keyword
https://read.qxmd.com/read/37179017/randomized-trial-of-biosimilar-xsb-001-versus-reference-ranibizumab-in-patients-with-neovascular-age-related-macular-degeneration
#21
JOURNAL ARTICLE
Anat Loewenstein, Norbert Czumbel, Jan Ernest, Jaroslava Dusová, Joel Pearlman, Agnieszka Nowosielska
OBJECTIVE: To evaluate the efficacy, safety, and immunogenicity of a ranibizumab biosimilar candidate (XSB-001) versus reference product (Lucentis®) for neovascular age-related macular degeneration (nAMD). DESIGN: Phase 3, multicenter, randomized, double-masked, parallel-group study. PARTICIPANTS: Patients with nAMD. METHODS: Eligible patients were randomized (1:1) to receive intravitreal injections of XSB-001 or reference ranibizumab (0...
May 11, 2023: Ophthalmology Retina
https://read.qxmd.com/read/37164394/central-retinal-vein-occlusion-after-covid-19-infection
#22
REVIEW
Ngoc-Chau Isabelle Nguyen, Chiara Eandi, Yan Guex-Crosier
INTRODUCTION: Central retinal vein occlusions are not well-known complications of SARS-CoV-2 infection. We describe a case of central retinal vein occlusion secondary to COVID-19, and a review of the literature was performed. HISTORY AND SIGNS: A 47-year-old woman with no underlying ocular or medical condition presented to the hospital complaining about sudden onset of multiple scotomas in her left eye. A COVID-19 infection was confirmed 2 days previously by a PCR test that was performed 2 days after the onset of symptoms...
April 2023: Klinische Monatsblätter Für Augenheilkunde
https://read.qxmd.com/read/37084932/morphovascular-changes-after-anti-vegf-intravitreal-injection-for-a-choroidal-neovascularization-secondary-to-covid-19-infection-in-a-pediatric-patient
#23
Gilda Cennamo, Luigi Massa, Lucia Montanaro, Adriano Magli, Ciro Costagliola
Choroidal neovascularization (CNV) is a common pathologic lesion that occurs in various chorioretinopathy. Although the incidence of CNV is quite rare in children and adolescents, these lesions have a severe impact on visual acuity and quality of life over patients' lifetime. The management of CNV in pediatric patients is challenging, clear guidelines are limited due to a lack of randomized clinical trials. However, the more promising option is the use of vascular endothelial growth factor (VEGF) inhibitors...
April 19, 2023: Photodiagnosis and Photodynamic Therapy
https://read.qxmd.com/read/37083292/stimuli-responsive-features-of-organic-rtp-materials-an-intriguing-carbazole-cyclic-triimidazole-derivative
#24
JOURNAL ARTICLE
Daniele Malpicci, Alessandra Forni, Chiara Botta, Clelia Giannini, Elena Lucenti, Daniele Marinotto, Daniele Maver, Lucia Carlucci, Elena Maria Cariati
Stimuli responsive luminescent materials possessing room temperature phosphorescence (RTP) are extremely desirable for various applications. The here investigated derivative of cyclic triimidazole (TT) functionalized with carbazole (Cz), namely TT-Ph-Cz, belongs to this class. TT-Ph-Cz possesses high conformational freedom resulting in rigidochromic and multi-stimuli responsive emissive behavior. It has been isolated as MeOH-solvated and de-solvated forms characterized by distinctive emissive features. In particular, the solvated form, in which hydrogen bonds with MeOH inhibit competitive non-radiative deactivation channels, possesses a higher quantum yield associated with a strong phosphorescence contribution which is preserved in DMSO/water solutions...
April 21, 2023: Chemistry: a European Journal
https://read.qxmd.com/read/37064960/biosimilar-versus-innovator-molecule-of-ranibizumab-in-neovascular-age-related-macular-degeneration-the-balance-trial-real-world-evidence
#25
JOURNAL ARTICLE
Debdulal Chakraborty, Soumen Mondal, Subhendu Boral, Arnab Das, Tushar Kanti Sinha, Saptorshi Majumdar, Ranabir Bhattacharya, Ritobroto Maitra
PURPOSE: To analyse outcomes of innovator ranibizumab (IRM) (Lucentis) and biosimilar ranibizumab (BRM) (Razumab) in Indian eyes with neovascular age-related macular degeneration (nAMD). METHODS: Retrospective observational study in nAMD patients, who were treated with IRM or BRM (3 loading doses followed by pro re nata (PRN). Primary outcome measures were change in best corrected visual acuity (BCVA) and central macular thickness (CMT) along with safety analysis...
