To view this email as a web page, click here

   Home

Subscribe

Advertise

 

 

 

 

March 29, 2018

Today's Rundown

Featured Story

Redx pauses WNT cancer trial after first patient suffers adverse events

Redx has hit pause on a phase 1/2a trial of its porcupine inhibitor after the first patient to receive the drug suffered “clinically significant” adverse events. The blow continues a rotten run for Redx, which spent half of last year fighting to resolve a debt crisis.

Top Stories

Unum IPO hits bottom of range, netting $62M for cell therapy cancer trials

Unum Therapeutics has netted $62 million in a Nasdaq IPO. The total falls short of the amount Unum set out to raise but leaves the biotech with enough cash to advance two cell therapy candidates in four clinical trials.

MediciNova's repurposed stroke drug flops in methamphetamine dependence trial

MediciNova's repurposed stroke and asthma drug ibudilast missed its primary endpoint of methamphetamine abstinence in a 12-week phase 2 trial.

[Sponsored] Highlighting Women Pioneers in Science & Medicine

As leaders in science and business, two high-profile female CEOs have been instrumental in advancing medical breakthroughs and are champions for issues that affect women around the world.

U.K. biotech C4XD leaps on $294M addiction drug deal with Indivior

Shares in U.K. biotech C4X Discovery almost doubled today after Reckitt Benkiser spinout Indivior agreed a $294 million deal for a drug candidate to treat addiction.

Mitsubishi Tanabe, Hitachi join forces in AI-enabled clinical trials

Through a new collaboration, Mitsubishi Tanabe Pharma will apply Hitachi’s artificial intelligence technology to make clinical trials more efficient and to drive down drug development costs.

Abbott backs Bigfoot, bringing series B haul up to $55M

Abbott has participated in diabetes startup Bigfoot Biomedical’s series B round. The involvement of Abbott and other investors means Bigfoot has $55 million to take its insulin pump and pen through clinical development and onto the market. 

Resources

[Whitepaper] Compliance Certificate and Training for Life Sciences Professionals

4-day interactive educational program trusted by multi-national companies as part of their compliance training for employees. Explore legal, regulatory and ethical issues faced by pharmaceutical, biotech and medical device manufacturers operating globally. Visit event homepage for session topics.

[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

.