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2 The first human study found that ALG-1001 caused complete PVD in six of 15 treated patients and Topline results from a prospective, double-masked, placebo-controlled phase-2b clinical study evaluating ALG-1001 (Luminate) in patients with diabetic macular edema. ARVO, May 2017. Bausch Health Investor Contact: Administered as an intravitreal injection, Luminate (previously known as ALG-1001) is a synthetic oligopeptide that inhibits 4 integrin receptor sites involved in angiogenesis and vitreolysis. The targeted receptors have functions both upstream and downstream of the VEGF pathways and can be manipulated to prevent new vascular sprouts, inhibit existing neovascularization and reduce fluid. Allegro began a double-blind, placebo-controlled, dose-ranging, international Phase II trial to Read the full 116 word article CHICAGO, IL, USA I October 16, 2014 I Allegro Ophthalmics, LLC, dedicated to establishing Integrin Peptide Therapy as the next-generation pharmaceutical category for the treatment of vitreo-retinal diseases, today announced that it is enrolling patients in a Phase 2 trial that will evaluate the safety and efficacy of Luminate®, previously known as ALG-1001, in patients with diabetic macular Top-line data from a Phase IIb study of a novel integrin peptide (ALG-1001) to treat diabetic macular edema (DME) has indicated encouraging visual acuity gains, including a reduction in central macular thickness (CMT) comparable to that observed with anti-VEGF therapy. Phase II clinical trial data from a study of integrin peptide therapy (referenced as “ALG-1001” or “Luminate”), conducted in 106 patients with vitreomacular traction (VMT) or vitreomacular adhesion (VMA), has reported that 3.2 mg of the intravitreal injection met the primary endpoint of a greater proportion of patients achieving release of VMT or VMA by day 90, versus placebo (65% vs Find your ALLEGRO WIPES WITH ALCOHOL 8INX11IN 50/BX at Grainger Canada, formerly Acklands-Grainger. We have been Canada's premiere industrial supplier for over 125 years with superior service and quality.
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Allegro began a double-blind, placebo-controlled, dose-ranging, international Phase II trial to Read the full 116 word article CHICAGO, IL, USA I October 16, 2014 I Allegro Ophthalmics, LLC, dedicated to establishing Integrin Peptide Therapy as the next-generation pharmaceutical category for the treatment of vitreo-retinal diseases, today announced that it is enrolling patients in a Phase 2 trial that will evaluate the safety and efficacy of Luminate®, previously known as ALG-1001, in patients with diabetic macular Top-line data from a Phase IIb study of a novel integrin peptide (ALG-1001) to treat diabetic macular edema (DME) has indicated encouraging visual acuity gains, including a reduction in central macular thickness (CMT) comparable to that observed with anti-VEGF therapy. Phase II clinical trial data from a study of integrin peptide therapy (referenced as “ALG-1001” or “Luminate”), conducted in 106 patients with vitreomacular traction (VMT) or vitreomacular adhesion (VMA), has reported that 3.2 mg of the intravitreal injection met the primary endpoint of a greater proportion of patients achieving release of VMT or VMA by day 90, versus placebo (65% vs Find your ALLEGRO WIPES WITH ALCOHOL 8INX11IN 50/BX at Grainger Canada, formerly Acklands-Grainger. We have been Canada's premiere industrial supplier for over 125 years with superior service and quality. Group 2 demonstrated the best efficacy among the ALG-1001 groups. Mean change in BCVA were 6.7 and 7.1 letters for 1.25mg bevacizumab and ALG-1001 1.0mg in sequential treatment, respectively. BCVA improved earlier than CMT improvements suggesting a new mechanism of action unlike anti-VEGF.