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Rigel Pharmaceuticals (RIGL) investor relations material
Rigel Pharmaceuticals Corporate Presentation summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Commercial performance and portfolio growth
Net product sales for Q3 2025 reached $64.1M, with TAVALISSE at $44.7M, GAVRETO at $11.1M, and REZLIDHIA at $8.3M, all showing strong year-over-year growth.
2025 net product sales guidance was raised to $225M–$230M, reflecting 55–59% growth and a 32% CAGR since 2021.
Global expansion includes commercial launches and regulatory approvals for TAVALISSE and REZLIDHIA in multiple international markets.
Collaboration revenues in Q3 2025 totaled $5.4M, with key partners including Grifols, Kissei, and Medison.
Total 2025 revenue is projected at $285M–$290M, with continued positive net income expected.
Product and clinical development highlights
TAVALISSE is indicated for chronic immune thrombocytopenia (CITP) and demonstrated efficacy across multiple lines of therapy, with a favorable safety profile.
REZLIDHIA is approved for relapsed/refractory AML with susceptible IDH1 mutation, showing a 35% CR+CRh rate and durable responses in a Phase 2 trial.
GAVRETO is approved for RET fusion-positive NSCLC and thyroid cancer, offering once-daily oral dosing and high response rates.
R289, a dual IRAK1/4 inhibitor, is in Phase 1b for lower-risk MDS, with Fast Track and Orphan Drug designations and promising early efficacy and safety data.
Strategic collaborations are advancing olutasidenib in AML, MDS, and glioma, with multiple ongoing studies and new indications under evaluation.
Financial and strategic outlook
Cash, cash equivalents, and short-term investments were $137.1M as of September 30, 2025.
The company is pursuing late-stage in-licensing and product acquisition opportunities to leverage existing capabilities.
Continued financial discipline is emphasized, with investment in both commercial and development programs.
The portfolio is positioned for further growth through expanded adoption, global access, and new clinical data presentations.
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