Rigel Appoints Alison L. Hannah, M.D. to Board of Directors

Rhea-AI Summary

Rigel Pharmaceuticals (Nasdaq: RIGL) announced the appointment of Dr. Alison L. Hannah to its Board of Directors. With over 30 years of experience in the pharmaceutical sector, she specializes in clinical development strategy for hematology and oncology, focusing on molecularly targeted therapies. Dr. Hannah has contributed to the regulatory approval of over 40 cancer treatments and served in key roles at various biotech firms. Her expertise is expected to enhance Rigel's clinical development initiatives as the company advances its hematology, immunology, and oncology programs.

Positive

• Dr. Alison L. Hannah brings over 30 years of pharmaceutical experience, enhancing Rigel's expertise in clinical development.
• Her background includes successful contributions to over 40 regulatory applications for cancer therapies, which can strengthen Rigel's strategic direction.
• Increased board expertise may lead to improved insights and guidance on drug development and regulatory strategies.

Negative

• None.

SOUTH SAN FRANCISCO, Calif., May 14, 2021 /PRNewswire/ -- Rigel Pharmaceuticals, Inc. (Nasdaq: RIGL) today announced that it has appointed Alison L. Hannah, M.D. to its Board of Directors. Dr. Hannah brings over three decades of pharmaceutical industry experience to Rigel, including a deep knowledge of clinical development strategy in hematology and oncology with a focus on molecularly targeted therapies.

"We are delighted to have Alison join our Board," said Raul Rodriguez, Rigel's president and CEO. "With her extensive expertise in areas of key focus for Rigel, including clinical development strategy and successful regulatory filings, she will provide valuable insights to our Board as we continue to advance and expand our hematology, immunology, and oncology programs."

Alison L. Hannah, M.D. currently serves as Chief Medical Officer for CytomX Therapeutics, a clinical-stage biopharmaceutical company developing conditionally activated therapies to treat cancer. Prior to joining CytomX, Dr. Hannah served as a consultant to nearly 30 pharmaceutical and biotechnology companies directing the development of investigational cancer therapies. In this capacity, Dr. Hannah has successfully filed over 40 regulatory applications for First-in-Human clinical testing and has played significant roles in the broad marketing approval of multiple anticancer therapeutics (including talazoparib, enzalutamide, defibrotide, carfilzomib, as well as tyrosine kinase inhibitors sunitinib and toceranib), including extensive experience interacting with global health and regulatory authorities. Earlier in her career, Dr. Hannah held the role of Senior Medical Director at SUGEN, Inc. (acquired by Pharmacia & Upjohn, now Pfizer) where she had oversight of clinical development, clinical operations, and pharmacovigilance, specializing in the development of tyrosine kinase inhibitors, including sunitinib (SUTENT) approved for the treatment of kidney cancer and imatinib-refractory gastrointestinal stromal tumors. Dr. Hannah began her career at Quintiles, a global contract research organization, where she specialized in overseeing early to registrational-stage oncology clinical trials. Dr. Hannah currently serves on the board of NeoGenomics, a publicly traded cancer diagnostic company. Dr. Hannah received her B.A. in biochemistry and immunology from Harvard University and her M.D. from the University of Saint Andrews.

"I have been very impressed by Rigel's scientific approach and its ability to discover and develop a portfolio of unique therapies for patients suffering from hematologic diseases, cancer and autoimmune disorders," said Dr. Hannah. "I'm looking forward to collaborating with Rigel's management team and other members of its Board to provide strategic guidance as the company continues to advance its innovative product candidates through clinical trials with the goal of delivering them to patients in need." 

About Rigel (www.rigel.com)
Rigel Pharmaceuticals, Inc., is a biotechnology company dedicated to discovering, developing and providing novel small molecule drugs that significantly improve the lives of patients with hematologic disorders, cancer and rare immune diseases. Rigel's pioneering research focuses on signaling pathways that are critical to disease mechanisms. The company's first FDA approved product is TAVALISSE^® (fostamatinib disodium hexahydrate) tablets, the only oral spleen tyrosine kinase (SYK) inhibitor for the treatment of adult patients with chronic immune thrombocytopenia who have had an insufficient response to a previous treatment. The product is also commercially available in Europe (TAVLESSE) and Canada (TAVALISSE) for the treatment of chronic immune thrombocytopenia in adult patients.

Fostamatinib is currently being studied in a Phase 3 clinical trial for the treatment of warm autoimmune hemolytic anemia (wAIHA)¹; a Phase 3 clinical trial for the treatment of hospitalized patients with COVID-19¹; an NIH/NHLBI-sponsored Phase 2 clinical trial for the treatment of hospitalized patients with COVID-19, in collaboration with Inova Health System; and a Phase 2 clinical trial for the treatment of COVID-19 being conducted by Imperial College London.

Rigel's other clinical programs include its interleukin receptor-associated kinase (IRAK) inhibitor program, and a receptor-interacting serine/threonine-protein kinase (RIP1) inhibitor program in clinical development with partner Eli Lilly and Company. In addition, Rigel has product candidates in development with partners AstraZeneca, BerGenBio ASA, and Daiichi Sankyo.

Please see www.TAVALISSE.com for full Prescribing Information.

¹The product for this use or indication is investigational and has not been proven safe or effective by any regulatory authority.

Rigel Contact:
Jodi Sievers
Phone: +1 (650)624-1232
Email: ir@rigel.com

 

View original content to download multimedia:http://www.prnewswire.com/news-releases/rigel-appoints-alison-l-hannah-md-to-board-of-directors-301291455.html

SOURCE Rigel Pharmaceuticals, Inc.

FAQ

Who is the new appointee to Rigel's Board of Directors?

Dr. Alison L. Hannah has been appointed to Rigel's Board of Directors.

What is Dr. Alison L. Hannah's background?

Dr. Hannah has over 30 years of experience in the pharmaceutical industry, focusing on clinical development in hematology and oncology.

What impact will Dr. Hannah's appointment have on Rigel Pharmaceuticals?

Her expertise in regulatory affairs and drug development is expected to enhance Rigel's strategic initiatives in hematology, immunology, and oncology.