Thermo Fisher plots Penn. expansion
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WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

While the year has not posted any major biopharma acquisitions so far, the drought has to break at some point—with some industry forecasters predicting a deluge of deals beginning this March. Many Big Pharmas have touted their abilities and appetites for large transactions in recent earnings calls—with a total of $1.7 trillion to spend among them—but as for who might be on the menu, Fierce Biotech has 10 predictions. And after a slump in 2021, analysts expect biopharma M&A to pick up the pace this year, with an “innovation deficit” spurring shopping for new assets. We’ll be watching.

 

Featured Story

Roche, Lilly push back against CMS painting their Alzheimer's meds with the same brush as Biogen's Aduhelm

In a rare moment of solidarity among fierce competitors, Biogen’s peers Roche and Eli Lilly are rallying behind the company’s troubled Alzheimer’s disease therapy, Aduhelm, in an effort to change the Centers for Medicare & Medicaid Services’ restrictive ruling against monoclonal antibodies for the condition.

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Top Stories Of The Week

Thermo Fisher dishes up $40M for Pennsylvania facility expansion, creating more than 100 jobs

Thermo Fisher, plowing ahead on a $650 million bioprocessing expansion, has unveiled a $40 million upgrade at its single-use technologies facility in Millersburg, Pennsylvania. The site is expected to employ more than 1,000 people once fully renovated in the middle of 2023.

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The top 10 M&A targets in biotech for 2022

All the biopharma world is talking about right now is M&A. Who’s going to buy? How much are they willing to spend? Who’s going to get bought? Here are our predictions.

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With $1.7T in the coffers, biopharma M&A expected to be 'a different animal' in 2022

Goodbye, lackluster 2021, and hello, "buoyant" 2022 for biopharma M&A. Biopharmas have $1.7 trillion to dish out on mergers and acquisitions, and the industry should expect a big year for M&A as big drugmakers must fill "innovation deficits" in their pipelines for the second half of this decade.

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Eli Lilly talks up 'long-term' game plan for tirzepatide launch, but don't expect major sales early on

Eli Lilly is taking the long view when it comes to the potential launch of its megablockbuster hopeful tirzepatide, and it's focusing on access programs to ensure patients can get their hands on the diabetes drug without being out-of-pocket.

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ASCO GU: AstraZeneca, Merck’s Lynparza one-ups J&J’s Zejula with prostate cancer win regardless of gene mutations

AstraZeneca and Merck & Co.’s Lynparza may have a narrower label than GlaxoSmithKline’s rival drug Zejula in ovarian cancer, but in prostate cancer, the situation could flip.

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Musk's Neuralink disputes accusations of animal abuse in brain implant experiments

The Physicians Committee for Responsible Medicine filed a federal complaint with the USDA regarding the alleged treatment of monkeys at the University of California, Davis in connection with Neuralink’s experiments.

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Illumina CEO: Here's why speeding Grail's cancer test to patients requires 'every part of our company'

The sequencing company’s $1.2 billion in sales marked a new quarterly high, but bigger spends on R&D and administrative expenses pushed net income down 56%. CEO Francis deSouza tells us that spending is key to innovation at Illumina—and he details the ways it will need to help Grail get its blood test to as many patients as possible.

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Novartis plots 400 job cuts in India after striking sales pact with Dr. Reddy's

Novartis India has forged a sales and distribution pact with Dr. Reddy’s Laboratories that puts 400 jobs on the chopping block, the Swiss drugmaker said late last week. The deal covers “a few” of Novartis’ established meds, such as pain-relief drug Voveran and Methergine, which is used to treat severe bleeding from the uterus after childbirth.

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FDA wallops Indian drugmaker with warning letter blasting API quality, equipment cleanliness and more

What not to do with active pharmaceutical ingredient (API) batch records? Tear them out of a company logbook ahead of an FDA inspection, for one. Earlier this month, Indian drugmaker Indiana Chem-Port learned that lesson the hard way. 

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Improving RNA editing for genetic diseases by recruiting the body's natural protein

In the search for more efficient and safer RNA-editing tools, two research teams from the U.S. and China have developed novel ways to recruit a naturally occurring protein inside the body to repair disease-causing mutations in RNA.

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Resources

Infographic: Providing comprehensive solutions for the most critical shipments

The United Cargo team has made a commitment to pharmaceutical and medical partners that we are equipped to support their vaccine transportation needs safely and effectively across our expansive global and domestic network. The safety and security of these commodities is our priority, and we are proud to be a trusted partner in these efforts. Download infographic now.

Whitepaper: Lipid-Based Drug Delivery System to Bring Poorly Soluble Drugs to Market

How can Lipid-Based Drug Delivery System help bring poorly soluble drugs to market?

Whitepaper: The Most Suitable Dosage Form Technologies for the Oral Delivery of Lipid-Based Formulations

What is the most suitable dosage form technology for the Oral Delivery of Lipid-Based Formulations?

Case Study: Versatility of Softgel Technology - Encapsulation of a Volatile Compound

Learn more about how the versatility of Softgel Technology helped a customer with a volatile compound.

Whitepaper: The CNS Market: 2021 Year in Review & Outlook for 2022

What’s in store for the CNS therapeutics market in 2022? This paper looks ahead in Alzheimer’s, Parkinson’s, DMD, psychiatric disorders, pain, and more.

Webinar: The Faster Path From Pre-Filled Syringe to Auto-Injector

Ypsomed and Catalent Biologics experts discuss strategies for integrated PFS manufacturing and auto-injector assembly to accelerate timelines and more in this webinar.

Whitepaper: Formulation Strategies When Transitioning From Vial to PFS

Learn how formulation development for a PFS affects manufacturing to drive the industry toward optimizing delivery of injectable products and, ultimately, improving patient care.