Good afternoon and welcome everyone to the GeoVax First Quarter 2023 Corporate Update Call. My name is Jack and I will facilitate today’s call. With me are David Dodd, Chairman and CEO; Mark Reynolds, Chief Financial Officer; Mark Newman, PhD, Chief Scientific Officer; Kelly McKee, MD, MPH, Chief Medical Officer; and John Sharkey, PhD, Vice President, Business Development. [Operator Instructions] As a reminder, this conference is being recorded. At this time, I am turning the call over to Gabby DeGravina of GC Capital.

Thank you. Please note the following. Certain statements in this presentation may constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act. These statements are based on management’s current expectations and are subject to uncertainty and changes in circumstances. Actual results may differ materially from those included in these statements due to a variety of factors, including whether GeoVax can develop and manufacture it’s product candidates with the desired characteristics in a timely manner and such products will be safe for human use; GeoVax’s vaccines will effectively prevent targeted infections in humans; GeoVax’s product candidates will receive regulatory approvals necessary to be licensed and marketed; GeoVax raises required capital to complete development of its products, there is development of competitive products that maybe more effective or easier to use than GeoVax’s products; GeoVax will be able to enter into favorable manufacturing and distribution agreements; and other factors over which GeoVax has no control. GeoVax assumes no obligation to update these forward-looking statements and does not intend to do so. More information about these factors is contained in GeoVax’s filings with the Securities and Exchange Commission, including those set forth as risk factors in GeoVax’s Form 10-K. It is now my pleasure to introduce the Chairman and CEO of GeoVax, David Dodd. David?

Good afternoon and thank you for participating in the GeoVax corporate update call. Since the start of 2023, we have expanded patient enrollment and supported the Gedeptin Phase 2 clinical trial and the two Phase 2 trials for GEO-CM04S1; also, the third Phase 2 clinical program in support of CM04S1, evaluating the vaccine as a booster among patients with chronic lymphocytic leukemia has viewed by the FDA and is expected to initiate soon. We also recently expanded our rights related to CM04S1 to include all omicron variants, monkeypox, and smallpox, further differentiating our COVID-19 vaccine. While the clinical development progress Gedeptin and the CM04S1 remain our priority, we are also focused on GEO-MVA, our vaccine against monkeypox and smallpox; as well as the implementation of the transformative MVA continuous cell line manufacturing process. Last year, we strengthened our balance sheet adding $37 million during a very difficult investment environment especially for the biotech industry. This enabled us to expand our current clinical programs, including additional sites, while also adding near-term opportunities related to further development opportunities, including our MVA manufacturing process, and expanding our oncology programs. We expect that our cash position will support our increased clinical program expansions and other initiatives through the remainder of this year. In the interim we will evaluate opportunities to further strengthen our balance sheet, resulting from supportive stock activities, business development opportunities, and non-dilutive opportunities related to government, and NGO funding. Gedeptin is a cancer therapy currently and has expanded multisite evaluation among patients suffering from advanced head and neck cancers. The product has received orphan drug designation and funding for the current clinical trial from the FDA orphan drug has clinical trials program. Our target population for the initial indication includes head and neck cancer patients, who are receiving palliative care, having…

