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Ultragenyx Pharmaceutical Inc. - RARE STOCK NEWS

Welcome to our dedicated page for Ultragenyx Pharmaceutical news (Ticker: RARE), a resource for investors and traders seeking the latest updates and insights on Ultragenyx Pharmaceutical stock.

Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE), founded in 2010, is a clinical-stage biotechnology company dedicated to developing and commercializing innovative therapies for the treatment of serious rare and ultra-rare genetic diseases. The company’s core focus is on debilitating metabolic genetic diseases, for which there are high unmet medical needs, and the biology for treatment is well-understood but lacks approved therapies. Ultragenyx's management team brings extensive experience in rare disease therapeutics.

The company’s diverse product portfolio includes approved medicines like Crysvita, Dojolvi, and Mepsevii. Crysvita is designed for the treatment of X-linked hypophosphatemia (XLH), a rare genetic bone disease, and has shown significant growth with revenue reaching $328 million in 2023. Dojolvi targets long-chain fatty acid oxidation disorders and saw a 27% revenue increase in 2023. Mepsevii treats Mucopolysaccharidosis VII, another severe genetic disorder.

Recent Achievements and Financial Performance

In 2023, Ultragenyx reported total revenues of $434 million, a 20% increase from the previous year. The company has a robust pipeline with several candidates in late-stage clinical trials. For instance, the Phase 3 Orbit study for UX143 (setrusumab) in Osteogenesis Imperfecta (OI) completed enrollment and showed promising interim results with a 67% reduction in fracture rates.

Ongoing Projects

  • GTX-102: An antisense oligonucleotide for Angelman syndrome showed significant improvements in clinical trials, with plans for a Phase 3 study in 2024.
  • UX701: A gene therapy for Wilson disease, with data expected in mid-2024.
  • DTX401: A gene therapy for Glycogen Storage Disease Type Ia (GSDIa), achieved its primary endpoint in a Phase 3 study.
  • Setrusumab (UX143): Demonstrated significant fracture rate reduction and bone mineral density improvement in OI patients.

Partnerships and Collaborations

Ultragenyx collaborates with various regulatory bodies and advocacy groups to support patients and ensure high-quality clinical trials. The company’s partnership with Mereo BioPharma on setrusumab exemplifies its collaborative approach to drug development.

Corporate Responsibility

Ultragenyx's 2023 Corporate Responsibility Report highlights its commitment to innovation, patient support, diversity, and environmental sustainability. The company has been recognized with several awards, including the Top Places to Work by the Boston Globe and Healthcare’s Best Companies to Work by U.S. News & World Report.

For more information, visit www.ultragenyx.com.

