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Metabolic Disorders

Amgen Reinvests Sales Gains In R&D As Phase II MariTide Readout Approaches

Amgen Reinvests Sales Gains In R&D As Phase II MariTide Readout Approaches

Amgen’s product sales grew 24% to $8.15bn in Q3 and its gains are being reinvested in R&D and manufacturing, including for MariTide, which will report Phase II obesity data in late 2024.

Winning With Partnerships: How To Turn A Three-Decade-Old Biotech Profitable

Winning With Partnerships: How To Turn A Three-Decade-Old Biotech Profitable

Since taking on the CEO role at Theratechnologies in 2020, Paul Lévesque has made it his priority to beef up the company’s commercial portfolio and look for partnerships on potentially high-value programs. Now, the Canadian biotech is turning a profit for the first time in many years.

Stealth’s Elamipretide Gets US FDA Panel Nod, But Not A Glowing Endorsement, For Barth Syndrome

Stealth’s Elamipretide Gets US FDA Panel Nod, But Not A Glowing Endorsement, For Barth Syndrome

The Cardiovascular and Renal Drugs Advisory Committee voted 10-6 that efficacy had been shown for the ultra-rare disease, but even panelists in the majority questioned whether the product satisfied the threshold requirement for an adequate and well-controlled study.

Sciwind Eyes Differentiation For Ecnoglutide In Highly Competitive Arena

Sciwind Eyes Differentiation For Ecnoglutide In Highly Competitive Arena

Chinese firm Sciwind has revealed additional Phase III findings for its promising once-weekly GLP-1 agonist ecnoglutide, just one asset in a burgeoning Chinese sector that could see the emergence of new rivals to current global leaders in obesity and diabetes.

Stealth’s Elamipretide Efficacy In Barth Syndrome Not Shown, US FDA Says

Stealth’s Elamipretide Efficacy In Barth Syndrome Not Shown, US FDA Says

The Cardiovascular and Renal Drugs Advisory Committee will consider whether open-label extension data from a randomized trial that failed its primary endpoint, along with a historical control comparison, are enough to support approval in the ultra-rare disease.

Viking Wins First Round In Legal Battle With Ascletis Over THRβ Agonist

Viking Wins First Round In Legal Battle With Ascletis Over THRβ Agonist

The US International Trade Commission looks set to ban the importation of Ascletis's THRβ agonist into the US for use in clinical trials due to an initial legal determination on potential infringement of trade secrets related to Viking's same-class candidate VK2809.

England Plans New Model For Use Of Lilly’s Mounjaro In Weight Loss

England Plans New Model For Use Of Lilly’s Mounjaro In Weight Loss

NHS England says it is proposing a “realistic but challenging uptake trajectory” that will make “this clinically and cost-effective drug” available to as many patients as possible without overwhelming health care providers.

Nxera: Building To Become Japan’s Global Biotech Champion

Nxera: Building To Become Japan’s Global Biotech Champion

CEO Chris Cargill talks to Scrip about Sosei Heptares’ new identity as Nxera, the ups and downs of being big pharma’s go-to small-molecule drug hunter and its move into commercialization in Japan.

Roche’s Plan To Muscle In On Obesity

Roche’s Plan To Muscle In On Obesity

The Swiss group’s head of cardiovascular, renal and metabolism aims to speed its incretins to market, and tackle the plateauing of weight loss and muscle wastage through combinations.    

Kailera’s $400m Series A Round Funds Ambitious Obesity Plans

Kailera’s $400m Series A Round Funds Ambitious Obesity Plans

A new contender emerges in obesity with pipeline assets from Jiangsu Hengrui, including a Phase III dual agonist, and an experienced team already focused on commercial hurdles.