Thank you, David. I’ll begin with a brief overview of our income statement. And I’ll first point out that we reported no grant revenues during 2023 as compared to a small amount in 2022, which is reflective of the wind down of our grant from the U.S. Army for our last fever preclinical program. I’ll note, however, that we are actively seeking additional non-dilutive government funding for our preclinical and clinical development programs, and we expect this to be an important component of our financing mix in the future. Research and development expenses were $2.8 million in the first quarter of 2023 versus $1.3 million in 2022. The increase was planned and expected and is associated with clinical trial activity for our CM04S1 and Gedeptin programs. The increase is also reflective of higher personnel and consulting costs as we staffed up during 2022. G&A expenses were $1.5 million in the first quarter of ‘23 as compared to $1.2 million in ‘22, with the increases also associated with higher personnel and consulting costs as well as patent costs. So, overall, net loss for the first quarter of 2023 was $4 million or $0.15 per share, versus $2.4 million in 2022 or $0.34 per share. Again, with the increases primarily associated with the ramp-up of organizational infrastructure and other costs associated with the CM04S1 and Gedeptin clinical trials. Turning now to the balance sheet, our cash balances at March 31 were $23.9 million, as compared to $27.6 million at December 31. The change in cash is reflective of $3.8 million used in operating activities. There were no significant financing or investing activities during the first quarter. Our outstanding common shares now stand at 26.4 million. Funding our three ongoing Phase 2 clinical programs is obviously the most important use of our cash and our top financial priority. Our cash runway is sufficient to fund these programs through the milestones expected to occur over the course of this year, as David previously mentioned. We believe the advancement of our clinical programs will create an attractive investment opportunity for new fundraising activities, and I’ll be happy to answer any questions during the Q&A period. So I will now turn the call back over to David.

Thank you, Mark. My colleagues and I will now answer your questions. Joining us for the Q&A session are Dr. Mark Newman, Kelly McKee, and John Sharkey, our Chief Scientific Officer, Chief Medical Officer, and Vice President of Business Development respectively. I will now turn the call back to the operator for instructions on the question-and-answer period.

Certainly. [Operator Instructions] Jason Kolbert with Dawson James, your line is open.

I am here. Thank you. Great job conserving capital resources and focusing on what’s important clinical expenses something that we couldn’t say about this company a couple of years ago. One really interesting question I have is what kind of discussions are you having with the government about what they are looking for in terms of a next-generation COVID vaccine? They are probably thinking something ubiquitous for the population, but have you caught their attention and have you had any of those discussions with them yet?

Sure, Jason. This is David and thanks for your question. The April 10, the federal government issued the RFI request for information related to Project Next Gen and that specifically outlined what they were looking for relative to criteria. And it was what I actually stated during my comments, about durability, a breadth of protection, and specifically focused on products that were already in the clinic or could enter the clinic within nine months. So, they are looking and recognizing that durability as a key issue, that the breadth of protection is an issue, and they are also – there are populations out there for whom current vaccines and therapies are inadequate. So, they laid that out, that the process for the RFI is that you completed and submitted, which we did very quickly, very well-prepared, I’d say, response to it. They will go through those and then decide with whom they’re going to follow-up for further information. At this stage, there was no discussion or providing information in terms of – or how much money are you seeking for what purposes, we have that all outlines. Now to address the question, we have had ongoing discussions with individuals within the federal government that includes those who are specifically part of the review team, et cetera, on Project Next Gen. We’ve been having such discussions for some time now, and had some even more recently on that, and have discussed with them, shared with them that we have accomplished thus far and what we’re proceeding towards with the continuous cell-line manufacturing process, which seem to really capture some interest. Ultimately, we’ll have to see how they respond. The process of submitting a response to the RFI is closed on May 25. So, right now, and still different companies are submitting, again, we submitted our very, very quickly. We were prepared for it, etcetera. And so, we are in the waiting. We still are engaging an outreach and discussion with various Federal government individuals, some of whom are part of Project Next Gen and some who are part of related entities, making sure that they are aware, not only of GeoVax, but of what we have already accomplished, where we are in the process of clinical development, and what our plans are in terms of moving forward with this new manufacturing system. So, I hope that answers the questions. So, the answer is yes, we have that dialogue. But we are also working through the process they have laid out also, but we are also working directly through other avenues to make sure we reach out to people.

Perfect. Thank you. And David, if you don’t mind, can you just touch on the sequence of milestones. I know you did mention it earlier, but given your CFO’s comments, I would just like to understand how they lay out over the next 12 months?

Okay. So, with Gedeptin, now, we have 8 patients of the 10 patients in the program. We had expanded it, as you recall, to three sites. And we anticipate bringing in the last two for this initial 10-patient trial. That’s the one that’s been funded fully by the FDA. Our plan is to have that accomplished sooner rather than later, clearly yet this year to review the data, we have already been in discussions with our advisors about the expanded program that we would propose to the FDA. So, we anticipate yet this year to review the data, to discuss the data, and hopefully initiate it and have initial discussions with the FDA.

