Vicarious Surgical (ticker: RBOT) announced its first-quarter financial results for 2024, highlighting advancements in its V1.0 surgical system and outlining its strategic focus on disciplined execution and testing. The company reported a decrease in operating expenses and a substantial cash reserve while preparing for clinical trials and FDA submissions.
Key Takeaways
- Vicarious Surgical's operating expenses in Q1 2024 were $16.1 million, down 28% from the previous year.
- The company reported an adjusted net loss of $15.1 million for the quarter.
- Research and Development (R&D) expenses amounted to $10 million, with general and administrative expenses at $5 million.
- Vicarious Surgical completed a successful cadaver lab in March, identifying areas for system refinement.
- The company expects to complete the V1.0 system by fall 2024, with a clinical trial planned for 2025.
- Vicarious Surgical ended the quarter with $84 million in cash and short-term investments.
- The estimated cash burn rate for 2024 is projected to be around $50 million.
Company Outlook
- Vicarious Surgical aims to fine-tune the V1.0 system in the coming quarters, leading to formal verification and validation testing.
- The unique technology of the V1.0 system, which reduces the need for multiple incisions, is anticipated to offer a competitive edge in the surgical robotics market.
- Clinical trials for the V1.0 system are scheduled for 2025, with preparations for FDA de novo submission underway.
Bearish Highlights
- The company encountered software bugs and issues with arm sensing during the cadaver lab testing.
- Vicarious Surgical reported an adjusted net loss, indicating ongoing investments in R&D and system refinement.
Bullish Highlights
- The successful cadaver lab in March validated the capabilities of the V1.0 system and provided valuable insights.
- The company's strong cash position supports its operational and development goals.
Misses
- Despite progress, the company still needs to address the identified technical challenges before proceeding with further testing.
Q&A Highlights
- CEO Adam Sachs expressed confidence in the company's teams and emphasized the importance of disciplined execution.
- Sachs noted that while there have been no direct updates from the FDA, other companies have received approvals based on non-U.S. data.
- Vicarious Surgical is in discussions for site selection for its OUS clinical trial, indicating a strategic approach to regulatory approval.
In summary, Vicarious Surgical is making strides in the development of its innovative V1.0 surgical system, with a focus on overcoming technical challenges and advancing towards clinical trials and regulatory submissions. The company's financial results reflect a commitment to R&D and a strong cash position to support its strategic initiatives.
InvestingPro Insights
Vicarious Surgical (ticker: RBOT) has shown a disciplined approach to its financials, as reflected in its first-quarter results for 2024. Here are some key metrics and insights from InvestingPro that provide a deeper look into the company's financial health and market performance:
InvestingPro Data:
- The company's market capitalization stands at $49.29 million, indicating its size within the surgical robotics sector.
- With a negative Price/Earnings (P/E) ratio of -0.7 for the last twelve months as of Q4 2023, investors should note that the company is not currently profitable.
- The Price/Book (P/B) ratio is at 0.51, which may suggest that the stock is undervalued relative to the company's book value.
InvestingPro Tips:
- Analysts have revised their earnings upwards for the upcoming period, which may signal optimism about the company's future performance.
- Despite a strong cash position, Vicarious Surgical is quickly burning through cash, a concern that investors should monitor closely.
For investors seeking more detailed analysis and additional insights, there are 9 more InvestingPro Tips available for RBOT, which can be found at InvestingPro Q1 2024:
Operator: Hello. And welcome to Vicarious Surgical’s 2024 First Quarter Earnings Call. My name is Elliot, and I’ll be coordinating your call today. [Operator Instructions] I’d now like to hand over to Kaitlyn Brosco, Head of Investor Relations. The floor is yours. Please go ahead.
Kaitlyn Brosco: Thanks Elliot, and thank you all for joining. With me today for prepared remarks are Adam Sachs, Co-Founder and Chief Executive Officer; and Bill Kelly, Chief Financial Officer. Later, Randy Clark, our new company President, will join for the Q&A portion of this call. Today after market closed, Vicarious Surgical released financial results for the three months ended March 31, 2024. A copy of this press release is available on the company website. Before we begin, I’d like to remind you that management will make statements during this call that include forward-looking statements within the meaning of federal securities laws, which are made pursuant to the Safe Harbor provisions of the Private Securities Litigation Reform Act of 1995. Any statements contained in this call that relate to expectations or predictions of future events, results or performance are forward-looking statements. All forward-looking statements, including without limitation, those relating to obtaining approval for the Vicarious Surgical system and timing for any such approval, our operating trends and future financial performance, expense management, market opportunity and commercialization are based upon our current estimates and various assumptions. These statements involve material risks and uncertainties that would cause actual results or events to materially differ from those anticipated or implied by these forward-looking statements. Accordingly, you should not place any undue reliance on these statements. For a list and description of the risks and uncertainties associated with the business, please refer to the risk factors set forth in our Securities and Exchange Commission filings, including our most recent Form 10-K and Form 10-Q. This conference call contains time-sensitive information and is accurate only of this live broadcast today, April 29, 2024. Vicarious Surgical disclaims any intention or obligation, except as required by law, to update or revise any financial projections or forward-looking statements, whether because of new information, future events or otherwise. Now, I’ll hand the call over to Adam for prepared remarks.
