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Wednesday, November 13, 2019

After decades of little progress, researchers may be catching up to sepsis

After decades of little or no progress, biomedical researchers are finally making some headway at detecting and treating sepsis, a deadly medical complication that sends a surge of pathogenic infection through the body and remains a major public health problem.
Researchers at Cincinnati Children’s Hospital Medical Center report in Science Translational Medicine they developed and successfully tested a new rapid blood assay that measures five biomarkers and accurately predicts which patients are at low, medium or high risk for death from sepsis (colloquially referred to as blood poisoning).
Called PERSEVERE, the test allows physicians to detect and stratify sepsis at its earliest moments, just as the body is about to unleash a storm of bacterial infection, according to study’s senior investigator, Hector Wong, MD, director of Critical Care Medicine at Cincinnati Children’s. By knowing which five proteins/genes make up the assay’s five-biomarker blood panel, physicians should be able to start medical interventions much earlier and with greater precision.
Wong said not only can patients be stratified into low, medium and high-risk groups, the biomarker test allows physicians to pick the right interventions for specific patients, including which drugs and dosages.
“The PERSEVERE platform focuses on stratification and prognostication, not diagnostics,” says Wong. “Prognostic enrichment is a fundamental tool of precision medicine. It allows us to predict the disease course and progression in individuals and tailor treatment to different groups of patients and individuals.”
Another benefit of the assay platform is it also gives researchers important clues for studying the underlying biological mechanisms of how sepsis gets started, ramps out of control and how it can be stopped with new therapeutic approaches, according to Christopher Lindsell PhD, a key collaborator on Wong’s team formerly with the University of Cincinnati School of Medicine and now at the Vanderbilt University Medical Center.
The research project is also expected to lead to the development of new therapeutic treatments, the researchers said.
The tool has been in development by the research team for more than a decade. They have able to progressively reduce the number of biomarkers in the assay platform from 80 down to five. This makes it easier to blend advanced technologies like computer-assisted biology and informatics with laboratory experimentation to look more efficiently for new therapies, according researchers.
A Heavy Toll
Sepsis usually strikes fragile young children and the elderly hospitalized in intensive care units. The complication kills more than 200,000 people a year and costs the health care system billions of dollars, according to research data published by the National Institutes of Health. In the current study, about 13 percent of patients did not survive, but PERSEVERE-based stratification effectively stratified the patients into three risk categories with widely different mortality rates. Wong said the goal of the research team’s work is to push those survival curves significantly higher among the higher risk patients.
A major hurdle frustrating researchers over the decades is that sepsis is known for its considerable clinical and biological heterogeneity, with the causes and outcomes varying greatly between different patients. PERSEVERE is designed to leverage today’s enhanced genetic and biological analysis technologies to make that variability more manageable.
Getting New Answers
Although more than 1,000 children have been tested by Wong and colleagues over the years, in the current study researchers used the latest version of PERSEVERE to test the blood samples from 461 children with sepsis as well as mouse models that faithfully mimic blood poisoning.
After receiving prior permission from patient families and Institutional Review Boards of participating institutions, the researchers used PERSEVERE to test children between ages 1 and 18 years who were already admitted to intensive care units and under care for sepsis at multiple pediatric hospitals, including Cincinnati Children’s. Because PERSEVERE is not yet approved for clinical use, it was not used to inform or influence patient care decisions. It was only tested for accuracy and potential future use.
Researchers said the five biomarkers in PERSEVERE were able to accurately predict with high reliability which patients would and would not develop severe cases of sepsis. When researchers next tested PERSEVERE in their mouse models of sepsis, the same five biomarkers were able to accurately predict which mice were at low or high risk. They also reported that mice at a greater risk of severe sepsis had significantly higher bacterial loads in their blood than lower-risk animals, and that higher doses of antibiotics were able to help contain the blood infections. The investigators also provide corroborating evidence that children with higher risk of mortality from sepsis also have higher bacterial loads in their blood.
Wong said the research team continues to test and refine PERSEVERE and study the biological clues it has uncovered so far to pinpoint the onset molecular bases of sepsis and find new treatments. The ability to study the biology of sepsis in mouse models that faithfully mimic the condition and have the same biomarkers as humans should allow the researchers to make significant new progress. Wong also said the technology has reached the point where it would benefit from a biotech industry partner and collaborator so the platform’s development can be accelerated and tested in clinic within the next few years.
To this end, the researchers have secured patents for the platform through the Cincinnati Children’s technology commercialization group, Innovation Ventures. Wong and Lindsell are listed as co-inventors. Wong said an adult version of PERSEVERE is also under development, and the researchers plan to concurrently test the platform as they conduct an NIH-funded clinical trial to use corticosteroids to treat sepsis.
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Funding support for the study came in part from the National Institutes of Health (R35GM126943) and a Research Innovation in Support of Excellence Award from Cincinnati Children’s. Wong serves on the scientific advisory boards for Inflammatix, Endpoint Health, and Eccrine Systems, Inc., companies that are not directly linked to development of the PERSEVERE platform.

