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Operator
As a quick reminder, there are three principal drivers for us joining forces with BD. First, to significantly improve our commercial reach, both in the U.S. and abroad. Second, to improve our selling effectiveness by combining our offerings with the BD portfolio to close more accounts. And lastly, to collaborate on future innovations. We are pleased with our improved commercial reach within the first several months of the partnership being launched in the U.S., as well as with the early days in EMEA. We are tracking commercial reach closely and are seeing big improvements with the volume of sales calls, as well as those calls turning into new FINO opportunities. In the U.S. alone during the first quarter, we added nearly as many new FINO opportunities to the funnel as we did throughout all of 2022. Turning to selling effectiveness, we are measuring effectiveness through sales funnel progression, funnel velocity, and ultimately account capture. We are seeing meaningful funnel stage progression, which has led to a significant increase in quotes and contracts being developed and presented compared to the prior year. In quarter two and beyond, we are expecting to deliver a significant increase in placements not seen since prior to the pandemic. This is exactly why we entered into a long-term partnership with Beck & Dickinson. In EMEA, we launched the Global Bloodstream Infection Campaign along with BD at the largest microbiology congress, ECMID, in Copenhagen last month. By showcasing Accelerate's ARC and Pheno with the breadth of BD's microbiology portfolio, customer enthusiasm was clear for end-to-end workflow complete solutions. Many current and prospective customers were eager to discuss implementing the BSI solution. This has led to a simplified contract offering for the combined BSI portfolio, which will include contracting and ordering to improve customer ease and speed of adoption. Turning more specifically to ARC, a customer from Italy will be presenting a poster on ARC workflow at the ASM Microbe coming up in June. The author also intends to publish a full study readout in a peer-reviewed European journal. We will leverage this customer's good work as part of our selling efforts in EMEA in the future. Bringing ARC to the U.S. market remains a priority as there are clear demands for an automated, cost-effective sample preparation solution for positive blood cultures. As discussed on our prior calls, we continue to pursue ARC as a Class II 510 device with the FDA and remain in active dialogue. We will not have a forecasted launch date in the U.S. until we begin clinical trials. Lastly, with our BD partnership, collaboration on future product development efforts remains a focus and early progress is being made on a number of fronts. Now turning my comments to our third strategic priority, delivering innovation with our next generation platform WAVE. We continue to make very good progress with our WAVE development program. As discussed previously, we have taken delivery of over 20 alpha instruments which are up and running in our core lab. Early instrument reliability is very good and the data being produced is quite promising. This is very exciting and has significantly sped up our development efforts. As a reminder, the WAVE platform will be able to provide rapid susceptibility test results for both positive blood culture and isolated colony samples and other sample types on a single system with significantly improved platform economics over Pheno. The WAVE system has complete random access and is capable of running 20 samples in a single shift from a single module. The system is fully scalable, which allows easy adoption by small and medium labs, while larger labs can integrate multiple modules into one system to manage all necessary volume and workflow needs. Our customers have confirmed a consolidated susceptibility approach will have a superior advantage over traditional isolated-based platforms on the market today. For Accelerate, WAVE significantly expands our revenue and wallet share per customer. while restating our platform economics. Our target is to deliver a pre-clinical data readout by the end of the year and start our clinical trials shortly thereafter. In summary, Q1 results were in line with our expectations, and we are very optimistic about the remainder of 2023 and beyond. By restructuring our debt and securing additional new capital, we can solely focus on driving our core business priorities. Our partnership with BD is off to a good start and will continue to gain momentum. Our R&D, regulatory, and manufacturing organizations are laser focused on wave development and achieving key milestones. And of course, we will continue to focus on organizational talent, infrastructure, and processes to scale up our business and support future growth. I would now be happy to answer questions from our analysts Should others on the call have questions not addressed today, we would welcome you to send these questions or request for a follow-up meeting to investors at axdx.com. Thank you.
