Summary of RAPT Therapeutics Conference Call (October 20, 2025) Company Overview - Company: RAPT Therapeutics (NasdaqGM:RAPT) - Focus: Development of innovative therapies for chronic spontaneous urticaria (CSU) and other IgE-driven disorders Key Points from the Call Industry and Product Development - Product: RPT-nine zero four (also known as JYB-nineteen oh four) - Indication: Chronic spontaneous urticaria (CSU) - Clinical Trial: Phase II trial conducted in China, comparing RPT-nine zero four to omalizumab - Results: Top line data showed RPT-nine zero four demonstrated comparable efficacy to omalizumab with potential for superior durability and less frequent dosing [5][6][7][10][38] Efficacy and Safety Data - Efficacy: - RPT-nine zero four showed a 22.1 improvement in UAS7 at week twelve compared to 18.5 for omalizumab [21] - At week sixteen, RPT-nine zero four arms showed improvements of 23.2 and 22.2, while omalizumab showed 19.1 [21] - Complete response (UAS7=0) at week twelve was 37% and 39% for RPT-nine zero four compared to 24.4% for omalizumab [23] - Safety: - No serious adverse events or anaphylaxis reported [24] - Treatment emergent adverse events were similar across groups, indicating a favorable safety profile [24] Competitive Landscape - Current Standard of Care: Omalizumab, which requires monthly dosing and has limitations in durability and convenience [10][11] - Market Research: Survey of allergists indicated that the advantages of RPT-nine zero four would likely drive it to become the preferred treatment option for CSU patients [13] Future Development Plans - Phase III Trials: Plans to engage with regulatory authorities to discuss registrational pathways for RPT-nine zero four in CSU [8][39] - Food Allergy Trials: Anticipated initiation of Phase IIb trial for food allergies before the end of the year, with top line data expected in 2027 [39][40] - Asthma Trials: Smaller Phase II study in moderate to severe asthma expected to read out data by the end of the year [42] Market Potential - Market Opportunity: RPT-nine zero four is positioned to address unmet needs in CSU and food allergies, with a focus on less frequent dosing and broader efficacy in patients who are ineligible for omalizumab [39][40] Regulatory Considerations - FDA Discussions: Plans to discuss data with the FDA to align on Phase III study designs, with confidence in the translatability of data from Asian populations to Western populations [117] Expert Commentary - Dr. Ana Maria Jimenez Arnaud: Highlighted the unmet need for effective treatments in CSU and the potential of RPT-nine zero four to improve patient compliance due to less frequent dosing [28][32][34] Conclusion RAPT Therapeutics is advancing RPT-nine zero four as a promising treatment for CSU, demonstrating comparable efficacy to the current standard of care, omalizumab, with a favorable safety profile and potential for improved patient adherence through less frequent dosing. The company is preparing for Phase III trials and exploring additional indications, including food allergies and asthma.
RAPT Therapeutics (NasdaqGM:RAPT) Update / Briefing Transcript