Merck Gains Preclinical Neurodegenerative Asset in $576M Buy

Merck plunked down $576 million to acquire San Diego-based Calporta to gain access to preclinical TRPML1 agonists that are seen as potential treatments for neurodegenerative disorders such as Alzheimer’s or Parkinson’s.
Calporta was launched as a collaboration between GlaxoSmithKline and Avalon Ventures. The company is located at COI Pharmaceuticals the Community Of Innovation site established by Avalon Ventures. GSK had the option to acquire Calporta as part of that collaboration but opted against that earlier this year, which opened the door to Merck.
Calporta Therapeutics focuses on the development of selective small-molecule agonists to TRPML1 (transient receptor potential cation channel, mucolipin subfamily), which is believed to play a role in lysosomal function by promoting autophagy and lysosomal exocytosis. The lysosome is a cellular compartment involved in the breakdown and recycling of cellular waste products, such as fats, proteins and other macromolecules, the company said. Damaged TRPML1 function has been implicated in several pathological conditions, including Niemann-Pick C Disease, as well as muscular dystrophy and Alzheimer’s disease. Calporta’s preclinical stage TRPML1 agonists are being evaluated for their potential to treat various lysosomal storage and neurodegenerative disorders, including Alzheimer’s and Parkinson’s disease. It is believed that activating TRPML1 signaling with small molecules could reestablish lysosomal processes and restore cellular function.
Jay Lichter, the managing director of Avalon Ventures and CEO of COI Pharmaceuticals said that TRPML1 was identified in 2014 as an important target for improving lysosomal function.
“We saw the potential to treat a number of diseases by activating this ion channel, and we launched Calporta in early 2015. Now four years later, we have an agreement with Merck, an industry leader in biopharmaceutical research and development, which is key to advancing these therapies to clinical trials and patients,” he said in a statement.
Fiona Marshall, vice president, neuroscience discovery Merck Research Laboratories, said in a brief statement that there is increasing evidence that shows the accumulation of toxic proteins are a common mechanism in neurodegenerative conditions such as Parkinson’s disease, amyotrophic lateral sclerosis (ALS) and Alzheimer’s. Marshall said Merck is excited about conducting its own research to evaluate the potential of TRPML1 agonists as a means to “activate a natural clearance mechanism the brain employs to clear toxic proteins.”
Under terms of the deal, Merck will pay up to $576 million for Calporta, including an undisclosed upfront payment and contingent milestone payments.
Calporta Chief Executive Officer Sanford J. Madigan called the deal with Merck an “important milestone” toward the development of novel therapeutics that could benefit millions of people with degenerative disorders that are caused by toxic accumulation of proteins, fats, or other cellular macromolecule. Madigan added that he was proud of the Calporta team for its diligence in advancing the preclinical research toward human trials.

Vertex deal with Wales expands cystic fibrosis treatment coverage to all of UK

Vertex Pharmaceuticals Inc’s drugs for lung condition cystic fibrosis will now be available to patients across the UK after the company reached a pricing deal with Wales on Wednesday.
The U.S. drugmaker has already reached similar agreements with the National Health Service in Northern Ireland, England and Scotland.
More than 10,000 people in Britain have cystic fibrosis, a debilitating, life-shortening inherited condition, making it the country with the second highest number of such patients in the world, according to the company.
Although the terms agreed with the countries have not been disclosed, UK government-run healthcare systems have been negotiating treatment supply with Vertex for years.

The company had wanted to charge around 100,000 pounds ($129,000) a year for a course of Orkambi, its combination drug that improves lung function, according to reports.
“This has been a hard-fought four year battle,” said David Ramsden, chief executive officer at UK-based charity the Cystic Fibrosis Trust.
However, Ramsden noted the company’s new drug, known as Trikafta in the United States, is likely to make a bigger difference for a wider group of cystic fibrosis patients.
“We must do all we can to ensure there is no repeat of the deadlock and delays in accessing these treatments when they are licensed,” he added.

Vertex said its agreement with Wales will allow about 270 eligible patients to be treated with Orkambi, as well as its other medicines Symkevi and Kalydeco.

NY insurance regulator notifies opioid makers, distributors of enforcement

New York’s insurance regulator has formally notified a group of opioid manufacturers and distributors that it will launch a civil enforcement action against them for contributing towards a rise in health insurance premiums in the state, said two sources familiar with the matter.
The New York State Department of Financial Services (NYDFS) has sent letters to around 23 opioid manufacturers and distributors, notifying them that the regulator would begin the process to hold a hearing on the issue in an administrative proceeding, the sources said.
New York Governor Andrew Cuomo said in September the state would launch a legal action against drug companies and distributors that sell opioids in order to recoup about $2 billion in insurance rate increases that were passed on to New York consumers because of opioids.
Premiums surged because insurers had to cover prescription costs and opioid-related issues such as emergency room visits and addiction treatments, Cuomo had said.
Opioids were involved in almost 400,000 overdose deaths in the country here between 1999 and 2017, according to the U.S. Centers for Disease Control and Prevention.

