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Today's Rundown

Featured Story

Precision reacquires rights to allogeneic CAR-Ts from Servier

Precision BioSciences has reacquired the global rights to its allogeneic CAR-T programs. The deal with Servier gives Precision control of assets including a clinical-phase CD19 candidate that it sold off back in 2016 for $105 million.

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Top Stories

EMA starts review of GSK and Vir's COVID-19 antibody therapy

The European Medicines Agency (EMA) has begun reviewing GlaxoSmithKline and Vir Biotechnology’s anti-SARS-CoV-2 antibody. The EMA is assessing the candidate in COVID-19 patients who do not require oxygen supplementation and are at high risk of disease progression.

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Rapha Capital Management launches $100M life science VC fund with an eye on early science

Life science venture capital firm Rapha Capital Management has launched its first managed venture capital fund with a target raise of $100M and “solely focused” on investment in early-stage life science companies.

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Sponsored: MyData-TRUST is becoming the undisputed world leader in Data Protection for Health Research

34.4% of worldwide data breaches come from the healthcare sector. Data Protection is no longer just a compliance issue, but a strategic topic. MyData-TRUST was created to support the sector.

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AI drug prospector Recursion bumps IPO up (again) to $374M

Recursion Pharmaceuticals ramped up its IPO target from $100 million to $306 million earlier this week, but the artificial intelligence biotech is scratching that plan. Now, it’s aiming to raise $374 million in its Nasdaq debut by adding 4 million more shares to the offering.

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Regenerative medicine biotech Surrozen aims for the Nasdaq in $212M SPAC deal

After banking two $50 million venture rounds about a year apart, Surrozen is ready to hit Wall Street. The company plans to go public via SPAC in a deal worth up to $212 million. If all goes to plan, the deal will close in the third quarter and the combined company will receive $92 million from the SPAC, as well as $120 million through a private round. It will list on the Nasdaq under the ticker “SRZN.”

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The dogtor is in: Study finds dogs can sniff out COVID-19 with 96% accuracy

A new study led by researchers from the University of Pennsylvania found that mass COVID-19 screening could be solved by a quick sniff from a dog—a dognostic test, if you will.

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Scientists make long-lasting but controversial human-monkey embryos for medical research

Scientists from the Salk Institute and China’s Kunming University of Science and Technology have created chimeric embryos by injecting human stem cells into monkey embryos. The approach could boost research into early human development, as well as drug discovery, the team said, but it also raised ethical questions.

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Fierce Pharma Asia—Sanofi's €400M vaccine site; BeiGene-Novartis' PD-1 data; India's remdesivir export ban

Sanofi laid out plans for a €400M vaccine site in Singapore. BeiGene is eyeing global filings for its Novartis-partnered PD-1 inhibitor after survival data in previously treated non-small cell lung cancer. India banned exports of Gilead's remdesivir as local demand surges. And more.

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Chutes & Ladders—Lilly, bidding adieu to Shah, lines up Apple exec as CDO

GSK's vaccine research lead is hitting the exit to run R&D at microbiome company Viome. Eli Lilly tapped an apple exec as its new CDO. And Gilead's oncology head is flying the nest for a post at biotech investor MPM.

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Resources

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

Whitepaper: Top 5 Benefits of a Cloud ELN

Discover the benefits of a cloud-native ELN that delivers better performance, security, connectivity, total cost of ownership PLUS sub-second search results through even the largest data volumes.

Annual Report: Why do US pharma come to Russia for clinical trials.

Find out why more than 400 clinical trials annually are initiated in Russia by US and EU pharma in the free annual report by OCT Clinical.

Special Report: The Marketer’s Guide to Taking the Vaccine Viral

Access this guide for the latest insights into how marketers can use data, technology, and personalized messaging to build vaccine confidence and drive successful immunization efforts.

Content Hub: How to improve the virtual work you do every day

We enable virtual work — offering over-time sessions where participants are more focused, insights are more diverse and business goals are met.

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.

Whitepaper: Roche to pick up GenMark Diagnostics in $1.8B infectious disease testing deal

Roche has inked a $1.8 billion, all-cash deal for GenMark Diagnostics, to acquire its molecular tests designed to screen patient samples for multiple infections simultaneously.

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. 

Whitepaper: Overcoming the hurdles of Real-World Data Access through a federated global network

Those wishing to unlock RWD’s true value must have access to a variety of data sources/types and the technological capabilities to use the data to uncover meaningful insights.

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.

Executive Summary: Manufacturing Strategies to Effectively Industrialize Autologous Cell Therapies

Autologous cell therapies have seen propelled growth since 2017, with the spotlight on the first FDA approval of a chimeric antigen receptor (CAR) T cell immunotherapy, Kymriah® (tisagenlecleucel), for the treatment of relapsed/refractory B-cell acute lymphoblastic leukemia.

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.

Whitepaper: The Art of Recognizing Clinical Supply Risk Factors

In a BioPharma Dive industry survey, planning and forecasting were identified as top concerns for trial sponsors. In response to this need, the CSM team at Catalent has developed a methodology for identifying, evaluating, and proactively managing the inherent risks involved in clinical trial supply chain management.

eBook: Expecting the Unexpected: Strategies for Efficient Clinical Supply Management and Forecasting

Learn how to drive excellence within the forecasting process and utilize forecasting throughout the clinical study to better plan clinical supply budgets and project timelines. Explore how to identify potential supply-related issues before they can negatively impact your study.

Events