2023: Clinical Ophthalmology
https://read.qxmd.com/read/36866850/do-published-trial-results-influence-physician-prescribing-patterns-intravitreal-antivascular-endothelial-growth-factor-usage-by-the-united-states-ophthalmologists-before-and-after-protocol-t-study
#26
JOURNAL ARTICLE
Serena Shah, Zahra Markatia, Arjun Watane, Alexandra Feldman, Lea Shah, Jayanth Sridhar
PURPOSE OF REVIEW: Clinical trial publications may influence physician prescribing patterns. The Diabetic Retinopathy Clinical Research Network (DRCR.net) Protocol T study, published in 2015, examined outcomes of intravitreal antivascular endothelial growth factor (VEGF) medications for treatment of diabetic macular oedema (DME). This study investigates if the Protocol T 1-year results were associated with changes in prescribing patterns. RECENT FINDINGS: Anti-VEGF agents have revolutionized treatment of DME by blocking angiogenesis signalled by VEGF...
March 2, 2023: Current Opinion in Ophthalmology
https://read.qxmd.com/read/36840191/brown-seaweed-extract-bse-application-influences-auxin-and-aba-related-gene-expression-root-development-and-sugar-yield-in-beta-vulgaris-l
#27
JOURNAL ARTICLE
Giovanni Bertoldo, Claudia Chiodi, Maria Cristina Della Lucia, Matteo Borella, Samathmika Ravi, Andrea Baglieri, Piergiorgio Lucenti, Bhargava Krishna Ganasula, Chandana Mulagala, Andrea Squartini, Giuseppe Concheri, Francesco Magro, Giovanni Campagna, Piergiorgio Stevanato, Serenella Nardi
The molecular and phenotypic effects of a brown seaweed extract (BSE) were assessed in sugar beet ( Beta vulgaris L.). Transcript levels of BSE-treated and untreated plants were studied by RNA-seq and validated by quantitative real-time PCR analysis (RT-qPCR). Root morphology, sugar yield, and processing quality traits were also analyzed to better elucidate the treatment effects. RNA-seq revealed 1019 differentially expressed genes (DEGs) between the BSE-treated and untreated plants. An adjusted p -value < 0...
February 13, 2023: Plants (Basel, Switzerland)
https://read.qxmd.com/read/36615335/crystallization-enhanced-emission-and-room-temperature-phosphorescence-of-cyclic-triimidazole-monohexyl-thiophene-derivatives
#28
JOURNAL ARTICLE
Daniele Malpicci, Alessandra Forni, Elena Cariati, Riku Inoguchi, Daniele Marinotto, Daniele Maver, Federico Turco, Elena Lucenti
The development of organic room-temperature phosphorescent (ORTP) materials represents an active field of research due to their significant advantages with respect to their organometallic counterparts. Two cyclic triimidazole ( TT ) derivatives bearing one and three hexyl-thiophene moieties, TT-HThio and TT-(HThio)3 , have been prepared and characterized. Both compounds display enhanced quantum yields in their crystalline form with respect to those in a solution state, revealing crystallization-enhanced emissive (CEE) behavior...
December 24, 2022: Molecules: a Journal of Synthetic Chemistry and Natural Product Chemistry
https://read.qxmd.com/read/36607595/physicochemical-and-biological-stability-assessment-of-sb11-ranibizumab-biosimilar-under-ambient-and-in-use-storage-for-intravitreal-administration
#29
JOURNAL ARTICLE
Peter K Kaiser, Jihoon Yun, Soyeon Kim, Jihyun Kim, Su Jin Park
INTRODUCTION: SB11 (Byooviz™) is a ranibizumab biosimilar that acts as a vascular endothelial growth factor (VEGF)-A inhibitor. Stability data for unopened SB11 vials at room temperature are limited and no data are available for SB11 withdrawn into syringes (in-use) for intravitreal administration. METHODS: SB11 stability was assessed in two different settings: unopened vials stored at 30 ± 2 °C/65 ± 5% relative humidity (RH) for 2 months, and in-use SB11 withdrawn into syringes stored at 5 ± 3 °C for 98 days and then 25 ± 2 °C/60 ± 5% RH for 24 h...
January 6, 2023: Ophthalmology and Therapy
https://read.qxmd.com/read/36520462/immunogenicity-with-ranibizumab-biosimilar-sb11-byooviz-and-reference-product-lucentis-and-association-with-efficacy-safety-and-pharmacokinetics-a-post-hoc-analysis-of-a-phase-3-randomized-clinical-trial
#30
JOURNAL ARTICLE
Neil M Bressler, Taehyung Kim, Inkyung Oh, Paola Russo, Mercy Yeeun Kim, Se Joon Woo
IMPORTANCE: SB11 and reference ranibizumab (RBZ) are monoclonal anti-vascular endothelial growth factor (VEGF)-A antibodies approved for the treatment of neovascular age-related macular degeneration (nAMD) and other retinal diseases. The association of ranibizumab immunogenicity and treatment outcomes in patients with nAMD is unclear but relevant regarding concerns about immunogenicity of anti-VEGF biological products. OBJECTIVE: To examine the association of immunogenicity to ranibizumab products (SB11 and RBZ) with efficacy, safety, and pharmacokinetics...
