AbbVie dumps Alector Alzhiemer’s therapy
To view this email as a web page, click here

WELCOME TO FIERCE LIFE SCIENCES WEEKLY DIGEST

After the FDA urged COVID-19 vaccine makers to tweak their shots and target omicron’s BA.4 and BA.5 subvariants, Moderna unveiled promising data showing its bivalent booster delivered more neutralizing antibodies than the original shot. Meanwhile, the agency has said it would allow pharmacists to prescribe Pfizer’s Paxlovid antiviral, but it did not extend the same privilege to Merck’s Lagevrio, even though they were both authorized a day apart last December. And MacroGenics has closed a phase 2 trial of its anti-cancer antibody, enoblituzumab, after learning of seven deaths potentially linked with major bleeding events. Those stories, plus our top reads of the week, follow below.

Featured Story

Moderna's omicron booster triggers stronger response against subvariants than its original shot, company says

Just a few weeks after the FDA recommended that vaccine makers update their boosters to protect against Omicron, Moderna unveiled positive data showing high neutralizing antibody responses in its updated booster trial.

read more

Top Stories Of The Week

MacroGenics closes solid tumor clinical trial after 7 people die

MacroGenics has closed a phase 2 clinical trial of its anti-cancer antibody enoblituzumab after learning of seven deaths potentially associated with hemorrhagic events. The setback means two of MacroGenics’ three attacks on B7-H3 have hit setbacks but the biotech is forging ahead with the third candidate.

read more

FDA is letting pharmacists prescribe Pfizer's Paxlovid but won't do the same for Merck's Lagevrio

After authorizing Pfizer’s COVID-19 oral antiviral Paxlovid to be prescribed by pharmacists, the FDA said it will not extend the same privilege to Merck and Ridgeback’s antiviral pill Lagevrio. The regulator cited Lagevrio’s side effect profile as reason to leave the decision in the hands of physicians.

read more

AbbVie dumps Alector's Alzheimer's immunotherapy after phase 1 review

Alector’s new approach to amyloid beta has ended the way of many of the old ideas for how to tackle the troublesome peptide. After going over data including phase 1 results, AbbVie has severed its ties to the potential Alzheimer’s disease immunotherapy—and the asset has vanished from Alector’s pipeline.

read more

Pfizer, Alnylam and BMS take note: The US is poised to see 'a staggering number' of cardiomyopathy cases this decade

There’s a new blockbuster heart disease market in town—and it's set to explode in size. As Pfizer, Bristol Myers Squibb and Alnylam are already fighting for their share of prescriptions, a new report finds they'll have millions more patients to treat in the coming years.

read more

SEC charges ex-Mazor exec with insider trading over $1.6B Medtronic buyout

The SEC filed charges against a former Mazor Robotics executive and two associates, alleging that they made more than $500,000 in profits through an insider trading scheme related to Mazor's 2018 acquisition by Medtronic.

read more

AstraZeneca escapes one Seroquel pay-for-delay claim but loses bid to scrap another

Apparently, a $107 million deal value isn't large enough to be considered anticompetitive when viewed in the context of delaying generics to a blockbuster brand. A Delaware federal judge reached that conclusion in throwing out an antitrust claim targeting a pay-for-delay deal involving AstraZeneca's antipsychotic Seroquel XR.

read more

Roche hands over $55M for licensing rights to Ionis' kidney disease candidate

Roche is handing over $55 million for the licensing rights to Ionis Pharmaceuticals’ rare kidney disease treatment candidate, an investigational med that the Big Pharma will advance into a phase 3 clinical trial.

read more

After building new plant and signing on with AbbVie, Regenxbio enters commercial phase

ROCKVILLE, MARYLAND—After building a new $65 million manufacturing facility and partnering with AbbVie in a $370 million deal, Maryland gene therapy biotech Regenxbio is entering a new phase as a burgeoning commercial business. The companies hope to bring a first-of-its-kind gene therapy to the market to treat wet age-related macular degeneration.

read more

Blood thinner's ability to boost fat burning could inspire new obesity therapies

Scientists in Germany have identified a molecular mechanism by which brown fat increases energy expenditure and showed how an anticoagulant may stimulate that process in mice.

read more

Resources

Whitepaper: Ensure Commercialization Success with TrialCard/Triangle Insights

Discover how the new partnership between TrialCard and Triangle Insights Group can help you bridge the critical gap between strategy and execution, ensuring commercialization success of your product or therapy.

Whitepaper: Through a CRO's Perspective: Innovative, Agile Solutions In Vaccine Efficacy Testing

Discover Nexelis’ first-hand perspective on how to develop innovative, agile solutions in vaccine efficacy testing in this exclusive e-book.

Case Study: Roche cuts feasibility process by 36%

Explore how Cognizant SIP helped Roche streamline its global feasibility process.

eBook: 12 Pitfalls in Europe

For an emerging biopharma company, Europe can be very attractive. But it can also be complex and confusing. This e-book covers the 12 most common pitfalls for companies entering European markets for the first time, offering guidance to help growing companies avoid them and succeed.

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?

eBook: Download the Cell Therapy Handbook

Explore the new cell therapy handbook from Thermo Fisher Scientific.

Article: 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.

Whitepaper: Catalent Pulmonary & Nasal Delivery Capabilities Sheet

Did you know Catalent has newly expanded in-house capabilities spanning clinical and commercial scale manufacturing for DPIs, unit-dose, bi-dose and preserved multi-dose nasal sprays?

Whitepaper: Jump Start for Biotech: New Lab Startup Guide

Sponsored by Thermo Fisher Scientific The journey for starting or expanding a lab can be exhilarating, while also being challenging--learn how this free program provides savings and solutions to support your goals.

Whitepaper: Intranasal Drug Product Development: Formulation to Manufacturing

What are key considerations for intranasal delivery in the treatment of acute and chronic conditions?

eBook: Orally Inhaled & Nasal Drug Delivery: A Pipeline of Opportunities

Orally Inhaled & Nasal Drug Delivery: A Pipeline of Opportunities

Events