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June 05, 2019___

Today's Rundown

Featured Story

Bristol-Myers unveils team to lead R&D after Celgene deal closes

Bristol-Myers Squibb has unveiled the new-look team that will lead its R&D group after the closure of its Celgene takeover. The Big Pharma is dividing the group up into early- and late-phase development, handing Celgene’s Rupert Vessey responsibility for the former and hiring Novartis’ Samit Hirawat to run the latter.

Thank you to Lonza for sponsoring this week's coverage of BIO.

Top Stories

BIO: In conversation with Sabrina Johnson, CEO of Daré Bioscience

Sabrina Johnson discusses her journey from a CNS-focused biotech to founding her own women's health company.

BIO: EpimAb bags $74M to push EGFR/cMET bispecific, build out pipeline

PHILADELPHIA—EpimAb Therapeutics reeled in a $74 million series B to build out its bispecifics pipeline and advance its lead program, an antibody that targets EGFR and cMET on track to enter phase 2 in 2020.

[Sponsored] How to Make the Most of Your Clinical Trial Data—All of it

Pharma and biopharma have endless data at their disposal. Why aren't they using it? Here's how to make the most of your data for clinical success.

Lung Therapeutics raises $36M to trial pleural effusion drug

Lung Therapeutics has raised a $36 million series C round to take a treatment for a serious complication of pneumonia through phase 2 studies.

Columbia University teams up with Deerfield for $130M R&D alliance

Venture capital firm Deerfield Management has committed up to $130 million for a long-term drug discovery collaboration deal with Columbia University.

Resources

[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.

[Executive Summary] Achieving a Successful Drug Product Tech Transfer

Download the executive summary to learn key considerations for a successful technology transfer for manufacturing drug products, including a case study on overcoming challenges in a process transfer for a sterile diluent.

[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.

Events