BIOSECURE Act clears House hurdle

Today’s Big News

Sep 10, 2024

Apple pitches sleep apnea detection, OTC hearing aid features


Genentech's cancer restructure was made 'for scientific reasons': exec


After BIOSECURE Act passes in House, targeted Chinese companies say they're 'deeply' concerned


Carisma, Moderna expand in vivo cell therapy collaboration to autoimmune diseases


Docs influenced by disease-specific leadership, corporate reputation when prescribing: survey

 

Featured

Apple pitches sleep apnea detection, OTC hearing aid features

The tech giant plans to add sleep apnea detection to its Apple Watch as well as bring long-anticipated over-the-counter hearing aid tech to its AirPods.
 

Top Stories

Genentech's cancer restructure was made 'for scientific reasons': exec

The recent decision to merge Genentech’s two cancer departments was made for “scientific reasons,” according to executives.

After BIOSECURE Act passes in House, targeted Chinese companies say they're 'deeply' concerned

Late Monday, the U.S. House of Representatives voted 306-81 in favor of the BIOSECURE Act, which was introduced in January and seeks to halt federal contracts with five named Chinese life-sci companies: WuXi AppTec, WuXi Biologics, BGI Group, MGI and Complete Genomics.

Carisma, Moderna expand in vivo cell therapy collaboration to autoimmune diseases

Carisma Therapeutics has been working for years to develop cell therapies using macrophages, immune cells that are better at attacking solid tumors than the T cells that currently dominate the industry. In a partnership with Moderna, now expanded to two undisclosed autoimmune targets, the biotech hopes to seriously simplify cell therapy by bypassing the need to culture patient cells out of the body.

Docs influenced by disease-specific leadership, corporate reputation when prescribing: survey

Physicians consider more than what a drug does when making prescribing decisions. They also look at who is behind the therapy. That is the conclusion of a WE Communications survey that found physicians are influenced by disease-specific leadership and corporate reputation when choosing which drug to use.

Viridian’s drug resolves eye disease symptoms in phase 3, advancing push to topple Amgen’s Tepezza

Viridian Therapeutics’ phase 3 thyroid eye disease clinical trial has hit its primary and secondary endpoints. But with Amgen’s Tepezza already on the market, the data leave scope to question whether the biotech has done enough to differentiate its asset and unseat the incumbent.

Johnson & Johnson consolidates medtech brands under single banner

Au revoir, Abiomed. Goodbye, DePuy. Bon voyage, Biosense. So long, Cerenovus. Adios, Ethicon.

Teva resolves Baltimore's opioid litigation with $80M settlement

The city scored its own deal after opting not to join in on Teva's $4.25 billion national opioid settlement.

Gilead inks $35M collab with AI drug discovery outfit Genesis

Gilead is paying $35 million to access Genesis' tech. The deal covers three targets, with an option for more down the line.

After previous data flop, Zealand Pharma links GLP-1/GLP-2 agonist to 8.3% weight loss

On the heels of disappointing low-dose data results, Zealand Pharma is back with separate findings for its GLP-1/GLP-2 receptor dual agonist that have emboldened the biotech to push the candidate into phase 2b development.

AbbVie's Ubrelvy to be top migraine seller in 2033 as total market to hit $16B-plus across biggest pharma countries

AbbVie’s migraine drug Ubrelvy (ubrogepant) is slated to be the top-selling drug in the migraine space in 2033 across the seven bigger pharma markets as total spend across those countries are set to rake in $16.4 billion.

FDA issues Form 483s to Japanese, Indian drugmakers in wake of plant inspections

Two Japanese drugmakers and another in India were hit with Form 483s from the FDA following inspections that uncovered issues ranging from a lack of sanitary procedures to improper data collection and monitoring.
 
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Resources

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Facing roadblocks in drug development? Uncover how phase-appropriate technology transfers can help you navigate challenges and speed up your journey to market.
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We interviewed dozens of biopharma leaders on the critical success factors for building a Best Practice commercial organization. This report shares what we learned.
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Finding an effective epilepsy treatment can be arduous. Download this brochure to delve into how IQVIA's expertise and innovative strategic approach can streamline the clinical trial process, helping to get new therapies to patients who need them sooner.
 

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On Helix

Date: ‌4 ‌July ‌2024 ‌- ‌Location: ‌Babraham ‌Research ‌Campus, ‌Cambridge ‌UK

 

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