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Roche Discontinues Development of Obesity Drug CT-173 Due to Lack of Competitiveness

WHAT'S THE STORY?

What's Happening?

Roche has decided to halt the development of CT-173, an investigational PYY analog for obesity treatment, citing insufficient competitiveness. The decision was announced during Roche's second-quarter earnings call, where Teresa Graham, CEO of the Pharmaceuticals Division, explained that the drug did not meet the company's criteria for further investment. CT-173 was acquired through Roche's $2.7 billion purchase of Carmot Therapeutics in 2023. Despite promising preclinical data, the molecule was deemed a very early-stage program with minimal impact on Roche's overall obesity portfolio. Roche remains confident in its competitive obesity pipeline, particularly with assets like CT-388, which showed significant weight loss in Phase Ib trials.
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Why It's Important?

Roche's decision to discontinue CT-173 highlights the competitive pressures in the pharmaceutical industry, particularly in the obesity treatment market. The move reflects Roche's strategic focus on investing in drug candidates with higher potential for success and market impact. The discontinuation may affect stakeholders involved in the development and potential commercialization of CT-173. However, Roche's robust pipeline, including CT-388, positions the company to capitalize on emerging subsegments within the obesity market. This strategic alignment is crucial for maintaining Roche's leadership in the field and ensuring long-term growth.

What's Next?

Roche will continue to advance its obesity portfolio, with expectations for Phase III-enabling readouts for CT-388 by the end of the year. The company aims to leverage its pipeline to address various subsegments of the obesity market, including comorbidities and varying degrees of weight loss. Roche's strategic focus on competitive assets is expected to drive future growth and enhance its position in the pharmaceutical industry.

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