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3 Reasons Why Buying Madrigal Pharmaceuticals Today Is a Wise Move

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When a company's shares shoot up 82% in 12 months, investors clearly think it's a good time to be a shareholder -- and that's exactly what's happened to the stock of Madrigal Pharmaceuticals (NASDAQ: MDGL). Earlier this year, the up-and-coming biotech received approval of a pioneering liver-disease treatment. And from how things looks right now, there isn't much reason to expect this budding player's growth to taper off anytime soon.

In fact, the bull thesis for buying it is still looking quite good. Here are three reasons why it's a canny move to buy the stock.

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1. Its first drug is rolling out quite efficiently

When it was approved in March 2024, Rezdiffra became the only medicine approved by the Food and Drug Administration (FDA) to treat metabolic-associated steatohepatitis (MASH), a disease that's characterized by fatty deposits on the liver, toughening and stiffening of liver tissue (fibrosis), and eventually scarring of the liver (cirrhosis).

Since then, Madrigal has been focused on getting more patients on treatment so that it can generate sales. In the third quarter, there were more than 6,800 patients taking Rezdiffra, which led to sales of $62.2 million. As the business had no revenue before the launch of the drug, that number should continue to grow at a rapid pace for at least the next couple of years.

By the middle of next year, the company should hear back from regulators in the E.U. regarding whether the medicine can be sold there. It's also actively working to network with specialist physicians who management thinks will be disproportionately important in terms of prescribing volume; so far, it's in touch with 40% of the doctors it's targeting during Rezdiffra's launch period.

That figure will likely keep climbing, and the ongoing success of the Rezdiffra rollout is a fair reason to consider buying the stock.

2. Efforts are underway to expand its addressable market

At launch, Madrigal set Rezdiffra's target market as the 315,000 or so patients in the U.S. who are already diagnosed with MASH, working with a specialist clinician, and who had moderate to advanced fibrosis of the liver. That makes sense, as that's the disease context where the drug was proven to work in its clinical trials. But, the total population of patients with MASH is much larger, with perhaps as many as 1.5 million people. And, with some additional research and development (R&D) work in the form of additional clinical trials, this biotech is keen on expanding its addressable market to capture a chunk of that larger group of patients, too.