14 Mar

Charged With Fraud, Theranos CEO Elizabeth Holmes Cuts Deal with Feds

Charged with what the U.S. Securities and Exchange Commission called “massive fraud,” Theranos CEO Elizabeth Holmes has cut a deal with the agency.

The SEC charged Holmes and the firm’s former president Ramesh “Sunny” Balwani with “an elaborate, years-long fraud,” in which they raised $700 million dollars from investors and enjoyed a multibillion-dollar valuation by misrepresenting the privately held firm’s diagnostic technology that was supposed to work with just a finger prick and a few drops of blood, and cost less than standard blood tests.

As the firm spread its product-walk-up centers were stationed at dozens of pharmacy chain… Read more »

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14 Mar

ICER Comes Under Renewed Scrutiny

As we enter a new and exciting era of medicine, there is an important question we need to answer: What if we could measure the efficacy of a medicine, and more broadly, the value a specific medicine will have on patients and society as a whole? To find an answer, efforts like the Innovation Value Initiative (IVI) are underway to develop value-assessment frameworks aimed to assess the worth of pharmaceuticals and other technologies. And as we are learning, not all value assessments are created equal.

In new blog featured in Health Affairs, Peter Neumann and Joshua Cohen of the Tufts University School of Medicine examine the Institute for Clinical and Economic Review (ICER), which has crafted its own way to measure the cost-effectiveness of drugs and technologies, but has come under scrutiny in recent years for their questionable processes and flawed methodology. Here’s why:

Doesn’t Reflect the Full Value of Treatments

Appropriately and accurately measuring value is increasingly important as our health care system seeks to reward quality over quantity and ensure patients have access to the medicines they need. These tools can help us better understand how biomedical innovations can improve the lives of patients and society more broadly, and these findings can help inform future health care decisions. However, ICER’s past ties to the insurance industry make us question who will ultimately benefit from their work. As Neumann and Cohen point out:

“[P]rivately funded assessment … raises questions, and given ICER’s expanding profile, it is important to consider them. A central one is: to whom is ICER accountable? As a private entity with private payers as a key target audience, ICER, however well intentioned, may downplay the “social good” aspect of health care-i.e., spillover effects on caregivers, families, and society at large. For example, treating a person’s cancer, Parkinson’s disease, or substance abuse can have broad benefits for society. Privately-led value assessments tend to ignore or discount such effects, as do private payers, a key audience of ICER’s reports, because the effects fall outside of their budgets.”  

Patient-Stakeholder Perspective Missing

One of ICER’s greatest flaws is its lack of sufficient input from the full breadth of stakeholders and patient advocates, which paints an incomplete picture of value. And while it’s true that ICER has made an effort to incorporate these voices more prominently in their work, the group must do more to ensure these viewpoints are included in the value measurement process. In a recent letter, BIO applauded these efforts as an encouraging step forward, yet groups like the Partnership to Improve Patient Care have noted that ICER’s use of the information these groups have provided is not consistent and their role is not formal.

Barriers to Critical Cures and Medicines Evident

By neglecting the full value and potential of a medicine and ignoring third-party perspectives, ICER’s flawed processes and methodology can detrimentally impact patient care by encouraging insurers to impose higher cost sharing requirements (or outright coverage denials) for some treatments. As Neumann and Cohen explain:

“[B]y identifying cost-effectiveness benchmarks (e.g., $100,000 to $150,000 per QALY) and budget thresholds to which a technology can be compared, ICER weighs in on what level of spending is appropriate. However, judgments about proper spending are better rendered by actual decision makers (payers and their enrollees) in consideration of specific budget constraints, preferences, and tradeoffs.”

Greater Transparency Needed

Believe it or not, until recently ICER had “no formal policy for updating its evaluations based on the availability of important new data,” the Partnership to Improve Patient Care found in a new report. And just this week, A report released by the President’s Cancer Panel highlighted this flaw and others in ICER’s work:

“Some efforts are under way, including those by the Institute for Clinical and Economic Review (ICER) … to develop value frameworks for use in the United States, but none of these is yet widely accepted or used. Limitations noted for one or more of these frameworks include lack of patient-centeredness, lack of systemwide perspective, inadequate provisions for updates as new data are obtained, lack of transparency about methodologies, and failure to engage all stakeholders.”

For a better approach, we should look at value-assessment tools like the IVI’s Open-Source Value Project (OSVP) – a transparent and holistic approach for estimating the value of medical technologies in a way that allows for a broad range of perspectives, incorporates the latest available evidence, and considers the full value of cures and treatments.

