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Monday, July 2, 2018

Well-known animal health drug could stop outbreaks of malaria and Zika


Medicines given to household pets to kill fleas and ticks might be effective for preventing outbreaks of malaria, Zika fever and other dangerous insect-borne diseases that infect millions of people worldwide, according to a new study led by scientists at Calibr, a non-profit drug discovery institute closely affiliated with Scripps Research and TropIQ Health Sciences, a Dutch social enterprise.
The researchers found that a class of drugs called isoxazolines, sold in veterinary products such as fluralaner (Bravecto ) and afoxolaner (NexGard ) to protect pets from fleas and ticks, also kills species of -carrying mosquitos that feed on human blood.
The research team, led by TropIQ’s Koen Dechering, Ph.D. and Calibr’s Matt Tremblay, Ph.D., determined via experimental studies on mosquitoes and computer modeling that giving isoxazoline drugs to less than a third of the population in areas prone to seasonal outbreaks of  could prevent up to 97 percent of all cases of infection. The results of the study were published today in the Proceedings of the National Academy of Sciences.
“Insect-borne infectious diseases remain primary causes of severe illnesses and fatalities worldwide, and new approaches to preventing outbreaks of these diseases are critically needed,” said Peter Schultz, Ph.D., chief executive officer of Calibr and Scripps Research. “Our findings suggest that isoxazolines might be effective at controlling outbreaks of diseases carried by mosquitos and other insects in regions with limited medical infrastructure.”
Millions of people each year contract malaria, Zika fever and other insect-borne diseases that are particularly prevalent in tropical and sub-tropical regions. In 2016, an estimated 216 million people contracted malaria worldwide and 445,000 died from the disease (mostly children in the African Region), according the US Centers for Disease Control. Zika, a mosquito-borne disease that can cause birth defects in infants born to infected mothers, has spread rapidly around the planet in recent years and is now found in 90 countries.
Mosquitoes aren’t the only carriers of such diseases. Leishmaniasis, caused by protozoan parasites transmitted by sandflies, is endemic to parts of Africa, South America, the Middle East and India. Though far less prevalent than malaria, forms of leishmaniasis that affect internal organs can be fatal if untreated.
“Research on insect-borne diseases has predominantly focused on control of insect populations through use of insecticides and prevention of bites through distribution of bednets, but these approaches have not been fully effective in controlling outbreaks” says Koen Dechering, CEO of TropIQ Health Sciences. “Vaccines are largely lacking for most diseases and drugs to treat people who have contracted the disease are losing efficacy because of emerging resistance.”
The international research team investigated a new strategy, the possibility of giving humans isoxazolines to block transmission of diseases by insect vectors. Isoxazolines are sold in veterinary products such as fluralaner (Bravecto ) and afoxolaner (NexGard ) that protect pets from fleas and ticks.
A well-known animal health drug could stop outbreaks of malaria and Zika virus
A female Aedes aegypti, a species of mosquito that carries Zika virus. Researchers at Calibr, a non-profit drug discovery institute closely affiliated with Scripps Research, and TropIQ Health Sciences found that drugs given to pets to kill …more
When administered orally the drugs absorb into the bloodstream and spreads throughout the animal’s body, where it remains active for up to three months. While well-tolerated in dogs and cats, the drugs kill blood-sucking fleas and ticks that feed on the blood of treated animals by damaging the insects’ nervous systems.
The Calibr and TropIQ scientists and their collaborators tested two of the drugs, fluralaner and afoxolaner, and found they also kill species of disease-carrying mosquitos and sand flies that feed on human blood infused with the insecticides. The drugs also were effective against insect strains that are resistant to common insecticides.
Based on existing data from studies of the drugs in animals, the researchers estimated that a single human dose of the drugs would convey an insecticide effect against mosquitos and sand flies lasting 50-90 days.
“In many regions where seasonal outbreaks are endemic, medical infrastructure is such that delivery of medical care is on an intermittent basis,” said Matt Tremblay, Ph.D., the chief operating officer of Calibr and Scripps Research and a senior author on the PNAS paper. “Isoxazolines could be administered prior to the beginning of seasonal disease outbreaks to convey protection until the threat diminishes at the end of the season.”
The drugs may not work as vaccines, since a treated person could still contract a disease from an insect bite. But an insect that bites an infected person taking the drugs would die before it could transmit the disease to other people, an effect that, when multiplied over a large population, would reduce the overall number of infections.
Working with collaborators at Imperial College London, in the UK, the researcher team used computer epidemiology models to estimate that that giving the drugs to just 30 percent of the population in a region where Zika fever is common could prevent more than 97 percent of cases. Looking at malaria incidence, their modelling showed that in areas with low and very seasonal transmission, such as Senegal, Sudan, Madagascar, Namibia, Botswana and Zimbabwe, giving isoxazolines to 30 percent of the population could prevent more than 70 percent of infections.
Regions with greater numbers of cases and year-round outbreaks would see a smaller percentage reduction, but the overall reduction in these areas could be dramatic. The Democratic Republic of the Congo has 16-20 million malaria cases annually, for instance, so a 30 percent reduction would prevent as many as 6 million cases.
Based on safety studies of isoxazoline use in animals, the drugs have a good chance of being safe if repurposed for human use. The research team is planning to evaluate the efficacy of the drugs in humans and anticipate these studies will take around two years.
More information: Marie Miglianico el al., “Repurposing isoxazoline veterinary drugs for control of vector-borne human diseases,” PNAS (2018). www.pnas.org/cgi/doi/10.1073/pnas.1801338115