Adam Sachs: Thanks, Kate, and thank you, everyone, for joining us. I’m proud to report a strong start to the year as we advance our mission to improve lives by transforming surgical robotics. In the first quarter, we made meaningful progress toward the finalization of our V1.0 system. The collective efforts of our development team culminated in the completion of our spring cadaver lab at the end of March. This lab marked the first use of our integrated V1.0 system in a cadaveric procedural setting, with the primary goal of validating the capabilities and potential of the new system’s feature set. I’m pleased to share that the lab proceeded as we had anticipated, verifying several advancements in development and yielding valuable insights across the system. During the lab, our V1.0 system showcased the tremendous potential inherent in our novel platform. Underpinned by the new fortified software, electronic and mechanical architecture, and supported by enhanced instrumentation and visualization technology, the V1.0 system exhibited the dynamic motion capabilities of our patient cart, facilitated maneuverability within the abdominal cavity and enabled 360-degree visualization and access to targeted surgical sites. We highlighted many of these specific V1.0 development goals in our remarks last year and I’m happy to report the success of our team’s diligent efforts since. As anticipated, in addition to our development success, the lab offered insight into the additional refinements required for our final system. Over the next few quarters, our team will focus on leveraging these insights to fine-tune the V1.0 system in preparation for formal verification and validation testing. Taking a step back, I’d like to contextualize the detailed development work we are performing against the broader landscape for surgical robotics to remind our stakeholders why we believe our offering is poised to take a disproportionate share of this market over time. Even with considerable progress over the past few decades, the field of surgical robotics is still in its infancy. Despite substantial growth and varying new market entrants, around 96% of the estimated $150 billion market opportunity remains white space. Recent strategic activity in the space continues to strongly support this notion that robotics is the future of surgery. And while existing robotic technology has notably augmented surgeons’ capabilities, these multi-port systems have amplified costs to the hospital system without addressing the technology’s fundamental limitations. For example, lack of instrument dexterity and range of motion constrains surgeons to utilizing wrist-on-a-stick instruments that necessitate multiple incisions to the patient and require cumbersome instrument triangulation by the surgeon. This approach introduces complexity both during the procedure and in preoperative steps, contributing to the steep learning curve for new users and the low 4% adoption rate for surgical robotics today. Vicarious Surgical was founded on the recognition of these limitations of multi-port surgical robots. Instead of building off legacy robotic technology, we reimagined surgical robotics from the ground up. Core to our reimagined architecture is our proprietary decoupled actuator technology, which prevents the force buildup in the joints of each instrument arm, significantly enhancing the dexterity and range of motion of our system, and thereby eliminating the need for multiple incisions required for instrument triangulation. Through a single 18-millimeter incision, our system is designed to achieve full intra-abdominal access with high force exertion for our targeted surgical indication. We believe this streamlined approach will enhance procedural efficiency and remove the training demands on new surgeons for every procedure. With today’s offerings predominantly limited to multi-port wrist-on-a-stick technology, we, along with our hospital system partners, see this as a distinct clinical and commercial advantage. We are confident that our technology’s unique capabilities will establish a lasting competitive edge for us in the robotic assisted surgery market and with the completion of our spring cadaver lab, we are excited to have taken another step towards finalizing our differentiated system. With that, I will turn it over to Bill to review our financial performance.