December 15, 2022: JAMA Ophthalmology
https://read.qxmd.com/read/36412625/comparative-study-of-curcumin-and-lucentis-on-retinal-neovascularization
#31
JOURNAL ARTICLE
Lu Yang, Ximei Zhang, Dongping Li, Guohong Zhou, Jiewei Liu, Yan Gao, Shufang Du, Yanyun Shi, Yong Li, Na Di
Introduction To investigate the effect of Curcumin on retinal neovascularization in mice with oxygen-induced lesions. Methods 7-day-old (P7) C57/BL6J mice were randomly divided into control group, OIR group, DMSO group, 100 mg/kg, 50 mg/kg and 25 mg/kg curcumin group and Lucentis group (15 mice per group). Mice in the experimental group were fed for 5 days in high oxygen partial pressure environment, and then in normal oxygen air environment for another 5 days. Corresponding interventions were given at 12-16 days of age (P12-16)...
November 21, 2022: Ophthalmic Research
https://read.qxmd.com/read/36278735/pain-education-in-the-management-of-patients-with-chronic-low-back-pain-a-systematic-review
#32
REVIEW
Rosario Ferlito, Chiara Blatti, Ludovico Lucenti, Umberto Boscarino, Marco Sapienza, Vito Pavone, Gianluca Testa
New prospective of chronic low back pain (CLBP) management based on the biopsychosocial model suggests the use of pain education, or neurophysiological pain education, to modify erroneous conceptions of disease and pain, often influenced by fear, anxiety and negative attitudes. The aim of the study is to highlight the evidence on the outcomes of a pain education-oriented approach for the management of CLBP. The search was conducted on the Pubmed, Scopus, Pedro and Cochrane Library databases, leading to 2673 results until September 2021...
September 26, 2022: Journal of Functional Morphology and Kinesiology
https://read.qxmd.com/read/36213057/application-and-mechanism-of-anti-vegf-drugs-in-age-related-macular-degeneration
#33
REVIEW
Dawei Song, Ping Liu, Kai Shang, YiBin Ma
Age-related macular degeneration (AMD) is the leading cause of blindness in the elderly. The incidence rate increases with age in people over 50 years of age. With the advent of China's aging society, the number of patients is increasing year by year. Although researchers have done a lot of basic research and clinical research on the pathogenesis and treatment of AMD in recent years, the pathogenesis of AMD is still controversialdue to the complexity of the disease itself. AMD is the primary cause of blindness in the elderly over 50 years old...
2022: Frontiers in Bioengineering and Biotechnology
https://read.qxmd.com/read/36127450/-prospective-noninterventional-blue-sky-study-evaluating-the-efficacy-of-brolucizumab-in-treatment-na%C3%A3-ve-and-previously-treated-patients-with-neovascular-amd
#34
JOURNAL ARTICLE
H Faatz, N Feltgen, M Gutfleisch, B Heimes-Bussmann, T U Krohne, S Liakopoulos, R Liegl, A Lommatzsch, P Mussinghoff, M Rehak, S Schmitz-Valckenberg, G Spital, B Stanzel, F Ziemssen, B Hägele, C Junkes, M Porstner, J Vögeler, B Gmeiner, D Pauleikhoff
Intravitreal injection of anti-vascular endothelial growth factor (VEGF) is the standard treatment for patients with neovascular age-related macular degeneration (nAMD). In addition to the approved substances ranibizumab (Lucentis®, Novartis) and aflibercept (Eylea®, Bayer), bevacizumab (Avastin®, Roche) is also available. Furthermore, brolucizumab (Beovu®, Novartis) has been approved and has been available in Germany since April 2020. The multicenter, noninterventional prospective BLUE SKY study investigates brolucizumab treatment with different schemes in 600 treatment-naive and pretreated nAMD patients in routine clinical practice over a 24-month period...
September 20, 2022: Ophthalmologie
https://read.qxmd.com/read/36043950/handover-methods-between-local-emergency-medical-services-and-accident-and-emergency-is-there-a-gold-standard-a-scoping-review
#35
REVIEW
Massimo Guasconi, Antonio Bonacaro, Emanuele Tamagnini, Silvia Biral, Linda Brigliadori, Sabrina Borioni, Daniele Collura, Sara Fontana, Giulia Ingallina, Maria Chiara Bassi, Enrico Lucenti, Giovanna Artioli
BACKGROUND: Pre-hospital emergency medical systems do not appear to work totally coordinated with Accident and Emergency (A&E). Often, patient admission to A&E is marked by scarce attention to the handover between the respective healthcare professionals. This phenomenon is potentially dangerous because it exposes patients to the risk of errors in a context where the patients' critical or progressing conditions must not be worsened by avoidable errors of communication between professionals...
