Neogen reports second quarter results

On December 23, 2019 Neogen Corporation (NASDAQ: NEOG) reported that its revenues for the second quarter of its 2020 fiscal year, which ended Nov. 30, were $107,803,000, compared to the previous year’s second quarter revenues of $107,098,000 (Press release, Neogen, DEC 23, 2019, View Source [SID1234552596]). Current year-to-date revenues were $209,227,000, compared to $206,724,000 for the same period a year ago.

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The second quarter was the 111th of the past 116 quarters that Neogen reported revenue increases as compared with the previous year — including all consecutive quarters in the last 14 years.

Second quarter net income was $16,276,000, or $0.31 per share, compared to the prior year’s $16,051,000, also $0.31 per share. Net income for the second quarter was benefitted by an effective tax rate of 15.3%; the rate in last year’s second quarter was 18.5%. Current year-to-date net income was $30,928,000, or $0.59 per share, compared to $31,288,000, or $0.60 per share, for the same period a year ago.

"For the quarter, we had strong performance in a number of our businesses, but we continue to fight challenges in our animal safety markets," said John Adent, Neogen’s president and chief executive officer. "Our overall genomics business continued to grow nicely, with revenues up 17%, driven by strong performance at our U.S. operations; these results were augmented by significant revenue increases at our newest global genomics locations in Australia and Canada.

"Our second quarter featured solid growth from our core food safety diagnostic product lines, including our food allergen, general sanitation, and foodborne pathogen testing products," Adent continued. "Despite continuing currency headwinds, our international revenues, which now include sales into 129 countries, increased 6% in the quarter."

Neogen’s gross margin was 47.3% of sales in its second quarter of the current year, compared to 46.7% recorded in the same quarter of the prior fiscal year. The change in margin percentage was the result of a product mix shift towards Food Safety products, which have higher margins, and gross margin improvements within our domestic genomics business. Operating income was $18,272,000, or 16.9%, for the second quarter, compared to $18,246,000, or 17.0%, in the same quarter a year ago.

"We continue to generate strong operating cash flow, but our sales results were again adversely affected by the impact of the strong dollar. In a neutral currency environment, we would have reported approximately $1 million more in revenues in the current quarter," said Steve Quinlan, Neogen’s chief financial officer. "Our balance sheet is strong, and our acquisition team is working on a number of opportunities that have the potential to drive future growth."

Revenues for the company’s Food Safety segment increased 6%, all organic, during the second quarter compared to the prior year quarter, from $53,750,000 to $56,854,000. The segment’s increase was led by a 14% rise in global sales of test kits to detect food allergens, with particular strength in sales of gluten, milk, egg and tree nut kits. This sales increase was aided by the introduction of a test kit for coconut in the past year, which represented the 19th allergen for Neogen’s comprehensive line of food allergen test kits.

Of note in the Food Safety segment’s current second quarter results was a 21% increase in sales of general sanitation tests. These tests include the product line to detect adenosine triphosphate (ATP) on food contact surfaces and in liquids. Sales of Neogen’s line of foodborne pathogen (e.g., Listeria and Salmonella) detection products also increased 11% in the current quarter compared to the prior year quarter. The increase was led by a 25% increase in sales of tests to detect Listeria, including Listeria Right Now, which detects and reports the bacteria in environmental samples in under 60 minutes — without the need to enrich samples. These increases were partially offset by a 29% decrease in sales of the company’s drug residue product line, the result of lower demand at our European distributor.

In the current quarter, revenues from international sources increased to 41% of total revenues, compared to 39% in the prior year quarter. Highlights of the current quarter included a 20% increase in revenues in our Brazilian operations, largely due to increased insecticide sales to governmental agencies, which overcame the loss of a large commercial lab customer that performs drug testing of truck and bus drivers in that country. Other international highlights within the quarter included a 7% revenue increase at our Neogen Europe operations; revenues that rose 5% at Mexico-based Neogen Latinoamerica; Neogen China’s increase of 40%, albeit from a smaller base; and Neogen Australasia’s quarterly revenue increase of 18%.

Neogen’s Animal Safety segment reported revenues of $50,949,000 for the second quarter of the 2020 fiscal year, compared to $53,348,000 in the prior year second quarter, a decrease of 4%, primarily the result of continued soft market conditions in our animal protein markets and inventory destocking within our distribution channels. Partially offsetting this was strong growth in the genomics testing business, a 28% increase in sales of the company’s disposable syringes, and a 15% increase in veterinary marking products.

Revenues from Neogen’s worldwide animal genomics business increased 17% in the second quarter of fiscal 2020 compared to the prior year. In the quarter, revenues from Neogen’s companion animal genomics business more than doubled as the company gained market share within the veterinary market. Neogen’s cattle genomics business remained strong, both for associations and for commercial producers, with revenues up from the prior year, and the company’s swine genomics business rose compared to the prior year quarter.

Neogen Corporation develops and markets products dedicated to food and animal safety. The company’s Food Safety Division markets dehydrated culture media and diagnostic test kits to detect foodborne bacteria, natural toxins, food allergens, drug residues, plant diseases and sanitation concerns. Neogen’s Animal Safety Division is a leader in worldwide biosecurity products, animal genomics testing, and the manufacturing and distribution of a variety of animal healthcare products, including diagnostics, pharmaceuticals and veterinary instruments.

SciTech Development, LLC Announces FDA Acceptance of Investigational New Drug (IND) Application for ST-001 nanoFenretinide in Patients with T-Cell Lymphoma

On December 23, 2019 SciTech Development reported that the U.S. Food and Drug Administration (FDA) has accepted Investigational New Drug (IND) Application for ST-001 nanoFenretinide, an experimental treatment for T-cell non-Hodgkin’s lymphoma (NHL) (Press release, SciTech Development, DEC 23, 2019, View Source [SID1234552595]).

