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Today's Rundown

    

Thank you to Janssen Oncology for sponsoring Fierce Biotech's ASCO coverage.

 

 

Featured Story

AdComm member quits over FDA approval of Biogen's Aduhelm

A member of the advisory committee that recommended rejecting Biogen’s aducanumab has quit over the FDA’s approval of the drug, Stat reports. Washington University neurologist Joel Perlmutter left “due to this ruling by the FDA without further discussion with our advisory committee.”

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Top Stories

AbbVie snags another preclinical Parkinson's program with $17M Caraway pact

Caraway Therapeutics wasn’t going to partner off its Parkinson’s program for a few more years, but AbbVie came along with an offer it couldn’t refuse. The Big Pharma handed over $17 million upfront for the option to license Caraway’s program targeting TMEM175, with the promise of $250 million more.

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Editor's Corner—The FDA's decision on aducanumab will drag down innovation for years to come

The amyloid theory just won’t die. In fact, by approving Biogen's new Alzheimer's disease drug, the FDA has just resurrected it for a long and healthy future. This is great news for Biogen, but it will decimate Alzheimer’s research, faith in the agency and the healthcare budget for decades to come.

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Sponsored: In a Year of Crisis, Maryland Biotech Responds with Leadership

Prior to the pandemic, nearly a quarter of Maryland’s biopharm and medical tech companies focused on infectious diseases. As COVID-19 spread, dozens of Maryland companies joined the global response.

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Kojin bags $60M to exploit weakness of drug-resistant cancers

Kojin Therapeutics has raised $60 million to use iron-dependent cell death to treat drug-resistant cancer. The series A round positions the biotech to build on the work its scientific founders did at institutions including Harvard University and Dana-Farber Cancer Institute.

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Sponsored: Innovative POC MATLOC Digital Device for CKD

Health Logic Interactive is working on advanced technology called MATLOC that has the potential to revolutionize the Chronic Kidney Disease treatment space from the ground up.

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Alcyone Therapeutics picks up $23M in hopes of being a star in treating CNS disorders

Alcyone Therapeutics looks to break into the severe CNS disorder landscape, include Rett Syndrome, with $23 million in funding and 12 adeno-associated virus gene therapy programs.

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Byondis ready to link up to bring Herceptin-booster to market after phase 3 win

A new linker drug from Byondis that boosts the targeting power of Roche's Herceptin helped patients with a certain type of advanced breast cancer live longer without disease progression in a phase 3 clinical trial. The Dutch biopharma is now ready to consider linking up with a partner to bring the therapy to market. 

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Boehringer Ingelheim taps into Lifebit's AI for global disease surveillance

Boehringer Ingelheim's ambitious project with AI developer Lifebit aims to use natural language processing to help chart a course among new global outbreaks of infectious diseases.

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Resources

Whitepaper: How to Launch a Successful BYOD Strategy in Any Phase

For faster deployment, improved patient engagement, and better-quality data — go where your patients are. GO BYOD with Lunexis™ from Clinical Ink.

Paid Marketplace: Story of Success: Ashfield Healthcare Empowers Field Sales to Grow Market Share based on Data

Discover how Ashfield Healthcare uses the power of data and analytics to enable pre-call planning, inform sales rep actions and drive higher market share for its target pharmaceutical products.

eBook: Improving Diversity and Inclusion in Clinical Trials

Create a more diverse and inclusive clinical trial enrollment and engagement environment by learning the barriers to participation and the strategies to overcome them.

Whitepaper: Closed Cell Processing System Benefits for Cell & Gene Therapy

Autologous cell and gene therapy workflows involve isolating cells from an individual, engineering the cells, expanding and concentrating them, and infusing them back into the patient. Optimized automation of certain steps of the workflow may decrease hands-on time and the cost of the cell manufacturing process.

Guide: Your Guide to Overcome Inconsistent Clinical Data Standards

Learn how to develop a standards program that has your full team’s buy-in and improves the efficiency and quality of your clinical trials.

eBook: The New Standard: Virtual Study Training in Clinical Trials

The new standards in study training help sponsors and CROs reduce costs by 60%, cut training time by 50%, and start enrollment 55 days faster – learn more today.

Report: New research indicates an accelerated shift to decentralized clinical trials

New research indicates an accelerated adoption of decentralized clinical trials due to COVID-19.

Content Hub: Process Intensification Resource Center

A one-stop hub for Cytiva resources to support process intesification

Whitepaper: COVID-19 Survey report: The Lasting Impact on Outsourcing Decisions

How has COVID-19 impacted CRO/CDMO customer (dis)satisfaction and outsourcing decisions for pharma and biotech companies in 2021 and beyond?

Content Hub: Emerging Biotech Resource Center

A one-stop hub for Cytiva resources to support process development and manufacturing of your novel molecule

Content Hub: Remarque Systems Resource Hub

Remarque Systems consolidates data, then layers on visualization and automated metrics to generate consistent, actionable data insights in real-time. Click here for more info. 

eBrief: Drug Product Process Development: Ensuring a Consistent, High-quality Biologic

Learn about drug product process development challenges and risks, the difference between innovator and biosimilar drug product process development, and more during the drug product process development phase.

Whitepaper: Achieving a Successful Drug Product Technology Transfer

Get insights on key considerations for a successful tech transfer process for manufacturing a biologic drug product, including a case study on overcoming challenges in a process transfer for a sterile diluent.

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