Selecta sheds staff and non-partnered gene therapies

Today's Big News

May 5, 2023

Acelyrin readies biggest biotech IPO so far this year with $540M upsized offering


AstraZeneca scraps pact with Riva-led Transgene in further blow to oncolytic viruses


Selecta lays off 25% as unpartnered gene therapies take a back seat


Boehringer Ingelheim to surf with Melbourne-based biotech in $181M neuropsychiatric therapy deal


Cellectis culls CAR-T cell therapy over cost of kick-starting crawling clinical trial


Chutes & Ladders—Cerevel CEO to exit as company nears inflection point

 

Featured

Acelyrin readies biggest biotech IPO so far this year with $540M upsized offering

In what looks set to be one of the biggest biotech IPOs of the year, Acelyrin has revealed that it’s expecting to raise $540 million to push its immune drug candidates through the clinic.
 

Top Stories

AstraZeneca scraps pact with Riva-led Transgene in further blow to oncolytic viruses

AstraZeneca is rowing back from its bet on oncolytic viruses. Four years after stepping up its presence in the immuno-oncology field through a five-asset pact with Transgene, the Anglo-Swedish drug developer has scrapped the partnership before moving a candidate into the clinic.

Selecta lays off 25% as unpartnered gene therapies take a back seat

An analyst has reiterated that Selecta’s portfolio is “promising” despite the biotech offloading a quarter of its workforce along with non-partnered gene therapy programs.

Boehringer Ingelheim to surf with Melbourne-based biotech in $181M neuropsychiatric therapy deal

Boehringer Ingelheim is heading out into the surf with Australia's Kinoxis Therapeutics in a $181 million biobucks deal to develop therapies for neuropsychiatric disorders.

Cellectis culls CAR-T cell therapy over cost of kick-starting crawling clinical trial

Cellectis has given up on its multiple myeloma CAR-T candidate UCARTCS1. With the phase 1 clinical trial two years behind schedule and heavy investment needed to accelerate enrollment, the off-the-shelf cell therapy specialist is stopping the study and focusing its resources on three other candidates.

Chutes & Ladders—Cerevel CEO to exit as company nears inflection point

Cerevel CEO Tony Coles, M.D., will be handing over the reins to Bain Capital’s Ron Renaud on June 12.

'The Top Line': Part 2 of a series on Narcan, the lifesaving nasal spray

This week on "The Top Line," we're continuing our miniseries on Narcan the nasal spray. It is the first naloxone product to be approved for use without a prescription.

Neuralink's animal research oversight board may pose conflicts of interest: Reuters

Already under fire for other aspects of its animal testing program, Neuralink is in the hot seat once again, this time for a Reuters report on potential conflicts of interest tied to the oversight board governing the animal research program.

Cigna boosts guidance as it reports $1.3B in profit in Q1 beat

The Cigna Group rounded out earnings for the large national insurers on Friday morning, where it reported $1.3 billion in profit for the first quarter of 2023.

After FDA rejection, Gilead's Hepcludex looks set for full EU nod

Six months after Gilead got a smackdown in the U.S. for its drug to treat hepatitis delta virus, bulevirtide has scored a regulatory win in Europe. The Committee for Medicinal Products for Human Use (CHMP) has given bulevirtide a thumbs up for patients with HDV and compensated liver disease.

Thermo Fisher lays off another 218 workers as 3 COVID test-making sites shutter

Just a few months after it began pruning back operations at a trio of its test-making facilities in San Diego, Thermo Fisher Scientific is now completely uprooting all three.

Fierce Pharma Asia—Astellas' eye drug buy; J&J's latest CAR-T deal; Sun's clinical hold

Astellas paid $5.9 billion to join the complement inhibitor battle in geographic atrophy. J&J put down $245 million upfront to partner with a CAR-T biotech with operations in China and the U.S. Sun Pharma's JAK inhibitor hit a partial clinical hold in alopecia. And more.
 
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'The Top Line': Part 2 of a series on Narcan

This week on "The Top Line," we're continuing our miniseries on Narcan the nasal spray. It is the first naloxone product to be approved for use without a prescription.

 

Resources

eBook

Decentralized Clinical Trials: The Complete Guide for 2023

Discover a game-changing approach to clinical research with Hybrid and Decentralized Clinical Trials (DCTs). Learn about the benefits, challenges, and key elements for success.
Research

How Lilly’s Legal and Library Services Empower Teams Across the Drug Development Pipeline

What role do the Library and Legal teams play in the drug development pipeline at Lilly? An import one – find out how.

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Medical Affairs Metamorphosis VI: The Changing Face of Stakeholder Engagement

This paper focuses on stakeholder engagement and how Medical Affairs teams’ responsibilities, goals, tools, and techniques are changing.
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Maximizing Clinical Trial Success

Strategies for Optimal Site Selection and Feasibility Research in Novel Therapies and Geographies
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eConsent: Flexible Consent Through Enabling Technologies

How can eConsent provide a more flexible approach to informed consent?

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Plan for scalable process liquid and buffer preparation

Preparation of critical process liquids and buffer components shifts resources away from core activities and can be filled with inefficiencies and risks that can increase time and costs across your workflow. Learn about the framework to help reduce your total costs beyond capital and operational expenditures and set a solid foundation for successful scale-up of buffer preparation.

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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.
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Key Clinical Supply Issues Sponsors Should Consider with their CRO

As sponsors increasingly look to CROs to support their clinical studies, making and addressing certain clinical supply considerations at the outset of the relationship can reduce the risk of potentially unforeseen impact to budget and time later. Discover key issues sponsors should consider to help their CRO or partner of choice better understand their clinical supply needs.

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Specialized Expertise for Management of Clinical Supply Budgets

For sponsors, cost is a key concern when it comes to managing the supply of their clinical trials. A financial project analyst (FPA) is a specialized expert who can help control clinical supply costs and keep the project within budget. Explore the critical role that a Financial Project Analyst plays in clinical trial supply and budget management.
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Clinical Supply Solutions for the Asia-Pacific Region

Learn how Catalent’s extensive network across APAC can meet a wide range of clinical supply needs for sponsors conducting trials within the region.
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Designing an Optimal APAC Clinical Supply Chain

Discover key considerations that every trial sponsor should know when navigating the complex clinical supply distribution landscape across Asia-Pacific.
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Roles and Responsibilities of Specialized Clinical Supply Experts

How can specialized expertise help you optimize your clinical supply chain? Learn about the roles and responsibilities of unique experts such as clinical supply management, project management, and financial project analysis.
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Supply Services to Support Clinical Trials in Japan & Beyond

Explore Catalent’s newest clinical supply facility in Japan, including the comprehensive services & solutions it offers to help support trials both in-country & around the world.
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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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