- |||||||||| Susvimo (ranibizumab port delivery system) / Roche, Lucentis (ranibizumab) / Roche, Novartis
Trial completion date, Trial primary completion date: PAVILION: A Multicenter, Randomized Study in Participants With Diabetic Retinopathy Without Center-involved Diabetic Macular Edema To Evaluate the Efficacy, Safety, and Pharmacokinetics of Ranibizumab Delivered Via the Port Delivery System Relative to the Comparator Arm (clinicaltrials.gov) - Feb 17, 2022 P3, N=160, Active, not recruiting, IVR 1 and 3 days before surgery can significantly reduce VEGF content in aqueous humor and effectively improve intraoperative conditions without causing TRD. Trial completion date: Jan 2023 --> Mar 2024 | Trial primary completion date: Jan 2023 --> Sep 2022
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Journal: Treat-and-Extend vs. Pro Re Nata Regimen of Ranibizumab for Diabetic Macular Edema-A Two-Year Matched Comparative Study. (Pubmed Central) - Feb 12, 2022 During the 2-year treatment periods, the T&E group received more injections than the PRN group (11.0 ± 3.2 vs. 6.2 ± 2.0; p < 0.001), while the PRN group had more recurrence of macular edema than the T&E group (71 vs. 41%; p = 0.015). After 2-year ranibizumab treatment for DME, better visual and anatomical improvement and less recurrence of macular edema were achieved in the T&E group, with more injections administered.
- |||||||||| Avastin (bevacizumab) / Roche
Review, Journal: A review of neovascular glaucoma. Etiopathogenesis and treatment. (Pubmed Central) - Feb 4, 2022 Anyway, the best treatment is prevention, so we must be very attentive at patients with risk factors for developing the NVG. Abbreviations: NVG = neovascular glaucoma, ICA = iridocorneal angle, IOP = intraocular pressure, TM = trabecular meshwork, AH = aqueous humor, AC = anterior chamber, PRP = panretinal photocoagulation, VEGF = vascular endothelial growing factor, Anti-VEGF = anti- vascular endothelial growing factor, PAS = peripheral anterior synechiae, CRVO = central retinal vein occlusion, PDR = proliferative diabetic retinopathy, DR = diabetic retinopathy, OIS = ocular ischemic syndrome, CRAO = central retinal artery occlusion, ROP = retinopathy of prematurity, FEVR = familial exudative vitreoretinopathy, PVR = proliferative vitreoretinopathy, MMPs = matrix metalloproteinases, VEGFR = vascular endothelial growing factor receptor, PDGF = platelet-derived growth factor, PIGF = placental growth factor, NRP = neuropilins, HIF = hypoxia-inducible factor, SDF1 = stromal cell-derived factor 1, DDL4 = delta like ligand 4, NICD = Notch intracellular domain, TIMMPs = tissue inhibitors of matrix metalloproteinases, ANGPT = angiopoietin, Tie 2 = tyrosine-protein kinase receptor for angiopoietins, IGF-1 = insulin-like growth factor 1, RPE = retinal pigment epithelium, IL = interleukin, TNF = tumor necrosis factor, bFGF = basic fibroblast growth factor, TGF = transforming growth factor, HGF = hepatocyte growth factor, TNFR 2 = tumor necrosis factor receptor 2, OIR = oxygen induced retinopathy, NVI = neovascularization of the iris, NVA = neovascularization of the iridocorneal angle, FA = fluorescein angiography, RAPD = relative afferent pupillary defect, CNP = capillary non-perfusion, NVE = neovascularization elsewhere in the retina, NVD = neovascularization of the optic disc, FFA = fundus fluorescein angiography, OCTA = optical coherence tomography angiography, B-scan US = B-scan ocular ultrasound, AS-OCT = anterior segment optical coherence tomography, ARC = anterior retinal cryotherapy, FDA = food and drug administration, United States of America, BVZ = bevacizumab, RBZ = ranibizumab, AFB = aflibercept, AMD/ ARMD = age related macular degeneration, DME = diabetic macular edema, GDDs = glaucoma drainage devices, MMC = mitomycin C, 5-FU = 5-fluorouracil, AGV = Ahmed glaucoma valve, AADI = Aurolab aqueous drainage implant, MIGS = minimally invasive glaucoma surgery, BCVA = best corrected visual acuity, TVT = Tube versus Trabeculectomy study, MPC = micro-pulse cyclophotocoagulation.
