Michael F. Brigham
Analyst · SER Asset Management. Please go ahead
Great, thanks Joe. I appreciate the opportunity to provide some updates on what is going on at ImmuCell. It's an exciting -- very exciting time here. The press release we disclosed last night covers the key financial highlights for the year ended December 31, 2020. We expect to file our Form 10-K providing much more detail around March 30th. As you may know we issued a press release covering our preliminary top line sales results on January 7th. We've been making these optional filings to give investors a very timely look at what I view as the most critical measure of our operations and financial performance early in the reporting period. There has been no change to our previously disclosed sales results. Product sales were up 12% for the year ended December 31, 2020 in comparison to 2019. This growth is very important for us and it comes with consistent market share gains as well. Simply put our sales team continues to disrupt the traditional scour vaccine market by replacing very old vaccine technology with our preformed antibodies. Beyond the top line results that I have just discussed and were previously disclosed, the three most important things that I want to talk to you about today are one, the status of our investment to expand our production capacity; two, the road to regulatory approval of Re-Tain; and three, our cash flows. So first, the status of our investment to expand our production capacity. We had a backlog of orders worth about $1.8 million as of 12/31/2020, compared to no backlog as of 12/31/2019. This strong indication of demand for our product is a good thing and confirms the need for our expanded production capacity because we need to get every dose that our customers want into their hands. The leasehold improvements to our new formulation fill an assembling facility were completed during 2020. The final phase of this project, which involves the 100% increase in our liquid processing operations and the 50% increase in our freeze drying operation is on budget and on schedule for completion during the second quarter of 2021. This work is being carefully coordinated to minimize disruption to our ongoing operations and product supply. Before this expanded capacity comes online we do expect to incur a decrease in sales during the first quarter of 2021 in comparison to the first quarter of 2020. This estimate of sales for the first quarter of 2021 amounts to about 92% of the 4.1 million that we estimate to be our current production capacity per quarter. We sold product equivalent to about 91% of this estimated quarterly capacity during the fourth quarter of 2020. We are working to fulfill this backlog and return to a growth mode during the second half of 2021 provided that we capture anticipated demand and end the year with available inventory on the shelf, ready for peak season sales during the first quarter of 2022, provided that we effectively complete our production capacity expansion investment. Second, the road to regulatory approval of Re-Tain, product development expenses continue to be our largest operating expense line item, increasing by 18% to 4.4 million during 2020, including a 1.5 million -- including 1.5 million of non-cash depreciation expense. Let's talk about Re-Tain a bit. It's been a long and expensive road, but we are nearing completion of the work required to achieve FDA approval of this novel subclinical mastitis treatment for lactating dairy cows without a milk discard. We recently submitted the last of five significant technical sections required for FDA approval. This one is known as the Chemistry Manufacturing and Controls or CMC Technical Section. This kind of submission is subject to a six-month review by the FDA that puts us at a huge fork in the road during the third quarter of 2021. If the FDA has questions for us, we could be required to respond through another submission, which would be subject to an additional six-month review. We do not anticipate that an additional submission would be required after that. Therefore, we are making plans for a mass market launch during the second quarter of 2022, while also being prepared to flex through an initial limited launch plan during the fourth quarter of 2021 if approval comes through in response to our first submission. Thirdly and last our cash flows. I think we should focus on our cash flows more than on our GAAP net loss at this stage in our development. Page 5 of last night's press release provides a look at the impact of non-cash expenses on our financial results. We reported increases in both EBITDA and what I describe as a measure of cash flows, which I believe is most relevant to tracking our performance. While both are important metrics to consider and understanding our cash flows, the most important measure is the statement of cash flows that will be included with our Form 10-K filing around the end of March. Subject to completion of our audit we do expect to see year-over-year increase in net cash provided by operating activities of approximately $1.1 million, which included the benefit of 938,000 in other income from the forgiveness of our paycheck protection program loan from the federal government. So in conclusion, I encourage you to review the press release that we filed last night, also please have a look at our corporate presentation slide deck, a February update was just posted to our website last night. I believe it provides a very good summary of our business strategy and objectives, as well as our current financial results. See the investor section on our website and click on corporate presentation or just contact our office and we can send you out a copy. With that said, I will be happy to take your questions. Let's have the operator open up the lines.