Valneva heads to FDA with chikungunya vax
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Today's Rundown

Featured Story

Novartis eyes next-gen AAV gene therapies in $1.75B Voyager biobucks pact

In Novartis’ perennial hunt for innovative therapies to bring under its wing, improving on gene therapy has always been kept top of mind. And the Swiss pharma continues to do just that thanks to a new biobucks deal with Voyager Therapeutics worth up to $1.75 billion.

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Top Stories

Sanofi deploying $1B to turn France into 'pioneer mRNA nation'

Sanofi will invest about $1 billion in its home country to beef up mRNA R&D and vaccines production in France. The move is part of the Big Pharma's broader $2.2 billion mRNA commitment revealed last summer.

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Valneva heads to FDA as durability of chikungunya vaccine holds up in phase 3 

The finish line is in sight for Valneva’s chikungunya virus vaccine candidate. With antibody levels holding steady out to six months in the phase 3 clinical trial, Valneva is set to start the pre-submission process with the FDA in the second quarter.

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Late-stage biotechs, Kurma has €160M to help you clear the final hurdles in the race to market

Kurma Partners has rounded up cash to help 15 companies clear the final hurdles in the race to market. Armed with an initial 160 million euros ($174 million), the Paris-based VC shop will primarily support unlisted European companies as they seek to transform from R&D- to commercial-stage organizations.

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J&J to celebrate Carvykti nod without Janssen oncology chief as Serge Messerlian nabs Teon CEO job

Serge Messerlian is probably missing out on a big celebration back at the offices of his former employer, Johnson & Johnson, after the approval of multiple myeloma med Carvykti last week. But instead, Messerlian has moved on to his next gig: CEO of oncology-focused biotech Teon Therapeutics. 

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Creyon joins wave of AI biotechs with $40M to create 'on demand' RNA-based medicines

Creyon Bio wants to create drugs "on demand" for patient populations that consist of one person with a rare disease, or "millions" of people with common diseases—and a $40 million series A will help get that mission underway. 

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BioNTech-Regeneron add 3rd tumor type to partnership testing cancer vaccines with Libtayo

BioNTech wants to run it back with Regeneron, extending a partnership first announced in 2020 to combine a cancer vaccine with the approved treatment Libtayo in the clinic, this time for advanced non-small cell lung cancer. 

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The top 10 drugs losing US exclusivity in 2022

With AbbVie’s megablockbuster Humira set to face an onslaught of biosimilars next year, industry watchers have long circled 2023 as the year of the major pharma patent cliff. But this year’s slate of top losses of exclusivity covers a hefty slate of brands worth more than $17 billion in annual sales.  

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NuCana's twist on chemo drug Gemzar fails in phase 3 again

NuCana’s retooled chemotherapy candidate Acelarin has come up short in phase 3 again. The latest failure wipes out hopes that NuCana’s attempt to improve on gemcitabine, sold by Eli Lilly as Gemzar, will drive improved outcomes in biliary cancer.

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Be 'recall ready': FDA asks companies to take potentially harmful products off the market faster

This month, the FDA finalized guidance outlining how makers of regulated products can become “recall ready” to minimize buyers’ and users’ exposure to any potential health risks.

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ViVE 2022: What collaboration looks like across CMS

MIAMI—Late last year, CMS set a goal of having all Medicare beneficiaries enrolled in both Part A and Part B in an accountable care model by 2030. Central to achieving that goal? The ability to coordinate and collaborate across different parts of the agency, leaders said Monday during a session at the ViVE conference.

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New pinhead-sized beads kill ovarian, colorectal cancers by producing interleukin-2: mouse study

Researchers at Rice University said they were able to eliminate ovarian cancer and colorectal cancer in mice using a beadlike implant that helped produce the cytokine interleukin-2. Avenge Bio has licensed the tech and will take the drug into the clinic in the second half of this year.

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Dopamine helps elicit dream time, could pave way to new sleeping disorder drugs

Dopamine plays a role in helping transition from non-rapid eye movement sleep to the portion of the night when your dreams come alive, according to new research from a team at University of Tsukuba. The findings could point to a new target for drugs that aim to treat sleeping disorders like narcolepsy.

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Resources

Whitepaper: The Long Game of Strategic Relationship Building with Medical Experts

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Whitepaper: Top 5 Challenges Of Decentralized Clinical Trials And How To Overcome Them

How to overcome top challenges faced in decentralized trials.

Paid Marketplace: United Cargo: 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: 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 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?

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.

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