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Tuesday, April 9, 2019

VALNEVA to Present on Lyme, Chikungunya Vax Candidates

Valneva SE (“Valneva” or “the Company”), a biotech company developing and commercializing vaccines for infectious diseases with major unmet needs, announced today it will present on its Lyme disease and chikungunya vaccine candidates on April 16th, 2019 at the 19th World Vaccine Congress in Washington, D.C.
Valneva’s Chief Executive Officer, Thomas Lingelbach, will provide an update and discuss next steps for VLA15, the Company’s vaccine candidate against Lyme disease. Lyme is the most commonly occurring vector borne illness in the Northern Hemisphere with an estimated 300,000 Americans contracting the disease each year[1]. VLA15 has been shortlisted in the “Best Prophylactic Vaccine” category of the 2019 Vaccine Industry Excellence (ViE) Awards, held in conjunction with the World Vaccine Congresseach year.
Valneva’s Chief Medical Officer, Dr. Wolfgang Bender, will also present on the Phase 1 development of the Company’s chikungunya vaccine candidate, VLA1553. He will also discuss next steps for the potential single-shot vaccine.

Encouraging Economic Outcomes for Medtronic HeartWare HVAD System

Medtronic plc (NYSE:MDT) today announced data showing promising economic outcomes for the Medtronic HeartWare HVAD System after analyzing multiple clinical studies.
The economic analyses of the HVAD System – a left ventricular assist device (LVAD) that helps a failing heart pump and increases the amount of blood that circulates through the body – were presented at the 2019 International Society for Heart and Lung Transplantation (ISHLT) Scientific Sessions.
The first analysis showed that heart failure patients who received the HVAD System through a less-invasive thoracotomy procedure in the LATERAL study incurred lower hospitalization and medical supply costs than patients who received a ventricular assist device (VAD) through the traditional sternotomy implant procedure. The average total cost per patient in the thoracotomy (LATERAL) study was $204,107 compared to $260,492 for (non-study) traditional median sternotomy VAD cases

FDA posts tentative approval of Teva’s Icatibant

https://thefly.com/landingPageNews.php?id=2890352

Frequency shows early positive results for small-molecule hearing loss therapy

Concertgoers, rejoice: An early safety study of Frequency Therapeutics’ hearing loss drug treatment has cleared its first hurdles while showing some signs of hearing improvement in certain patients.
Frequency’s lead candidate, FX-322, is a cocktail of small-molecule drugs designed to activate the body’s healing abilities. By triggering dormant cells within the ear, the treatment hopes to spur the growth of the fine hairs that sense and translate sound waves, which can be damaged over time. The drug showed no serious adverse events in the phase 1/2 study following a single injection given through the eardrum.
Additionally, some adult patients with stable sensorineural hearing loss—with a history of either chronic noise exposure or sudden hearing loss—showed improvements in hearing range tests and word scores compared to placebo, the company said.
Frequency said it plans to publish and present the full study results at an upcoming otolaryngology meeting and launch a phase 2a study of FX-322 before the end of the year.
“While the focus of this study was safety, we are excited to see initial results in sensorineural hearing restoration as there are currently no treatments to restore hearing for these patients,” Frequency’s CEO, president and co-founder David Lucchino said in a statement.
“Furthermore, this data provides support for our small-molecule-driven regenerative medicine platform, which has the opportunity to address numerous degenerative diseases,” Lucchino added.
The double-blind phase 1/2 study randomized 23 patients to high- and low-dose FX-322, as well as placebo. Participants were evaluated two weeks after the injection, and were monitored for three months.
“If successful, our lead development program would represent the first time ever that hearing could be restored in humans with a therapeutic,” said Marc Cohen, Frequency’s executive chairman. “We are defining a new mode of regenerative medicine: activating progenitor cells within your body to repair damaged tissue.”
Frequency secured $42 million in funding through a series B round this past January to advance FX-322’s clinical testing and the company’s regenerative medicine work in other applications.
The round was led by Taiwania Capital Management and Axil Capital, a healthcare-focused venture fund spun out of Mizuho Securities. New backers included Yonjin Capital and DF Investments, while previous investors Polaris Founders Capital, Alexandria Venture Investments, CoBro Ventures, Korea Investment Partners and Emigrant Capital also participated, bringing the company’s total funding to $87 million.
Meanwhile, Frequency’s rival in the space, Decibel Therapeutics, recently brought on the company’s former chief medical officer for its own. There, Peter Weber will oversee Decibel’s gene therapy approach to treating hearing loss as well as inner-ear balance issues and tinnitus being developed in partnership with Regeneron Pharmaceuticals.
Frequency instead hired Bill Chin, formerly CMO and executive VP for science and regulatory advocacy at PhRMA, executive dean for research at Harvard Medical School and senior VP for discovery research and clinical investigation at Eli Lilly & Co.