Rhea-AI Summary
Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) announced that Emil D. Kakkis, M.D., Ph.D., the company's CEO and president, will present at the 42nd Annual J.P. Morgan Healthcare Conference on January 8, 2024. The webcast will be accessible from the company’s website, with a replay available for 30 days.
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Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) grants 30,325 restricted stock units to new non-executive officers under the Ultragenyx Employment Inducement Plan.
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Andelyn Biosciences, a cell and gene therapy CDMO, has been selected by Ultragenyx (NASDAQ: RARE) to perform late-stage Process Performance Qualification (PPQ) manufacturing of the company's UX111 gene therapy for the potential treatment of Sanfilippo Syndrome (MPS IIIA), leveraging their extensive experience in AAV technology.
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Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) receives approval from the European Commission to extend the use of Evkeeza (evinacumab) as a treatment for children aged 5 to 11 years with homozygous familial hypercholesterolemia (HoFH). The approval is based on the results of a Phase 3 open-label study showing a 48% reduction in LDL-C levels in children with HoFH after 24 weeks of treatment. Evkeeza is the first angiopoietin-like 3 (ANGPTL3) inhibitor treatment indicated for children as young as 5 years old to control dangerously high levels of low-density lipoprotein cholesterol (LDL-C) caused by HoFH. The treatment is delivered via 60-minute intravenous infusion once monthly and is now reimbursed and commercially available to prescribe for appropriate patients with HoFH in the U.S., Canada, Italy, and Germany, with early access schemes in Austria and France.
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Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) announced its participation in two upcoming investor conferences, the 6th Annual Evercore ISI HealthCONx on November 28 in Miami and the Piper Sandler 35th Annual Healthcare Conference on November 29 in New York City. The company will host 1x1 meetings at both events, and CEO Emil Kakkis, M.D., Ph.D., will participate in a fireside chat at the Piper Sandler conference. The live and archived webcast of the chat will be accessible from the company’s website.
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Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) has reported the grant of 22,765 restricted stock units to eight newly hired non-executive officers under the Ultragenyx Employment Inducement Plan. The awards were approved by the compensation committee and vest over four years, with 25% of the shares vesting on each anniversary of the grant date.
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Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE) CEO to participate in fireside chat at Jefferies London Healthcare Conference on November 14, 2023. The company focuses on developing therapies for rare genetic diseases. Webcast accessible at company website.
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Ultragenyx Pharmaceutical Inc. reported total revenue of $98.1 million for Q3 2023, with Crysvita revenue of $74.9 million and Dojolvi revenue of $16.6 million. The company reaffirmed its 2023 revenue guidance of $425 million to $450 million. Positive updates were presented on three lead clinical programs. The net loss for Q3 2023 was $159.6 million.
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Ultragenyx Pharmaceutical Inc. will host a conference call on November 2, 2023, to discuss its financial results and corporate update for Q3 2023.
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Ultragenyx Pharmaceutical Inc. announced the closing of its underwritten public offering, raising approximately $326.1 million. The offering included the sale of common stock and pre-funded warrants.
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FAQ

What is the current stock price of Ultragenyx Pharmaceutical (RARE)?

The current stock price of Ultragenyx Pharmaceutical (RARE) is $44.22 as of December 20, 2024.

What is the market cap of Ultragenyx Pharmaceutical (RARE)?

The market cap of Ultragenyx Pharmaceutical (RARE) is approximately 4.0B.

What is the primary focus of Ultragenyx Pharmaceutical Inc.?

Ultragenyx focuses on developing therapies for serious rare and ultra-rare genetic diseases, especially debilitating metabolic genetic diseases.

What are some key products of Ultragenyx?

Key products include Crysvita for X-linked hypophosphatemia (XLH), Dojolvi for long-chain fatty acid oxidation disorders, and Mepsevii for Mucopolysaccharidosis VII.

What were the financial highlights for Ultragenyx in 2023?

Ultragenyx reported $434 million in total revenues in 2023, marking a 20% growth compared to the previous year.

What recent achievements has Ultragenyx made in clinical trials?

Recent achievements include the Phase 3 Orbit study for UX143 showing significant reduction in fracture rates in Osteogenesis Imperfecta patients.

Who leads Ultragenyx Pharmaceutical Inc.?

Ultragenyx is led by a management team experienced in rare disease therapeutics, with Emil D. Kakkis, M.D., Ph.D., serving as the CEO and President.

What partnerships does Ultragenyx have?

Ultragenyx collaborates with various regulatory bodies and advocacy groups and has a notable partnership with Mereo BioPharma for the development of setrusumab.

What is Ultragenyx's commitment to corporate responsibility?

Ultragenyx is committed to innovation, patient support, diversity, and environmental sustainability, as highlighted in its 2023 Corporate Responsibility Report.

How does Ultragenyx engage with the rare disease community?

Ultragenyx works closely with advocacy groups to support and engage affected individuals and families in the clinical testing process.

What are the future plans for GTX-102?

GTX-102, an antisense oligonucleotide for Angelman syndrome, showed significant improvements in clinical trials, with plans for a Phase 3 study in 2024.

Where can I find more information about Ultragenyx?

You can find more information on Ultragenyx's official website at www.ultragenyx.com.

Ultragenyx Pharmaceutical Inc.

Nasdaq:RARE

RARE Rankings

RARE Stock Data

4.01B
88.07M
3.62%
97.49%
3.62%
Biotechnology
Pharmaceutical Preparations
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United States of America
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