Perfect. Thank you so much. We appreciate all these upgrades.

Okay. Thank you.

Vernon Bernardino, H.C. Wainwright.

Hi, David, and Mark, everyone. Thanks for taking my question, and congrats on the process, especially with the manufacturing for MVA based vaccines and immunotherapies. It’s really important piece. A lot of my questions were asked by Jason, so I don’t have anything other than – just wanted to get your take, as you know, on the Federal Register, did you see as ACIP is going to have a meeting next month – and one of the things, David, intend to discuss is Mpox or formally called monkeypox. I was wondering if there is anything there as well as the other vaccine recommendations that they may have that could help you with your programs. What are you looking for, and what made you change it, as far as your programs are concerned, such the candidates could be advanced into the clinic in the near-term future such as next 6 months to 12 months?

Thank you, Vernon. We are not aware of anything on that agenda that relates to what we are doing, but I am going to ask John Sharkey to weigh in, since he is leading our MVA vaccine program, that is specifically what we in-licensed or acquired the rights to and are developing against Mpox and smallpox. John?

Sure. Hey, thanks for the question, Vernon. As we have mentioned before, our desire for the MVA is – the monkeypox and smallpox has become U.S. based manufacturer, eventually switch to continuous cell-line platform, so that we can manufacture on large scale in quick timeframes. Our regulatory strategy, as we have mentioned, is that there is a number of countries outside the U.S. that were unable – were or are still unable to get access to the MVA vaccine. And so we see a market opportunity there. Our strategy right now is engaging. We have retained an outside regulatory consulting group that’s well-known, respected in this space. And we are putting together a strategy to see what regulatory agencies around the world would be open to working with us, given the known safety and efficacy of MVA against smallpox and monkeypox to put together as we have referred an expedited pathway, whether that’s an accelerated pathway or that’s a biosimilar, whatever it is. What that is going to be available to get approval from a recognized regulatory agency that we could then use with NGOs and other countries, that will be confident with that approval, would now allow use of MVA within their territories. So, that’s our general strategy. Right now, we are in the – we are past the information gathering. We are beginning now to reach out to regulatory agency to engage discussions with them about our thinking, and how we would like to work with them to accelerate on approval process to get this product to the market, because we believe there is a need in many parts of the world.

Terrific. Thanks for that information. And as a follow-up, do you anticipate making further progress and announcing progress on those kinds of things you might get as far as what the governments need outside the U.S., outside the Western World such as Europe, later this year?

Yes. It will definitely be within the next two months. We have looked at this for a couple of months now, and kind of reading the regulations of working with our consultants. We have mapped out proposed strategies that we want to present to them, as well as engage them and see what their thinking is on how we might adjust them or tweak them or is there a pathway we may not be familiar with that they would be willing to work with us on. So, this is going to move quickly forward into the engagement phase with the regulators.

Perfect. That’s very exciting. Looking forward to further news on that front. And thanks for taking my question.

You’re welcome.

Kumar Raja with Roth Capital, your line is open.

Thanks for taking my questions and congratulations on the progress. Just a follow-up on Gedeptin, will you be enrolling more than 10 patients if they are screened by Q2? And in terms of the interactions with the regulator, following those interactions, how quickly do you think you can expand the program, if expectation that in the expanded program, there will be arm which will include a checkpoint inhibitor? Thank you.

Okay. I am going to ask Kelly McKee, our Chief Medical Officer to provide some guidance on there. And then he and John Sharkey may want to discuss the status related to what is currently still preclinical, but with immune checkpoint inhibitors. Kelly?

