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April 06, 2018

Today's Rundown

Featured Story

Body blow for Incyte as Merck-partnered melanoma trial bombs

The combination of Incyte’s epacadostat and Merck & Co.’s Keytruda was supposed to pose a major threat to rival Bristol-Myers Squibb’s melanoma franchise—but the data tell a different story.

Top Stories

Unity files for $85M IPO to take anti-aging drugs into phase 1

Unity Biotechnology has filed for an $85 million IPO. Hitting the target would bring the preclinical anti-aging startup’s fundraising haul up toward $300 million and set it up to move two assets into the clinic.

Novo moves into sickle cell with $400M EpiDestiny deal

Novo Nordisk has moved into sickle cell disease through a licensing deal with EpiDestiny. The $400 million deal gives Novo worldwide rights to an epigenetic treatment of the disease that is closing in on the start of a phase 2 trial.

[Sponsored] Personalized Medicine Requires Personalized Measurement

How we measure outcomes will evolve from applying one solution to finding an empirical basis for a highly customized application of all of them. Personalized medicine needs a more personalized approach to measurement. Read more.

Hydrogel delivery enables long-lasting, ‘flare-responsive’ arthritis treatment

Injectable drugs used to treat inflammatory arthritis are usually cleared quickly from joints, limiting their effectiveness. A PureTech startup is developing an immune-responsive hydrogel system that releases a corticosteroid into arthritic joints based on their level of inflammation.

EuroBiotech Report—Sofinnova’s fund, ITB bags $67M, Nanovector delay, AstraZeneca’s I-O deal and more

In this week's EuroBiotech Report, Sofinnova Partners raised €275 million on later-stage bets, while ITBMed raised $67 million. Meantime, Nordic Nanovector delayed a pivotal lymphoma trial readout. 

FiercePharmaAsia—U.S.-China trade battle, Takeda-Shire deal insight, China’s generics push

A long list of biopharma products from China are proposed targets for additional U.S. tariffs, analysts now think the Takeda-Shire deal is "more likely than not," China puts forward a policy package that favors generics over brands and more.

Chutes & Ladders—Celgene COO abruptly resigns amid immunology setbacks

Celgene COO Scott Smith steps down after recent setbacks, former Kite leaders Belldegrun and Chang are back at a new CAR-T shop, former GSK Dermatology executive Rubenstein is among several C-suite hires at Dermavant, plus more hirings, firings and retirings throughout the industry.

Enrollment Showcase

Online Graduate Programs Designed for Your Career

Drexel University’s online graduate programs in biomedicine, clinical research, drug discovery, and molecular medicine were developed with working professionals in mind, providing you with the education, practical skills, and competitive edge you need to be successful in your career. Learn more.

Resources

[Whitepaper] 2018 Life Sciences Trends

What are the biggest trends in life sciences this year?

[Whitepaper] For Fixed-Dose Combination Manufacturing, Confidence Matters

Why does confidence matter when outsourcing Fixed-Dose Combination products? Download Halo Pharma’s white paper on the importance of product design, technology, and analyticals tools for FDC.

[Whitepaper] Not Like Everyone Else: Unique Challenges for Small Biopharma Companies

Small biopharma companies are conducting almost 50% of the clinical trials in the US today, yet they face unique challenges that large pharma do not. In this paper, we explore some of those challenges, and solutions that can reduce the pressure on small biopharma teams and timelines.

[Whitepaper] The Future of Life Sciences Events Management

Explore a new model for events management, and learn how to deliver more value.

[Video] So Many Choices: What’s the Right Biomanufacturing Strategy for Me?

Patheon's Stephen Lam reviews the formidable challenges and decisions facing biopharma manufacturing executives. Watch as he shares unique insights and perspectives and demonstrates how there is really no one-size-fits-all solution in biomanufacturing, regardless of company size.

[Meeting] AACR Annual Meeting 2018

How do you get your oncology therapy to the clinic? The path isn’t always clear. In vitro, ex vivo, xenograft, syngeneic, PDX, humanized models, immunology considerations, safety regulations – which do you need to plan for and when?

[Whitepaper] Digitizing the Global Life Sciences Supply Chain: The Critical Role of Digital Transaction Management

Life science companies are experiencing a significant transformation in how they bring new products to market.

[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] 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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