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The obesity drug market is a battlefield of innovation, and
Therapeutics' recent Phase 2 trial results for VK2735 have sparked a critical debate: Is the company's 12.2% average weight loss a breakthrough or a red flag in a race dominated by and Novo Nordisk? With Viking's stock plummeting 30% post-announcement, investors must weigh whether this is a buying opportunity or a warning sign of a flawed strategy.Viking's VK2735, a dual GLP-1/GIP oral drug, delivered a headline-grabbing 12.2% weight loss in its highest dose (120 mg) over 13 weeks—a figure that rivals Eli Lilly's orforglipron (12.4% at 36 mg) and outpaces Novo Nordisk's semaglutide (9.39% over 104 weeks). However, the catch lies in tolerability. Viking's trial reported a 28% dropout rate due to gastrointestinal (GI) adverse events, with nausea and vomiting affecting 58% and 26% of participants, respectively. By contrast, Eli Lilly's 36 mg orforglipron had a 10.3% discontinuation rate, while Novo's semaglutide saw 16.6% attrition.
The key question is whether Viking's efficacy justifies its side effects. While 12.2% weight loss is impressive, the high dropout rate raises doubts about long-term adherence. Patients are unlikely to stick with a drug that causes nausea in nearly 60% of users, especially when alternatives like Eli Lilly's once-daily pill or Novo's once-weekly injection offer comparable or better tolerability.
Eli Lilly's orforglipron has a critical advantage: a 72-week trial duration, demonstrating sustained efficacy and safety over a year. Viking's 13-week trial, while promising, lacks long-term data. Novo Nordisk's semaglutide, though subcutaneous, has a robust 104-week SELECT trial showing a 20% reduction in major cardiovascular events—a value proposition that extends beyond weight loss.
Viking's exploratory dosing strategy—transitioning patients to lower maintenance doses (30 mg) after initial high-dose treatment—could mitigate dropout risks. However, this approach remains unproven in real-world settings. Investors must ask: Can Viking replicate the success of Eli Lilly's titration model, which gradually increases doses to minimize side effects?
Viking's stock has taken a hit, but this could be a strategic entry point for risk-tolerant investors. The company's dual GLP-1/GIP mechanism offers a unique angle in a market dominated by single-agonist therapies. If Viking can refine its dosing strategy to reduce GI side effects—perhaps through formulation tweaks or slower titration—it could carve out a niche.
However, the path is fraught. Eli
is on track to submit orforglipron for regulatory approval by year-end, while Novo Nordisk's semaglutide already has a strong foothold in the injectable market. Viking's oral format is a differentiator, but only if it can match the tolerability of its rivals.Viking Therapeutics' setback is not a death knell but a crossroads. The company's dual-agonist approach and oral format remain compelling, but the path to commercialization hinges on improving tolerability. For investors, the sharp sell-off offers a chance to bet on a bold innovation—if Viking can prove it can fix its GI issues. However, those seeking safer bets should look to Eli Lilly's near-term regulatory milestones or Novo Nordisk's entrenched market position.
In the end, the obesity drug race is not just about weight loss percentages—it's about who can deliver the most sustainable, patient-friendly solution. Viking has the potential to be a contender, but it must first clear the hurdle of real-world adherence.
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