ADC eyes 2nd FDA nod for lymphoma med
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Today's Rundown

Featured Story

GSK hails phase 3 win for RSV vaccine in older adults, sparking race to regulators

GSK’s respiratory syncytial virus (RSV) vaccine has hit the mark in a phase 3 trial in older adults, teeing the company up to file for approval by the end of the year. But the data-devoid statement leaves the big question of how the vaccine will fare in a competitive, blockbuster market unanswered.

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Top Stories

The hangover: Caribou's allogeneic CAR-T hit by durability doubts as half of patients relapse

Caribou Biosciences is nursing a hangover. Weeks after celebrating a 100% overall response rate, the CRISPR biotech has revealed 50% of patients relapsed within six months of receiving its allogeneic CAR-T cell therapy, sending its stock suddenly into a 13% dive that largely erased earlier gains.

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On the hunt for next FDA nod, ADC Therapeutics scores high response for Hodgkin lymphoma drug

Following the company’s first drug approval in 2021, ADC Therapeutics is looking for FDA nods, and appears to have landed on phase 2 data for a Hodgkin lymphoma drug that could do just that. 

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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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AACR calls for policy changes to reduce cancer care inequities, improve trial access for minority communities

The issue is well documented by now: minorities are not getting the same chances to participate in cancer clinical trials as White patients and at the same time face overall disparities in care. The American Association for Cancer Research has put out a call for funding, data collection, cancer control initiatives and access to healthcare in an effort to finally turn things around.

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Bluebird gene therapy overcomes safety worries to snag a win at FDA advisory panel

One vote down, another to go: After facing serious safety doubts from FDA reviewers on its gene therapy prospect eli-cel, bluebird bio has convinced an expert panel that the drug's benefits outweigh its risks—at least in some patients. A second bluebird therapy faces scrutiny Friday.

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Alcon nabs MVP Cooper Kupp as football star joins Pataday allergy eye drop team

Alcon's Pataday allergy eye drops are the latest eye care med to enlist a celebrity to help promote the product. This time, Los Angeles Rams wide receiver and Super Bowl LVI MVP, Cooper Kupp, joins the Pataday team.

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Brain circuits behind movement and mood could inspire new Parkinson’s disease treatment

A team led by MIT identified three distinct brain circuits underlying motor and nonmotor symptoms of Parkinson’s disease. The scientists also identified specific receptors on the circuits that could be targeted by drugs.

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Can biosimilars tear down AbbVie's Humira rebate wall? Just look at Viatris' Lantus copy: analyst

AbbVie’s megablockbuster TNF blocker Humira is about to face biosimilars next year. But will those biosims succeed? According to analysts who examined Viatris and Biocon’s two biosimilar versions of Sanofi’s popular insulin Lantus, both high- and low-list-priced Humira copycats actually could steal market share.

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Bristol Myers pays $80M to AI firm Owkin as part of cardiovascular trial accord

Bristol Myers Squibb will work with French biotech AI developer Owkin to design and optimize cardiovascular drug trials under a deal announced June 8.

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Oracle, Cerner plan to build national medical records database as Larry Ellison pitches bold vision for healthcare

Oracle's chairman Larry Ellison outlined a bold strategy Thursday for the database giant to use the combined tech power of Oracle and Cerner to make access to medical records more seamless.

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Tempus ties up Eli Lilly collab to bring free genomic testing to lung cancer patients

Tempus fugit, but the Chicago medtech of the same name is aiming to stop the clock on cancer with its genomic sequencing tests.

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'The Top Line' podcast: ASCO data that wowed, rising stars blurring the line between traditional and tech-enabled drugs, plus this week’s headlines

This week on "The Top Line," we discuss our special report on the rising stars in the digital health sector. We also talk about surprising data from this weekend’s ASCO meeting and the week's other big headlines. Plus, we're back in person at the biggest conferences!

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Chutes & Ladders—Forte taps Chen to be president, CSO amid shareholder dissent

Forte taps Chen to be new president and CSO amid dissent from top shareholder. Goldstein continues his tour of ocular biotechs, jumping to Aurion. Third Harmonic brings aboard Conner as CMO to guide the development of its hives program.

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Fierce Pharma Asia—Enhertu's standing ovation; Tessa's $126M CAR-T financing; Samsung's manufacturing deal

AstraZeneca and Daiichi Sankyo's Enhertu showed strong data in a new breast cancer category: HER2-low. CAR-T specialist Tessa Therapeutics raised $126 million in series A funding. Samsung Biologics and Novartis teamed up for the first time. And more.

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Resources

eBook: Streamline HCP interactions management

Don’t miss these critical considerations when evaluating your HCP interactions management program.

White Paper: 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.

eBook: Download the Cell Therapy Handbook

Explore the new cell therapy handbook from Thermo Fisher Scientific.

Whitepaper: Gain Operational Speed and Velocity by Sharing Quality Incident Data

Quality operations guide your organization through regulatory compliance processes and safeguard your products, processes, and reputation. But your team is capable of so much more. Quality incident data and processes can be a driver of significant business value if shared with other stakeholders.

Whitepaper: Medical Affairs Metamorphosis: Trends Driving Change & What They Mean

Recent trends are driving big changes in Medical Affairs. This paper explores why, and what MA teams can do to stay ahead of the curve.

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?

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

Orally Inhaled & Nasal Drug Delivery: A Pipeline of Opportunities

Whitepaper: Intranasal Drug Product Development: Formulation to Manufacturing

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

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