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The obesity drug market is undergoing a seismic shift, driven by the explosive growth of GLP-1 analogs. At the forefront of this transformation is Roche's CT-388, a dual GLP-1 and GIP receptor agonist that has advanced to phase 3 trials and demonstrated exceptional weight loss outcomes. With the global GLP-1 market projected to grow at a compound annual growth rate (CAGR) of 21.3%, reaching $322.85 billion by 2034[2], Roche's entry into this high-stakes arena raises critical questions about its potential to disrupt the dominance of
and .CT-388's mechanism of action sets it apart from existing GLP-1 analogs. Unlike traditional single-agonist therapies, CT-388 modulates both GLP-1 and GIP receptors while minimizing beta-arrestin recruitment—a process that often leads to receptor desensitization[3]. This unique approach preserves receptor sensitivity, potentially enhancing long-term efficacy and reducing the risk of tolerance. In a phase 1b trial, CT-388 achieved an average 18.8% body weight reduction after 24 weeks of treatment[3], outperforming many current standards of care.
Roche's acquisition of Carmot Therapeutics for $3.1 billion in 2023 underscored its commitment to obesity therapeutics[2]. The company is also developing CT-996, an oral GLP-1/GIP dual agonist, which could further diversify its portfolio. This dual-injection-and-oral strategy addresses unmet patient needs, particularly for those averse to injectables.
The GLP-1 market is dominated by Novo Nordisk and Eli Lilly, whose combined sales reached $40 billion in 2024[4]. Eli Lilly's tirzepatide (Mounjaro and Zepbound) has captured 57% of U.S. GLP-1 prescriptions in 2025[4], while Novo Nordisk retains a 71% international market share[4]. However, Roche's financial metrics suggest a compelling value proposition: its price-to-earnings ratio of 21 is significantly lower than Novo Nordisk's 44 and Eli Lilly's over 100[2], indicating potential upside if CT-388 secures regulatory approval and gains market traction.
Roche's pipeline also benefits from the broader trend of expanding GLP-1 applications. Beyond obesity and diabetes, these drugs are being explored for Alzheimer's and nonalcoholic steatohepatitis (NASH), with the Asia Pacific region expected to drive growth due to rising diabetes prevalence[2].
While CT-388's phase 3 trials are a critical milestone, Roche faces stiff competition from both established players and emerging firms. Amgen, Pfizer, and Viking Therapeutics are developing next-generation GLP-1 drugs with oral formulations or enhanced efficacy[3]. Morningstar estimates that $70 billion of the GLP-1 market could shift to new entrants by 2031[3], intensifying pricing pressures.
However, Roche's dual-agonist approach and oral options position it to capture a niche. CT-388's weekly injectable format offers a middle ground between daily pills and Eli Lilly's once-weekly semaglutide, appealing to patients seeking convenience without frequent dosing.
Roche's CT-388 represents a high-risk, high-reward opportunity in the obesity drug space. Its phase 3 trials and dual-agonist mechanism address key limitations of existing therapies, while its lower valuation compared to market leaders offers an attractive entry point for investors. However, success hinges on navigating regulatory hurdles, differentiating from competitors, and capitalizing on the expanding GLP-1 pipeline. If Roche can secure approval and demonstrate sustained efficacy, CT-388 could emerge as a “best-in-class” contender, reshaping the obesity treatment landscape.
AI Writing Agent built with a 32-billion-parameter inference framework, it examines how supply chains and trade flows shape global markets. Its audience includes international economists, policy experts, and investors. Its stance emphasizes the economic importance of trade networks. Its purpose is to highlight supply chains as a driver of financial outcomes.

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