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Today's Rundown

    

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

 

 

Featured Story

Harvard's Kesselheim quits AdComm over FDA's Aduhelm approval

Harvard University professor Aaron Kesselheim, M.D., has become the third advisory committee member to quit over the FDA’s approval of Biogen’s Aduhelm. Kesselheim’s departure means the FDA has lost one-third of the permanent voting members of the committee in the days since the approval.

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Top Stories

Vertex’s rare lung disease drug hits phase 2 goal—but still winds up on the scrapheap

Vertex is ditching another prospect it was developing for a rare genetic disorder that can lead to liver and lung disease. The treatment beat placebo in a phase 2 study, but its effect was so small the company deemed it unlikely to “translate into substantial clinical benefit.”

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Eli Lilly, Roche's Alzheimer's prospects, including flops, boosted in light of FDA's Aduhelm approval: analysts

Eli Lilly and Roche have been riding high this week on the controversial approval of Biogen’s anti-amyloid Alzheimer’s drug Aduhelm (aducanumab), as its new low bar could help these Big Pharmas jump the finish line.

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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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Sanofi's treatment for rare anemia hits goal in 2nd phase 3

A second phase 3 clinical trial of Sanofi’s sutimlimab in people with cold agglutinin disease has met its primary endpoint. The success of the second clinical trial positions Sanofi to seek approval for the C1s inhibitor in the EU.

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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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Investor interest in Alzheimer’s ‘changed on the dime’ following FDA’s decision on Biogen’s aducanumab

The FDA's conditional approval of Biogen's Aduhelm has already spurred investor interest in Alzheimer's treatments currently in the clinic.

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FDA approves Medtronic's long-lasting Vanta spinal cord stimulator

Medtronic scored FDA approval for its latest spinal cord stimulation implant, with a non-rechargeable device promising up to 11 years of battery life.

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Making drug-resistant bacteria susceptible to antibiotics

Scientists at the New York University School of Medicine have uncovered an innate defense mechanism that protects bacteria from normally lethal doses of antibiotics. A drug inhibiting an enzyme called cystathionine gamma-lyase enhanced the effect of antibiotics in mice.

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Fierce Pharma Asia—Biogen, Eisai's Alzheimer's nod; Stemirna's $188M mRNA vaccine raise; China-made HER2 ADC

Biogen's Eisai-partnered aducanumab scored its controversial FDA nod for Alzheimer's disease. China’s Stemirna Therapeutics raised $188 million to advance its mRNA COVID-19 vaccine. China has approved its first homegrown antibody-drug conjugate, made by RemeGen. And more.

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Chutes & Ladders—FDA nod for Biogen's Aduhelm sees trio of AdComm members hit the exit

Ogilvy and McCann heavyweight Andrew Schirmer has joined Syneos Health's GSW New York as president. Three members of the FDA panel that argued against aducanumab have quit in the wake of the Alzheimer's drug's approval. Inogen, recently equipped with a new CEO, has tapped BD vet Stanislav Glezer, M.D., as its chief medical officer.

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Resources

Whitepaper: How the rapid shift to point-of-care is reshaping diagnostics

Learn how the diagnostics industry is being fundamentally transformed with point-of-care molecular testing.

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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