- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma
Trial completion, Trial completion date: Intravitreal Conbercept After Vitrectomy (clinicaltrials.gov) - Apr 29, 2019 P1, N=50, Completed, The regression of neovascularization reaches a plateau 3 days after IVC. Active, not recruiting --> Completed | Trial completion date: Jul 2018 --> Feb 2019
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma, Visudyne (verteporfin) / Novartis
Trial primary completion date, Combination therapy: Initial Versus Delayed PDT Combination With Conbercept in PCV (clinicaltrials.gov) - Apr 23, 2019 P4, N=80, Recruiting, Active, not recruiting --> Completed | Trial completion date: Jul 2018 --> Feb 2019 Trial primary completion date: Jan 2019 --> May 2019
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Retrospective data, Journal: Treatment of retinopathy of incontinentia pigmenti by anti-vascular endothelial growth factor (Pubmed Central) - Apr 20, 2019 The efficacy of anti-vascular endothelial growth factor in the treatment of retinopathy of incontinentia pigmenti was prelininarily confimed.However,the optimal use timing,dosage,local and systemic safety issues were needed to be further studied. (Chin J Ophthalmol, 2019, 55:294-301).
- |||||||||| Eylea (aflibercept intravitreal) / Bayer, Regeneron, conbercept (KH902) / Chengdu Kanghong
Clinical, Review, Journal: The efficacy and safety of aflibercept and conbercept in diabetic macular edema. (Pubmed Central) - Mar 25, 2019 Advantages have been shown for aflibercept and conbercept, the two recombinant decoy receptors that can bind VEGF with high specificity and affinity, in DME treatment in clinical trials conducted both worldwide and in People's Republic of China. This review introduces the structural characteristics and molecular mechanisms of action of these two anti-VEGF drugs, and summarizes the clinical trials evaluating their efficacy and safety, with the hope to provide clues for designing optimal and personalized therapeutic regimens for DME patients.
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma
Enrollment open, Trial initiation date: Efficacy and Safety Trial of Conbercept Intravitreal Injection for Neovascular AMD (PANDA-2) (clinicaltrials.gov) - Mar 5, 2019 P3, N=1140, Recruiting, This review introduces the structural characteristics and molecular mechanisms of action of these two anti-VEGF drugs, and summarizes the clinical trials evaluating their efficacy and safety, with the hope to provide clues for designing optimal and personalized therapeutic regimens for DME patients. Not yet recruiting --> Recruiting | Initiation date: Sep 2018 --> Dec 2018
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Biotech
New trial: PRP vs PRP+IVC for Severe nPDR (clinicaltrials.gov) - Mar 4, 2019 P=N/A, N=40, Recruiting,
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma, Visudyne (verteporfin) / Novartis
Trial primary completion date, Combination therapy: Initial Versus Delayed PDT Combination With Conbercept in PCV (clinicaltrials.gov) - Jan 25, 2019 P4, N=80, Recruiting, Not yet recruiting --> Recruiting | Initiation date: Sep 2018 --> Dec 2018 Trial primary completion date: Jan 2018 --> Jan 2019
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma
Trial completion date, Trial primary completion date: CRVO: Conbercept Ophthalmic Injection for Patients of Central Retinal Vein Occlusion (clinicaltrials.gov) - Sep 21, 2018 P3, N=237, Recruiting, Trial completion date: Jul 2018 --> Dec 2020 | Trial primary completion date: Jan 2018 --> Dec 2019 Trial completion date: Oct 2018 --> Dec 2020 | Trial primary completion date: Apr 2018 --> Dec 2019
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma, Visudyne (verteporfin) / Novartis
Enrollment open, Combination therapy: Initial Versus Delayed PDT Combination With Conbercept in PCV (clinicaltrials.gov) - Jan 4, 2017 P4, N=80, Recruiting, Active, not recruiting --> Enrolling by invitation | Initiation date: Sep 2016 --> Oct 2017 Not yet recruiting --> Recruiting
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma, Visudyne (verteporfin) / Novartis
Trial initiation date, Trial primary completion date, Combination therapy: Initial Versus Delayed PDT Combination With Conbercept in PCV (clinicaltrials.gov) - Dec 15, 2016 P4, N=80, Not yet recruiting, Not yet recruiting --> Recruiting Initiation date: Jul 2016 --> Jan 2017 | Trial primary completion date: Jul 2017 --> Jan 2018
- |||||||||| Lucentis (ranibizumab) / Roche, Novartis
Trial completion, Head-to-Head: RELIANCE: Head to Head Study of Anti-VEGF Treatment. (clinicaltrials.gov) - Aug 2, 2016 P4, N=12, Completed, Initiation date: Jul 2016 --> Jan 2017 | Trial primary completion date: Jul 2017 --> Jan 2018 Recruiting --> Completed
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma
Enrollment closed: SHINY: A Randomized, Double-blind, Multicenter, Sham-controlled, Safety and Efficacy Study of Conbercept in Patients With mCNV (clinicaltrials.gov) - Mar 20, 2014 P3, N=176, Active, not recruiting, Recruiting --> Active, not recruiting Recruiting --> Active, not recruiting
- |||||||||| Lumitin (conbercept) / Chengdu Kanghong Pharma
Trial completion: A Randomized, Double-masked, Multicenter,Sham-controlled, Safety and Efficacy Study of KH902 in Patients With Wet AMD (clinicaltrials.gov) - Mar 20, 2014 P3, N=125, Completed, Recruiting --> Active, not recruiting Active, not recruiting --> Completed
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