Chobani combats sad breakfast experiences with new product
BY Ryan Chavis
NEW YORK — Stale muffins, soggy cereals and singed toast — the trappings of a sad breakfast experience. But it doesn't have to be. Greek yogurt brand Chobani is taking a stand with mission #StopSadBreakfast, which will be supported with the launch of new Chobani Greek Yogurt Oats. The product contains 10 g of protein, 8 g of whole grain and 3 g of fiber from steel-cut oats and real fruit.
Reality television star Lauren "Lo" Bosworth will help kick off the brand's #StopSadBreakfast mission at a pop-up shop in New York City's Grand Central terminal. Commuters can stop by for free Chobani Oats beginning today, Oct. 7 through Thursday, Oct. 9. Chobani also is treating sad breakfast consumers near Bryant Park.
"If there's one thing I've learned as a new business owner and chef, it's how important it is to start your day off with the right fuel! That's why I'm thrilled to join Chobani on their mission to stop sad breakfast and offer a better way to start mornings. As a chef, I am passionate about sharing good food made from only natural ingredients. I've been using Chobani to cook with for years and now with Chobani Greek Yogurt Oats, I can start my days off with a delicious cup to keep me going all morning long," Bosworth said.
Chobani Oats is available in four flavors — Apple Cinnamon, Banana Maple, Blueberry and Cranberry — and can be found in grocery stores and mass merchants across the country, including Walmart, Target, Kroger and Safeway, among many others.
Actavis strengthens emerging infectious disease franchise with acquisition of Durata
DUBLIN — Actavis and Durata Therapeutics on Monday announced that they have entered into a definitive merger agreement under which a subsidiary of Actavis will commence a tender offer to acquire all of the outstanding shares of Durata common stock for $23 per share in cash, or approximately $675 million in the aggregate, and contingent value rights entitling the holder to receive additional cash payments of up to $5 per share if certain regulatory or commercial milestones related to Durata's lead product Dalvance are achieved.
Actavis expects the acquisition to be accretive by the end of the first year.
The acquisition of Durata enhances Actavis' Infectious Disease portfolio with the addition of Dalvance (dalbavancin) for injection, the an IV antibiotic for acute bacterial skin and skin structure infections with once-a-week dosing for two weeks. Dalvance was approved by the Food and Drug Administration on May 23, and was the first drug approved as a Qualified Infectious Disease Product. A Marketing Authorization Application for dalbavancin is under review with the European Medicines Agency, with a decision anticipated in the first half of 2015.
A single-dose regimen of Dalvance also is in late-stage development for ABSSSI, with a supplemental New Drug Application filing expected by mid-2015. Durata also has plans to continue the development of Dalvance for additional indications, such as hospitalized community-acquired pneumonia and pediatric osteomyelitis.
"The acquisition of Durata is a strong strategic fit that strengthens Actavis' emerging infectious disease franchise and aligns with our stated goal to make smart, targeted investments that complement our existing businesses and position the Company for continued long-term growth," said Brent Saunders, CEO and president of Actavis. "Dalvance is a novel antibiotic that can be used in multiple sites of care. It complements our Teflaro product and ceftazidine-avibactam, currently in late-stage development, which are intended for use in the inpatient setting. Dalvance is also a highly differentiated product with documented efficacy, safety and tolerability, and its acceptance by health care providers will be enhanced by Actavis' best-in-class commercial infrastructure and complementary product line."
"With the addition of Dalvance, we deliver on our commitment to build an anti-infective franchise with true scale. Actavis will be in an enviable position to offer innovative solutions to physicians while providing value to hospitals and healthcare systems in advancing the treatment of patients in the outpatient and inpatient settings," he said.
For the six-month period of January to June 2010, an estimated 9.2 million patients were treated in U.S. hospitals for infections of any type, and nearly 17% of the diagnostic category presentations were for skin and skin structure infections. With its once-a-week dosing for two weeks, and potential single-dose formulation, Dalvance's unique dosing regimen offers a more convenient and potentially less costly approach to the treatment of serious skin infections by allowing patients, healthcare professionals and hospitals to move beyond the standard daily or twice-daily IV antibiotic infusions.
"Actavis recognizes Dalvance as a strong development asset with significant potential. By joining Actavis, we gain additional resources, commercial reach and scale to expand patient access and realize the full potential of Dalvance in the marketplace," said Paul Edick, Durata's CEO. "This transaction will provide Durata shareholders with a strong immediate return on their investment with meaningful longer-term opportunities to participate in the future upside of Dalvance through the CVRs. We look forward to working with the highly experienced Actavis team as we continue the successful launch of Dalvance."
Under the terms of the definitive merger agreement, if Dalvance is approved in Europe for ABSSSI, holders of the CVR will receive $1 per share. If Dalvance is approved for single dose administration by the FDA, holders of the CVR will receive $1 per share. If a net global Dalvance revenue threshold is met over a designated time period, holders of the CVR will receive $3 per share.
BofA Merrill Lynch is serving as financial advisor to Durata, and Wilmer Cutler Pickering Hale and Dorr is serving as Durata's legal advisor. Debevoise & Plimpton is serving as Actavis' legal advisor.
Chimerix gets emergency FDA approval for Ebola antiviral
BY Ryan Chavis
DURHAM, N.C. — Biopharmaceutical company Chimerix on Monday announced that brincidofovir has been provided for potential use in patients with Ebola virus at the request of treating physicians. Emergency investigational new drug applications were granted by the Food and Drug Administration.
"Chimerix is committed to working with global health organizations and government agencies in the fight against the Ebola virus outbreak," said M. Michelle Berrey, M.D., M.P.H., president and CEO of Chimerix. "Based on in vitro data from work conducted by the CDC and the National Institutes of Health suggesting brincidofovir's activity against Ebola, we are hopeful that brincidofovir may offer a potential treatment for Ebola Virus Disease during this outbreak. Data collected over years of clinical development of brincidofovir have allowed us to progress this compound into Phase 3 programs for cytomegalovirus and adenovirus infections, and provided information on the safety and dosing of brincidofovir to allow it to be explored as a potential therapy for Ebola Virus Disease."
The company said it is working with the FDA to finalize clinical trial protocol this week to assess the safety and efficacy of the drug in patients who are confirmed to have Ebola.
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