David
We'll now begin the question and answer session. The first question comes from Andrew Brackman with William Blair. Please go ahead.
Andrew Brackman
Hi, guys. Good afternoon. Thanks for taking the questions. Jack, you talked about the momentum that you're seeing here with BD on the commercialization front. Maybe peel back the onion there a little bit and tell us exactly where you're starting to see that momentum, anything in terms of specific customer types where you're starting to see some increased interest there. Thanks.
Operator
Sure. Thanks, Andrew. Appreciate the question. Yeah, as I said in my opening remarks, really good activity and the momentum is building with BD. As I mentioned, we've been live since January. We've trained an entire sales organization of a large number of people, regions, and so forth. And so what we're starting to see now is more and more accounts coming into the funnel. Specifically, I mean, they're across the U.S., They're really, I mean, where we're starting to see, you know, early, early success with BD is naturally in the accounts where BD already has a very strong relationship, where they have systems in place, whether it be blood culture systems or whether it be MALDI systems or even, you know, in some cases, the Phoenix susceptibility system that they have as well. With those accounts, we're really getting entry, we're getting reach, we're getting access. We're immediately, with our small team of specialists that support the BD salespeople, we're able to go in and get very quickly into dialogue. And those are where the accounts are starting to not only just become introductory calls, but also advancing very rapidly through the sales funnel because of the relationships, because of the trust that's already been built in BD. And so, again, what we're seeing is, and what we believe will happen, and what I've talked about is, as we move into quarter two here, we're almost halfway through the quarter, and then Q3 and Q4, we're going to start seeing more and more funnel growth, funnel progression through the funnel, and then ultimately more and more account closes as we progress throughout the year.
Andrew Brackman
That's perfect and good to hear. Maybe just turning the wave here, it sounds like things are progressing nicely with development efforts there. Can you maybe just sort of take a step back and just sort of talk about the critical steps that are needed here to get that to the market? And then if you're successful there, just sort of talk to us high level about what this does to your opportunity size with customers. Thanks.
Operator
Yeah, absolutely. Let me take the second part of that first. I mean, just a reminder on why wave. So Wave is a completely new, innovative platform that builds on the great experience that we've learned in rapid ID and AST testing over the years. We're using a significant amount of our AI that we've built relative to organism and bug drug combination learnings that we have already. But the actual system and the technology that we're using relative to image capture, throughput, random access, all of that is unique to Wave. It's different than Fino. And then also, from a business model standpoint, Wave will dramatically change our overall cost position because of cost of goods sold and the way that we're able to capture images. So we believe with this then, with WAVE, what will happen is we have the opportunity to open up not only positive blood culture, which we're clearly doing today with Pheno, that will be available on WAVE, but also it will also take it to the next level, which is the much higher volume testing in the isolate market and other future samples that is a much, much higher lower acuity, but much higher volume testing segment within microbiology, which will significantly expand our footprint within microbiology. It will allow us to not only compete in rapid positive blood culture, but also the much broader segment. It will allow customers to consolidate instrumentation that they have today in their laboratory and bring that together. As far as the program goes, we're very happy with the way the program is progressing. We have over 25 systems live today in our clinical laboratory we're running samples on. We're getting very good results. Reliability looks very good. The next phases, Andrew, are we'll be looking at having beta units here over the coming months. We'll be getting those units live as well. That is on track. And then from there, we look to prepare for really the preclinical studies that we'll be doing, and we expect to produce that preclinical readout sometime in Q4. From there, we'll prepare our clinical trial that we're already working on today, but we'll prepare that and get started on the clinical trial work thereafter.
Andrew Brackman
Okay, perfect. And then just sort of last one for me. just on the RSA that was announced a few weeks ago. It sounds like you're increasingly confident that that's going to get done. I recognize you probably don't want to say too, too much on that, but can you maybe just sort of provide a high-level detail around what's driving that confidence? Thanks.