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The FDA approved IND provides clearance for ST-001 nanoFenretinide to enter the clinic. SciTech’s Phase I clinical trial will be conducted at the Rush University Medical Center (Chicago, IL) under the guidance and direction of Timothy M. Kuzel, MD, FACP, Samuel G Taylor III MD Professor of Oncology, Chief, Division of Hematology/Oncology/Cell Therapy; Deputy Director, Clinical Affairs, Rush University Cancer Center (Principal Investigator, PI). The study is planned to enroll patients with relapsed/refractory (R/R) T-Cell NHL and is scheduled to begin in mid-2020 with the potential to advance to a registration trial in late 2021.

"The IND approval is an important step to enabling the collection of first-in-human safety data for nanoFenretinide. We hope to provide required data for eventual full registration of this potential treatment for cutaneous T-cell lymphoma to meet the continuing unmet needs of this rare disease population," said Dr. Kuzel.

SciTech’s ST-001 nanoFenretinide technology is a cancer drug employing a nanoparticle suspension for intravenous administration. ST-001 is comprised of nanoparticle-sized fenretinide in a patented combination with carefully selected phospholipids. SciTech’s product pipeline includes nanoFenretinide formulations for the treatment of several cancer indications.

"FDA approval of our IND for ST-001 is a significant milestone in the development of our SciTech Drug Delivery Vehicle (SDV) program," said Earle Holsapple, President of SciTech Development. "Moving forward, and in addition to the previously granted Orphan Drug Status (Feb. 1, 2018) for the treatment of peripheral T-cell lymphoma (PTCL) and cutaneous T-cell lymphoma (CTCL), we intend to make use of other FDA expedited programs including fast track designation, priority review and expedited new drug application (NDA) approval in bringing ST-001 nanoFenretinide to market."

SciTech Development will present an update at the Biotech Showcase on Monday, January 13, 2020 at 11:15am (PST) at the Hilton San Francisco Union Square Hotel (Room: Franciscan B), 333 O’Farrell Street, San Francisco, CA. Qualified investors can register to attend Biotech Showcase free of charge and SciTech personnel will be available during the annual JPMorgan Healthcare Conference in San Francisco. For ST-001 nanoFenretinide investment and partnering opportunities contact Earle Holsapple | +1-313-263-4887 | [email protected]

Asia Matters presents "Special Award to Investors in Ireland" to WuXi Biologics

On December 23, 2019 WuXi Biologics ("WuXi Bio") (2269.HK), a leading global open access technology platform for biologics, the all-in-one solution for research, development and manufacturing offers biological preparations, reported the "Special Award to Investors in Ireland " at the Asia Matters Global Business Summit 2019 (Press release, WuXi Biologics, DEC 23, 2019, View Source [SID1234552594]). This is Ireland’s only Asian think tank that specifically deals with trade, investment and economic issues, as well as international relations between the EU and Asia.

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The "Special Award to Investors in Ireland " is given to a newly established company that invests in Ireland. The emphasis is on a long-term and significant contribution to economic growth, employment, research and corporate social responsibility (CSR). Last year, WuXi Biologics a "Factory of the Future" for the production of biologicals was built in Dundalk. A second investment was announced last month by its subsidiary WuXi Vaccines. A new vaccine production facility is to be built at the Dundalk site.

"We are extremely pleased to receive this award from Asia Matters . It demonstrates the great progress we are making in Ireland, "said Dr. Chris Chen , CEO of WuXi Biologics, speaking at the summit." Based on our leading expertise and expertise in the high-growth biology business, we will continue to be our local and global partners provide a robust and world-class supply chain for the benefit of patients around the world. "

Universal Health Services, Inc. To Present At The 38th Annual J.P. Morgan Healthcare Conference

On December 23, 2019 Universal Health Services, Inc. (NYSE: UHS) reported that Steve Filton, Executive Vice President and Chief Financial Officer will present at the 38th Annual J.P. Morgan Healthcare Conference in San Francisco, CA, on Monday, January 13, 2020 at 2:00 p.m. (Pacific Time) (Press release, Universal Health Services, DEC 23, 2019, View Source [SID1234552593]). A live audio webcast of the presentation will be available on the Company’s website (www.uhsinc.com). For those unable to listen to the live webcast, a replay will be available on the Company’s website for 90 days following the conferences.

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Universal Health Services (NYSE: UHS) is one of the largest and most respected hospital management companies in the nation. For nearly 40 years, UHS and its affiliates have focused on meeting patients’ healthcare needs across hundreds of local communities. Today, UHS subsidiaries own and/or operate 394 inpatient and outpatient facilities including acute care hospitals, behavioral health facilities, ambulatory centers, freestanding emergency departments, and urgent care centers in 37 states, Washington, D.C., the United Kingdom, Puerto Rico, and the U.S. Virgin Islands. For additional information on the Company, visit our web site: View Source

Illumina to Webcast Upcoming Investor Conference Presentation

On December 23, 2019 Illumina, Inc. (NASDAQ:ILMN) reported that its executives will be speaking at the following investor conference and invite investors to participate via webcast (Press release, Illumina, DEC 23, 2019, View Source [SID1234552592]).

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J.P. Morgan Healthcare Conference in San Francisco, CA on Monday, January 13, 2020
Presentation at 8:30am Pacific Time followed by a Q&A Session at 9am Pacific Time

The live webcasts can be accessed in the Investor Relations section of Illumina’s website under the "company" tab at www.illumina.com. Replays will be posted on Illumina’s website after the event and will be available for at least 30 days following.