Bill Kelly: Thank you, Adam. As expected, our 2023 initiatives to streamline resources, optimize spending and restructure the company for maximum efficiency are yielding a benefit to our 2024 expense profile. As a result, total operating expenses for the first quarter of 2024 were $16.1 million, a 28% decrease, compared to $22.3 million in the first quarter of last year. R&D expenses for the first quarter of 2024 were $10 million, compared to $13.4 million in the first quarter of 2023. General and administrative expenses for the first quarter of 2024 were $5 million, down from $7 million in the first quarter of 2023. In first quarter 2024, sales and marketing expenses were $1.1 million versus $2 million in the first quarter of 2023. Again, the year-over-year reduction in operating expenses reflects the diligent efforts made throughout last year to optimize our burden and prioritize capital efficiency. Continuing on, adjusted net loss for the first quarter of 2024 was $15.1 million, equating to a net loss of $0.09 per share, as compared to an adjusted net loss of $20.8 million or $0.17 per share, in the first quarter of 2023. GAAP net loss for the first quarter of 2024 was $17 million, equating to a net loss of $0.10 per share and this compares to a net loss of $26.9 million or $0.21 per share, in the first quarter of 2023. For a reconciliation of all non-GAAP measures to GAAP, please review our earnings press release. We ended the first quarter of this year with approximately $84 million of cash, cash equivalents and short-term investments on our balance sheet. This represents a first quarter cash burn rate of approximately $14 million. Note that while first quarter cash burn was slightly elevated as a result of a few seasonally timed payments, we continue to expect full year 2024 cash burn to be approximately $50 million and remain committed to disciplined capital allocation. 2024 is off to a strong start and our team is executing with the urgency and discipline needed to achieve our development timeline, including the completion of the V1.0 system build and integration this fall. We look forward to updating you as we progress with our business initiatives in the coming quarters. And with that, I’ll turn the call back to Adam for closing remarks. Adam?
Adam Sachs: Thank you, Bill. I’d like to close by reemphasizing the way in which we as a company have differentiated ourselves within the broader robotics market. While many surgical robotics companies continue to iterate on legacy platforms, we are taking a new path forward. While this approach takes careful time and consideration, we remain steadfast in the value of our unique technology. I’d like to thank all of our stakeholders, particularly our employees, for their continued support of our mission and vision. Elliot, we’re now happy to take any questions.
Operator: Thank you. [Operator Instructions] First question comes from Ryan Zimmerman with BTIG. Your line is open. Please go ahead.
Ryan Zimmerman: Thanks. Thanks for taking my questions. Good afternoon. Just maybe a few for me. Your R&D expenses came in a little higher. SG&A was certainly lower than I think we expected. But overall, really good expense management this quarter. Just kind of help us understand kind of how you’re balancing the needs on kind of both sides of that P&L as you think about your progress and kind of what you have planned for the balance of this year?
Bill Kelly: Great question. Obviously, as we’ve made a number of cost reductions year-over-year, the focus has really been on building a quality robot and getting it to market as fast as possible and such, really where we try and draw the line there, focus and prioritize spending there. As noted in the call, our burn rate was probably a little bit higher than otherwise the run rate would be, but that was really due to the seasonality of certain spending. As you can imagine, certain material expenses and things like that, they happen in one period versus another. That’s why you’re seeing that. But we still remain committed to $50 million cash burns for the year.
Ryan Zimmerman: Okay. And then, correct me if I’m wrong here, Adam, but the V1.0 wraps up in the fall of this year. Talk to us about kind of next steps from there, how that dovetails into potentially the establishment of a clinical trial. I think, slated for maybe mid to late 2025, if I’m not mistaken and kind of what you need to do once we get all the design and testing done for V1.0?
Adam Sachs: Yeah. I think that’s a really important question. So, as we finalize our V1.0 system and go into more sort of preliminary verification and validation testing, we’re going to then roll that into all of the formal testing that’s required. As I’m sure you’ll recall, we’re focused primarily on outside the U.S. data collection and our clinical trial. And one of the advantages of that is in the verification and validation process, we need to do primarily the all of the essential performance and safety testing rather than all verification and validation testing. So, once essential performance and safety testing is complete for our system, we’ll then be able to start up our clinical trial in 2025.
Ryan Zimmerman: Thank you.
Operator: We now turn to Adam Maeder with Piper Sandler. Your line is open. Please go ahead.
Adam Maeder: Hi, Adam, Bill, Randy. Thank you for taking the questions and congrats on the progress. I wanted to start with the spring cadaver lab experience and just ask a little bit more color there. So, I guess, the first question would be multi-part here. How many cadavers were performed? Who was doing the procedure? Was it surgeons that you guys partner with? Talk about kind of setting a care. And then just bigger picture, maybe just what were the learnings from the spring cadaver lab? What went better than planned and what were some of the challenges, if any, that may have arisen? And then I had a follow-up. Thanks.
Adam Sachs: Yeah. Super fair question. So, overall, it was the very first cadaver that we performed. This was a single cadaver and will be the first of a number that we do over the course of this year. Overall, the procedure was designed to really test out the core functionality of our system, and burn down and evaluate any potential issues and risks with it as early as possible, which is one of the reasons that we did it, frankly, on the earlier side of the spring. It was done by internal surgeons and surgeon partners, and with a collaboration between two physicians. And overall, there were a number of things across, frankly, each subsystem that came up that we needed to focus on revising over the next two to three quarters, and that is why we’ve scheduled in this time over the next couple of quarters to make those revisions before we actually lock our V1.0 system.
