Fierce Biotech’s Rotten Tomatoes 2021
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Today's Rundown

Featured Story

GSK pulls off clean sweep of endpoint hits in anemia phase 3, positioning it to leapfrog AstraZeneca

GlaxoSmithKline has boosted its challenge for the anemia due to chronic kidney disease market, revealing a clean sweep of hits on key endpoints across two phase 3 clinical trials. But with the FDA rejecting AstraZeneca’s rival drug, doubts remain about GSK’s chances of getting to market. 

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Top Stories

Blade runs toward Nasdaq in $353M SPAC deal for 2 2022 trials, money from BMS, Pfizer

Pfizer Ventures and Bristol Myers Squibb contributed financing for Blade Therapeutics' special purpose acquisition company merger as the biotech gears up for two clinical trial starts in 2022. The $254 million in cash will bankroll trials in fibrosis and neurodegenerative conditions.

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Fierce Biotech’s Rotten Tomatoes 2021

The biopharma industry has received acclaim during the COVID-19 pandemic. But while some companies have been working hard on life-saving therapies, others' actions have further stained the industry's already shaky reputation.

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Sponsored: A New Reference Model for Clinical Trial Recruitment, Enrollment and Retention Success

Rare diseases demand a modern recruitment approach grounded in uncovering the ideal, medically-eligible patient population with the highest propensity for study enrollment and retention.

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Blackstone bets on Autolus' CD19 CAR-T in $250M deal, clearing path to pivotal readout in 2022

Autolus Therapeutics has found a deep-pocketed supporter of its CD19 CAR-T therapy. Having seen Autolus’ stock halved over the past year, Blackstone Life Sciences has stepped in with a $250 million package to support the British biotech through to a pivotal readout and beyond.

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Provention Bio, hit by AdComm rejection for lead drug, hires early research exec from Gossamer

Provention Bio has come out with a little bit of good news amid a tough 2021 as it hires former Gossamer Bio early R&D lead Miguel Sanjuan, Ph.D., to help shore up its early shots on goal.

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Gyroscope spins the wheel again as it taps Sanofi for $60M months after ditching IPO attempt

The biotech IPO window, at the start of the year at least, was wide open, leaving more than a few people scratching their heads when the eye disease biotech said back in May it was ditching its plans because of “market conditions.”

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ATP fuels Marengo with $80M for battle against cancers with former Merck KGaA oncology head in driver's seat

With $80 million to fuel its battle against cancer, Marengo Therapeutics will bring its first candidate into the clinic in late 2022. Former Merck KGaA global oncology leader Zhen Su will lead the way for the biotech, named after the French battle and Napoleon Bonaparte's horse.

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Once-failed cancer drug from BioXcel ramps up immunotherapy in mouse models of pancreatic cancer

Georgetown researchers reported that combining BioXcel's DPP inhibitor talabostat with a PD-1 blocker in mouse models of pancreatic cancer slowed tumor growth and increased the recruitment of cancer-fighting immune cells. They're working to advance the combo into clinical trials.

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iRhythm picks up the tempo with 19% revenue boost despite Medicare pricing letdown

For the third quarter in a row, iRhythm Technologies continued its streak of increasing revenues amid a host of challenges ranging from staffing shortages to lower-than-expected Medicare reimbursement rates to the ongoing COVID-19 pandemic.

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Many expectant mothers unlikely to get vaccinated for COVID-19, survey finds

Ovia Health, a family benefits solution, conducts monthly surveys of 4,500 users across each of its various apps on their attitudes toward the COVID-19 vaccine. Most remain hesitant, though most have discussed the benefits with their provider.

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With oncology spinoff done, bluebird bio moves to new digs better suited to its future

With many of its employees working from home and others having left for a new spinoff venture, Massachusetts-based bluebird bio has decided to move its headquarters from Cambridge three miles north to Somerville. The shift will save bluebird $120 million in overhead during the next six years, the company said.

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Resources

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

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Whitepaper: Formulation Strategies When Transitioning From Vial to PFS

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Whitepaper: How the Chronic Insomnia Market Raises Big Questions About Digital Therapeutics

Paper describing how the chronic insomnia market offers big lessons for any biopharma company thinking about getting into digital therapeutics in any therapeutic area.

Whitepaper: Create a seamless experience across eConsent, eCOA & more

Find out how to improve clinical protocol adherence, and thus patient outcomes, by 15%+ with Medable’s latest White Paper.

Whitepaper: A Checklist for eCOA Solution Deployment

Every detail is important when selecting a new eCOA solution; learn more about the current eCOA landscape, best practices, and crucial considerations for successful eCOA solution deployment in this white paper.

2021 Report: Clinical Trial Management in a Post-Pandemic World

New market research provides valuable insight into the impact of adaptations made in clinical trials during the pandemic.

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

Paid Marketplace: Online Graduate Programs Designed for Your Career

Drexel University’s online graduate programs in biomedicine, clinical research, drug discovery, and molecular medicine were developed with working professionals in mind, providing you with the education, practical skills, and competitive edge you need to be successful in your career. Learn more.

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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