Operator
Yeah, great. I'll turn it over to David and let him take that one.
David
Sure. Andrew, thank you for the question. So, you know, this is the question that we're getting a lot these days, and, you know, it is a pending transaction, so I want to start there, that nothing's been finalized and it's a proposal. And so what we have here is, as you know, we've agreed to a restructuring support agreement with a vast majority of our note holders. And so really once that subsequently was announced, we got to work on three main priorities. The first one was the subsequent documentation and the agreements that we're working on with both us and the note holders to bring this transaction to closure. And so that includes many, as I said, the securities purchase agreements, and there's many subsequent transactions as a part of this proposal. So we're working on that every day. Secondarily, we're working with our current RSA signers, if you will, that we're going to go on and get more folks signed on to the deal. We work on this every single day. And really, getting progress there is twofold. It's ongoing and active dialogue with the folks that aren't yet signed on. Additionally, it is going to bringing up those note holders up to speed on what the terms and the conditions are of the transaction, walking them through kind of the series of transactions, why certain things were done. And so those have been good and productive dialogues. And thirdly, as well, is we have a shareholder meeting next Friday, which is May 19th. And part of our outstanding proxy statement is we have several proposals out there that will help facilitate the transactions that are within the RSA proposal. And so, you know, we're working on all three of those, you know, of those work streams every single day and continue to work. So, you know, and we've had a lot of great dialogue. And so from there, you know, we keep working it every day.
Andrew Brackman
Very clear. Thanks, guys.
David
The next question comes from Alex Nowak with Craig Hallam. Please go ahead.
Alex Nowak
Good afternoon, guys. This is Chase Don for Alex. I'll start now with one for David. I mean, looking at, you know, OpEx in the quarter up a little bit sequentially, I know kind of, you know, optimization of that spend is certainly a big focus for you guys. I guess walk me through the moving pieces of the increase sequentially. And then you had mentioned some one-time expenses from the debt restructuring. Kind of walk me through what comes out and then what we should be thinking about for OpEx on the go forward.
David
Thank you very much, Chase. Great question. When we look at OpEx, that is one of our focuses as Jack talks about financial strength. Once we work through the debt restructuring and the proposed transaction, this is going to be the laser focus moving forward. We did have a hefty amount of professional fees associated with the debt restructuring in the quarter. We do anticipate that to bleed into this quarter a bit. as we work to close the transaction as previously discussed. That said, we are also seeing savings from the restructuring of our commercial organization back last year, and so that will continue to streamline as well. So overall, SG&A will streamline over the subsequent quarters for those reasons. Moving to R&D, and most importantly, another laser focus for us, is the great progress we're making with WAVE. So as Jack mentioned, we just began ordering beta units which will essentially be very close to our production units that we'll be using in a post-FDA setting. So these beta units we're actually purchasing will be used in the clinical trial. And so from there, we're bringing the project timeline in from that standpoint, but that also brings in costs. So for us, it's a very exciting time, but also bringing in some of the project costs has led to higher incurred costs earlier in the year than we anticipated. And for us, you know, that's very exciting. But as we're exiting development and entering, you know, B and D, you know, we'll see, you know, the costs, you know, be reduced. And that's because we're entering trial. And with the significantly lower cost of goods sold, it'll be a much more cost-effective clinical trial than FINA was. And so with that, we anticipate both SG&A and R&D coming down in the subsequent quarters this year.
Alex Nowak
Got it. Maybe relaying that into a question for Jack. Assuming that the RSA closes and everything gets squared away there, without drastic OPEX cuts, we've got another capital raise in our model needed at some point in the future here. Certainly, though, it gets pushed out meaningfully. Update investors where you'll be able to get to from a business perspective with traction with BD and with this restructuring and additional capital that's going to flow into the model.