August 31, 2022: Acta Bio-medica: Atenei Parmensis
https://read.qxmd.com/read/36010147/diagnostic-tools-in-the-detection-of-physical-child-abuse-a-systematic-review
#36
REVIEW
Vito Pavone, Andrea Vescio, Ludovico Lucenti, Mirko Amico, Alessia Caldaci, Xena Giada Pappalardo, Enrico Parano, Gianluca Testa
Child abuse is a critical social issue. The orthopedic surgeon's role is essential in noticing signs and symptoms of physical abuse. For this reason, several authors have proposed scoring systems to identify abuse early on and reduce undiagnosed cases. The aim of this systematic review is to overview the screening tools in the literature. In 2021, three independent authors performed a systematic review of two electronic medical databases using the following inclusion criteria: physical child abuse, questionnaire, survey, score, screening tool and predictive tool...
August 20, 2022: Children
https://read.qxmd.com/read/36010012/mid-long-term-outcomes-of-surgical-treatment-of-legg-calv%C3%A3-perthes-disease-a-systematic-review
#37
REVIEW
Alessia Caldaci, Gianluca Testa, Eleonora Dell'Agli, Marco Sapienza, Andrea Vescio, Ludovico Lucenti, Vito Pavone
BACKGROUND: Legg-Calvè-Perthes disease (LCPD) is a common childhood disease that usually occurs in 4- to 12-year-old children. Surgical treatment consists of femoral, pelvic, or combined osteotomies. This comprehensive review aimed to investigate the mid- and long-term outcome of the surgical treatment. METHODS: A systematic review of PubMed, Science Direct, and MEDLINE databases was performed by two independent authors, using the keywords "outcome", "surgical treatment", "pelvic osteotomy", "femoral osteotomy", and "Legg-Calvè-Perthes disease" to evaluate studies of any level of evidence that reported the surgical outcome of LCPD...
July 27, 2022: Children
https://read.qxmd.com/read/35958912/prognostic-evaluation-of-vitrectomy-assisted-by-lucentis-in-diabetic-retinopathy-and-neovascular-glaucoma
#38
JOURNAL ARTICLE
Xuli Zhao, Yakun Wang
For verifying the prognosis of Lucentis-assisted vitrectomy (PPV) in diabetic retinopathy (DR) and neovascular glaucoma (NVG), a retrospective analysis of DR and NVG patients who were admitted to our hospital from July 2019 to December 2020 was conducted. According to the treatment protocol, subjects who had PPV intervention were in the control group (CG; n  = 38) and those receiving Lucentis adjunctive PPV were included in the intervention group (RG; n  = 40). The indicators between groups were listed: treatment success rate, postoperative complication rate, surgical outcome indicators, BCVA, intraocular pressure (IOP) change, foveal thickness, and VEGF level in aqueous humor...
2022: Evidence-based Complementary and Alternative Medicine: ECAM
https://read.qxmd.com/read/35918963/commentary-a-prospective-randomized-parallel-group-double-blind-multicenter-study-to-compare-the-efficacy-safety-and-immunogenicity-of-lupin-s-ranibizumab-with-lucentis-in-patients-with-neovascular-age-related-macular-degeneration
#39
RANDOMIZED CONTROLLED TRIAL
https://read.qxmd.com/read/35918962/a-prospective-randomized-parallel-group-double-blind-multicenter-study-to-compare-the-efficacy-safety-and-immunogenicity-of-lupin-s-ranibizumab-with-lucentis-%C3%A2-in-patients-with-neovascular-age-related-macular-degeneration
#40
RANDOMIZED CONTROLLED TRIAL
Ramandeep Singh, Rohan Chauhan, Ashish Saxena, Anup Shah, Laxshmi Mondal, Dhananjay Bakhle, Chirag Shah, Arpit Shah, Shashank Deoghare, Neelakant Krishnan, Neelima Godse
Purpose: The present study compares the efficacy, safety, and immunogenicity of Lupin's biosimilar ranibizumab with that of Lucentis® in patients with neovascular age-related macular degeneration. Methods: This prospective, double-blind, multi-centric phase-III study was conducted across 19 centers in India. A total of 202 patients with neovascular age-related macular degeneration were randomized (1:1) to receive either Lupin's biosimilar ranibizumab or Lucentis® , 0...
August 2022: Indian Journal of Ophthalmology
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