oncology
ITM's radiopharmaceutical notches late-stage win
ITM Isotope Technologies Munich SE said this morning that it will seek FDA approval for its radiopharmaceutical to treat rare gastrointestinal cancers, after showing that the therapy halted tumor progression for nearly two years.
The drug, called ITM-11, is being developed for gastroenteropancreatic neuroendocrine tumors (or GEP-NETs). In a Phase 3 trial, patients with the earliest forms of this cancer who took the treatment lived for 23.9 months without their tumors growing, while patients taking an existing treatment on the market went a median 14.1 months before their cancer progressed.
Biopharma companies have been racing to develop candidates in the class of cancer drugs called radiopharmaceuticals. Novartis is currently the only company with radiopharmaceuticals on the market, one of which, Lutathera, treats GEP-NET cancers.
Read more from STAT's Allison DeAngelis.
obesity
Novo follows Lilly with direct-to-patient offering
Novo Nordisk said yesterday that it will start selling its obesity drug Wegovy directly to patients at a reduced price, following a similar move from Eli Lilly, though Novo's offering is broader.
Wegovy normally carries a list price of about $1,350 a month, but Novo will sell the treatment through its new direct-to-consumer offering called NovoCare Pharmacy at $499 a month for all doses to cash-paying patients, meaning patients who are paying on their own without insurance. Meanwhile, Lilly sells all but the highest doses of Zepbound through LillyDirect, and at different prices ranging from $349 to $699 a month.
Novo also said that in the "near future," it will extend the reduced price to cash-paying patients who fulfill their orders at traditional pharmacies. Lilly hasn't indicated it will take such a step.
Read more.
obesity
Amgen starts late-stage studies of MariTide
Elsewhere in the obesity space — Amgen has initiated Phase 3 trials of its obesity drug MariTide, one in overweight and obese people without diabetes and another one for people with diabetes.
The company's chief scientific officer, Jay Bradner, said at a health care conference yesterday that it will study three doses of "low, medium, and high." He disclosed little about the exact dosing scheme that will be tested, but said that "you can think of a titration scheme as starting lower."
Recall that late last year, Amgen reported that in a Phase 2 trial, MariTide led to roughly 20% weight loss over a year. Many investors didn't view the result as competitive enough, especially since executives had said they were "very encouraged" by an interim analysis of that study. Still, though, Amgen's leadership has said it continues to see the treatment, designed to be dosed monthly, as being "differentiated."
"The progression of the MariTide Phase 3 program is going very, very well," Bradner said.
Correction: Yesterday's newsletter incorrectly described the target of a BioAge therapy. The drug, azelaprag, targeted apelin receptors.
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