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Haemonetics (HAE) News & Sentiment

Haemonetics Announces Executive Leadership Updates
Haemonetics Announces Executive Leadership Updates
Haemonetics Announces Executive Leadership Updates
HAE
prnewswire.comMarch 3, 2025

Frank Chan joins Haemonetics as Executive Vice President, Chief Operating Officer;  Roy Galvin named Executive Vice President, Chief Commercial Officer BOSTON , March 3, 2025 /PRNewswire/ -- Haemonetics Corporation (NYSE: HAE), a global medical technology company focused on delivering innovative medical solutions to drive better patient outcomes, today announced updates to its Executive Leadership team. Frank Chan, Ph.D.

Haemonetics to Present at Raymond James 46th Annual Institutional Investors Conference
Haemonetics to Present at Raymond James 46th Annual Institutional Investors Conference
Haemonetics to Present at Raymond James 46th Annual Institutional Investors Conference
HAE
prnewswire.comFebruary 24, 2025

BOSTON , Feb. 24, 2025 /PRNewswire/ -- Haemonetics Corporation (NYSE: HAE) announced that Chris Simon, President and CEO, will participate in a fireside chat with investors at the Raymond James 46th Annual Institutional Investors Conference on Tuesday, March 4, 2025 at 2:50 p.m. ET. The public may access a live webcast of the fireside chat at Haemonetics' Investor Relations website or at the following link: https://wsw.com/webcast/rj131/hae/1437678.

The European Medicines Agency (EMA) Has Approved an Additional Subcutaneous Administration Option for TAKHZYRO® (lanadelumab) for Patients Aged 12 Years and Above with Recurrent Attacks of Hereditary Angioedema (HAE)
The European Medicines Agency (EMA) Has Approved an Additional Subcutaneous Administration Option for TAKHZYRO® (lanadelumab) for Patients Aged 12 Years and Above with Recurrent Attacks of Hereditary Angioedema (HAE)
The European Medicines Agency (EMA) Has Approved an Additional Subcutaneous Administration Option for TAKHZYRO® (lanadelumab) for Patients Aged 12 Years and Above with Recurrent Attacks of Hereditary Angioedema (HAE)
HAE
prnewswire.comFebruary 24, 2025

TAKHZYRO Solution for Injection in 2 mL Pre-Filled Pen is Now Approved to Facilitate Subcutaneous Administration in Adolescent (Aged 12 Years and Above) and Adult Patients with HAE.1 The Pre-Filled Pen Option is Designed to Allow for An Individualized Treatment Approach for Adolescent and Adult HAE Patients. In the EU, TAKHZYRO is Approved for Routine Prevention of Recurrent HAE Attacks in Patients Aged 2 Years and Older.1 ZURICH , Feb. 24, 2025 /PRNewswire/ -- Takeda (TSE: 4502) (NYSE: TAK) announced today that the EMA has approved an additional 2 mL pre-filled pen option for TAKHZYRO® (lanadelumab) for subcutaneous administration in adolescents (aged 12 years and above) and adult patients with Hereditary Angioedema (HAE).1 The additional subcutaneous administration option expands Takeda's offering in this space, showing dedication to the HAE community while providing individualized treatment options to support patients with a life-threatening disease, by helping to reduce HAE burden and improving their Quality of Life.

CSL Receives Approval in Japan for ANDEMBRY® (garadacimab) Subcutaneous (S.C.) Injection 200mg Pens, a Novel Human Anti-Activated Factor XII Monoclonal Antibody for the Prevention of Acute Attacks of Hereditary Angioedema (HAE)
CSL Receives Approval in Japan for ANDEMBRY® (garadacimab) Subcutaneous (S.C.) Injection 200mg Pens, a Novel Human Anti-Activated Factor XII Monoclonal Antibody for the Prevention of Acute Attacks of Hereditary Angioedema (HAE)
CSL Receives Approval in Japan for ANDEMBRY® (garadacimab) Subcutaneous (S.C.) Injection 200mg Pens, a Novel Human Anti-Activated Factor XII Monoclonal Antibody for the Prevention of Acute Attacks of Hereditary Angioedema (HAE)
HAE
prnewswire.comFebruary 20, 2025

