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June 12, 2019___

Today's Rundown

Featured Story

Sobi to buy Novimmune R&D assets, lay off 90 staff 

Sobi is exiting drug discovery and early research outside of hematology and immunology, putting 90 people out of work. It also announced the $518 million acquisition of immunology R&D capabilities from Novimmune. 

Top Stories

ADC Therapeutics bumps up series E by $76M, prepares lead drug for 2020 filing

ADC Therapeutics has expanded its series E by $76 million, extending its runway through the end of 2020 when it plans to file its lead program for FDA approval.

BIO: CEOs weigh in on biotech companies going public earlier and earlier

We caught up with some CEOs at this year’s BIO International Convention to get their take on increasingly large biotech IPOs and an increase in companies going public at earlier stages.

[Sponsored] Advancing a Diabetes Multi-Registration Program

Read the case study to learn how Covance helped a sponsor who wanted to get all sites for a 2,700 patient study up and running as quickly as possible. Covance leveraged their proprietary historical investigator performance database to see which investigators outperformed their peers on a consistent basis and had the capacity to run multiple studies at the same time.

Prelude Therapeutics nabs $60M series B, gains biopharma veteran as CMO

Prelude Therapeutics has completed a $60 million series B round, boosting its total raised to $95 million as it looks to deepen its cancer work into the clinic.

Synlogic, Ginkgo expand synthetic biology research pact

Synlogic has tapped Ginkgo Bioworks for a cell programming platform to support development of its pipeline of engineered microbes. 

Could a pufferfish toxin be a safe alternative to opioids?

Scientists have been exploring the potential of pufferfish toxin in pain management. Now, researchers at Boston Children’s Hospital believe they have developed a feasible method for delivering the drug as a painkiller.

Resources

[Webinar] Why do US sponsors come to Russia? New options for clinical trials.

Fast and cost-efficient patient-enrollment,100% success strategy for obtaining a CTA, unified market authorization across the EEU countries. Find out the key compelling reasons to conduct studies in Russia.

[Whitepaper] Agile Competitive Intelligence Strategies For Healthcare

What is agile competitive intelligence, and how can it help take market research to the next level?

[POCKET GUIDE] Reference and Literature Management Made Easy

Get 5 quick tips for faster research and better results!

[Report] Precision medicine from concept to clinic

In this publication, Blue Latitude Health maps the journey of stakeholders impacted by the rise of precision medicine today. Download the report.

[Whitepaper] Flow Chemistry: A Scale-Up Solution for Modern API Development & Manufacturing

Increase Safety & Flexibility with Flow Chemistry

[On-Demand Webinar] Lessons Learned Implementing an End-to-End RIM Solution

IONIS shares best practices for implementing an end-to-end RIM solution in this on-demand webinar. Watch now.

[Whitepaper] Site-specific, Patient-centered and Whip-smart: Enrollment Assistants Adapt to a Shifting Landscape

Increasingly complex clinical trials place a tremendous burden on study sites, exacerbating already-troubling recruitment and enrollment issues. Overwhelmed, many sites may not be up to the task or have the appropriate infrastructure, creating costly delays that keep new therapies from patients.

[Case Study] Clinical Supply Management

Download the case study to learn about the clinical supply management tools that helped a small sized pharma company during phase III of a multi-arm oncology study.

[Video] Demand Led Services and Clinical Supply Efficiency

Watch a short video on demand led supply model. It is designed to meet the needs of patients, clinical sites, clinical team and sponsors and results in shorter lead time, less waste, less stock out risk and no booklet labels.

[eBook] Strategies for Efficient Clinical Supply Management and Forecasting

Download the eBook to explore a proactive approach for clinical supply management.

[Whitepaper] Choosing the Best Sterile Dosage Form for Phase I Clinical Supply Needs

Choosing the Best Sterile Dosage Form for Your Phase I Clinical Supply Needs.

[Whitepaper] Delivering oral solid dose product to Phase I Clinic in 14 weeks

Designed with speed & flexibility,Quick to Clinic™ for Oral Solid Dose helps deliver products to Phase I Clinic in as little as 14 weeks.

[Paid Marketplace] Accelerating DoD’s Fielding of Prototypes for Medical Countermeasures

MCS is currently seeking broad-based industry/academia collaboration on research and prototype work in technical areas related to developing medical countermeasures for the Joint Warfighter.

Events