Caribou CAR-Ts take on the competition

Today's Big News

Jul 14, 2023

Hungry for more, Lilly tops off weight loss pipeline with $1.9B deal to acquire Versanis


Nominations for Fierce Biotech's 2023 Fierce 15 close TODAY—last day to enter


CAR-Ts are 'working wonders.' Caribou CEO says latest lymphoma data show they can be even better 


Roche lining up potential $7B Roivant licensing deal to join Merck in bowel disease race: WSJ


Industry, not NIH, fronts most of the cash for clinical trials: report


Apogee, Sagimet overshoot IPO expectation as both biotechs land on Nasdaq


Nymox fights back mutiny, defending its actions and throwing jabs at former execs


Theseus struggles to escape toxicity labyrinth as safety signal sinks cancer program and share price


Korro Bio merges with off-pitch Frequency, hits Wall Street with $117M


CEL-SCI's multi-decade Multikine journey extends with FDA request for new trial


Chutes & Ladders—Flagship plucks former BMS R&D exec Rupert Vessey to be chief scientist


'The Top Line': The state of digital phenotyping, plus this week's headlines

The Top Line Podcast: don’t miss out on the newest episode where we discuss ASCO data, rising health tech stars, and more. Listen now.

 

Featured

Hungry for more, Lilly tops off weight loss pipeline with $1.9B deal to acquire Versanis

Eli Lilly just can't get enough weight loss therapies or acquisitions to bolster its pipeline. The Indianapolis-based company has signed off on a $1.92 billion deal, which covers an upfront payment and potential milestones, for Boston-based Versanis and lead asset bimagrumab.
18-19
Jul
July 18-19, 2023 | Jersey City, NJ
 

Top Stories

Nominations for Fierce Biotech's 2023 Fierce 15 close TODAY—last day to enter

Fierce Biotech is once again seeking your nominations for the best, most exciting and innovative private biotechs.

CAR-Ts are 'working wonders.' Caribou CEO says latest lymphoma data show they can be even better

Caribou Biosciences CEO Rachel Haurwitz, Ph.D., has nothing but praise for the autologous CAR-T cell therapies that have provided another option for lymphoma patients. It’s just that her CRISPR gene editing company would like to do it better with an off-the-shelf approach.

Why this boutique biotech agency is the future of clinical recruitment

Using behavioral data science and social algorithms, this boutique biotech agency creates therapeutic-specific and patient-centric content to bypass traditional channels and speak directly to patients.

Roche lining up potential $7B Roivant licensing deal to join Merck in bowel disease race: WSJ

Is Roche ready to bet $7 billion to challenge Merck & Co. for a red-hot bowel disease space? That is the assertion of the Wall Street Journal, which reports that the Swiss drug developer is in talks with Roivant Sciences about acquiring the rights to an ex-Pfizer candidate.

Clinical trial technologies support recruitment efforts

Hear why sponsors should equip sites with technology that makes securely capturing pre-screening, recruitment, and enrollment data easier.

Industry, not NIH, fronts most of the cash for clinical trials: report

A new analysis shows that the NIH spent $8.1 billion on phased clinical trials of drugs approved between 2010 and 2019—about 10% of what the pharma and biotech industry committed over the same period.

Apogee, Sagimet overshoot IPO expectation as both biotechs land on Nasdaq

If the sight of two biotechs hopping onto the Nasdaq on the same day isn’t enough of a sign that the freezing IPO waters may be thawing, then the fact both companies have overshot expectations may help warm up sentiment further.

Nymox fights back mutiny, defending its actions and throwing jabs at former execs

Nymox Pharmaceutical has spoken out against two ex-leaders who formed a rebellion based around the company’s refusal to accept a proposed partnership. The biotech said the proposal would have created debt and blamed the two leaders for pushing the deal for their own personal benefit.

