Will an Alzheimer’s moonshot ever land?
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WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

The FDA said it would need three more months to consider Cytokinetics’ heart failure therapy after getting their hands on additional data, pushing a decision into early 2023. Meanwhile, not content with a mere stake in Seagen, Merck is reportedly considering buying out the cancer-focused biotech. However a deal may not be imminent, and Merck may not be the only suitor. Merck, along with BMS and Pfizer, all face patent cliff exposure later this decade—but they also have the cash for major acquisitions to potentially head off the loss. Those stories, plus our other top reads of the week, follow below.

Featured Story

Cytokinetics' heart failure drug delayed as FDA seeks more time for review

The FDA needs more time to consider Cytokinetics’ omecamtiv mecarbil after getting a look at some additional data.

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Top Stories Of The Week

Merck eyes Seagen purchase amid quest to diversify from star cancer drug Keytruda: WSJ

Merck & Co. already owns a stake in antibody-drug conjugate specialist Seagen. But now, the New Jersey pharma appears to want the whole thing, according to The Wall Street Journal.

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Will we ever land the Alzheimer's moonshot? Genentech's crenezumab partners reflect on failure

In a moment of public reflection, the partners on Genentech's failed Alzheimer's disease therapy consider what happened, what they learned and what happens next.

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BMS, Pfizer and Merck face steep patent cliffs but all have the financial flexibility for M&A: Moody's

Bristol Myers Squibb, Pfizer and Merck will face extreme patent cliff exposure later in this decade. But those companies also have the financial flexibility to strike mergers and acquisitions to address the anticipated losses, according to recent research from Moody's Investors Service.

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Eli Lilly taps Sidekick Health to tailor smartphone apps for breast cancer patients

Eli Lilly has joined forces with the digital therapeutics developer Sidekick Health to offer tailored apps that help patients with breast cancer stick to their medication regimens.

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As biosimilars gain steam, Amgen exec lays out its Humira copycat plans

As the industry sees more biosimilar uptake, Amgen says it's well prepared. Last week, the company presented a preview of its annual trends in biosimilars report at the BIO 2022 convention in San Diego. Next year, Amgen is planning to really make its mark with the industry's first US biosimilar of AbbVie's Humira.

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Galapagos finally takes M&A plunge, spending $251M for 2 biotechs in CAR-T push

Galapagos CEO Paul Stoffels, M.D., has finally taken the plunge on M&A. The newly minted chief executive has signed not one but two deals in an attempt to right the ship, bringing two small biotechs aboard for a combined 239 million euros ($251.4 million).

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Amid death risk fears, Clovis pulls Rubraca in 3rd-line ovarian cancer as PARP player plugs away at earlier setting

A death risk signal has taken a toll on Clovis Oncology’s already lagging ovarian cancer drug, Rubraca. The company has taken FDA's hint, withdrawing the med in a late-line setting, but it remains undeterred in newly diagnosed patients despite an FDA warning.

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GSK opens doors at $110M biologics smart factory in UK

GSK has cut the ribbon at its new aseptic smart manufacturing plant in Barnard Castle, England, local news outlet Business Live reported Tuesday. Bankrolled by a £90 million ($110.45 million) investment, the facility—dubbed Q Block—will add another fixture to one of GSK’s biggest U.K. manufacturing sites, the publication said.

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Enzyme inhibitor could counter bad 'seeds' that let leukemia bounce back

Leukemia is notorious for being very aggressive and hard to eradicate from the body. The culprits are leukemic stem cells—known as “seed” cells—that drive resistance to chemotherapy and can trigger a relapse of the cancer.

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'The Top Line' podcast: Why we need an Alzheimer's moonshot, a controversial take on a diversity in biotech, plus this week's headlines

This week on "The Top Line," we discuss why scientists say we need an Alzheimer's moonshot. We also talk about a controversial take on a diversity during a panel at the BIO conference. Plus, we'll hear award-winning ads that tug at our heartstrings.

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Resources

Whitepaper: Medical Affairs Metamorphosis II: Medical Affairs’ Evolving Role as Insight Generator

Medical Affairs plays a critical role in generating insights to inform strategic decisions, but that role is changing. This paper explores why, and how MA teams can stay ahead of the curve.

eBook: Streamline HCP interactions management

Don’t miss these critical considerations when evaluating your HCP interactions management program.

eBook: Download the Cell Therapy Handbook

Explore the new cell therapy handbook from Thermo Fisher Scientific.

Whitepaper: Gain Operational Speed and Velocity by Sharing Quality Incident Data

Quality operations guide your organization through regulatory compliance processes and safeguard your products, processes, and reputation. But your team is capable of so much more. Quality incident data and processes can be a driver of significant business value if shared with other stakeholders.

White Paper: Jump Start for Biotech: New Lab Startup Guide

Sponsored by Thermo Fisher Scientific The journey for starting or expanding a lab can be exhilarating, while also being challenging--learn how this free program provides savings and solutions to support your goals.

Whitepaper: Catalent Pulmonary & Nasal Delivery Capabilities Sheet

Did you know Catalent has newly expanded in-house capabilities spanning clinical and commercial scale manufacturing for DPIs, unit-dose, bi-dose and preserved multi-dose nasal sprays?

Whitepaper: Intranasal Drug Product Development: Formulation to Manufacturing

What are key considerations for intranasal delivery in the treatment of acute and chronic conditions?

eBook: Orally Inhaled & Nasal Drug Delivery: A Pipeline of Opportunities

Orally Inhaled & Nasal Drug Delivery: A Pipeline of Opportunities

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