Response Pharmaceuticals' Ex-Sanofi Asset Shows Promise in Post-GLP-1 Weight Management

Response Pharmaceuticals has unveiled promising phase 2 data for its investigational drug RDX-002, demonstrating potential benefits for patients who have discontinued GLP-1 receptor agonist treatments for obesity. The oral iMTP inhibitor, originally licensed from Sanofi, has shown efficacy in reducing blood-fat levels and mitigating weight gain in individuals who previously used popular obesity medications like Eli Lilly's Zepbound and Novo Nordisk's Wegovy.
Phase 2 Trial Results
The 12-week randomized trial involved 68 participants who had lost at least 10% of their body weight or 10 kg while taking Zepbound or Wegovy before discontinuing treatment. RDX-002 achieved its primary endpoint, demonstrating a statistically significant reduction in postprandial blood-fat levels compared to placebo. Additionally, the drug met a key secondary endpoint related to weight gain prevention following GLP-1 discontinuation.
Safety data from the trial were encouraging, with no serious adverse events reported and no patients discontinuing treatment due to side effects. Mild to moderate gastrointestinal adverse events were observed but generally resolved early in the treatment course.
Mechanism of Action and Market Potential
RDX-002 targets a protein involved in triglyceride transfer, a mechanism that has been explored by other pharmaceutical companies, including Bristol Myers Squibb. The FDA previously approved Aegerion Pharmaceuticals' Juxtapid, another MTP inhibitor, as a lipid-lowering drug in 2012.
Dr. William Sasiela, Chief Medical Officer at Response Pharmaceuticals, highlighted the potential of RDX-002, stating that the mechanism may offer a "differentiated and complementary approach to help patients maintain and, over the long term, enhance the health benefits they achieve with GLP-1s." The company is exploring opportunities to test the drug candidate in combination with GLP-1 receptor agonists, addressing a growing need in the obesity treatment landscape.
Addressing Post-GLP-1 Treatment Challenges
The development of RDX-002 addresses a significant challenge in obesity management. While GLP-1 receptor agonists like Zepbound and Wegovy have shown remarkable efficacy in promoting weight loss, studies indicate that many patients discontinue these medications and subsequently regain lost weight. Response Pharmaceuticals initially targeted antipsychotic-induced weight gain but has pivoted to focus on the post-GLP-1 market, recognizing the need for interventions that can help patients maintain their weight loss after stopping GLP-1 therapy.
As the obesity treatment market continues to evolve, RDX-002 represents a potential solution for maintaining the long-term benefits of GLP-1 receptor agonist therapy. Response Pharmaceuticals plans to present full data from the phase 2 study at an upcoming medical meeting, which will likely provide further insights into the drug's efficacy and safety profile.
References
- Response’s ex-Sanofi asset hits midphase goal in post-GLP-1 patients
Response Pharmaceuticals has shared phase 2 data in post-GLP-1 patients, linking its ex-Sanofi asset to reductions in blood-fat levels and weight gain in previous users of obesity drugs.
Explore Further
What are the key differences in safety and efficacy between RDX-002 and other MTP inhibitors like Juxtapid?
What is the potential market size for RDX-002 in addressing post-GLP-1 weight management challenges?
How does the mechanism of RDX-002 compare to GLP-1 receptor agonists in terms of long-term weight management?
What are the current annual sales figures for GLP-1 receptor agonists such as Zepbound and Wegovy?
What are the strategic plans of Response Pharmaceuticals to commercialize RDX-002 if phase 3 trials are successful?