengend Snippet: Results of USP <51> Antimicrobial Effectiveness Testing for micronized SEFM The limit of detection for this assay was 50 CFU/mL. Values observed below this limit are presented as <5.00E+01 in the table above. USP = United States Pharmacopeia; SEFM = synthetic electrospun fiber matrix; m-SEFM = micronized synthetic electrospun fiber matrix; CFU = colony forming units.

Article Snippet: The SEFM is a soft, white, conformable, nonfriable, absorbable material available in both sheet form (s-SEFM) and in micronized form (m-SEFM) (MiniMatrix®, Acera Surgical, Inc., St. Louis, Mo) [ ].

Techniques:

Table of study acronyms

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Table of study acronyms

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques: Injection, Inhibition

Treatment groups in included trials

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Treatment groups in included trials

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques: Injection

Summary of findings: bevacizumab versus  ranibizumab

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Summary of findings: bevacizumab versus ranibizumab

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Summary of findings:  anti‐VEGF  treatment versus control

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Summary of findings: anti‐VEGF treatment versus control

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Forest plot of comparison: 2 Ranibizumab versus control, outcome: 2.1 Gain of 15 or more letters visual acuity at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Forest plot of comparison: 2 Ranibizumab versus control, outcome: 2.1 Gain of 15 or more letters visual acuity at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Forest plot of comparison: 2 Ranibizumab versus control, outcome: 2.2 Gain of 15 or more letters visual acuity at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Forest plot of comparison: 2 Ranibizumab versus control, outcome: 2.2 Gain of 15 or more letters visual acuity at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Adverse events up to 1 year:  ranibizumab  versus control

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Adverse events up to 1 year: ranibizumab versus control

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Adverse events up to 2 years:  ranibizumab  versus control

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Adverse events up to 2 years: ranibizumab versus control

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 1 Gain of 15 or more letters visual acuity at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 1 Gain of 15 or more letters visual acuity at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Forest plot of comparison: 4 Bevacizumab versus ranibizumab, outcome: 4.1 Gain of 15 or more letters visual acuity at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Forest plot of comparison: 4 Bevacizumab versus ranibizumab, outcome: 4.1 Gain of 15 or more letters visual acuity at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 2 Gain of 15 or more letters visual acuity at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 2 Gain of 15 or more letters visual acuity at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Forest plot of comparison: 4 Bevacizumab versus ranibizumab, outcome: 4.2 Gain of 15 or more letters visual acuity at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Forest plot of comparison: 4 Bevacizumab versus ranibizumab, outcome: 4.2 Gain of 15 or more letters visual acuity at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 3 Loss of fewer than 15 letters visual acuity at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 3 Loss of fewer than 15 letters visual acuity at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 4 Loss of fewer than 15 letters visual acuity at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 4 Loss of fewer than 15 letters visual acuity at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 5 Visual acuity better than 20/200 at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 5 Visual acuity better than 20/200 at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 6 Visual acuity better than 20/200 at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 6 Visual acuity better than 20/200 at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 7 Mean change in visual acuity at 1 year (number of letters).

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 7 Mean change in visual acuity at 1 year (number of letters).

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 8 Mean change in visual acuity at 2 years (number of letters).

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 8 Mean change in visual acuity at 2 years (number of letters).

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 9 Reduction in central retinal thickness at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 9 Reduction in central retinal thickness at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 10 Reduction in central retinal thickness at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 10 Reduction in central retinal thickness at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 11 No problems in quality of life domain at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 11 No problems in quality of life domain at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 12 No problems in quality of life domain at 2 years.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 12 No problems in quality of life domain at 2 years.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Adverse events up to 1 year: bevacizumab versus  ranibizumab

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Adverse events up to 1 year: bevacizumab versus ranibizumab

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Adverse events up to 2 years: bevacizumab versus  ranibizumab

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Adverse events up to 2 years: bevacizumab versus ranibizumab

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

Comparison 2 Bevacizumab versus ranibizumab, Outcome 13 Loss of fewer than 30 letters visual acuity at 1 year.

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Comparison 2 Bevacizumab versus ranibizumab, Outcome 13 Loss of fewer than 30 letters visual acuity at 1 year.

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques:

 Anti‐VEGF  treatment versus control

Journal: The Cochrane Database of Systematic Reviews

Article Title: Anti‐vascular endothelial growth factor for neovascular age‐related macular degeneration

doi: 10.1002/14651858.CD005139.pub4

Figure Lengend Snippet: Anti‐VEGF treatment versus control

Article Snippet: Notes , Full study name: Minimally Classic/Occult Trial of the Anti‐VEGF Antibody Ranibizumab in the Treatment of Neovascular Age‐Related Macular Degeneration Trial registration: {"type":"clinical-trial","attrs":{"text":"NCT00056836","term_id":"NCT00056836"}} NCT00056836 Funding sources: Genentech, USA, and Novartis Pharma, Switzerland Declarations of interest: various authors reported that they had received consulting fees from Genentech, Eyetech, Novartis Ophthalmics, Novartis, QLT, Alcon Laboratories, Pfizer, Regeneron, Theragenics, VisionCare, Protein Design Labs, Allergan, BioAxone, Tanox, Genaera, Jerini, Oxigene, Quark, Genzyme, iScience, ISTA, and Athenagen; lecture fees from Genentech, Eyetech, Pfizer, Jerini, Allergan, and Novartis Ophthalmics; grant support from Genentech, Novartis, Eyetech, Pfizer, Theragenics, and Genaera and Alcon Laboratories; and/or equity interest in Pfizer and/or were employees of Genentech and owned Genentech stock Study period: enrollment March 2003 to December 2003 Reported subgroup analyses: by baseline lesion (4 or fewer optic disc areas; more than 4), type of lesion (minimally classic; occult with no classic), and baseline VA (fewer than 55 letters; 55 or more letters) Contacting study investigators: trial authors contacted and contributed information for this review , .

Techniques: