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March 08, 2018

Today's Rundown

Featured Story

Roche promotes Pao to replace departing pRED head Reed

John Reed, M.D., Ph.D., is leaving Roche for personal reasons. William Pao, M.D., Ph.D., has stepped up to fill the head of Roche pharma research and early development (pRED) post vacated by Reed.

Top Stories

Pfizer calls it quits on CytomX deal as research comes to naught

Pfizer has been slowly backing out of its $635 million armed antibody tech deal with CytomX over the last few months, and during the biotech’s financials posted late yesterday, the final nail was drilled into this fruitless pact.

JW Therapeutics, a China CAR-T biotech formed by Juno and WuXi, gains $90M series A

Back in 2016, Juno Therapeutics (now owned by Celgene) and WuXi AppTec joined forces to create a new CAR-T biotech. Today, it got off a meaty $90 million series A with Chinese backing as it eyes clinical trials of its new cancer therapy.

Sanofi, Evotec in major infectious disease R&D transfer and license deal

Big Pharma Sanofi and German CRO-biotech drug discovery hybrid Evotec are penning a deal that will see Sanofi license out a host of infectious disease assets to the biotech, with 100 staffers also moving into its R&D engine.

Merck KGaA BTK inhibitor beats placebo in phase 2 multiple sclerosis trial

A phase 2a trial of Merck KGaA’s BTK inhibitor evobrutinib has hit its primary endpoint. The prospect chalked up the win by reducing gadolinium-enhancing T1 lesions by more than placebo, but Merck has yet to quantify the difference or say how it fared against rival multiple sclerosis drug Tecfidera.

VBL Therapeutics sees Avastin-VB-111 phase 3 combo flop in brain cancer

Israeli biotech VBL Therapeutics has joined a long and depressing line of companies that have failed to move the needle in a test against a form of aggressive brain tumor.

Parkinson’s startup Prevail raises $75M for gene therapy programs

The biotech will use the funds to advance programs for Parkinson's and other neurodegenerative diseases caused by lysosomal dysfunction.

Cyteir reels in $29M to target DNA repair in cancer, autoimmune disease

The funding will propel Cyteir's lead program, small-molecule RAD51 inhibitors, into clinical trials in cancer, as well as boost its preclinical work in autoimmune disease.

Helix to grow DNA test ‘app store’ on first close of planned $200M series B

As next-generation technologies continue to drive down costs for DNA sequencing, DNA tests have become more accessible to the masses. Illumina spinout Helix, which runs an online marketplace for such tests, has held the first close of a planned $200 million funding round.

Resources

[Webinar] Driving Market Access through Patient Advocacy: Trends & Opportunities

There’s no magic bullet to successful access but insights from patient advocates and industry experts can help shape future strategies. Learn how in this webinar. Sign up now!

[Whitepaper] Medical Device Innovation: Are You Outrunning The Competition?

The competitive landscape in medical device R&D is tough. And simply investing in R&D is no guarantee for profitability. So how do you accelerate time-to-market?

[Whitepaper] How Life Sciences Companies Use Box for Regulated Content in the Cloud

Learn how biopharma and medical device companies can now collaborate on, manage and distribute regulated clinical, lab and manufacturing content in Box. That means all of your content is standardized on a single content repository that meets regulatory and compliance standards, so you can eliminate inefficient silos, enable seamless collaboration and accelerate the validation process.

[Whitepaper] CFO's, Is This Part Of Your Corporate TO DO List?

Employee stock option trading & administration, Restricted stock transactions (Rule 144), Affiliated trading plans (10b5-1), Directed share plans, Equity comp plan administration — private to public

[Whitepaper] Choosing the Right Solution: Improving the Site Feasibility Process

Selecting the right sites to conduct your clinical trials will determine the success or failure of meeting your enrollment goals.

[Whitepaper] How Do Sponsors Ensure Quality in Global Clinical Trials?

Global clinical trials are the trend and gaining in popularity, but running a global trial is not a straightforward process. This white paper explores some of the challenges associated with global clinical trials and considerations for ensuring that the collected data comply with the trial's overall objectives.

[Webinar] Validating a 7 Day Membrane Filtration Sterility Test using Celsis®

Join us as we discuss how Charles River Celsis® helped Labor L+S AG validate a 7-day membrane filtration sterility test using existing protocols.

[Infographic] Evolution of Flexible Commercial Biologics Manufacturing

Learn how Catalent Biologics is paving the way for flexible biologics development and manufacturing through advanced technologies and fully integrated multi-product facility.

[eBook] Developing Site-specifically Modified ADCs: Using a Chemoenzymatic Approach

Download the eBook to get articles from various Elsevier journals highlighting developments in ADC technology.

[Article] Optimizing titer and use of a specific enzyme for generating a fully processed antibody

Learn how cell development and process scale-up can be optimized for antibodies requiring additional processing.

[Webinar] Within-Subject Clinical Trials: Intro to New Methods & Stat. Models

In this webinar, we will introduce the rapidly-evolving within-subject clinical trial (WSCT) methods for early phase evidence generation that require fewer people, less time, and usually less funding than traditional early phase methods.

Events

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