Operator
Yeah, thank you. So, I mean, a couple things on that front. First of all, as David highlighted, I mean, we're actively looking at our cash burn and continuing to conserve cash wherever possible. We're doing a good job with that on many fronts, and we're going to continue to do that. The second thing that you mentioned is absolutely getting the the commercial business cranking and doing that through our partnership with BD. As I mentioned, that's going, we're very happy and encouraged about how it's going. It just, as you look at training an entirely new sales organization, these things take time, but what we're starting to see is the opportunity for revenue growth, new account places, new account placements closes, leading the revenue growth into the future. So we're looking closely at that clearly. And all of those things put together will ultimately lead us to at what point should we need to raise additional capital. We'll make that decision in the future as we look at all these different levers.
Alex Nowak
Got it. But at that point, you know, BD is going to be an attraction. There's going to be a much different place. I guess digging in a little bit more on kind of the funnel that started to grow now with BD. I mean, let's kind of separate out that customer base that's coming into the funnel. Is it kind of where, you know, BD is out there currently doing RFPs for, you know, certain customers and build outs or expansions in the lab? Or is it existing customers that are kind of being cross-sold with existing BD devices, might not need upfront capital from them, but they're kind of being cross-sold your instruments and your solutions?
Operator
Yeah, it's a combination of all of the above. So in EMEA, for example, just this week alone, we participated in several very key, very large tenders. that were completely driven by BD. It was a tender for a much bigger group of product offerings than just the Pheno and Arc, but it included Pheno and Arc as well. And so we've got that happening in EMEA. And then in the U.S., we definitely have very specific accounts where BD customers are upgrading or renewing contracts, and as part of that, they're very interested in closing the gap relative to rapid susceptibility. And that's where Pheno comes in, and that's where we are effectively combining the Pheno along with other solutions. And then I would say equally, we have you know, very specific pointed customers that are interested solely in Rapid ID and AST. These may be accounts that we've known or were working previously, and now we're working those along with BD. And those are accounts that are, I would call them our more traditional accounts that we had before our partnership with BD. that are more standalone opportunities that are looking for rapid ID AST or they're looking for AST only, an AST only solution. They're looking for a combination of things. And that's where we're continuing to drive that along with BD as well.
Alex Nowak
Got it. That's helpful. I appreciate the questions, guys.
Operator
Thank you.
David
This will conclude our question and answer session. I'll turn the conference back over to Mr. Jack Phillips for any closing remarks.
Operator
Thank you, and thanks to everyone for dialing in to the call today. Just in summary, a few things from my side. As I mentioned a few times today, our BD Partnership, you know, the reason why we came to this partnership was to grow market share globally, to really create great reach, to improve our selling effectiveness by combining the rapid IDAST along with other solutions to create an end-to-end bloodstream infraction solution for customers, and then ultimately to collaborate on much broader innovation for the future. And I would say while this partnership was a big stepwise change for Accelerate, it took a lot of effort and continues to take a lot of effort as it relates to training, bringing all the key stakeholders up to speed from regional sales managers, marketing managers, salespeople, et cetera, up to speed. We've done so much of that legwork along with BD, and I would say right now it's going extremely well And what we're looking for into the future here, we're starting to look to the future for more closes, more effective opportunities, and ultimately, reagent growth and more account penetration. And then on the wave front, we could not be happier about how our next generation innovation is advancing that will dramatically improve our footprint in microbiology. It will allow customers to consolidate and add not only rapid positive blood culture susceptibility, but also consolidate that high volume isolate testing as well. We are on track with our program. We continue to innovate every day and we expect to continue to update on this very important innovation program as we go throughout the year. And then as David talked about today, our debt restructuring continues to go along. We expect this to be closed out over the coming weeks, and we plan to update on that as well. And that will clearly open us up to truly focus on all the other key aspects of the business around market share growth and innovation, et cetera. So with that, I'll bring this earnings call to a close. Thank you for your support of Accelerate Diagnostics, and we'll talk to you all soon. Thank you.
David
The conference is now concluded. Thank you for attending today's presentation.
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