Source: Pfizer Investor Insights
Shares of Pfizer Inc. (PFE) slipped by over 1% in premarket trading after the company announced it was discontinuing the development of danuglipron, an experimental oral weight loss drug taken daily. The decision came after clinical trial data revealed a potential link to liver injury, raising serious safety concerns.
Pfizer made the call to end development of oral danuglipron after a clinical trial participant developed signs of liver injury, which the company believes may be drug-related. The patient’s condition brought into question the long-term safety of daily dosing.
Dr. Chris Boshoff, Pfizer’s Chief Scientific Officer, stated:
“While we are disappointed to discontinue the development of danuglipron, we remain committed to evaluating and advancing promising programs in an effort to bring innovative new medicines to patients.”
This isn’t Pfizer’s first shift in strategy for obesity treatments. In late 2023, the company also scrapped a twice-daily version of danuglipron due to side effects like nausea and vomiting. The more recent decision effectively halts any further clinical advancement of the daily oral formulation, though injectable or other formulations may still be under consideration.
The move comes as pharmaceutical companies race to dominate the booming global weight loss drug market, projected to exceed $100 billion by 2030, according to Goldman Sachs. Popular drugs like Novo Nordisk's Wegovy and Ozempic, and Eli Lilly’s Mounjaro, have already demonstrated massive success in both weight loss and diabetes control.
Unlike these injectable GLP-1 receptor agonists, Pfizer hoped to offer a pill-based alternative that could make obesity treatment more accessible. However, this recent setback shows the difficulty in balancing efficacy with tolerability and safety—especially with oral medications that are taken daily.
Pfizer’s weight loss strategy has hit multiple roadblocks in recent months. The company, best known for its COVID-19 vaccine, has been seeking to diversify revenue streams amid a decline in pandemic-related product sales.
The termination of danuglipron’s development leaves a gap in its metabolic disease pipeline, but Pfizer assures investors and the public that it’s still committed to the obesity space. Analysts expect Pfizer to possibly redirect investments into next-gen GLP-1 alternatives or partner with other biotech firms working on obesity therapeutics.
As of now, the company has not announced any immediate replacements for danuglipron but continues to evaluate other compounds in early-stage trials.
Following the announcement, Pfizer’s stock experienced a modest decline of around 1.2% in premarket trading. While not a significant drop, it reflects investor concern over the company’s ability to compete in the lucrative weight loss space.
However, some analysts remain cautiously optimistic.
“While this is a setback, Pfizer’s broad pipeline and deep R&D capabilities suggest it’s far from out of the game,” said an industry analyst at Morningstar.
Pfizer’s decision to end its pursuit of a daily weight loss pill underscores the critical importance of safety in drug development, especially in a competitive sector like obesity treatment. Although the company faces short-term challenges, it remains to be seen how it adapts its long-term strategy and whether it can still secure a foothold in this fast-growing market.