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Thursday
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16 January, 2025 |
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Eli Lilly CEO Dave Ricks told delegates at the JPM confab that it is considering another manufacturing expansion in the next few months to boost production for its incretins, including Zepbound and Mounjaro. This comes as the company faced destocking challenges from its wholesale customers in the second half of 2024. Read more below. |
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Anna Brown |
Biopharma Breaking News Reporter, Endpoints News
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Rendering of Samsung Biologics' Plant 5 at its Bio Campus II plot in Songdo, South Korea (Credit: Samsung Biologics) |
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by Anna Brown
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Following a blockbuster 2024, Samsung Biologics is considering building a sixth manufacturing facility to meet the rising demand for biologics as it gears up to open its fifth site in April. During the annual JP Morgan Healthcare Conference in San Francisco this week, Samsung Bio hinted that it might construct its sixth
factory to bring its total capacity to 964,000 liters, according to a Tuesday press release. The CDMO is awaiting board approval for the new site. Last year, the company seemed to buck the trend of CDMOs struggling: Merck KGaA, Catalent, Avid Bioservices and Thermo Fisher Scientific all saw
manufacturing revenue dip during at least one quarter in 2024. Samsung Bio, by contrast, secured multiple billion-dollar contracts with customers and reported
quarterly revenue jumps. Samsung intends to build on this growth by opening its fifth manufacturing facility, dubbed Plant 5, in April this year. |
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by Anna Brown
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Charles River Laboratories is predicting 2025 to be as tough as last year for CDMOs as pharma customers continue to cut costs with manufacturers. The company expects its revenue for 2025 to decline in a similar fashion as last year, according to an SEC filing published on Tuesday. Charles River’s overall revenue declined during each quarter of 2024, most recently by 1.6% in Q3, 3.2% in Q2 and 1.7% in Q1. Charles River’s stock $CRL was down 6.2% Tuesday morning. William Blair analysts were “disappointed” in the company’s outlook for this year, which missed their revenue growth estimate of 1%, according to an analyst report. The service provider anticipates pharma customers will continue to cut their spending with third-party
manufacturers as they restructure programs and reprioritize their pipelines. The company’s CEO James Foster had already warned investors these headwinds would persist into 2025 during its second-quarter earnings in August. |
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David Ricks, Eli Lilly CEO (Jeenah Moon/Bloomberg via Getty Images) |
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by Nicole DeFeudis
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Eli Lilly expects to miss its recent revenue estimate for 2024 by about $400 million, according to a preliminary report. The company’s estimates have varied widely this year. Lilly raised its 2024 revenue projections multiple times before tempering those expectations in the third quarter. Now executives are saying the actual figure will be around $45 billion, which is $400 million below the low end of its third-quarter projection, but still above the midpoint of its first-time estimate. Investors sent Lilly’s stock LLY down 7% on Tuesday afternoon, following the announcement. David Risinger, an analyst with the investment bank Leerink Partners, said in a note to investors that this is the “second quarter in a row of disappointing results" for Lilly. However, he added that the company’s financial and R&D prospects in 2025 and beyond are
“encouraging,” specifically Lilly’s Phase 3 oral GLP-1 candidate for weight loss and diabetes, orforglipron. |
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by Lei Lei Wu, Max Gelman
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US regulators have rejected a T cell therapy for a rare and serious transplant complication related to Epstein-Barr virus from Atara Biotherapeutics and Pierre Fabre. The therapy, known as tabelecleucel or tab-cel, was turned away after the FDA inspected a third-party manufacturing site, Atara said in a Thursday press release. FDA's rejection letter "did not identify any deficiencies" related to the manufacturing of the therapy itself, nor any concerns over efficacy or safety data, Atara said. Additionally, it will not be required to run another clinical trial. Atara's stock price ATRA fell more than 45% on Thursday morning. |
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by Anna Brown
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Indian CDMO Aragen Life Sciences has secured a $100 million investment from Singapore-headquartered private equity firm Quadria Capital. Aragen will use the investment to expand its facilities to meet growing demand from US and European customers for its discovery and manufacturing capabilities, CEO
Manni Kantipudi said in a Monday press release. No further details were given. Aragen has six locations in India as well as sales offices in Tokyo, Japan and South Korea. Quadria will get a minority stake in the manufacturer, valued at around $1.4 billion, according to the release. The private equity firm will be the second investor in Aragen, following Goldman Sachs who invested in May 2021. Quadria has invested in other
CDMOs previously, including Indian-based Akums Drugs and Encube Ethicals, as well as Malaysia-based Straits Orthopaedics. |
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