Amgen and a small company called Viking Therapeutics are “set up perfectly” for obesity plus heart disease and NASH, respectively, says [Oppenheimer’s Jay] Olson.
…both companies have their own obesity meds in the works. …Amgen’s drug has potential as a monthly injection; current drugs on the market are injected weekly. Viking is working on a pill version of its drug, making it “one of the front-runners” in that race, says Olson.
Amgen already has a blockbuster drug called Repatha for treating high levels of the bad kind of cholesterol. The company hasn’t said whether it plans to combine Repatha, also a monthly injection, with its future obesity treatment, or whether such a combination is even feasible. But Olson views such a combination as likely. “Now you’re talking about a really potent cardiovascular risk-factor reduction combination,” he says.
The same goes for Viking and NASH. It has a pill in development that was shown this year to have sharply reduced liver fat in Phase 2 trials. Results compare well to those of a further-along drug from Madrigal Pharmaceuticals that is expected to be the first to win approval. Viking hasn’t indicated whether it plans to combine its NASH drug with its future obesity treatment, but Olson believes that the two drugs could eventually be taken as a single daily pill.
I've included a link to the latest version of this compilation in the Intro box of the Biotech Values board. The link is immediately below the link for Recent Biotech Buyouts.
Hat tip to Mufaso for maintaining this compilation!
12/9/23 – Added Roche/Carmot’s CT996. I’m speculating that of the $2.7B plus $400 mill in milestones Roche is paying for Carmot, the majority was for their ORAL CT996 compound based on the market cap of GPCR. In addition to CT996, Roche also got an injectable Obesity NME with a different MOA (CT388 GLP1/GIP completed ph1) and a Type 1 Diabetes drug (CT868 GLP1/GIP completed ph1). Added some observations. Also cleaned up formatting.
This has become a very crowded field. Structure Therapeutics (GPCR) currently has the most interesting compound. Others which have we will soon find out more on are VKTX's VK2809, AZN's ECC5004, Kallyope's Hormone NME's and Roche/Carmot’s CT-996.
Here is an updated list of ORAL weight loss drugs currently in trials listed in possible commercial success tiers:
Most Interesting NME's
Owner Drug MOA Comments
GPCR GSBR-1290 GLP1 Structure Therapeutics -Significant weight loss in 28day Phase 1 (up to 4.9%) VKTX VK2809 GLP1/GIP In phase 1- peptide PFE PF-06954522 GLP-1 GLP1 for Type 2 Diabetes - just entered Ph1- very little info AZN ECC5004 GLP-1 In Phase 1- small molecule GLP1- AZN paid 185mill + up to 1.8B milestones + royalties for compound. Kallyope K757&K833 Hormone New oral nutrient receptor agonists that stimulate the secretion of multiple appetite-suppressing satiety hormones AMGN Not Named Undisclosed Probably oral version of AMG 133 which activates GLP1 but inhibits GIP RHHBY CT996 GLP1 In phase 1- small molecule. From Carmot- Roche paid 2.7B for Carmot to acquire this Ph1 asset and 2 others
May surprise
LLY Orforglipron GLP1 In phase 3- No comment at last CC NOVO Rybelsus GLP1 Semaglutide- approved for Diabetes only but used off label TERN TERN-601 GLP1 Management discussing this drug in combination- not competitive standalone?
Not going forward
PFE Lotiglipron GLP1 Discontinued due to elevated liver enzymes PFE PF-06882961 GLP1 Danuglipron BID- Small Molecule- completed ph1 and in ph2b
Here are some observations:
PFE is trying very hard in this arena.
Kallyope is private but someone may buy them or strike a deal.
Viking Therapeutics is only public company with a NME having a potentially successful ORAL (possibly best in class tolerability). All other public companies are already "Big Pharma".
Structure Therapeutics (GPCR) market cap of $2.87B is primarily based on GSBR-1290 in Obesity
Roche paid an eye opening $2.7B for Carmot Therapeutics and prevented Carmot from going public
Again, anyone with knowledge of new Oral weight loss drug candidates is encouraged to reply to this post.