Adam Maeder: Yeah. That’s good color, Adam. And sorry to press here a little bit, but just to the extent that you’re willing to share, I think, you called it additional refinements in the prepared remarks to the final system. What are some of those things that you guys need to kind of smooth out before you go into final system integration in the fall?
Adam Sachs: Yeah. I’ll give you a few examples of a few different things. So, within the software, there were a handful of bugs that we encountered, including one on firmware within the arms and the sensing of the arms that caused some challenges along the way. That one has actually already been resolved. A few small things between interaction between the lubrication of the trocar seals and the arm itself, and the sensing of the arm. Just to name, I’d say two out of, frankly, a decent handful of similar things. So, either one of the two of those are fairly easy to resolve. It’s just that, there are a number that we need to tackle and that’s why we want to give ourselves a couple of quarters to do that and to really heavily test out the implementation of each solution.
Adam Maeder: Yeah. That makes sense to me. Thank you for that. And then just one last one, if I may, maybe for Randy, and congratulations on the new role, by the way. I wanted to ask, you’ve been in the seat now for a few months, maybe just talk about some of the early impressions from your vantage point of the company and the technology, and how will you look to put your fingerprints on the broader organization going forward? Thanks again for taking the questions.
Randy Clark: Yeah. No. I appreciate the new person question, Adam. So, as you mentioned, since joining at the end of January, I’ve really just been fully immersing myself into the intricacies of our business and really trying to familiarize myself with each team and taking deep dives into all aspects of our operations, as you can imagine. And I can tell you, it’s been an incredibly exciting journey so far, especially where you’re going with Adam. I had the privilege of observing the team’s unwavering dedication and hard work and commitment that led up to our spring cadaver lab, and that’s one of my first takeaways that I want to double down on, is just the talent that we have here at Vicarious Surgical is absolutely incredible, let alone the work ethic and commitments from the teams to really drive towards our mission. And I’m just focusing right now and being very committed to just disciplined execution of our current objectives and consistently achieving our milestones. That’s going to be key to ensuring our success in the long run.
Adam Maeder: Thank you.
Operator: [Operator Instructions] We now turn to Josh Jennings with TD Cowen. Your line is open. Please go ahead.
Josh Jennings: Hi. Good afternoon. Thanks a lot for taking the questions. I wanted to just get an update on the plans for the OUS clinical trial to support the de novo submission. Any -- I know it’s only been two months since the last call and the last update and less than that since our healthcare conference, but any further communications with the FDA on that trial design? And just, I guess, the second part of the question is thinking about international sites and how do you go about, I know we’re not until next year, but how do you go about establishing those relationships or maybe they’re already in hand in terms of finding investigator sites and finding the right ones and developing those surgeon relationships or center relationships with vicarious.
Adam Sachs: Yeah. Thanks, Josh, and two great questions there. So, I’ll start with the FDA side. So nothing that we have to share on that front directly, but what I will say is, as we’re seeing the broader robotics space continue to develop, we are seeing other filings and frankly other approvals come through, many of which are occurring with entirely outside the U.S. data, as well as with about 30 patients each in each trial. So this is further confirming that unsurprisingly the guidance and support that the FDA is giving to us is being given in exactly the same way to the other new entrants in the space and they are following through on their commitments there. So that is very reassuring for us to see. As far as specific site selection and country selection, we are in conversations with a number of different locations. We do have time, but we are well on the way to working through this already, and one of the goals here is to maintain optionality for as long as we can. We actually view that as a distinct advantage, especially when frankly regulatory environments in specific countries do change and we’d like to maintain that optionality to choose the specific sites and even the specific countries out of a few that we’re working with at the latest point that wouldn’t impact our schedule.
Josh Jennings: Great. And then just to follow up on the cadaveric testing results and some of the refinements that you’re going to put in play, is there -- are there more cadaveric lab sessions that are required before you get to that fully integrate -- fully integrated, I guess, era and move forward with the pre-V&V testing? Thanks for taking all the questions.
Adam Sachs: Yeah. So the answer to that is certainly yes. We’re well on the way to implementing a lot of these refinements already and they’re being primarily implemented into this next build, which will then be tested through robust cadaveric testing, as well as a number of other tests.
Josh Jennings: Great. Thank you.
Operator: Ladies and gentlemen, this concludes our Q&A and today’s conference call. We’d like to thank you for your participation. You may now disconnect your lines.
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