Innovent obesity drug enters Big Pharma race
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Moderna eyes fall vaccine season for omicron booster after phase 2/3 success

Moderna hopes that the successful readout from a phase 2/3 trial of its omicron-targeting COVID-19 shot means the booster will be ready for people’s arms by the late summer.

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Top Stories

Precision hails phase 1/2 data as proof it could deliver the first approved off-the-shelf CAR-T

Gene editing biotech Precision BioSciences is touting phase 1/2 results as proof it could bring the first approved allogeneic CAR-T drug to market. The promising, albeit early, data from the study found that 100% of evaluable patients whose cancer had relapsed had responded to the treatment.

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Weight watcher: Innovent catching up with Lilly, Novo Nordisk thanks to phase 2 obesity data

Innovent is catching up with the likes of Eli Lilly and Novo Nordisk as the Chinese pharma’s own obesity drug passes strong results in a phase 2 trial. A placebo-controlled trial of the drug, mazdutide, in 230 Chinese participants met the primary endpoint of a percentage change in baseline body weight at week 24.

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Sponsored: Tech-Enabled Trials Don't Have to Mean Loss of Human Connection

DCTs hold the promise of reducing site and patient burdens but at what cost to human connection? Vault says it doesn't have to be a compromise.

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DBV patches up prospects with phase 3 win in infants with peanut allergies

DBV Technologies has chalked up a win for its beleaguered peanut allergy patch candidate, hitting the primary endpoint in a phase 3 clinical trial in infants to send its battered share price past its prior high for 2022.

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Mineralys hauls in $118M series B to advance hypertension med through phase 2 trial

Mineralys has raised $118 million in series B funds off of the promise of its sole asset, a hypertension med that's progressing through a phase 2 trial slated to read out in a matter of months. As for future development, the company says it would likely first work on expanding the indication of the drug, MLS-101, to other cardio-metabolic disorders.

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After late-study endpoint switch, Aldeyra hails success of phase 3 dry eye disease trial

Aldeyra Therapeutics’ late-study primary endpoint switch has paid off. Weeks after disclosing the change to its dry eye disease phase 3, the biotech has reported a hit against the new primary endpoint, teeing it up to find out what the FDA makes of the data set.

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Roche's bispecific blood cancer drug Lunsumio treads on CAR-T's turf with first global approval

After Rituxan's fall off the patent cliff, Roche is looking to new assets to replenish its blood cancer arsenal. With a first-in-class nod, the Swiss pharma is introducing a novel bispecific lymphoma drug that will first compete with powerful CAR-T therapies.

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As monkeypox cases rise, BD pairs up with Spain-based CerTest for diagnostic

The project aims to have CerTest’s CE-marked test operate on the BD MAX automated PCR system.

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AHA: Nonprofit hospitals provided community benefits 9 times higher than 2019 tax exemptions

An average 13.9% of hospitals’ total expenses went toward community benefits in 2019, according to a recent report from the American Hospital Association and Ernst & Young.

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Lilly, Novo Nordisk's weight loss meds could replace surgery for obesity patients: specialist

Tirzepatide weight loss data presented this week by Eli Lilly are so compelling that the drug and Novo Nordisk's Wegovy could in many circumstances replace sleeve bariatric and gastric bypass surgeries—often seen as last resorts for those who are morbidly obese. That is the belief of a key opinion leading obesity specialist who was consulted by SVB Securities.

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Ginkgo Bioworks picks up Bitome's AI to bolster its cell engineering platform

Ginkgo Bioworks has acquired certain assets from Bitome, which is developing machine learning technology to track how well individual cell lines are performing throughout the programming process.

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Residents of Republican counties more likely to die of COVID-19 regardless of own political beliefs, study finds

A lack of implementation or compliance with public health measures "played a significant role" in mortality, which was likely driven by individual political beliefs.

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Better late than never? Novavax's COVID shot gets endorsement from FDA expert panel

An FDA panel of independent experts voted 21-0, with one abstention, to recommend the Novavax COVID-19 vaccine for authorization for those 18 and older. The endorsement leaves the fate of the shot in the hands of the FDA, which could sign off on it as early as this week.

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