Logotype for RAPT Therapeutics Inc

RAPT Therapeutics (RAPT) Investor Update summary

Event summary combining transcript, slides, and related documents.

Logotype for RAPT Therapeutics Inc

Investor Update summary

10 Jan, 2026

Strategic 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.

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