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Approval window: Based on a Q1 2027 filing, FDA action is expected between Q3 2027 (priority review scenario) and Q1Q2 2028 (standard review scenario)

In both our sites, we did see increased risks of developing these events, and both our studies do show statistical significance in terms of increased risk

A Phase IIb trial of mRNA-4157 in combination with pembrolizumab for patients with resected high-risk melanoma showed that this combination therapy prolonged recurrence-free survival compared with pembrolizumab monotherapy and had a manageable safety profile

Research is currently being conducted to evaluate the long-term safety of Mazdutide in larger populations