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Rigel Pharmaceuticals RIGL · USD

Health Care · US listing · 🇺🇸 United States

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42.05

+6.05%

Close of 9 Nov 2026, in USD

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About Rigel Pharmaceuticals

From its filings with the US Securities and Exchange Commission

SEC filings

Rigel Pharmaceuticals is based in South San Francisco, California and is incorporated in Delaware. Its shares trade on Nasdaq under the ticker RIGL. The SEC classifies its business as pharmaceutical preparations. In the fiscal year to 31 December 2025, it reported revenue of $294.3m and net income of $367.0m. At that date it held total assets of $513.6m and shareholders' equity of $391.5m.

In its own words

We are a biotechnology company dedicated to developing and providing novel therapies that significantly improve the lives of patients with hematologic disorders and cancer. We focus on products that address signaling pathways that are critical to disease mechanisms.

TAVALISSE® (fostamatinib disodium hexahydrate) is our first FDA-approved product and is the only approved oral spleen tyrosine kinase (SYK) inhibitor for the treatment of adult patients with chronic immune thrombocytopenia (ITP) who have had an insufficient response to a previous treatment. The product is also commercially available in Europe and the United Kingdom (UK) (as TAVLESSE), and in Japan, the Republic of Korea (Korea), Canada and Israel (as TAVALISSE) for the treatment of chronic ITP in adult patients.

REZLIDHIA® (olutasidenib) is our second FDA-approved product and indicated for the treatment of 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. We in-licensed REZLIDHIA from Forma Therapeutics, Inc., now Novo Nordisk (Forma), with exclusive, worldwide rights for its development, manufacturing and commercialization, pursuant to a license and transition services agreement entered in July 2022.

Quoted from its 10-K, filed 3 Mar 2026. Read the filing on SEC.gov ↗

Company facts

Sector
Health Care
Industry
Biotechnology
Listed since
29 Nov 2000
Employees
172
Website
rigel.com ↗
Head office
611 GATEWAY BOULEVARD, SUITE 900, SOUTH SAN FRANCISCO, CA, 94080
Incorporated in
DE
Classification
Pharmaceutical Preparations
Filer status
Accelerated filer

Leadership

Pay as last reported

  • Mr. Gregg LapointeIndependent Chairman of the Board$170,254
  • Mr. Raul RodriguezPresident, Chief Executive Officer, Director, since 2000$3.0m
  • Mr. Dean SchornoChief Financial Officer, Executive Vice President$1.4m
  • Mr. Raymond FureyExecutive Vice President, Chief Compliance Officer, General Counsel, Corporate Secretary$1.3m
  • Dr. Lisa RojkjaerExecutive Vice President, Chief Medical Officer$1.1m
  • Mr. David SantosExecutive Vice President, Chief Commercial Officer$1.4m
  • Ms. Kamil Ali-JacksonIndependent Director$120,254
  • Dr. Mark FrohlichIndependent Director
  • Dr. Alison HannahIndependent Director$113,254
  • Dr. Walter MoosIndependent Director$118,254
  • Ms. Jane WasmanIndependent Director$125,254

Environmental, social and governance

Scores out of 100, from our data supplier

ESG
Overall
50
Environment
24
Social
56
Governance
71
Carbon reduction policy
No
Human rights policy
No

SWOT analysis

AI-generated by our data supplier. Not written or checked by our editors.

AI-generated

Strengths

  • Rigel Pharmaceuticals employs 172 employees in the Health Care sector.
  • TAVALISSE is an oral SYK inhibitor for immune thrombocytopenia treatment.
  • Rigel has clinical programs in autoimmune hemolytic anemia and IgA nephropathy.

Weaknesses

  • Rigel's IPO was on 29 November 2000 with 169 employees.
  • Rigel's headquarters is in South San Francisco, California.
  • Rigel has no products approved for cancer or rare diseases.

Opportunities

  • Rigel's clinical programs include Phase 2 studies for fostamatinib.
  • Rigel partners with BerGenBio AS, Daiichi Sankyo, and Aclaris Therapeutics.
  • Rigel's research focuses on signaling pathways for disease mechanisms.

Threats

  • Rigel's product TAVALISSE is for immune disorders only.
  • Rigel's clinical programs are in Phase 2 and Phase I stages.
  • Rigel has no approved products for cancer or rare diseases.

Sources and methodology

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