Michael Brigham
Analyst · Shattemac Capital. Please go ahead
Thank you, Joe, and thanks to all of you participating on today’s call. All of us, at ImmuCell, greatly appreciate your time and interest. I have a few prepared remarks and observations before turning to the Q&A. This was a very positive year for us. I feel that our business continues to be headed in the right direction. As you may know, we provide significant disclosures about the company and our financial results in our SEC filings. Today's press release includes significant details about the financial results and we expect to file our Form 10-K for the year ended December 31, 2015 before the end of March. I encourage you to review these reports for the full details, but I will touch on five highlights here. First, let's talk about the fourth quarter of 2015, all of the following numbers compare the three-month period ended December 31, 2015, to the three-month period ended December 31, 2014. Product sales increased 22% or $489,000 to $2.7 million. In addition to these sales out our door, we also had a backlog of orders aggregating approximately $381,000 as of December 31, 2015. We are proud of this significant and consistent sales growth. Gross margin increased by 23% or $315,000 to $1.7 million equaling 62% of product sales. Product development expenses decreased by 28% or $132,000 to $331,000. Net income increased by 121% or $158,000 to $289,000. The earnings per diluted share increased to $0.09 from $0.04. Second, let’s talk about the full-year ended December 31, 2015. All of the following numbers compare the year ended December 31, 2015, to the year ended December 31, 2014. Product sales increased 35% or $2.6 million to $10.2 million. As I noted, in addition to these sales out our door, we also had a backlog of orders aggregating approximately $381,000 as of December 31, 2015. Again, we are proud of this significant and consistent sales growth. Gross margin increased by 41% or $1.8 million to $6.3 million equaling 61% of product sales. Product development expenses decreased by 43% or $944,000 to $1.2 million. Net income increased to $1.2 million in contrast to a net loss of $167,000. Earnings per diluted share were $0.38 in contrast to a loss per share of $0.06. Third, I would like to comment on the market dynamics and the drivers to this improved financial performance. Above all, we are benefiting from an increase in sales of First Defense and the resulting increase in gross margin from these growing sales. A competitive product experienced interruption of its supply to the market during the early part of 2015, beef prices are strong, more than anything I believe our sales and marketing team is doing excellent job in the field. This is evidenced by the 36% increase in year-over-year sales of First Defense. This sales growth has created a backlog of orders since the first quarter of 2015. We have responded to this backlog by increasing our production capacity. The investment to increase our First Defense liquid processing capacity by 50% was completed during the fourth quarter of 2015. The investments increased our First Defense freeze-drying capacity by 100% is proceeding on schedule and is expected to be completed before the end of the first quarter of 2016. Additionally, product development expenses were higher through the first half of 2014 as we incurred expenses to construct a pilot plant for the production of Nisin, our active ingredient in Mast Out. Fourth, I would like to talk about our financing strategy to build the commercial scale plant for the production of Nisin, our active ingredient in Mast Out. We investigated several strategic options, including a contract manufacturer that we found to be prohibitively expensive, as well as several possible corporate partnerships that would have taken a large share of the gross margin from sales of the product. After much deliberation with our Board of Directors, we settled on a combination of debt and equity financing to augment our available cash and cash to be generated from operations. On January 19, 2016, we signed a commitment letter with TD Bank covering $4.3 million credit facility which is subject to customary closing conditions. On February 3, 2016, we raised $5.9 million in gross proceeds from an underwritten public offering of 1.1 million shares of common stock at a price to the public of $5.25 per share. The net proceeds from the common stock issuance were approximately $5.3 million after deducting underwriting discounts and other expenses incurred in connection with the offering. Craig-Hallum Capital Group LLC of Minneapolis acted as our sole underwriter and placed approximately 27% of our stock, largely with institutional investors, resulting in an increase in our shares outstanding to almost $4.2 million. As a result, we now for the first time, have a clear roadmap to complete the development of Mast Out and bring the product to market. Our preliminary estimate for the cost of this project is approximately $17 million to $18 million and we aim to complete the construction and installation work in late 2017 or 2018. This is an important milestone in the history of ImmuCell and we look forward with great anticipation. Fifth, and lastly, our balance sheet has been strengthened principally by our continued profitability. We closed on the purchase of land intended for the Nisin facility. In December 2015, we had cash and investments of $6.5 million, and equity of $10.6 million as of December 31, 2015. These balances are before the effect of the new debt and equity financing discussed above. To summarize, we continue to execute on the two core components of our business strategy, as to the first core strategic action, we are expanding the market penetration of First Defense our best-in-class treatment for calf scours. The addition of a bovine rotavirus disease claim to our existing claims against E. coli and coronavirus infections could allow us to bring the first passive antibody product with this breadth of disease claims to market in 2017. As to our second core strategic action, we are advancing the development of Mast Out, our novel treatment for subclinical mastitis in lactating dairy cows. Our groundbreaking product innovation is unlike all other mastitis treatments on the market today, and they're all sold subject to a milk discard period. Our goal is to revolutionize the way mastitis is treated by making earlier treatment of subclinical infections economically feasible by not requiring a milk discard or meat withhold during or for a period of time after treatment. No other product presently on the market can offer this value proposition. Work is underway to complete the two remaining technical sections required for approval of the new animal drug application for Mast Out by the U.S. Food and Drug Administration is presently uncertain, when our FDA approval of this product will be achieved. But we have disclosed a timeline of events that could lead to our achieving this approval during late 2018 or 2019. Again, we provide extensive additional details in our press release, and will provide more detail in our Annual Report on Form 10-K. I encourage interested investors to review these filings. With that, I would like to move on to the Q&A. Let's open up the call for your questions. Denise, could you help us with that?