- |||||||||| Eylea (aflibercept intravitreal) / Regeneron, Lucentis (ranibizumab) / Roche, Novartis, Lumitin (conbercept) / Chengdu Kanghong Pharma
New trial, Real-world evidence, Real-world: Anti-VEGF in Real-world (clinicaltrials.gov) - Feb 2, 2022 P=N/A, N=1000, Recruiting,
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Clinical, Journal: Ranibizumab for the treatment of diabetic retinopathy. (Pubmed Central) - Feb 1, 2022 A comprehensive presentation of randomized clinical trials evaluating ranibizumab for DR indicates that it is effective and safe, offering improvement of DR severity in both non-proliferative and proliferative form. However, there is no general consensus regarding the exact treatment regimen in patients with DR, while the effect of ranibizumab on the progression of retinal ischemia remains unclear.
- |||||||||| Byooviz (ranibizumab biosimilar) / Samsung, AffaMed Therap, Biogen, Lucentis (ranibizumab) / Roche, Novartis
Journal: Evaluation of the Structural, Physicochemical, and Biological Characteristics of SB11, as Lucentis (Ranibizumab) Biosimilar. (Pubmed Central) - Jan 28, 2022 The cytokines TNF, IL-1, IL-10, and IL-12 did not show significant variation. Based on the comprehensive analytical similarity assessment, SB11 is highly similar to the EU/US-ranibizumab with respect to structural, physicochemical, and biological properties.
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
To study the effect of process parameters on titre and expression ratio of heavy and light chains of ranibizumab in Escherichia coli (Pacific Ballroom: Section 19 (Marriott Marquis San Diego Marina)) - Jan 28, 2022 - Abstract #ACSSp2022ACS_Sp_12168; The product identification was performed with LC-MS and expression level was quantified using RP HPLC, product quality and impurity level was also quantified by RP HPLC and further analysed by LC-MS. The optimum range was predicted for each parameter and found to be satisfactory for obtaining higher protein titre with equal expression and minimal impurities.
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Ethanol as an additive enhances expression of Ranibizumab in Escherichia coli: Impact on cellular physiology and transcriptome (Pacific Ballroom: Section 18 (Marriott Marquis San Diego Marina)) - Jan 28, 2022 - Abstract #ACSSp2022ACS_Sp_235; LC-MS confirmed correct disulfide bond formation and Surface plasmon resonance confirmed the formation of active recombinant protein via binding to its target VEGF. Transcriptomic analysis and RT-qPCR validation indicated that changes in membrane properties and DNA synthesis results in growth, gene amplification and enhances synthesis of inducible proteins in case of the optimized medium.
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis, Fovista (pegpleranib) / IVERIC bio, Roche
Clinical, P1/2 data, Journal: Intravitreous treatment of severe ocular von Hippel-Lindau disease using a combination of the VEGF inhibitor, ranibizumab, and PDGF inhibitor, E10030: Results from a phase 1/2 clinical trial. (Pubmed Central) - Jan 27, 2022 In addition, treatment was able to positively influence anxiety via VA improvement. Combination intravitreous injection with ranibizumab and E10030 demonstrated a reasonable preliminary safety profile, but limited treatment effect.
- |||||||||| LY09004 (aflibercept biosimilar) / Luye Group, Ocumension Therap, Lucentis (ranibizumab) / Roche, Novartis
Biomarker, Retrospective data, Journal: Recurrence and visual prognostic factors of polypoidal choroidal vasculopathy: 5-year results. (Pubmed Central) - Jan 27, 2022 In addition, patients with recurrence, large lesion, and cluster polyps had worse final visual acuity than those without these factors. CVI and CVH may be used to predict recurrence of PCV.
- |||||||||| Avastin (bevacizumab) / Roche
Clinical, Retrospective data, Journal: Visual Outcome of Anti-vascular Endothelial Growth Factor Injections at the University College Hospital, Ibadan. (Pubmed Central) - Jan 27, 2022 This retrospective study included 182 eyes of 172 patients managed in the vitreoretinal unit between 2016 and 2019 who were treated with intravitreal anti-VEGF bevacizumab (1.25 mg/0.05 ml) with at least 1 year of follow-up...Visual acuity gain was recorded in patients who had intravitreal anti-VEGF injections in 1 year. It is recommended that patients should have more than one injection.
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Journal, HEOR, Real-world evidence: Real-World Evidence for Treat-and-Extend Regimen of Ranibizumab Therapy for Macular Oedema Secondary to Branch Retinal Vein Occlusion. (Pubmed Central) - Jan 26, 2022 We found statistically significant differences between complete and incomplete responders on the average number of injections during the second year (2.46 ± 2.18 compared to 5.43 ± 1.27; p = 0.007) and change of the BCVA and CMT between both groups (p < 0.001) at 6, 12, 18 and 24 months. T&E seems to be effective in MO secondary to BRVO, improving visual function and decreasing CMT, with less need for injections.
