LGBTQ+ progress in biotech: 'We're getting there'
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Today's Rundown

Featured Story

Adicet soars on early responses to gamma delta CAR-T therapy

Adicet Bio has laid down a marker for the nascent gamma delta CAR-T cell therapy space, reporting its off-the-shelf candidate ADI-001 triggered responses in a small clinical trial of B-cell non-Hodgkin lymphoma patients. Shares in Adicet jumped 45% to above $14 in premarket trading.

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Top Stories

Investors punish Aeglea for missed rare disease secondaries, sending stock spiraling despite primary endpoint success

Aeglea BioTherapeutics found itself in an unusual position going into the readout from its pivotal rare disease clinical trial. With Aeglea expected to meet its primary endpoint, investors were focused on whether it could show clinical improvement of a secondary measure—and were swift to punish the stock when it fell short of expectations.

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'We're getting there': LGBTQ+ progress in biotech lingers in the 'diagnose' stage

The biotech industry is "getting there" in terms of advancing LGBTQ+ inclusion, but it's an effort that remains in the early innings. Fierce Biotech spoke with more than 20 LGBTQ+ leaders in biopharma to learn where the industry stands on incorporating the LGBTQ+ community into its diversity and inclusion work.

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Biohaven pain spray aces test as C-suite shake-up sees incoming CFO, chief in chairman role

Biohaven is eyeing filing for approval early next year for its experimental pain spray after new data showed it hit its primary endpoints in a phase 3 test.

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Gilead-partnered Goldfinch Bio snags 13-year Ardelyx vet to lead scientific operations of kidney assets

Goldfinch Bio hopes a 13-year Ardelyx veteran can help it advance mid-stage and early-phase kidney disease drugs. Jeff Jacobs joins the Gilead-partnered biotech after helping Ardelyx get its own kidney disease drug approved in autumn 2019, but the company has been mired by a recent rejection for the same drug and mass layoffs.

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BenevolentAI to take drug discovery tech public in Europe's largest SPAC deal, valued at €1.5B

In the course of its combination with special purpose acquisition company Odyssey—which went public in a 300 million euro IPO of its own earlier this year—BenevolentAI will rake in up to 390 million euro in net proceeds.

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AstraZeneca weighs spinning out COVID-19 products into separate company: Bloomberg

AstraZeneca recently bundled its COVID-19 vaccine and antibody treatment into a separate division. But there’s a chance that the new unit might not stay with the British drugmaker for long, as the firm is reportedly considering various options including a potential spinoff, Bloomberg reported.

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Black patient inclusion in clinical trials improves, but Asian, Latino and other groups 'significantly' underrepresented

Clinical trials had more Black patients in the past decade, but studies of investigational drugs continued to underrepresent patients from Asian, Latino, Hispanic and Native American backgrounds. Clinical development data provider Phesi analyzed trials that began in the past decade, sifting through data on 1.3 million U.S. patients.

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Improving CAR-T cell therapies for cancer by targeting a protein 'brake'

CAR-T cells to treat cancer have precious little time to proliferate in the body, which often limits their anti-tumor efficacy. A team at the Curie Institute pinpointed the protein SOCS1 as an inhibitor of CAR-T expansion and survival and suggested it could be targeted to improve T-cell therapies.

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Resources

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A variety of genetic analysis methods are valuable in ensuring that ex vivo human cells to be used for cell-based therapies are correctly identified, have the correct characteristics, and are free of contaminants.

Research: How Buffer Prep Services Alleviate Sudden Spikes in Campaign Volume

Learn how a CDMO partnered with Thermo Fisher Scientific to manage high-volume process liquid and buffer preparation scale-up. Download the free case study from Thermo Fisher Scientific

Whitepaper: Modernizing Key Clinical Trial Processes with Artificial Intelligence

This whitepaper addresses where AI can make the biggest impact in clinical trials. The stakes are too high for patients to leave decision-making to machines, but AI can lend administrative support that empowers staff and medical experts alike to carry out their jobs more effectively.

Whitepaper: Medable was able to cut costs in multiple clinical trials by over US$25,000,000

Find out how to improve clinical protocol adherence, and thus patient outcomes, by 15%+ with Medable’s latest White Paper.

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Learn how to elevate your omnichannel marketing strategy with Next Best - a combination of data and analytics, deployed to facilitate decision making.

Webinar: The Faster Path From Pre-Filled Syringe to Auto-Injector

Ypsomed and Catalent Biologics experts discuss strategies for integrated PFS manufacturing and auto-injector assembly to accelerate timelines and more in this webinar.

Whitepaper: Formulation Strategies When Transitioning From Vial to PFS

Learn how formulation development for a PFS affects manufacturing to drive the industry toward optimizing delivery of injectable products and, ultimately, improving patient care.

2021 Report: Clinical Trial Management in a Post-Pandemic World

New market research provides valuable insight into the impact of adaptations made in clinical trials during the pandemic.

Whitepaper: Enhance the cost-effectiveness of your cGMP chemical supply chain

Learn how to develop a high-performing supply chain for cGMP chemicals used throughout your biologics workflow. Download the free whitepaper from Thermo Fisher Scientific

eBook: Get solutions to market faster

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