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Biomea Fusion Announces Late-Breaker Oral Presentation Showing New Analysis From The Escalation Portion Of COVALENT-111 Presented At The 1st Annual Asian Conference On Innovative Therapies For Diabetes Management; Icovamenib Achieves A Mean Reduction...

Biomea Fusion Announces Late-Breaker Oral Presentation Showing New Analysis From The Escalation Portion Of COVALENT-111 Presented At The 1st Annual Asian Conference On Innovative Therapies For Diabetes Management; Icovamenib Achieves A Mean Reduction...

Biomea Fusion宣佈在首屆亞洲糖尿病管理創新療法大會上,展示COVALENt-111升級部分的新分析的快報口頭報告;Icovamenib實現了平均降低...
Benzinga ·  11/18 21:21

Biomea Fusion Announces Late-Breaker Oral Presentation Showing New Analysis From The Escalation Portion Of COVALENT-111 Presented At The 1st Annual Asian Conference On Innovative Therapies For Diabetes Management; Icovamenib Achieves A Mean Reduction In HbA1c Greater Than 1% At Week 26 Following 4 Weeks Of Dosing In Type 2 Diabetes Patients Characterized By Insulin Deficiency

Biomea Fusion宣佈在第一屆亞洲創新糖尿病治療研討會上進行了遲報口頭報告,展示了COVALENt-111升級部分新分析;Icovamenib在第26周取得了超過1%的HbA1c平均減少,經過4周對2型糖尿病患者進行劑量治療,特徵爲胰島素缺乏

Icovamenib Achieves a Mean Reduction in HbA1c Greater than 1% at Week 26 Following 4 Weeks of Dosing in Type 2 Diabetes Patients Characterized by Insulin Deficiency

Icovamenib在第26周取得了超過1%的HbA1c平均減少,經過4周對2型糖尿病患者進行劑量治療,特徵爲胰島素缺乏

  • 32 patients from the 100mg and 200mg cohorts, doses selected for the expansion phase, were characterized based on baseline biomarkers and analyzed for efficacy. Patients identified as insulin deficient (approx. 50% of the broader patient population) and insulin resistant were compared to examine the mean reduction in HbA1c at Week 26, following 4 weeks of dosing.
  • 83% of patients with insulin deficiency responded to icovamenib, and showed a greater mean HbA1c reduction at Week 26 compared to baseline, than those that were found to be more insulin resistant (-1.23% vs -0.48%, placebo-adjusted, 22 weeks after last dose of icovamenib).
  • These two patient groups are pre-specified in the upcoming read out of the Phase IIb expansion portion of COVALENT-111 in December, reporting over 200 persons with type 2 diabetes (T2D) with 8 and 12 weeks of icovamenib treatment.
  • 從100mg和200mg隊列的32名患者中選擇了劑量以進行擴展階段的特徵基準生物標誌物分析。鑑定爲胰島素缺乏(約佔更廣泛患者群體的50%)和胰島素抵抗者的患者進行比較,以研究第26周的HbA1c平均減少,在接受4周劑量治療後
  • 83%的胰島素缺乏患者對icovamenib有反應,並顯示了第26周HbA1c的平均減少優於基線,與被發現更具胰島素抵抗性的人相比(-1.23% vs -0.48%,安慰劑調整,icovamenib最後劑量後22周)。
  • 這兩個患者群在12月即將公佈的COVALENt-111第IIb擴展部分的結果中預先指定,報告超過200名接受了8和12周icovamenib治療的2型糖尿病(T2D)患者。

譯文內容由第三人軟體翻譯。


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