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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://repozitorij.uni-lj.si/IzpisGradiva.php?id=144586"><dc:title>Continuous glucose monitoring-based time-in-range using insulin glargine 300 units/ml versus insulin degludec 100 units/ml in type 1 diabetes</dc:title><dc:creator>Battelino,	Tadej	(Avtor)
	</dc:creator><dc:creator>Danne,	Thomas	(Avtor)
	</dc:creator><dc:creator>Edelman,	Steve V.	(Avtor)
	</dc:creator><dc:creator>Choudhary,	Pratik	(Avtor)
	</dc:creator><dc:creator>Renard,	Eric	(Avtor)
	</dc:creator><dc:creator>Westerbacka,	Jukka	(Avtor)
	</dc:creator><dc:creator>Mukherjee,	Bhaswati	(Avtor)
	</dc:creator><dc:creator>Pilorget,	Valerie	(Avtor)
	</dc:creator><dc:creator>Coudert,	Mathieu	(Avtor)
	</dc:creator><dc:creator>Bergenstal,	Richard M.	(Avtor)
	</dc:creator><dc:subject>basal insulin</dc:subject><dc:subject>continuous glucose monitoring</dc:subject><dc:subject>glycaemic control</dc:subject><dc:subject>insulin analogues</dc:subject><dc:subject>randomized trial</dc:subject><dc:subject>type 1 diabetes</dc:subject><dc:description>Aim: To use continuous glucose monitoring (CGM)-based time-in-range (TIR) as a primary efficacy endpoint to compare the second-generation basal insulin (BI) analogues insulin glargine 300 U/ml (Gla-300) and insulin degludec 100 U/ml (IDeg-100) in adults with type 1 diabetes (T1D). 
Materials and Methods: InRange was a 12-week, multicentre, randomized, active-controlled, parallel-group, open-label study comparing glucose TIR and variability between Gla-300 and IDeg-100 using blinded 20-day CGM profiles. The inclusion criteria consisted of adults with T1D treated with multiple daily injections, using BI once daily and rapid-acting insulin analogues for at least 1 year, with an HbA1c of 7% or higher and of 10% or less at screening. 
Results: Overall, 343 participants were randomized: 172 received Gla-300 and 171 IDeg-100. Non-inferiority (10% relative margin) of Gla-300 versus IDeg-100 was shown for the primary endpoint (percentage TIR ≥ 70 to ≤ 180 mg/dl): least squares (LS) mean (95% confidence interval) 52.74% (51.06%, 54.42%) for Gla-300 and 55.09% (53.34%, 56.84%) for IDeg-100; LS mean difference (non-inferiority): 3.16% (0.88%, 5.44%) (non-inferiority P = .0067). Non-inferiority was shown on glucose total coefficient of variation (main secondary endpoint): LS mean 39.91% (39.20%, 40.61%) and 41.22% (40.49%, 41.95%), respectively; LS mean difference (non-inferiority) −5.44% (−6.50%, −4.38%) (non-inferiority P &lt; .0001). Superiority of Gla-300 over IDeg-100 was not shown on TIR. Occurrences of self-measured and CGM-derived hypoglycaemia were comparable between treatment groups. Safety profiles were consistent with known profiles, with no unexpected findings. 
Conclusions: Using clinically relevant CGM metrics, InRange shows that Gla-300 is non-inferior to IDeg-100 in people with T1D, with comparable hypoglycaemia and safety profiles.</dc:description><dc:date>2023</dc:date><dc:date>2023-03-02 14:14:44</dc:date><dc:type>Članek v reviji</dc:type><dc:identifier>144586</dc:identifier><dc:language>sl</dc:language></rdf:Description></rdf:RDF>