- |||||||||| LY09004 (aflibercept biosimilar) / Luye Group, Ocumension Therap, Lucentis (ranibizumab) / Roche, Novartis
Clinical, Retrospective data, Journal: Three-Year Outcomes of Wet Age-Related Macular Degeneration Treatment in Polish Therapeutic Programs. (Pubmed Central) - Jan 26, 2022 After the first year, central retinal thickness in treatment-naïve eyes was significantly reduced. Regular treatment of wet age-related macular degeneration as part of the treatment program achieves functional stabilization and significant morphological improvement over a long-term, three-year follow-up, with significantly fewer injections needed after the first year of treatment.
- |||||||||| Avastin (bevacizumab) / Roche
Journal: Real-Life Data of Patients with Exudative Age-Related Macular Degeneration. (Pubmed Central) - Jan 26, 2022 Anatomical and functional success was achieved with anti-VEGF treatment after fewer injections and visits than have been reported in randomized, controlled, clinical studies in the literature. The number of injections and visits recorded in this study was consistent with the data of other real-life studies.
- |||||||||| Actemra IV (tocilizumab) / Roche, JW Pharma, Eylea (aflibercept intravitreal) / Bayer, Regeneron, LY09004 (aflibercept biosimilar) / Luye Group, Ocumension Therap
Journal: Tocilizumab and Aflibercept as a Treatment Option for Refractory Macular Edema after Acute Retinal Necrosis. (Pubmed Central) - Jan 26, 2022 A combination treatment of tocilizumab, an interleukin-6 receptor inhibitor, and intravitreal aflibercept was successful to control the CME. In selected patients with treatment-refractory CME following ARN a therapy with tocilizumab and intravitreal aflibercept might be considered.
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Journal: Factors Associated With the Presence of Foveal Bulge in Eyes With Resolved Diabetic Macular Edema. (Pubmed Central) - Jan 26, 2022 A total of 165 eyes with complete integrity of ellipsoid zone (EZ) at the fovea and resolved DME were divided into two groups according to the presence of FB at 6 months after intravitreal injection of ranibizumab treatment...At 6 months, better BCVA and longer OS length were significantly correlated with the existence of FB (all P < 0.05). Factors associated with the presence of FB after the resolution of DME include younger age, better baseline BCVA and lower baseline CFT, and better post-treatment BCVA and longer post-treatment OS length.
- |||||||||| Eylea (aflibercept intravitreal) / Bayer, Regeneron, LY09004 (aflibercept biosimilar) / Luye Group, Ocumension Therap, Lucentis (ranibizumab) / Roche, Novartis
Journal: Risk of Myocardial Infarction, Stroke, or Death in New Users of Intravitreal Aflibercept Versus Ranibizumab: A Nationwide Cohort Study. (Pubmed Central) - Jan 26, 2022 Factors associated with the presence of FB after the resolution of DME include younger age, better baseline BCVA and lower baseline CFT, and better post-treatment BCVA and longer post-treatment OS length. Aflibercept and ranibizumab appear to have similar safety profiles with respect to the risk of MI, stroke, or death under real-world conditions of use.
- |||||||||| HLX04-O (bevacizumab biosimilar) - Fosun Pharma, Essex Bio / Technology
Enrollment open: Compare the Efficacy and Safety of HLX04-O With Ranibizumab in Subjects With wAMD (clinicaltrials.gov) - Jan 25, 2022 P3, N=388, Recruiting, Aflibercept and ranibizumab appear to have similar safety profiles with respect to the risk of MI, stroke, or death under real-world conditions of use. Not yet recruiting --> Recruiting
- |||||||||| Nevanac (nepafenac) / Novartis, Lucentis (ranibizumab) / Roche, Novartis
Clinical, Journal: Prophylaxis of macular edema after cataract surgery in diabetic patients, topical Nepafenac versus intravitreal Ranibizumab. (Pubmed Central) - Jan 21, 2022 In postoperative visits, cystoid macular edema occurred in three patients (7.9%) in Nepafenac group, one patient (2.7%) in Ranibizumab group, and seven patients (17.07%) in control group. Both postoperative topical Nepafenac and intra-operative intra-vitreal Ranibizumab are effective adjunctive to phacoemulsification in diabetic patients for prophylaxis of macular edema.
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