Theseus struggles to escape toxicity labyrinth as safety signal sinks cancer program and share price

A safety signal has derailed Theseus Pharmaceuticals’ quest to develop a gastrointestinal stromal tumor treatment. The dose-limiting toxicity drove the biotech to stop enrollment and end development, sending its stock down 65% and leaving its hopes of navigating the R&D maze resting on other assets.

Korro Bio merges with off-pitch Frequency, hits Wall Street with $117M

Korro Bio is hitting Wall Street via reverse merger with Frequency Therapeutics, adding $117 million in new financing as well. Frequency has struggled this year after flunking a phase 2 trial of its hearing loss med, spurring reprioritizations and layoffs.

CEL-SCI's multi-decade Multikine journey extends with FDA request for new trial

CEL-SCI will need to conduct another clinical trial for its Multikine head and neck cancer drug—which the company has long trumpeted as a promising treatment, despite data that says otherwise.

Chutes & Ladders—Flagship plucks former BMS R&D exec Rupert Vessey to be chief scientist

Former BMS R&D czar Rupert Vessey will be the first chief scientist at venture creation firm Flagship Pioneering. Eisai's Ivan Cheung to depart after Leqmebi nabbed full FDA approval. Pfizer CEO Albert Bourla to lead international trade group.

'The Top Line': The state of digital phenotyping, plus this week's headlines

This week on "The Top Line," we discuss the state of digital phenotyping, plus the vaccine patent lawsuits, the smallest insulin pump, and the rest of the week's headlines.

FDA rolls back warnings of death risks for paclitaxel-coated balloons, stents

The agency was previously leery of some of the devices, recommending alternatives after analyses showed possible increases in long-term death risks.

UnitedHealth kicks off Q2 earnings with $5.5B in profit, double-digit revenue growth

Healthcare giant UnitedHealth Group kicked off insurer earnings for the second quarter Friday morning, when it reported $5.5 billion in profit alongside double-digit revenue growth.

Fierce Pharma Asia—BeiGene, Novartis' TIGIT divorce; Takeda's FDA withdrawal; Eisai's new Alzheimer's lead

Novartis walked away from BeiGene's TIGIT inhibitor. Takeda pulled the FDA filing for its dengue vaccine after the FDA requested more data. Eisai's Alzheimer's chief Ivan Cheung is handing the baton to group CEO's son. And more.
 
Fierce podcasts

Don't miss an episode

'The Top Line': Digital phenotyping, plus this week's headlines

This week on "The Top Line," we discuss the state of digital phenotyping, plus the vaccine patent lawsuits, the smallest insulin pump, and the rest of the week's headlines.

 

Resources

Research

Develop a cost-effective cGMP chemical sourcing strategy

The right sourcing strategy can help save of millions of dollars—learn about developing a strategy for sourcing the cGMP chemicals critical to your processes.
Whitepaper

Discovering High-Affinity, Functional Anti-GLP-1R Antibodies

Learn how a GPCR-focused library with a cell-based biopanning strategy led to the discovery of 13 high-affinity and selective anti-GLP-1R antibodies with highly developable therapeutic properties.
eBook

Medical Affairs Metamorphosis

This eBook identifies the trends driving major change in the Medical Affairs (MA) function. It also outlines the strategic and tactical implications for MA leaders and team members.
eBook

6 Tools Trial Sponsors Need to Take Action Earlier in Enrollment

Take a look at the reporting tools sponsors need to access insights earlier in the clinical trial enrollment funnel, so you can take informed actions.
Whitepaper

Enhance the cost-effectiveness of your GMP chemical supply chain

Learn how to develop a high-performing supply chain for cGMP chemicals used throughout your bioprocessing workflows.
Whitepaper

Running Decentralized Trials at Scale

Explore how clinical supply can be scaled up as decentralized programs progress, and how technological solutions can accelerate trial deployment.
Whitepaper

Questions You Need to Ask Your CRO About Clinical Supply

Planning on using a CRO to support your next clinical study? This infographic outlines critical areas to address at the start of the relationship in order to ensure that budget and timelines keep on track for the duration of the trial.
 

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