Opioid litigatihere is playing out across the United States, including some 2,600 lawsuits brought by states, towns, cities, counties and tribal governments over the opioid epidemic.
The two sources familiar with the NYDFS action declined to name the companies to which the letters were sent.
Cuomo, on Sept. 10, published a list of entities the regulator had subpoenaed here including Purdue Pharma Inc, Johnson & Johnson, Teva Pharmaceuticals USA Inc, McKesson Corp, AmerisourceBergen Drug Corp and Janssen Pharmaceuticals Inc.
“Janssen acted as a responsible manufacturer and seller of its opioid pain medications, which play in an important role in the lives of patients with severe pain,” the company said.
Other companies mentioned above could not immediately be reached for comment.

A letter of intent to bring an enforcement action follows a determination by the regulator that there is sufficient evidence to bring the case, the sources said.
The entities will first have an opportunity to try to convince the regulator not to start the proceeding. The case would be heard by a hearing officer within the agency.
Funds that New York would collect from the suits would be returned to consumers, possibly in the form of rebates of lower insurance premiums, NYDFS Superintendent Linda Lacewell has said.

Apple Watch detects irregular heartbeats in U.S. study

Apple Inc’s Heart study, the largest yet to explore the role of wearable devices in identifying potential heart problems, found the device could accurately detect atrial fibrillation, the most common type of irregular heartbeat, U.S. researchers reported on Wednesday.
The results, published in the New England Journal of Medicine (NEJM), come as technology companies increasingly strike up partnerships with drugmakers as a way to gather large amounts of real-time health data on individuals.
Earlier this month, Alphabet Inc’s Google bought the health tracking company Fitbit for $2.1 billion. That followed Fitbit’s alliance in October with U.S. drugmakers Bristol-Myers Squibb Co and Pfizer Inc to develop their own technology to spot atrial fibrillation, a condition that significantly increases the risk of stroke.
Smaller players such as AliveCor have paved the way. AliveCor’s KardiaBand, a mobile phone accessory that can take medical-grade electrocardiograms (EKG) to detect dangerous heart rhythms, won U.S. approval in 2017.
The Apple study, conducted by researchers at Stanford University School of Medicine, tested the Apple Watch’s heart rate sensor and algorithm in more than 400,000 participants who used an app to sign up for the eight-month trial.

During the study, only 0.5% of participants received a warning that they had an irregular pulse, a finding study authors believe should ease concerns that the device would result an excess of notifications in healthy participants.
People flagged for an irregular pulse were sent an EKG patch to wear. Of those, 34% were found to have atrial fibrillation.
Dr. Mintu Turakhia, a Stanford cardiologist and study co-author, said the aim was to evaluate how good the algorithm was and whether it was safe.
“If you turn this on out in the wild, how many people are going to get notified and what does that mean for patients, the healthcare system, payers, and patients themselves?” he said.
On that score, Turakhia said, the trial was a success.

NEJM editor Dr. Edward Campion noted in an editorial, however, that everyone in the study had to own both an iPhone and an Apple Watch, making all participants customers of the study sponsor.
Dr. Daniel Cantillon, a Cleveland Clinic cardiologist who was not involved with the study, called the technology promising, but said more than half of the people who signed up were under 40, a group already at low risk for atrial fibrillation.
“The overarching concern is are we identifying the sick, or are we scaring the healthy?”

NY opioid trial pushed back three months

The start of the second state-level trial related to certain companies’ role in the U.S. opioid epidemic, slated to begin on January 20, 2020, in New York has been extended to March 20, 2020 according to Susquehanna International Group. The move, if confirmed, is surprising since the start date was moved up two months to January 20 last week.
The case against privately held Purdue Pharma, maker of Oxycontin (oxycodone), is being conducted separately through U.S. Bankruptcy Court.
Selected tickers: AmerisourceBergen (ABC +0.8%), Cardinal Health (CAH +0.8%), McKesson (MCK +1.1%), Endo International (ENDP +4.5%), Johnson & Johnson (JNJ -0.4%), Mallinckrodt (MNK +4.1%), Teva Pharmaceutical Industries (TEVA +1.7%)

Qiagen up 7% on rumored Thermo Fisher interest

Diagnostic gear maker QIAGEN (QGEN +7.4%) perks up on almost triple normal volume in apparent reaction to unconfirmed reports that Thermo Fisher Scientific (TMO +1.4%) is mulling a bid.
QGEN is clawing back from a four-month selloff that trimmed ~40% off the share price before the recent reversal.