Sensorion tries to flip mid-stage flop
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Today's Rundown

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AstraZeneca throws open doors to new ideas in global postdoc challenge

AstraZeneca is throwing open its doors to ideas from scientists near the start of their careers. Through its global R&D Postdoctoral Challenge, the Anglo-Swedish drugmaker will equip researchers to pursue novel approaches to treating diseases.

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Top Stories

Silence stops enrollment in blood cancer arm of RNAi trial over 'recruitment challenges'

Silence Therapeutics’ stuttering effort to generate clinical data on SLN124 in myelodysplastic syndrome (MDS) has conked out. Facing recruitment challenges, the RNAi specialist has decided to stop enrollment in the MDS arm of an early-phase clinical trial to focus on thalassemia and polycythemia vera.

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Sensorion spins hearing loss flop into exploratory win in attempt to revive lead program

If at first you don’t succeed, try a sub-population analysis, the biotech playbook goes. That’s exactly what Sensorion is doing after its phase 2 hearing loss treatment—and lead program—flopped a key study in January.

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NIH squashes Synairgen’s COVID therapy from ACTIV-2 trial after omicron shakes up study

The NIH has kiboshed Synairgen’s arm of the ACTIV-2 trial testing the company's SNG001 in nonhospitalized patients due to a “significant shift” in the pandemic (read: the omicron variant). The announcement from Synairgen Tuesday that recruitment was being halted came two weeks after the company first said the NIH had told it to slow its roll while the two tweaked the trial.

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Eiger eager to send COVID-19 drug to FDA after hospitalizations, deaths slashed—including against omicron

Eiger BioPharmaceuticals' drug, licensed from Bristol Myers Squibb in 2016, halved the risk of hospitalizations or emergency room visits lasting longer than six hours in patients with COVID-19, including those with the omicron variant, in a phase 3 trial. 

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Shionogi's COVID-19 antiviral heads to phase 3 backed by NIH after receiving FDA go-ahead

Shionogi's COVID-19 treatment, backed by the National Institutes of Health, is moving on to phase 3 after the FDA finalized the study design, a positive step after several clinical pauses and discontinuations have marred pandemic research funded by the NIH in March. 

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Athenex cuts jobs, narrows focus to cell therapies in continued fallout from 2021 FDA rejection

Athenex has been trying to stem the damage since receiving a complete response letter from the FDA in February 2021 with pipeline changes and other measures. But now, it's come to layoffs and a slimmed focus on cell therapies. 

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BioNTech, CureVac part of $3.14B deal to bolster German vaccine capacity through 2029: report

Germany will pay upward of 2.86 billion euros ($3.14 billion) to lock up local vaccine production capacity through 2029, Reuters reports, citing the country’s economy ministry. On Wednesday, the German government approved plans to sign contracts with mRNA specialists BioNTech and CureVac-GSK plus contract manufacturers Wacker and CordenPharma, Celonic and IDT.

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Invitae launches personalized cancer blood tests to spot tumor relapses

The company’s Personalized Cancer Monitoring platform includes a set of assays that are tailored to a patient’s particular tumor.

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After Alexion buyout, AstraZeneca pays Roche $775M to settle Ultomiris patent brawl

AstraZeneca and Roche recently decided to end a patent infringement fight around Ultomiris. Now we know the price of the deal.

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Thermo Fisher says buoyant demand prompted clinical lab expansion

Thermo Fisher Scientific is embarking on a clinical bioanalytical lab expansion thanks to 'buoyant' pipelines and continued demand.

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Glooko picks up Diabnext to launch digital diabetes management platform in France

In its second acquisition of the year so far, Glooko is forging ahead in its mission not only to bulk up its digital diabetes management offerings but also to expand their reach around the world.

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Here are the top health systems by patient reviews

Reputation analyzed more than 2.7 million patient reviews of the 25 largest health systems by revenue. Those with higher scores had more engagement with feedback.

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MIT-made COVID-19 vax produced by yeast could address global vaccine inequity

Researchers from MIT and Beth Israel Deaconess Medical Center say their yeast-produced COVID-19 vax generated antibody levels comparable to J&J's one-shot jab. The team hopes the results bolster the use of the easy-to-manufacture vaccine in regions where global vaccine inequity has permeated.

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Resources

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.

Industry Report: The Top Four Barriers to Successful KOL Engagement

Read why many MSLs are still challenged in developing integrated strategies to increase the volume of meaningful engagements. Download this industry report to find out what the top challenges are and suggestion strategies to solve them. Download now.

eBook: Leveraging Clinical Data for Study Success

The landscape of clinical trials has been permanently changed. Today's trials require sponsors to modernize their use of technology and data to adapt. This eBook provides an overview of how sponsors can empower trials with real-time performance data to improve study integrity, reduce risks, optimize patient safety, and increase trial success rates.

Whitepaper: Autologous CAR T-Cell Manufacturing: Semiautomatic, Closed, Modular Workflow

Learn how to navigate the top manufacturing challenges and achieve a seamless transition from discovery to clinical manufacturing across the CAR T-cell therapy workflow.

eBook: EMEA Regulatory Roadblocks around Decentralized Trials

Learn about ways to break down regulatory roadblocks and get closer to 100% clarity on regulatory positions to advance decentralized clinical trials in research.

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

How to overcome top challenges faced in decentralized trials.

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.

Events