RAPT Therapeutics (RAPT) Investor Update summary
Event summary combining transcript, slides, and related documents.
Investor Update summary
10 Jan, 2026Strategic partnership and license agreement
In-licensed RPT904 (JYB1904), a long-acting anti-IgE antibody, from Jemincare for territories outside China, Taiwan, Macau, and Hong Kong, with $35M upfront, up to $672.5M in milestones, and mid-single to low double-digit royalties.
RPT904 is a half-life-extended omalizumab biobetter, designed for less frequent dosing and improved compliance in food allergy and other allergic disorders.
The agreement positions the company to address significant unmet needs in food allergy and allergic disorders, leveraging omalizumab's market success.
$150M financing secured from top-tier investors, extending cash runway into mid-2027, past the phase 2b food allergy data readout.
Clinical development and trial plans
Phase 2b study in food allergy planned to start in H2 2025, with top-line data expected in H1 2027; parallel PK/PD studies will refine dosing.
Jemincare is running phase 2 studies in asthma and CSU in China, with data expected in H2 2025 and H1 2026, respectively.
RPT904's phase 1 data showed a twofold longer half-life (63 vs. 27 days) and deeper IgE suppression compared to omalizumab, supporting Q8- or Q12-week dosing.
Phase 2b food allergy trial will use a simplified dosing table and include patients currently excluded from omalizumab label.
Jemincare's Phase 2 and 3 trials in asthma and CSU in China are designed to establish optimal dosing and demonstrate non-inferiority to omalizumab.
Product profile and differentiation
RPT904 uses YTE mutation for over twofold half-life extension and affinity maturation for about fourfold higher affinity over omalizumab.
Improved manufacturability, stability, and reduced immunogenicity through targeted molecular modifications.
RPT904 offers less frequent dosing (Q8W/Q12W) compared to omalizumab (Q2W/Q4W), with potential to treat patients with high weight or IgE levels.
PK/PD simulations support Q12W dosing for most patients, potentially improving compliance.
Latest events from RAPT Therapeutics
- RPT904 targets major allergy markets with extended dosing and broad patient coverage, with pivotal data due by 2027.RAPT
Stifel Virtual Immunology and Inflammation Forum3 Feb 2026 - Ozureprobart advances with strong phase 2 data, targeting broad allergic disorders and unmet needs.RAPT
44th Annual J.P. Morgan Healthcare Conference14 Jan 2026 - RPT904 aims to transform food allergy and CSU treatment with superior dosing and strong market potential.RAPT
43rd Annual J.P. Morgan Healthcare Conference 202510 Jan 2026 - RPT-904 aims to transform allergy and urticaria care with less frequent dosing and broad access.RAPT
Wells Fargo 20th Annual Healthcare Conference 20255 Jan 2026 - Phase IIB trials for a long-acting omalizumab biobetter in food allergy and CSU begin year-end.RAPT
Leerink’s Global Healthcare Conference 202526 Dec 2025 - RPT904 targets food allergy and CSU with extended dosing, aiming for market leadership and premium pricing.RAPT
Barclays 27th Annual Global Healthcare Conference 202526 Dec 2025 - 176.5M shares registered for resale after $143.5M private placement to fund immunology drug development.RAPT
Registration Filing16 Dec 2025 - RPT904 showed durable, superior or comparable efficacy and safety to omalizumab with less frequent dosing.RAPT
Study Result12 Dec 2025 - Proxy seeks approval for director, auditor, reverse split, and equity plan changes; Board supports all.RAPT
Proxy Filing2 Dec 2025