STOCK TITAN

Ultragenyx to Participate at Investor Conferences in March

Rhea-AI Impact
(Low)
Rhea-AI Sentiment
(Neutral)
Tags
conferences
Rhea-AI Summary
Ultragenyx Pharmaceutical Inc. (RARE) will participate in three investor conferences in March 2024, including the 44th Annual Cowen Healthcare Conference, Leerink Partners Global Biopharma Conference, and Barclays 26th Annual Global Healthcare Conference. Management will engage in fireside chats and 1x1 meetings to discuss the company's focus on developing therapies for rare genetic diseases.
Positive
  • None.
Negative
  • None.

44th Annual Cowen Healthcare Conference on March 4

Leerink Partners Global Biopharma Conference on March 12

Barclays 26th Annual Global Healthcare Conference on March 13

NOVATO, Calif., Feb. 27, 2024 (GLOBE NEWSWIRE) --  Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE), a biopharmaceutical company focused on the development and commercialization of novel therapies for serious rare and ultrarare genetic diseases, today announced that management will be participating in three upcoming investor conferences.

44th Annual Cowen Healthcare Conference (Boston, MA)

  • Monday, March 4, 2024, Eric Crombez, M.D., Chief Medical Officer, will participate in a fireside chat and host 1x1 meetings.

Leerink Partners Global Biopharma Conference (Miami, FL)

  • Tuesday, March 12, 2024, Emil Kakkis, M.D., Ph.D., CEO and President and Howard Horn, Chief Financial Officer, will participate in a fireside chat and host 1x1 meetings.

Barclays 26th Annual Global Healthcare Conference (Miami, FL)

  • Wednesday, March 13, 2024, Emil Kakkis and Howard Horn will participate in a fireside chat and host 1x1 meetings.

The live and archived webcast of the fireside chat will be accessible from the company’s website at https://ir.ultragenyx.com/events-presentations.

About Ultragenyx

Ultragenyx is a biopharmaceutical company committed to bringing novel products to patients for the treatment of serious rare and ultrarare genetic diseases. The company has built a diverse portfolio of approved therapies and product candidates aimed at addressing diseases with high unmet medical need and clear biology for treatment, for which there are typically no approved therapies treating the underlying disease.

The company is led by a management team experienced in the development and commercialization of rare disease therapeutics. Ultragenyx’s strategy is predicated upon time- and cost-efficient drug development, with the goal of delivering safe and effective therapies to patients with the utmost urgency.

For more information on Ultragenyx, please visit the company's website at: www.ultragenyx.com.

Contacts – Ultragenyx
Investors
ir@ultragenyx.com

Media
media@ultragenyx.com


FAQ

When will Ultragenyx Pharmaceutical Inc. (RARE) participate in the 44th Annual Cowen Healthcare Conference?

Ultragenyx Pharmaceutical Inc. (RARE) will participate in the 44th Annual Cowen Healthcare Conference on Monday, March 4, 2024.

Who will represent Ultragenyx Pharmaceutical Inc. (RARE) at the Leerink Partners Global Biopharma Conference?

Dr. Emil Kakkis, CEO and President, and Howard Horn, CFO, will represent Ultragenyx Pharmaceutical Inc. (RARE) at the Leerink Partners Global Biopharma Conference on Tuesday, March 12, 2024.

Where can the webcast of the fireside chat be accessed?

The live and archived webcast of the fireside chat can be accessed on Ultragenyx Pharmaceutical Inc.'s (RARE) website at https://ir.ultragenyx.com/events-presentations.

Ultragenyx Pharmaceutical Inc.

NASDAQ:RARE

RARE Rankings

RARE Latest News

RARE Stock Data

3.55B
72.17M
4.11%
101.15%
4.76%
Pharmaceutical Preparation Manufacturing
Manufacturing
Link
United States of America
NOVATO

About RARE

ultragenyx is a clinical-stage biotechnology company committed to bringing to market novel products for the treatment of rare and ultra-rare diseases, with an initial focus on serious, debilitating metabolic genetic diseases. founded in 2010, the company has rapidly built a diverse portfolio of product candidates with the potential to address diseases for which the unmet medical need is high, the biology for treatment is clear, and for which there are no approved therapies. our company is led by an experienced management team in rare disease therapeutics. recognizing that our primary responsibility is to our patients, we are working with advocacy groups to provide support and outreach to individuals and families affected by these disorders and engage them in the clinical testing process. we are also working with regulatory agencies to design and conduct high quality clinical studies that meet the requirements for approval. we are creating an improved model for successful rare disease d