Rigel Pharmaceuticals, Inc., a biotechnology company, develops and provides therapies that enhance the lives of patients with hematologic disorders and cancer in the United States. The company offers TAVALISSE, an oral spleen tyrosine kinase inhibitor for the treatment of adult patients with chronic immune thrombocytopenia; REZLIDHIA, a non-intensive monotherapy to treat adult patients with relapsed or refractory (R/R) acute myeloid leukemia (AML) with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation as detected by an FDA-approved test; and GAVRETO, a once daily, small molecule, oral, kinase inhibitor for the treatment of adult patients with metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer (NSCLC), as well as to treat adult and pediatric patients twelve years of age and older with advanced or metastatic RET fusion-positive thyroid cancer. It also develops R289, an oral interleukin receptor-associated kinases 1 and 4 (IRAK1/4) inhibitor, which is being advanced to Phase 1b study for the treatment of hematology-oncology, autoimmune, and inflammatory diseases, as well as to treat lower-risk myelodysplastic syndrome. The company has strategic development collaboration with The University of Texas MD Anderson Cancer Center (MDACC) for the development of olutasidenib in AML and other hematologic cancers with IDH1mutations; and the Collaborative Network for Neuro-Oncology Clinical Trial (CONNECT) to conduct a Phase 2 clinical trial to evaluate olutasidenib in combination with temozolomide in patients with high-grade glioma harboring an IDH1 mutation. Rigel Pharmaceuticals, Inc. was incorporated in 1996 and is headquartered in South San Francisco, California. Show more
611 Gateway Boulevard, South San Francisco, CA, 94080, United States
Market Cap
479.4M
52 Wk Range
$15.50 - $52.24
Previous Close
$26.60
Open
$26.87
Volume
415,910
Day Range
$25.53 - $27.16
Enterprise Value
377.7M
Cash
155M
Avg Qtr Burn
N/A
Insider Ownership
3.10%
Institutional Own.
90.07%
Qtr Updated
12/31/25
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| Drug & Indication | Stage & Event | Catalyst Date |
|---|---|---|
GAVRETO (pralsetinib) Details Non-small cell lung carcinoma | Approved Quarterly sales | |
TAVALISSE® (fostamatinib disodium hexahydrate) Details Adult Chronic Immune Thrombocytopenia (ITP) | Approved Quarterly sales | |
REZLIDHIA (Olutasidenib) (FT-2102) Details Glioma, Acute myeloid leukemia, Cancer | Approved Quarterly sales | |
REZLIDHIA (Olutasidenib) (FT-2102) Details Cancer, Acute myeloid leukemia | Approved Quarterly sales | |
Phase 3 Update | ||
REZLIDHIA (Olutasidenib) (FT-2102)+ temozolomide Details Glioma, Cancer | Phase 2 Data readout | |
REZLIDHIA (Olutasidenib) (FT-2102) (IDH1 Inhibitor) Details Relapsed Or Refractory IDH1-Mutated Myeloid Malignancies | Phase 2 Initiation | |
Ocadusertib (previously R552) Details Rheumatoid arthritis, Autoimmune disease | Phase 2a Update | |
REZLIDHIA (Olutasidenib) [triplet therapy] Details Cancer, Acute myeloid leukemia | Phase 1/2 Update | |
R289 Details Lower-risk myeloid dysplastic syndrome | Phase 1b Data readout | |
TAVALISSE® (fostamatinib disodium hexahydrate) Details Blood disorder | Failed Discontinued | |
Failed Discontinued |
