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(Glucagon + insulin human) by Abvance Therapeutics for Hypoglycemia: Likelihood of Approval

Pharmaceutical Technology

(Glucagon + insulin human)is under clinical development by Abvance Therapeutics and currently in Phase I for Hypoglycemia.

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Phase 3 trial dashes Oramed’s oral insulin hopes

pharmaphorum

Oramed Pharma has conceded defeat in its attempt to bring an oral formulation of insulin to market for people with type 2 diabetes, after its ORMD-0801 candidate missed the mark in a phase 3 trial. The post Phase 3 trial dashes Oramed’s oral insulin hopes appeared first on.

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Once-weekly insulin icodec demonstrates superior reduction in HbA1c vs insulin degludec in people with type 2 diabetes in ONWARDS 2 phase 3a trial

The Pharma Data

Novo Nordisk today announced headline results from the ONWARDS 2 trial, a phase 3a, 26-week efficacy and safety treat-to-target trial investigating once-weekly insulin icodec vs insulin degludec in 526 people with type 2 diabetes switching from daily insulin. events per patient year exposed to once-weekly insulin icodec and 0.27

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(LAI-287 + semaglutide) by Novo Nordisk for Type 2 Diabetes: Likelihood of Approval

Pharmaceutical Technology

(LAI-287 + semaglutide) is under clinical development by Novo Nordisk and currently in Phase III for Type 2 Diabetes. LAI-287 + semaglutide) overview A fixed dose combination of GLP-1 analogue semaglutide and LAI-287, long-acting basal insulin is under development for the treatment of type 2 diabetes.

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RZ-358 by Rezolute for Hyperinsulinemia: Likelihood of Approval

Pharmaceutical Technology

RZ-358 is under clinical development by Rezolute and currently in Phase II for Hyperinsulinemia. RZ-358 overview RZ-358 (XOMA-358) is under development for the treatment of hyperinsulinemic hypoglycemia post gastric bypass surgery, and hypoglycemia associated with congenital hyperinsulinism.

Insulin 100
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RZ-358 by Rezolute for Hyperinsulinemia: Likelihood of Approval

Pharmaceutical Technology

RZ-358 is under clinical development by Rezolute and currently in Phase II for Hyperinsulinemia. RZ-358 overview RZ-358 (XOMA-358) is under development for the treatment of hyperinsulinemic hypoglycemia post gastric bypass surgery, and hypoglycemia associated with congenital hyperinsulinism.

Insulin 100
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Lilly’s new drug Mounjaro (tirzepatide ) wins US FDA approval

pharmaphorum

The findings were made via Lilly’s SURPASS phase 3 global clinical development programme, which comprised studies ranging from 40 to 52 weeks. These examined Mounjaro in 5mg, 10mg and 15 mg doses in five clinical trials, used either as a stand-alone therapy or as an add-on to other diabetes medicines. more than semaglutide, 0.9%