COVID-19 lessons drive new clinical trial not-for-profit
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Today's Rundown

Featured Story

Merck's chronic cough med gets a nay from FDA, potentially clearing first-to-market path for Bellus

The FDA rejected Merck's chronic cough treatment, potentially setting up more breathing room for competitor Bellus Health in a first-to-market battle. 

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Top Stories

Does the world need more COVID-19 vaccines? These companies think there's still room for improvement

The ultimate COVID-19 vaccine will be able to tackle all emerging coronavirus strains, easy to store and quick to manufacture. And yes, there's still time for the stragglers who were beaten to the punch by Pfizer, BioNTech and Moderna—at least according to the companies still trying to get in line.

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New clinical trial organization launches with promise to conduct randomized trials at fraction of the cost

After quickly identifying an existing medication would be an effective COVID-19 treatment using a large randomized clinical trial design, a leading epidemiologist has formed a new not-for-profit organization out of the U.K. to apply the same approach to other conditions.

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1b, or not 1b: FDA hits Viking with clinical hold over mix-up in phase of rare disease trial

Viking Therapeutics thought it was running a phase 1b clinical trial. The FDA thought otherwise, leading it to slap a clinical hold on the metabolic disorder study while Viking does the preclinical work needed to enter phase 2. 

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MaaT wraps up cancer microbiome trial early to power into phase 2/3 this year

MaaT Pharma is racing its microbiome therapy into a late-phase cancer clinical trial. Rather than take the current phase 1b to its planned conclusion, MaaT is wrapping the trial up early to accelerate its push into a larger study of acute myeloid leukemia patients.

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In biopharma VC world, what does it mean to take a 'leap'? For Leaps by Bayer, it's 'fewer, but maybe bigger bets'

Sparking innovation at a Big Pharma with a 150-year history can be difficult, so sometimes it takes some outside perspective to get the ball rolling. That's where Leaps by Bayer comes in.

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Gilead's Veklury expands FDA nod to patients outside the hospital as oral version heads to trial

Gilead Sciences’ Veklury has extended its reach to outpatients at a time when effective COVID-19 therapies against omicron are in high demand. To overcome the inconvenience factor—Veklury is injectable, compared with newer oral antivirals— the company has started clinical trials with an oral version.

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Casana lands $30M to take its heart-scanning smart toilet seat to the FDA

Casana aims to provide people with a regular heart health scan without intruding on their daily routine, with electronic sensors for logging heart rate and blood pressure built directly into the cushion.

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The eviction moratorium in New York has ended. Here's how one practice is prepared to serve affected patients

The practice works with Phreesia, a patient intake software, to screen for social determinants. It also refers patients in need to community partners who do work in areas like housing or food security.

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You say Trintellix, I say Brintellix: Why a drug name in the US won't always translate across the pond

As a British citizen living in England but writing on American drug names, I’m in the perfect position to know that many drugs approved in Europe and the U.K. can have very different names from those in the U.S.

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Global digital health funding skyrockets to $57.2B with record cash for mental health, telehealth

Digital health investment around the world hit an all-time high of $57.2 billion in funding in 2021, fueled by the growing need to provide digital solutions and delivery models to patients during the pandemic.

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Resources

Whitepaper: Tailored, Dedicated Support Expedites COVID-19 Vaccine Trial

Sites receiving augmentation support enroll more than 30,000 patients in just over three months. See how additional site resources can make a difference.

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.

Events