To view this email as a web page, click here

December 19, 2016

Subscribe

Our Team

Contact Us

FierceBiotech Logo

 

Today's Rundown

  1. Loxo sets clock ticking on filing for first-in-class cancer drug

  2. Bankrolled by Chinese VCs, ex-Sanofi execs buy Cambridge antibody shop to create global immuno-oncology startup

  3. Northern Biologics merges with Mosaic Bio as Versant, Celgene boost involvement

  4. Sanger spinout gets $10M to work on live bacteriotherapies

  5. Purdue inks Shionogi collab on constipation med as it awaits FDA approval

  6. MicroPort invests in Lombard, lands rights to stent grafts

  7. Matt Kapusta named CEO of gene therapy pioneer UniQure, its third leader in a year

Featured Story

Loxo sets clock ticking on filing for first-in-class cancer drug

Loxo Oncology reckons it could be just a year or so away from being able to file for approval of its lead drug, just months after reporting phase 1 data.


Top Stories

Bankrolled by Chinese VCs, ex-Sanofi execs buy Cambridge antibody shop to create global immuno-oncology startup

Harbour BioMed has bought an Atlas Venture-backed antibody player to further its ambition to build a pipeline of immuno-oncology programs. The deal sees Chinese VCs teaming with Big Pharma veterans to gain control of transgenic mouse platforms developed and commercialized in Cambridge, Massachusetts, and Rotterdam, the Netherlands.

Northern Biologics merges with Mosaic Bio as Versant, Celgene boost involvement

Canadian biotech Northern Biologics has signed a “transformative” merger deal with Spain’s Mosaic Biomedicals as the new player looks to become a global cancer company, eyeing 2017 in-human testing for its lead candidate.

Sanger spinout gets $10M to work on live bacteriotherapies

A spinout from the Wellcome Trust Sanger Institute’s microbiome research group has raised $10 million to advance live bacteriotherapy programs. The startup, Microbiotica, is helmed by a former GlaxoSmithKline executive and built on years of work to sequence the genomes of the thousands of bacteria that inhabit the guts of humans.

Purdue inks Shionogi collab on constipation med as it awaits FDA approval

Purdue has signed a new deal with Japanese drugmaker Shionogi that will see the pair work together to sell in the U.S. the latter’s opioid-induced constipation candidate Symproic (naldemedine).

MicroPort invests in Lombard, lands rights to stent grafts

MicroPort Scientific has invested $15 million in Lombard Medical as part of a deal that gives it rights to stent grafts in China and Brazil. The pact gives Lombard a partner capable of commercializing its Aorfix and Altura stent grafts in key global markets, plus an infusion of capital and component supply pact.

Matt Kapusta named CEO of gene therapy pioneer UniQure, its third leader in a year

Hoping to gain some stability, Dutch gene therapy company UniQure has awarded the CEO role to Matthew Kapusta, who took over as interim leader in September, and who now becomes the company's third CEO in a year.

News of Note

German biotech Medigene told Reuters it has been "drawing more interest from prospective alliance partners" for its tech after a Bluebird Bio deal. Reuters story

The EMA said it is working on "tailored scientific advice" to help support step-by-step development of new biosimilars for biopharmas. Statement

Vivo Capital and ZQ Capital signed a pact to buy out medical device company Angiotech Pharmaceuticals. Release

Resources

[Infographic] Bridging the Patient ID Accuracy Gap

Get the stats you need to start down the path to a more secure infrastructure, today.

[Checklist] Customized Care Anywhere with Digital Signage

What's the first step to a better patient experience? The patient experience starts well before the exam room or even reception - it begins as soon as your patients pull into the parking structure.

[Whitepaper] The Paperless Future of Healthcare and Life Sciences

DocuSign’s eSignature solutions modernize healthcare and life science organizations by eliminating paper and antiquated signature processes while meeting compliance requirements and reducing costs and errors.

[Whitepaper] DocuSign Life Sciences eBook: Reducing Cycle Time with Digital Transaction Management

The patients who rely on your scientific leadership are expecting more.

[Whitepaper] Streamline Regulatory Compliance in Life Sciences with Digital Transaction Management

The U.S. Department of Justice has collected upwards of $17 billion in settlements from the healthcare industry since 2009, including more than $2 billion from a single life sciences company.

[Whitepaper] THE Rx FOR NEXT-GEN LIFE SCIENCES: How Technology Can Treat Industry Pain Points

Life sciences companies, like many industries today, face new challenges across the board. Read More.

[Research] Bioprocessing Services and Technologies Market Trends and Outsourcing Dynamics

Make essential outsourced bioprocessing decisions by staying informed of industry outsourcing practices and contract manufacturer usage patterns with ISR’s Bioprocessing Services and Technologies Market Trends and Outsourcing Dynamics report.

[Research] Biosimilars in the US Oncology Market (2nd Edition)

ISR’s Biosimilars in the US Oncology Market (2nd Edition) report provides data and insights from 101 US-based, board-certified oncologists/hematologist oncologists as to their expectations, fears, and aspirations for biosimilars in oncology.

[Research] Medical Science Liaisons in Oncology (2016)

Pinpoint the information oncologists find most valuable and the best sales channels for delivering specific types of data/information.

[Research] Bioprocessing Market Trends and Outsourcing Dynamics: 2016-2021

ISR’s Bioprocessing Market Trends and Outsourcing Dynamics: 2016-2021 report provides an overview of the current market dynamics for bioprocessing as well as an outlook on what the marketplace will look like in five years.

[Research] Phase II/III CRO Quality Benchmarking

ISR’s CRO Quality Benchmarking – Phase II/III Service Providers (8th Edition) report provides a Consumer Reports-style analysis of Phase II/III CRO service quality from hundreds of users who rated 44 Phase II/III CROs across 26 critical dimensions of quality.

[Whitepaper] Ensuring the Greatest Return From Your Poorly Soluble Molecule

Can you avoid a risky trial-and-error approach to find the right path for your poorly soluble molecule by utilizing a CDMO? Download this complimentary Whitepaper to learn more!

[Whitepaper] Complimentary IDMP Report from Gartner

Gartner research on short- and long-term strategies for IDMP compliance.

Events

.