XOMA Acquires Royalty Rights to Five Hematology Candidates

XOMA Corporation (NASDAQ: XOMA) announced today it has agreed to acquire the rights to potential royalty payments and a portion of the potential milestone payments associated with five hematology assets from Aronora, Inc. Three of the assets are anti-thrombotic candidates that are covered by a collaboration with Bayer, a global leader in hematology therapeutics. Two of the collaboration assets are in early to mid-stages of development and the third is a Phase 2 candidate that is subject to an option. In addition, XOMA agreed to acquire the rights to potential royalty payments and a portion of the potential upfront and milestone payments associated with two unpartnered hematology programs from Aronora.
The transaction diversifies XOMAs royalty interest portfolio by expanding into hematology indications, and these innovative anti-thrombotic candidates have the potential to address very large market opportunities. The fact that three assets are part of an ongoing collaboration between Aronora and Bayer, a company for whom we have tremendous respect, strengthens our belief in the potential of these therapies to address significant unmet medical needs, said Jim Neal, Chief Executive Officer at XOMA. These assets possess the characteristics we have established for our royalty aggregator business model: outstanding development partner, mid-stage to early clinical stage of development, important therapeutic categories, and sizable potential royalty opportunities. Aronoras expertise in hematology, with an advanced focus on anti-thrombotic monoclonal antibodies, intrigued our team.
The five royalty interest assets XOMA acquired from Aronora are:
Three Bayer collaboration monoclonal antibody (mAb) programs targeting factor XI/XIa: BAY1213790 in Phase 2 clinical development; BAY1831865 in early clinical development; and Aronoras AB023 (xisomab 3G3) in Phase 2 development; and,
Two proprietary hematology programs at Phase 1 and preclinical stage: AB002, a thrombin analog, and AB054, a factor XII mAb, positioned for acute cardiovascular events, medical device associated clots, and/or inflammation.
Under the terms of the agreement, XOMA will make an initial $6 million payment subject to closing conditions defined in the agreement. XOMA will make an additional payment of up to $3 million to Aronora upon fulfillment of certain other conditions. In return, XOMA will receive, on average, low single-digit royalties on future sales of these five products and 10 percent of the milestones associated with each of the assets. In addition, XOMA could pay Aronora sales-based milestones on each asset if XOMAs royalty receipts related to each program exceed certain thresholds. XOMA expects this transaction to close within the next 90 days.

Cerner upgraded to In Line from Underperform at Evercore ISI

https://thefly.com/landingPageNews.php?id=2890261

Piper encourages investors to start positions in Neuronetics

After hosting an investor call with the management team of Greenbrook TMS, a domestic transcranial magnetic stimulation provider, Piper Jaffray analyst Matt O’Brien reiterates an Overweight rating on Neuronetics with a $28 price target. Greenbrook’s goal of reaching 100-plus centers by Q1 of 2020 is on track and the company expects “robust” organic growth this year with further market development efforts, O’Brien tells investors in a research note. He points out that the majority of Greenbrook’s mix is weighted towards Neuronetics’ NeuroStar. Given the “variety of positives” on Neuronetics and the underlying TMS market landscape, investors “can put to bed any competitive concerns,” says the analyst. He encourages investors to start positions in the name.