14 Mar

Crinetics Closes $63.5M Financing to Back Rare Hormone Disease Drug

Crinetics Phamaceuticals team 2017 (photo used with permission)

Crinetics Pharmaceuticals, a San Diego biotech focused on developing new drugs for endocrine disorders and endocrine-related cancers, said today it has raised $63.5 million in a Series B financing led by Perceptive Advisors, the New York biotech fund.

Two new investors, RA Capital and OrbiMed, joined the round, along with existing investors 5AM Ventures, Versant Ventures, and Vivo Capital. With the latest funding, CEO Scott Struthers, who founded Crinetics in 2008, said the company has raised over $100 million, including private investments and non-dilutive funding such as Small Business Innovation Research Grants.

In a statement Tuesday, Crinetics said it plans… Read more »

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13 Mar

2nd FOOD 2030 HIGH-LEVEL EVENT: Research and Innovation for Food and Nutrition Security – Transforming our food systems – 14-15 June 2018, Plovdiv, Bulgaria

[Source: Research & Innovation] The second FOOD 2030 high-level event will take place on 14-15 June 2018 during the Bulgarian Presidency of the European Council. It will be dedicated to research and innovation (R&I) as a driver of food systems transformation; such that our food systems become sustainable, resilient, inclusive, responsible, resilient, diverse and competitive.
In the plenary session and 6 parallel sessions the speakers will demonstrate the status quo of Food research and innovation policy and its vision of shaping tomorrow’s food and nutrition systems. The high level events will provide a dialogue platform and recommendations for the following actors:

• policy makers and R&I funders
• researchers and educators
• the private sector
• civil society

Besides structured plenary and parallel sessions the high-level event for FOOD 2030 will offer the opportunity to visit an open exhibition on the “Food R&I Domain” showcasing innovative research projects, networks, regional initiatives, start-ups and sustainable agriculture and food technologies.
In addition to the main sessions 3 interesting side events in the afternoon of 13 June will be open to participants and can be selected in the registration form:

• Showcasing Sustainable Food for Cities
• Food in Regions – one health, from regionality to functionality
• Future-Proofing Food Systems – joint workshop between SCAR Food Systems Strategic Working Group and JPIs – HDHL and FACCE.

13 Mar

Two new biotech related podcast episodes. I would love some feedback.

One week since I launched the podcast and there has been a lot of buzz. I want to thank everyone who shared, left a review, and interacted with my previous posts. I want to do my part to help show the different avenues of success in biotech and other science related industries, and at the same time shine a light on those doing fantastic work to make all of our lives better.


I learned a lot since the launch. Specifically how to better set up show statistics and how goofy itunes feed updaters can be. One thing I did learn is that there is an easier way than just Itunes to leave reviews, which is Stitcher. All you need is an email and maybe 20 seconds. It’s pretty nice. I made a guide on how to leave a review for either. I’m open to feedback on different players/feeds you all listen to. I can get on google play for instance.


For the next 5 weeks because of the great response I’ve been getting I will be putting out two episodes every Tuesday. Two new episodes are up right now, which brings us to the reason behind the post today. I did the intros and the audio editing a little different in these episodes. I’m looking for feedback.

** Questions: 1) What do you like/hate, 2) what do you want to see next, and 3) topics/guests you’d love to see on the show?**


Podcast Episode 011: Paul Berning Employee of the year & #1 Sales person at Formulatrix

He grew up underprivileged and with a disabled mom. They lived on food stamps and struggled a lot. Paul says that he wasn’t the type of person you would think would grow into success, but that’s exactly what he did. Tune in to this episode to hear his story and advice on how he worked to become the employee of the year and #1 sales person at Formulatrix. There are a lot of nuggets of advice and suggestions in here. If you’re looking to work your way into biotech, then I’d suggest you start here. Link to episode. Also, I struggle to say Formulatrix in the intro, so feel free to make fun of me for it 🙂


Podcast Episode 012: Ali and Ignacio Co-founders of Hackscience

Ali and Ignacio founded Hackscience in London to save scientists time and mental energy. They found a great way to do that by developing a cell culture automation machine. Scientists can now cut their time in the lab down significantly. Tune in to hear their story, the story of their company, and how they developed their product. (Excuse some of the noise in the background. A few things fall suddenly). Episode link.


What are everyone’s thoughts? I share what ever I learn in blog posts, guides, and the like. Let’s all work together to shine a greater light on the amazing things happening with science every day!

