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1020 First Avenue King of Prussia, PA 19406 US
CSL Behring, a Business Unit of CSL, is a global biotherapeutics leader driven by its promise to save lives.
Headcount: 32,452 Year Established: 1916 Revenues: $14,744 (+11%) Net Income: $2,818 (+26%) R&D expenses: $1,428 (+12%) *Numbers based on CSL Half Year Results February 2025
Despite the impact of declines in U.S. influenza vaccination rates, demand for CSL’s plasma products is rising and supply is improving. Also, with the recent approval of Andembry, expanding its HAE franchise, CSL’s outlook is progressing.
As one of only a handful of providers of plasma products, sourcing and supply can be a challenge. CSL Behring’s new plasma processing facility in Broadmeadows, Victoria recently began operations, increasing its plasma processing capacity in Australia by nine times. It is now able to handle more than 10 million liters of plasma per year. This helps produce key components for medicines that treat immune disorders, bleeding conditions like hemophilia, and other serious health issues.
In June, the U.S. FDA approved CSL’s Andembry, becoming the only prophylactic Hereditary Angioedema (HAE) treatment targeting Factor XIIa with once-monthly dosing for all patients from the start. Andembry inhibits the top of the HAE cascade by targeting factor XIIa and provides sustained protection from attacks. Additionally, the once-monthly dosing was shown to reduce HAE attacks by a median of more than 99 percent compared to placebo.
This profile references CSL’s 2025 half year results, released February 2025. When looking at CSL’s performance by business, CSL Behring, overseeing biotherapeutics, had the highest revenue of $10.6 billion, up 14% in consistent currency. CSL Behring sales were strong in emerging markets, with solid growth in China, the U.S., and Europe.
CSL’s largest franchise, the immunoglobulin (Ig) portfolio, largely contributed to company growth. Ig revenue reached $3.2 billion, increasing 15% with strong growth recorded across all geographies. Privigen and Intragam increased by 15%, and Hizentra increased by 16%.
The Albumin segment increased by 9% to $672 million in revenue, with strong growth in China. Revenue for CSL’s Hemophilia franchise reached $731 million, an 11% increase. Idelvion remained a market leader with a 6% increase, Hemgenix saw an uptake in acceleration, and Plasma-derived coagulants grew 6%, led by Von Willebrand Factor (VWF).
However, Specialty products sales were down 5% to $921 million, mainly impacted by the loss of a substantial contract for Kcentra, with sales down 20%. In this segment, Haegarda sales grew by 1% and Berinert sales grew 6%.
Headcount: 24,660 Revenues: $13,310 (+31%) Net Income: $7,250 (+32%) R&D: $1,232 (+22%)
Melbourne, Australia-based CSL develops and delivers innovative medicines that help people with serious and life-threatening conditions through three businesses: CSL Behring, a global biotherapeutics leader; CSL Seqirus, a leading influenza vaccine provider; and the recently acquired CSL Vifor, a global partner for pharmaceuticals and innovative therapies in iron deficiency and nephrology.
Revenue for fiscal year 2023 was $13.31 billion, up 31% when compared to the prior comparable period, delivered against a challenging operating environment. In particular, the CSL Behring business rebounded strongly driven by growth in immunoglobulin sales and record plasma collections.
Early 2023 was marked by a major leadership transition as Paul Perreault retired from his role as CEO and managing director after 10 years in the position. Dr. Paul McKenzie was appointed as the new chief executive and managing director in March 2023, bringing more than 30 years of leadership experience in the global biotechnology industry, including his time at CSL as the chief operating officer.
In March 2023, CSL celebrated the opening of a new plasma fractionation facility in Marburg, Germany, a $470 million project that took five years to construct. With optimized process flows, modern technologies and automation, the new fractionation facility quadruples the current capacity.
In June 2023, the first patient received FDA approved gene therapy Hemgenix for hemophilia B in the U.S. In March 2024, the FDA approved Vafseo tablets for the treatment of anemia due to chronic kidney disease (CKD) in adults who have been receiving dialysis for at least three months.
Most recently, in June, CSL Seqirus was selected by the Health Emergency Preparedness and Response Authority (HERA), part of the European Commission (EC), to provide 665,000 pre-pandemic vaccine doses for fifteen EU and EEA member states as well as to the “Union Civil Protection Mechanism.”
Headcount: 25,000 Revenues: $8,951 Net Income: $2,117 R&D: $857 *CSL does not report annual results until 30 June, so data is estimated.
TOP SELLING DRUGS
Headcount: 10,500 Bio/Pharma Revenue: $4,550 (10%) Total Revenues: $4,747 (11%) Net Income: $1,009 (8%) R&D Budget: $364 (13%)
Top Selling Drugs
Account for 61% of total biopharma sales, down from 63% in previous year.
NOTE: Fiscal year ends June 30, so these results are based on previous fiscal year, ending June 30, 2011
NOTE: Australian dollar appreciated 4% from year to year, creating jumps in results in USD
Headcount: 10,000 Pharma Revenues: $3,930 (23%/4%*) Total Revenues: $4,082 (8%/-8%*) Net Income: $929 (8%/-8%*) R&D Budget: $280 (20%/2%*)
* Converted at avg. exch. rate / based on reported currency (AUD)
Fiscal year ends June 30, so these results are based on previous fiscal year, ending June 30, 2010
Australian dollar appreciated 17% from year to year, creating extreme jumps in results in USD
Top-Selling Drugs in 2010
Drug
Indication
(+/- %)
Immunoglobulins
$1,049
9%
Plasma-derived coagulants
Helixate/Recombinant FVIII
Albumin
$309
n/a
Account for 56% of total biopharma sales, same as previous year..
Previous Profile: Biogen Idec. // Next Profile: Genzyme
Williamson offers experience building innovative life sciences companies and delivering strong commercial and operational outcomes.
By: Charlie Sternberg
New alliance is dedicated to advancing lipid nanoparticle (LNP) technology and accelerating the development of next-generation therapeutics.
The site is also expanding its High Potency Active Pharmaceutical Ingredient and Antibody Drug Conjugate capacity.
By: Rachel Klemovitch
Collaboration complements Bayer's precision oncology development portfolio in the areas of pancreatic, colorectal, and lung cancer.
Avista will leverage Forge’s FUEL platform to manufacture AAV for AVST-101, Avista’s lead gene therapy to treat patients with X-linked retinoschisis (XLRS).
Collaboration aims to scale OBD's analytical framework by leveraging Google Cloud's infrastructure.
Certifies ElevateBio’s compliant and scalable manufacturing capabilities for advanced therapies using U.S. and E.U. commercial-level evaluation standards.
The new facility designs, develops and manufactures research-grade pDNA materials to support the cell and gene therapy field.
Sartorius supports commercialization and joint development of solutions based on Nanotein’s NanoSpark platform.
If approved, gepotidacin would offer a new oral option to U.S. patients currently relying on injectable treatments for uncomplicated urogenital gonorrhea.
AVTOZMA IV now aligns with all indications approved for ACTEMRA IV in the United States.
Strategic expansion is designed to advance gene therapy development and manufacturing.
CureVac and GSK will receive $740 million and single-digit royalties on COVID-19 vaccine sales in the U.S. going forward.
CEO Dr. Johannis Willem van Vliet will leave the company shortly as the company transitions to a CDMO.
Meeting Global Injectable Demand
Released By Rovi Pharma Industrial Services
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