Novartis nixes JAK after seeing clinical data
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Today's Rundown

Featured Story

Gilead's CD47 clinical hold expands as CEO O'Day expresses 'sense of urgency' in getting trials back on track

Gilead revealed that a partial clinical hold for its CD47 targeted cancer hopeful is larger than originally thought. Disclosed in the fine print of the pharma giant’s fourth-quarter earnings presentation Tuesday was that two more studies are subject to the hold, bringing the total number of affected trials to seven.

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Top Stories

Pfizer poaches Roche's pharma R&D leader to fill MacKenzie's shoes as chief development officer

Pfizer's new development leader is on the way from Roche. Replacing 35-year Pfizer veteran Rod MacKenzie, Ph.D., as chief development officer will be William Pao, M.D., Ph.D.

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Novartis JAKs in rival to Incyte's topical eczema drug after seeing clinical data

Strike Novartis from the list of rivals to Incyte’s topical eczema drug Opzelura. After getting a look at early clinical data, Novartis has dumped its topical pan-JAK inhibitor CEE321 over an unfavorable risk-benefit profile.

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Sponsored: Taking a Different Approach to Drug Development

Dive into the unique history of TD2 and learn how their approach to cancer drug development impacts clinical and partner success.

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Biden revives Cancer Moonshot program to seek 50% drop in cancer death rate by 2047

President Joe Biden unveiled his second attempt at a "cancer moonshot" with a renewed program focused on slashing the cancer death rate by more than 50% in the next 25 years.

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Sponsored: Choose wisely. Biospecimens can make or break your biomarker-driven cancer research

Advances in cancer biomarker discovery, validation and clinical applications hinge on one critical resource: Quality biospecimens. Optimize and accelerate program success by sourcing and selecting the right samples.

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FDA puts LogicBio genome editing therapy trial on hold after 2nd infant suffers adverse event

LogicBio Therapeutics’ bid to develop a genome editing therapy in infants has hit more trouble. Months after the first infant to receive the therapy suffered a serious adverse event, LogicBio has revealed the second subject has experienced the same clinical syndrome, prompting the FDA to impose a clinical hold. 

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AliveCor's credit-card-sized ECG snags FDA clearance for 30-second arrhythmia detection

Thin is in for AliveCor: The personal electrocardiogram tech maker scored FDA clearance for its slimmest heart monitor yet, which is the size and shape of a credit card and is aptly named the KardiaMobile Card.

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Unvaccinated 23 times more likely than boosted to be hospitalized during omicron wave

New Los Angeles County public health surveillance data reaffirm vaccines and boosters' protection against COVID-19, and particularly against severe illness.

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Gilead's COVID-19 antiviral Veklury blew past sales estimates in late 2021 as omicron surged, vaccinations lagged

The omicron variant has fueled a surge in demand for Gilead's Veklury, the company said on Tuesday when it reported fourth quarter and 2021 sales. The COVID-19 antiviral treatment rang up 2021 sales to $5.6 billion. The company is projecting Veklury to generate $2 billion in revenue in 2022.

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Shkreli and Vyera settle for $28M in yet another Daraprim antitrust suit

Blue Cross and Blue Shield of Minnesota has settled a class-action lawsuit against Martin Shkreli, his former company and another ex-CEO for $28 million, the insurance system said this week. The news comes after a federal judge ordered the "pharma bro" to pay nearly $65 million in disgorgement and exit the pharma industry for life.

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Paragonix's lung transport system completes 4,700-mile, cross-country transplant

The high-stakes transplant procedure set a new record for the company’s LUNGguard system, pushing past its intended organ storage time of up to eight hours.

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Kindbody hits unicorn status with Vios Fertility Institute acquisition, new leadership additions

Fertility startup Kindbody hit a $1.15 billion valuation with its acquisition of Vios Fertility Institute, a deal that gives the company 13 more clinics, doubling its national footprint.

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Resources

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.

Research: How Buffer Prep Services Alleviate Sudden Spikes in Campaign Volume

Learn how a CDMO partnered with Thermo Fisher Scientific to manage high-volume process liquid and buffer preparation scale-up. Download the free case study from Thermo Fisher Scientific.

Whitepaper: QC for ex vivo manipulated cell lines and tissues

A variety of genetic analysis methods are valuable in ensuring that ex vivo human cells to be used for cell-based therapies are correctly identified, have the correct characteristics, and are free of contaminants.

Webinar: Using Next Best to Elevate your Omnichannel Marketing Strategy

Learn how to elevate your omnichannel marketing strategy with Next Best - a combination of data and analytics, deployed to facilitate decision making.

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.

Whitepaper: Enhance the cost-effectiveness of your cGMP chemical supply chain

Learn how to develop a high-performing supply chain for cGMP chemicals used throughout your biologics workflow. Download the free whitepaper from Thermo Fisher Scientific.

eBook: Get solutions to market faster

Read Get to Know Cloud Content Management for Life Sciences and learn how to eliminate silos across all workflows, from R&D to commercialization.

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