New types of cancer immunotherapy shows promise in early tests


Much cancer immunotherapy research has focused on harnessing the immune system’s T cells to fight tumors, “but we knew that other types of immune cells could be important in fighting cancer too,” says Ashish Kulkarni at the University of Massachusetts Amherst. Now he and colleagues at Brigham and Women’s Hospital, with others, report that in preclinical models they can amplify macrophage immune responses against cancer using a self-assembling supramolecule.
As  usually eat foreign invaders including pathogens, bacteria and even cancer cells, Kulkarni explains, but one of the two types do not always do so. Macrophage type M1s are anti-tumorigenic, but M2s can be recruited by  to help them grow. Also, tumor cells overexpress a protein that tells the macrophages, “don’t eat me.” In this way, pro-tumorigenic macrophages may make up 30 to 50 percent of a tumor’s mass, says the biomedical engineer and lead author of the new study.
Kulkarni adds, “With our technique, we’re re-programming the M2s into M1s by inhibiting the M2 signaling pathway. We realized that if we can re-educate the macrophages and inhibit the ‘don’t eat me’ protein, we could tip the balance between the M1s and M2s, increasing the ratio of M1s inside the tumor and inhibiting tumor growth.” Details appear in the current online issue of Nature Biomedical Engineering.
To address both the M2 “re-education” problem and to enhance the macrophages’ capacity to eat tumor cells, the researchers used what they call a bi-functional or “one-two punch,” says Kulkarni. He and research technician Anujan Ramesh, with colleagues in India and at Harvard Medical School’s Brigham and Women’s Hospital, used a multi-component supramolecular system that self-organizes at the nanoscale to deliver an antibody inhibitor plus a drug inside the tumor. “This is the first time anyone has combined these two, a drug that targets M2 macrophages and an antibody that inhibits ‘don’t eat me signal,’ in one delivery system,” Kulkarni notes.
He adds, “We feel this new approach provides a complementary one that can be used along with other therapies. We tested it in melanoma and breast cancer , two aggressive cancers, and we plan to try it on different types of cancer and in combination with other current therapies like T-cell-based therapies now used in clinics.”
The researchers tested the supramolecular therapeutic in animal models of the two forms of cancer, comparing it directly with a drug currently available in the clinic. Mice that were untreated formed large tumors by Day 10, they report. Mice treated with currently available therapies showed decreased  growth. But mice treated with the new supramolecular therapy had complete inhibition of . The team also reported an increase in survival and a significant reduction in metastatic nodes.
Co-author Shiladitya Sengupta at Brigham and Women’s Hospital says, “We can actually see macrophages eating ,” citing confocal microscopy images in the paper that show macrophages engulfing .
Kulkarni says next steps are to continue testing the new therapy in preclinical models to evaluate safety, efficacy and dosage. The supramolecular therapy they have designed has been licensed and they hope to move the therapeutic into clinical trials if preclinical testing continue to show promise.
More information: Ashish Kulkarni et al, A designer self-assembled supramolecule amplifies macrophage immune responses against aggressive cancer, Nature Biomedical Engineering (2018). DOI: 10.1038/s41551-018-0254-6

Rockwell Medical files suit against former CEO Chioini,former CFO Klema


Rockwell Medical filed a lawsuit in the United States District Court for the Eastern District of Michigan against the company’s former CEO Rob Chioini, former CFO Thomas Klema, board member Ron Boyd and former board member Patrick Bagley.The Lawsuit alleges that Chioini, Klema, Boyd and Bagley have for years mismanaged the company, promoting self-enrichment and poor corporate governance at the expense of Rockwell Medical’s shareholders, employees and patients in need of the Company’s life-changing drug, Triferic. Their recent continued attempts to paralyze the Board’s and the Company’s ability to operate follows a long-line of wrongful acts that are outlined in the Lawsuit. In addition, the Lawsuit outlines the timing and rationale for the Board’s decision to terminate Chioini and Klema. Ben Wolin, Chairman of the Board, said, “Importantly, the five independent directors of the Board are continuing to make progress on the significant efforts underway to put the company on stable footing, including identifying and hiring a new CEO and CFO, engaging a new audit firm and implementing our new Triferic commercialization strategy.” Mr. Wolin added, “We recognize how both upsetting and confusing these events resulting from the harmful actions taken by Chioini, Klema, Boyd and Bagley must be for our investors. We will continue to vigorously defend the Company and take actions that are in the best interest of the Company and all our stakeholders.”

