Ventyx grabs $152M IPO to challenge Bristol Myers
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Today's Rundown

Featured Story

FDA slaps clinical hold on AstraZeneca cancer drug amid heart safety scare in combo test

We found out, via a small and almost unnoticed ClinicalTrials.gov update today, that AstraZeneca suspended trial work on its experimental blood cancer drug AZD5991. Now, we have learned that things are in fact bleaker for the therapy.

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Top Stories

Another $80M: mRNA biotech ReCode matches 2020 series A with Pfizer, Sanofi money for cystic fibrosis trial

ReCode Therapeutics is back with its second $80 million financing round, this time a series B from Pfizer, Sanofi and VC shops, to bring its lead programs into human trials. Up first are cystic fibrosis and primary ciliary dyskinesia, another lung disease.

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Ventyx nabs a $152M upsized IPO to challenge BMS' Zeposia—and a backer with intimate knowledge of its rival

Ventyx Biosciences is in the fast lane: Less than a year ago, the biotech emerged from stealth with big plans to dampen down some blockbuster autoimmune/inflammation targets. Then last month, it sprinted to Wall Street with the now standard $100 million IPO ticket.

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Sponsored: Considerations for Laboratory-Related Operational and Patient Burden in Decentralized Clinical Trials. Clinical Lab Testing in Your Home: Fact or Fiction?

Clinical lab testing at home - fact or fiction? Many operational and patient-related considerations must be taken when using a decentralized approach to specimen collection at or near the trial participant's home.

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Menarini, chased by 3 Big Pharmas, records win in breast cancer phase 3, plots path to FDA

Menarini and Radius Health have gained a lead over AstraZeneca, Roche and Sanofi in the race to bring a new class of oral breast cancer drugs to market, posting phase 3 data and outlining plans to seek approvals on both sides of the Atlantic next year. 

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GSK-backed Atreca inks license with Gates Medical Research Institute for malaria monoclonal antibody

Oncology biotech Atreca is linking arms with the Bill & Melinda Gates Medical Research Institute to work on a monoclonal antibody for the potential treatment of malaria. The licensing deal comes just two weeks after the WHO signaled a breakthrough in the fight against malaria with a recommendation for broader rollout of GlaxoSmithKline's vaccine.

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VCs back Leucid to trial CAR-T twist in ovarian cancer patients

John Maher has secured funding to put his ideas about CAR-Ts to the test. As chief scientific officer of Leucid Bio, Maher has pushed the idea that the configuration of co-stimulatory modules is the secret to success in CAR-T—and now he has the cash to run a phase 1 clinical trial in ovarian cancer.  

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FDA contracts Aetion’s real-world evidence platform to assess COVID-19 treatments

Clinical trials, though critical to the scientific process, can take a long time, which can be a problem in the face of a public health crisis. The FDA announced today it's partnering with the Aetion Evidence platform, which will allow the agency to analyze data about COVID-19 from real patients in real-time.

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Pfizer strong-armed governments in COVID-19 vaccine supply talks, report says

Pfizer is playing a leading role in producing vaccines against COVID-19, but new documents released by Public Citizen shine a light on the company's aggressive tactics when negotiating supply deals.

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Medtronic issues EU safety warning for Percept PC deep brain stimulation implant

Medtronic identified an issue in which its Percept PC deep brain stimulation implant may stop working and need to be removed after an implanted patient undergoes a cardioversion.

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Princeton and MIT gene-editing pioneers uncover clues for improving CRISPR and other tools

Scientists at Princeton and MIT, including gene-editing pioneer David Liu, used a new screening method called Repair-seq to identify pathways that affect different outcomes in CRISPR/Cas9, prime editing and base editing. The findings could help design more accurate and efficient gene-editing systems, they say.

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Resources

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Report: New research indicates an accelerated shift to decentralized clinical trials

New research indicates an accelerated adoption of decentralized clinical trials due to COVID-19.

Whitepaper: Transform LIMS Data into Action-Ready Insights with Advanced Analytics

Shift from data collection to data science. Add advanced analytics to your lab informatics platform to yield valuable, action-ready insights from LIMS and other data.

Whitepaper: Clinical trial simulation: Advanced modeling techniques enable data-driven supply chain planning

Integrate supply chain simulation into your early clinical trial planning to minimize risk in an uncertain supply chain environment, improve supply chain outcomes, and help streamline time-to-market for innovative therapies.

Whitepaper: Big Challenges for Small Sponsors: Competition in Oncology Research

Every biopharma sponsor faces the challenge of initiating, running and closing trials on time, but oncology studies pose several unique hurdles.

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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