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May 22, 2017

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Today's Rundown

  1. Shock for Amgen and UCB as side effects undermine romo trial

  2. Celgene touts ozanimod MS data, but disability benefit weak over rival drug

  3. Shire, Xenetic see hemophilia A candidate flunk key test

  4. [Sponsored] The Impact of Data and Informatics Technologies Throughout the Clinical Trial Journey

  5. La Jolla posts mixed bag of phase 3 data, raising hopes of FDA approval but calling commercial potential into question

  6. Merck KGaA, Ablynx push osteoarthritis asset toward clinic

  7. Nektar pens sweetened Takeda cancer drugs deal

  8. Startup Tilos to develop cancer-fighting antibody that emerged from MS research

  9. Connected thermometer data used to predict flu outbreaks

  10. Amgen's romosozumab red flag on heart safety means a boost for new Radius bone drug

Featured Story

Shock for Amgen and UCB as side effects undermine romo trial

Amgen and UCB's romosozumab trounced a comparator drug in a trial in osteoporosis, but there's a big catch: The therapy seems to cause side effects that will delay and could scupper its chances of reaching the market.

Top Stories

Celgene touts ozanimod MS data, but disability benefit weak over rival drug

Celgene has posted some new late-stage data from its second pivotal test in multiple sclerosis for its $7.2 billion oral candidate ozanimod, showing it could beat out Biogen’s marketed MS med Avonex in reducing annualized relapse rates in a head-to-head, hitting its primary endpoint.

Shire, Xenetic see hemophilia A candidate flunk key test

Shire and drug partner Xenetic have released new data for their collab bleeding disorder drug SHP656 and the news isn’t good.

[Sponsored] The Impact of Data and Informatics Technologies Throughout the Clinical Trial Journey

With pressures to fast-track clinical development, the pharmaceutical industry recognizes the value of improving internal clinical data management processes. Learn how using comprehensive analytical capabilities helps to advance clinical trial execution.

La Jolla posts mixed bag of phase 3 data, raising hopes of FDA approval but calling commercial potential into question

La Jolla Pharmaceutical has posted a full look at data from a phase 3 trial of its vasodilatory shock candidate LJPC-501. Key findings are in line with the earlier, positive top-line data drop but the picture becomes muddier beyond the primary endpoint, with the lack of improvement to mortality and total organ function raising doubts about whether LJPC-501 can win over physicians.

Merck KGaA, Ablynx push osteoarthritis asset toward clinic

Ablynx and Merck KGaA have moved their osteoarthritis candidate to the cusp of the clinic. Merck accepted the preclinical package for single-domain antibody ALX-1141, triggering a €15 million ($17 million) milestone payment to Ablynx and teeing it up to start clinical development.

Nektar pens sweetened Takeda cancer drugs deal

Perennial biotech investor and backer Takeda has signed its latest collaboration with Nektar Therapeutics that will see the pair work on combo cancer approaches with NKTR-214, a CD122-biased agonist, as well as five Takeda oncology compounds.

Startup Tilos to develop cancer-fighting antibody that emerged from MS research

Serendipity can play a key role in scientific discovery, and it certainly did for a group of neuroscientists at Brigham and Women's Hospital in Boston who were searching for clues to the development of multiple sclerosis when they found an antibody with cancer-fighting properties.

Connected thermometer data used to predict flu outbreaks

Researchers have used data gathered by connected thermometers to predict the onset of an influenza outbreak. An analysis of data from users of the iThermometer wearable and companion app in China predicted the spike in the 2015-16 flu season one month before the country’s public health body.

Amgen's romosozumab red flag on heart safety means a boost for new Radius bone drug

When Radius Health scored an early approval for its osteoporosis med Tymlos last month, industry watchers thought it wouldn't be long before the drug had to contend with another newcomer from Amgen. But now, Amgen says it’ll be a while before its drug hits the market—if ever.

News of Note

Tim Mayleben, president and CEO of Esperion, has penned an unusual rebuttal to a recent report from an investment firm that had "misinterpretations or intentionally inaccurate statements regarding Esperion and bempedoic acid." CEO's blog

Otsuka says its additional phase 3 data for tolvaptan in ADPKD saw positive results for its primary and key secondary endpoints versus placebo. Release

PCI Biotech and RNAi biotech RXi Pharmaceuticals have extended their preclinical research collaboration first inked back in 2015. Statement

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[Whitepaper] Run the Trial You Want with Modern EDC

To thrive in a fiercely competitive market, life sciences companies need to set themselves apart by designing and executing the best trial and successfully deliver drugs to market first. Learn how a modern EDC can help.

[Whitepaper] Solving the Knowledge Management Puzzle in Biopharma

Puzzled by Scientific Literature Access? Here is your guide for navigating knowledge management’s twists and turns! If yours is a small- or medium-sized biopharma business, we can help you putting the pieces together. Learn the secrets of top knowledge management experts who will show you how to search, discover, acquire and manage knowledge in new ways.

[Whitepaper] Immuno-Oncology and the Role of Biomarkers, Companion and Complementary Diagnostics

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

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