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Ionis announces expanded licensing agreement with Otsuka in Asia Pacific for investigational medicine donidalorsen in hereditary angioedema Otsuka will be responsible for commercialization efforts for donidalorsen across

Key Takeaway: Ionis Pharmaceuticals has announced an expanded licensing agreement with Otsuka Pharmaceutical for donidalorsen, an investigational therapy for hereditary angioedema (HAE). Under this agreement, Otsuka will be responsible for developing and commercializing the medicine in the Asia-Pacific region, following similar efforts in Europe. Ionis plans to file for FDA approval later this year and has reported positive Phase 3 trial results, positioning donidalorsen as a potentially significant treatment option for HAE. The deal includes a $20 million upfront payment with milestone payments based on regulatory achievements.

Market Sentiment Analysis

POSITIVE FACTORS

  • Expanded licensing agreement enhances Ionis's market reach for donidalorsen.
  • Otsuka's expertise in the Asia-Pacific region bolsters commercialization efforts.
  • Ionis anticipates regulatory submissions for donidalorsen based on positive Phase 3 results.

CONCERNS & RISKS

  • Forward-looking statements carry inherent risks and uncertainties.
  • Regulatory approvals are still pending, which may delay commercialization.

Full Press Release Details

Ionis announces expanded licensing agreement with Otsuka in Asia Pacific for investigational medicine donidalorsen in hereditary
CARLSBAD, Calif., June 18, 2024 -- Ionis Pharmaceuticals, Inc.
(Nasdaq: IONS) today announced that it has entered into a license agreement with Otsuka Pharmaceutical Co., Ltd. (Otsuka) under which Otsuka obtains
exclusive rights across the Asia-Pacific region for donidalorsen, an investigational RNA-targeted prophylactic medicine for hereditary angioedema (HAE). Ionis will maintain primary responsibility for the development of donidalorsen, while Otsuka
will be responsible for territory-specific development, regulatory filings and commercialization in the Asia-Pacific region and Europe.
Ionis plans to file a New Drug Application with the U.S. Food and Drug Administration (FDA)
this year, and will independently launch donidalorsen in the U.S., if approved. Ionis and Otsuka previously announced a licensing agreement for donidalorsen in Europe, and Otsuka is also preparing to
submit a Marketing Authorization Application to the European Medicines Agency this year.
"Ionis and Otsuka share a steadfast commitment to bring donidalorsen to as many people living with HAE as possible," said Brett P. Monia, Ph.D., chief
executive officer of Ionis. "We look forward to working alongside Otsuka to advance regulatory discussions across Europe and the Asia-Pacific region based on our positive Phase 3 results for donidalorsen, which were presented late last month. In
the U.S., we've built a robust commercial infrastructure in preparation for our near-term anticipated launches for olezarsen in familial chylomicronemia syndrome and donidalorsen in HAE."
Under the terms of the Asia-Pacific agreement, Ionis will receive a $20 million upfront
payment and milestone payments based on achievement of regulatory and sales targets. Ionis is also eligible to earn tiered royalties, with similar economic terms to the previous agreement for Europe. Originating in Japan, Otsuka brings deep knowledge of regional and local regulations across the Asia-Pacific region, as well as global expertise in delivering rare disease medicines to patients and a robust commercial infrastructure.
Ionis recently reported positive results from the Phase 3 OASIS-HAE and OASISplus studies, presented at the 2024 European Academy of Allergy and Clinical Immunology (EAACI) Annual Congress in
Valencia, Spain and published in The New England Journal of Medicine.
About Hereditary Angioedema (HAE)
HAE is a rare and potentially life-threatening genetic condition that involves recurrent attacks of severe swelling (angioedema) in various parts of the body, including
the hands, feet, genitals, stomach, face and/or throat. HAE is estimated to affect more than 20,000 patients in the U.S. and Europe. In the U.S., doctors frequently use prophylactic treatment approaches to prevent and reduce the severity of HAE
attacks in patients.
Donidalorsen is an investigational LIgand-Conjugated Antisense (LICA) medicine designed to target prekallikrein (PKK), which plays an
important role in activating inflammatory mediators associated with acute attacks of hereditary angioedema (HAE). By reducing the production of PKK, donidalorsen could be an effective prophylactic approach to preventing HAE attacks.
About Ionis Pharmaceuticals, Inc.
For three decades, Ionis has invented medicines that bring better futures to people with serious diseases. Ionis currently has five marketed medicines and
a leading pipeline in neurology, cardiology, and other areas of high patient need. As the pioneer in RNA-targeted medicines, Ionis continues to drive innovation in RNA therapies in addition to advancing new approaches in gene editing. A deep
understanding of disease biology and industry-leading technology propels our work, coupled with a passion and urgency to deliver life-changing advances for patients.
Ionis Forward-looking Statements
This press release includes forward-looking statements regarding Ionis' business, financial guidance and the therapeutic and commercial potential of our
commercial medicines, donidalorsen, additional medicines in development and technologies. Any statement describing Ionis' goals, expectations, financial or other projections, intentions or beliefs is a forward-looking statement and should be
considered an at-risk statement. Such statements are subject to certain risks and uncertainties including those inherent in the process of discovering, developing and commercializing medicines that are safe and effective for use as human
therapeutics, and in the endeavor of building a business around such medicines. Ionis' forward-looking statements also involve assumptions that, if they never materialize or prove correct, could cause its results to differ materially from those
expressed or implied by such forward-looking statements. Although Ionis' forward-looking statements reflect the good faith judgment of its management, these statements are based only on facts and factors currently known by Ionis. Except as required
by law, we undertake no obligation to update any forward-looking statements for any reason. As a result, you are cautioned not to rely on these forward-looking statements. These and other risks concerning Ionis' programs are described in additional
detail in Ionis' annual report on Form 10-K for the year ended December 31, 2023, and most recent Form 10-Q, which are on file with the Securities and Exchange Commission. Copies of these and other documents are available from the Company.
In this press release, unless the context requires otherwise, "Ionis," "Company," "we," "our" and "us" all refer to Ionis Pharmaceuticals and its
Ionis Pharmaceuticals is a registered trademark of Ionis Pharmaceuticals, Inc.
Ionis Investor Contact:
D. Wade Walke, Ph.D.
Ionis Media Contact:

Frequently Asked Questions

What is donidalorsen used for?

Donidalorsen is an investigational medicine aimed at treating hereditary angioedema (HAE).

Who is partnering with Ionis for donidalorsen?

Otsuka Pharmaceutical Co., Ltd. is partnering with Ionis for donidalorsen in the Asia-Pacific region.

What are the next steps for donidalorsen's approval?

Ionis plans to file a New Drug Application with the FDA and a Marketing Authorization Application with the EMA.

How much is the upfront payment Ionis will receive?

Ionis will receive a $20 million upfront payment as part of the licensing agreement.

What is hereditary angioedema (HAE)?

HAE is a rare genetic condition characterized by recurrent, severe swelling attacks.

Last updated: Jun 18, 2024