Here is my [last post] on reddit.(https://www.reddit.com/r/biotech/comments/82peic/started_a_biotech_podcast_and_would_love_feedback/)

submitted by /u/iwashere23
[link] [comments]

13 Mar

Goldfinch Bio Names Peter Mundel Chief Scientific Officer

Goldfinch Bio has appointed Peter Mundel to serve as chief scientific officer of the Cambridge, MA, kidney disease drug developer. Mundel, a nephrologist, comes to Goldfinch from Massachusetts General Hospital and Harvard Medical School, where his research focused on developing treatments for kidney diseases. He was also a consultant to Third Rock Ventures, the venture capital firm that incubated Goldfinch and provided the startup with $55 million in funding when it formally launched in 2016.

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13 Mar

National Women’s History Month: Rosalind Franklin Nomination Opens

Each March, the U.S. celebrates National Women’s History Month, recognizing the great contributions women have made to our nation. It’s a fitting time to announce that BIO is now accepting nominations for the 2018 Rosalind Franklin Award. Every year at the BIO World Congress, BIO honors women who’ve made significant contributions to the field of industrial biotechnology and the advancement of the biobased economy by presenting the Rosalind Franklin Award in Industrial Biotechnology and Agriculture.

While sometimes overlooked, Rosalind Franklin is credited with discovering the structure of DNA. In 1952, while a research associate at King’s College in London, Franklin conceived and captured Photograph 51 of the “B” form of DNA. The photograph was acquired through 100 hours of X-ray exposure from a machine Dr. Franklin herself refined. The discovery was an important advance in modern biology and helped establish the field of biotechnology. Without Franklin’s critical discovery, the biotechnology industry would not be what it is today.

“Rosalind Franklin’s contribution to the discovery of DNA’s structure has been vital to the advancement of the field of biotechnology, but her legacy has often been overlooked,” said Brent Erickson, Executive Vice President, Industrial and Environmental at BIO. “In presenting this award we hope to not only honor Rosalind Franklin’s legacy but also honor and inspire the women working in the field of industrial biotechnology today.”

Nominations for the 2018 Rosalind Franklin Award will be open throughout much of National Women’s History Month, closing on March 28. The Award is sponsored by the Rosalind Franklin Society whose goal is to support and showcase the careers of eminent women in science.

Past recipients of the Rosalind Franklin Award include:

  • Vonnie Estes, Independent Consultant, in 2017
  • Anna Rath, President and CEO of NexSteppe, in 2016
  • Dr. Jennifer Holmgren, CEO of LanzaTech, in 2015
  • Dr. Debbie Yavers, Director of Expression Technology, Genomics and Bioinformatics at Novozymes, in 2014

To submit a nominee, or for more information, click here. Also, don’t forget to register for the 2018 World Congress at the Pennsylvania Convention Center in Philadelphia from July 16-19.

13 Mar

Nasdaq’s Head of Healthcare Listings Shares 2018 Predictions for Biotech IPOs

Nasdaq: What is the current market environment for biotech initial public offerings and biotech listings overall? Saxe: I expect that 2018 will demonstrate positive momentum for biotech listings overall, and specifically on Nasdaq. We predict 30-plus biotech IPOs this year and a strong first half of 2018 …

12 Mar

Information and Communication Technologies

[Source: http://ec.europa.eu/health/ageing/innovation/index_en.htm] Identifier: H2020-ICT-2018-2020Pillar: Industrial LeadershipPlanned Opening Date: Deadline: Wed, 14 Nov 2018 17:00:00 (Brussels local time)Modification Date: Mon, 12 Mar 2018Latest information: We would like to inform you that until 12 March 2018, there was a small problem with the template provided in the submission tool for the Innovation-Action (IA) proposals: the template for sections 1 to 3 of the technical annex erroneouly also contained sections 4 & 5. This has been changed on 12 March so that now one template unites sections 1 to 3 and the other one secthions 4 & 5. Please make sure that your proposal is split along the same line so that your sections 1 to 3, which are subject to a page limit, are not impacted by sections 4 & 5.

12 Mar

Gilead CSO Bischofberger to Step Down, McHutchison Named Successor

Norbert Bischofberger, executive vice president of research and development and chief scientific officer of Gilead Sciences (NASDAQ: GILD), is stepping down after nearly 30 years with the company. Foster City, CA-based Gilead says Bischofberger will leave his position at the end of April but remain with the company through July. John McHutchison, who is currently executive vice president of clinical research, has been named Bischofberger’s successor.

In other moves, Gilead announced that Andrew Cheng, executive vice president of clinical research and development operations, will be appointed chief medical officer. Gilead says Cheng will continue leading the company’s HIV clinical research… Read more »

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