Celyad’s CAR-T Pipeline Has Potential: Wainwright


CELYAD SA/ADR CYAD 4.34% bolstered its entirely bullish cohort of analysts Monday with a fresh buyer.

The Rating

HC Wainwright analyst Edward White initiated coverage of Celyad with a Buy rating and $45 price target.

The Thesis

The chimeric antigen receptor therapy, or CAR-T,  pipeline is led by CYAD-01, a treatment for solid and liquid tumors that’s in a Phase 1 dosing escalation study.
“We believe that by targeting eight different ligands, CYAD-01 is differentiated from currently approved CAR-T therapies and those in development,” the analyst said, noting that early safey data is “compelling.”
The drug demonstrated the world’s first complete response in relapsed/refractory acute myeloid leukemia, White said. The affected patient was still surviving 10 months after treatment, well beyond median the AML survival rate of below four months, he said.
If Phase 1 results prove positive, White said he expects a Phase 2 pivotal trial to begin in 2020 on a trajectory for 2022 approval.
In solid tumors, CYAD-01 demonstrates the potential to disrupt blood supply and modulate the immunosuppressive environment, according to HC Wainwright.
Early data from the dose escalation portion of the Phase 1 study in colorectal cancer yielded promising activity, and full figures are expected in November, White said.
“CYAD-01 could usher in a paradigm shift in cell-based immuno-oncology for solid tumors.”
Assuming 2022 approval, HC Wainwright forecast 2026 revenue of $596 million for colorectal cancer and $239 million for AML.

Apollo Medical: Units acquire 50% ownership in LA hospital


Apollo Medical announced that two of its affiliates, Network Medical Management, or NMM, and Allied Pacific of California, or APC, have acquired a 50% ownership stake in the 128-bed French Hospital, the oldest hospital in Los Angeles, for $17M. ApolloMed partnered on the acquisition with AHMC Healthcare, which operates seven hospitals in Los Angeles County and Orange County. The total cost of the 2.5-acre, 90,000-square foot facility was $33M. The French Hospital was acquired from the non-profit Societe Francaise De Bienfaisance Mutuelle De Los Angeles. The hospital closed in November 2017 after its operators chose not to renew the lease with the French society because state law required the facility to complete nearly $100M of earthquake renovations. ApolloMed and AHMC plan to convert the facility into an integrated care center, complete with a 24-hour urgent care center, multispecialty clinics, imaging center, diagnostic lab, pharmacy, behavioral care center, infusion center and will also provide telemedicine services.

New York’s top court defends city’s flu vaccine mandate for children


New York state’s highest court said today that the New York City Board of Health and Health Department can mandate annual flu vaccines for children in city-regulated day care and preschool, reversing lower court rulings.
The decision clears the way for the Health Department to enforce the rule, first adopted in December 2013 by the city Board of Health, that all children ages 6 months old to 5 years old must get a flu shot by Dec. 31 each year, and families must show proof their children have received it.
“The rules challenged here do not relate merely to a personal choice about an individual’s own health but, rather, seek to ensure increased public safety and health for the citizenry by reducing the prevalence and spread of a contagious infectious disease within a particularly vulnerable population,” Leslie Stein, associate judge of the Court of Appeals, wrote in her opinion.
A group of five families filed a lawsuit in 2015 to block the rule, and two previous court decisions ruled in their favor, leading the Board of Health to make a final appeal.
City Health Commissioner Dr. Mary Bassett hailed the decision as improving safety for the 150,000 children who would be affected. Five city children died from the flu last year. The Health Department said the mandate would be effective immediately.
“Vaccines save lives and are an effective public health tool to prevent the spread of disease,” she said in a statement. “The severity of this past influenza season reminds us of how deadly influenza can be.”

Regeneron has ‘substantial’ opportunity for Q2 upside, says Piper

Piper Jaffray analyst Christopher Raymond says that with Dupixent script trends indicated up almost 30% quarter-over-quarter, Regeneron’s (REGN) opportunity for Q2 upside is “substantial.” Further, Regeneron and Sanofi (SNY) over the weekend raised the list price by 3% for the drug’s first ever price increase, Raymond tells investors in a research note. He thinks Dupixent remains well positioned to outperform expectations “this quarter and beyond.” The analyst maintains an Overweight rating on Regeneron with a $450 price target.