ANDEMBRY® is a first-in-class monoclonal antibody treatment that inhibits activated Factor XII (FXIIa), the initiating factor in the HAE pathway, and offers the first pre-filled pen presentation enabling once-monthly subcutaneous administration The approval is based on the results of the international pivotal Phase 3 VANGUARD trial, which included HAE patients from Japan CSL is dedicated to improving the lives of those with HAE – a community that we have proudly supported for more than 40 years TOKYO , Feb. 20, 2025 /PRNewswire/ -- CSL Behring K.K. (Headquarters: Minato-ku, Tokyo; President and Representative Director: Izumi Yoshida) today announced that it has received manufacturing and marketing approval from Japan's Ministry of Health, Labour and Welfare (MHLW) for ANDEMBRY® (garadacimab) Subcutaneous (S.C.

Astria Therapeutics: A High-Conviction Bet On HAE
Astria Therapeutics: A High-Conviction Bet On HAE
Astria Therapeutics: A High-Conviction Bet On HAE
HAE
seekingalpha.comFebruary 17, 2025

Astria Therapeutics' strong cash position and efficient spending provide a financial runway through mid-2027, reducing dilution risk and supporting pivotal trials for navenibart and STAR-0310. Navenibart, targeting hereditary angioedema, shows promising Phase 1b/2 data with a 90-95% reduction in attack rates, positioning it as a potential best-in-class treatment. STAR-0310, aimed at atopic dermatitis, leverages OX40 inhibition and YTE half-life extension technology, though it faces stiff competition and must prove differentiation.

Haemonetics (HAE) Q3 Earnings: Taking a Look at Key Metrics Versus Estimates
Haemonetics (HAE) Q3 Earnings: Taking a Look at Key Metrics Versus Estimates
Haemonetics (HAE) Q3 Earnings: Taking a Look at Key Metrics Versus Estimates
HAE
zacks.comFebruary 6, 2025

Although the revenue and EPS for Haemonetics (HAE) give a sense of how its business performed in the quarter ended December 2024, it might be worth considering how some key metrics compare with Wall Street estimates and the year-ago numbers.

Haemonetics (HAE) Q3 Earnings Meet Estimates
Haemonetics (HAE) Q3 Earnings Meet Estimates
Haemonetics (HAE) Q3 Earnings Meet Estimates
HAE
zacks.comFebruary 6, 2025

Haemonetics (HAE) came out with quarterly earnings of $1.19 per share, in line with the Zacks Consensus Estimate. This compares to earnings of $1.04 per share a year ago.

Haemonetics 3rd Quarter Fiscal Year 2025 Earnings Release Available on Investor Relations Website
Haemonetics 3rd Quarter Fiscal Year 2025 Earnings Release Available on Investor Relations Website
Haemonetics 3rd Quarter Fiscal Year 2025 Earnings Release Available on Investor Relations Website
HAE
prnewswire.comFebruary 6, 2025

Financial release accessible online BOSTON , Feb. 6, 2025 /PRNewswire/ -- Haemonetics Corporation (NYSE: HAE) announced that financial results for its third quarter fiscal year 2025, which ended December 28, 2024, are available on its Investor Relations website. The Company will host a conference call and webcast with investors and analysts to discuss and answer questions about the results at 8:00 a.m.

Completion of Whole Blood Assets Sale to GVS Likely to Boost HAE Stock
Completion of Whole Blood Assets Sale to GVS Likely to Boost HAE Stock
Completion of Whole Blood Assets Sale to GVS Likely to Boost HAE Stock
HAE
zacks.comJanuary 20, 2025

Haemonetics completes the sale of whole blood assets to GVS, S.p.A.

HAE or ABT: Which Is the Better Value Stock Right Now?
HAE or ABT: Which Is the Better Value Stock Right Now?
HAE or ABT: Which Is the Better Value Stock Right Now?
HAE
zacks.comJanuary 20, 2025

Investors interested in Medical - Products stocks are likely familiar with Haemonetics (HAE) and Abbott (ABT). But which of these two companies is the best option for those looking for undervalued stocks?