Yes. Hi. With regard to whether or not we would continue enrolling after we hit our current target of 10 patients, I think that’s a bit of an open question. We don’t have any current plans to do that, but I think it would probably depend on sort of the dynamics of enrollment. If we have an opportunity to add one or two additional patients within a reasonable timeframe, for example, if there are – if our investigators have people identified that are waiting and willing and available to enroll without delaying the final closure of the study, then we would probably consider that. But I think, at the present time, we really are targeting 10 total patients for this study, get it closed up to get the data reviewed in front of the regulators for furthering our discussions.

John, do you want to comment some on the ICIs and where that stands, and what we learn?

Sure. So, as David said, it’s still in preclinical that would be – the scheduling of the ICIs in combination with Gedeptin, I think and Kelly can speak to it more, is still somewhat open. Our focus right now is to see the data from the 10 patients, see what’s actually there, have the discussions with the agency on what we could do to get Gedeptin approved as a monotherapy. At what point we would now win the ICI, with that, I think is going to be very dependent on how that discussion goes with the regulatory agency. Preclinical data is highly suggestive, because always never show as you go from a small animal to humans that there will be a synergistic effect between the two. But that’s the discussions we have with the regulators to decide how – in concert with them, how would you want to proceed. And I will let Kelly add any other insight to that.

Well, only that I think we are very optimistic that this is going to be a sort of major advancement for our program. You are well aware of the success that Moderna and Merck that had with – in [indiscernible]. There was some recent data on bladder cancer, where they have oncolytic virus paired up with a checkpoint inhibitor, which in many ways is sort of similar to the concept or conceptually similar to what we have got in mind, exposing neoantigens. And so, I think we are optimistic that this offers a potential for us to target patients with head and neck cancer in earlier stages of the disease, as well as other solid tumor types with this approach. So, we are going to move as quickly as we can to advance this. But again, it’s going to depend on our discussions with the regulators about what’s required for us to get there.

Okay. That’s great. Thanks so much.

James Molloy with Alliance Global Partners, your line is open.

Hi, this is Laura in for Jim Molloy. Thank you for taking our questions. So, for enrollment for the Phase 1/2 trial of Gedeptin expected to be completed on soon this quarter. When should we anticipate a last patient in or last patient visit announcement? And then also on top of the ICIs that were already mentioned in the previous question, what might the protocol for the subsequent expanded trial look like, or will this be determined following the completion of the ongoing Phase 1/2 trial?

Let me just comment. Once we have the 10th patient enrolled, there are five cycles. So, it’s basically five months. So, that gives you a time period depending on when that 10th patient is enrolled, then we look forward to then through the five cycles and then the evaluation of the data. So, if we are successful when they come in – as the soon as they come in, then the more likely is we will be able to see the results of the completion through the five cycles yet this year. I mean that’s just the metrics, so it depends on that. And that’s what we are working on, let’s see. Obviously, when we expanded to the three sites from the initial one that and opened up greater opportunity to be able to move this along and complete this initial 10 patient study. There has been no discussions about clinical protocol related to in conjunction or in combo therapy with ICIs, mainly because our focus is really on determining if there is a basis which we hope to see from the 10th patient to then look at an expanded Phase 2 trial. And that may be anywhere depending on what the final protocol structure, but less, I think we are thinking less than 100 patients and all. But again, that will be based upon the discussions we have with review of the data. I will ask if Kelly would like to add anything at this point.

No, I think that that pretty much summarizes it. Just to note that enrolling these patients is not as simple and straightforward as it might appear on the surface. Remember that our trial is targeting patients with essentially the terminal stages of their disease. So, it’s more or less palliative therapy for these folks. And in order for us to find eligible patients, they have to have exhausted all of their other therapeutic options, and they have to be healthy enough to enroll in a study that’s going to take them through, again, six months – five months to six months of treatment. And we found that those patients tend to be few and far between. And so we are trying as hard as we can to get eligible patients identified and enrolled. But it’s taking a little bit longer than we had initially anticipated. But as David said, I mean once we get this study fully enrolled, get our data analyzed, and in front of the agency, and have our discussions about what they would like to see for us to continue in this patient population and then what they would also like to see for us to take a sort of a parallel approach with a checkpoint inhibitor or potentially other combination strategies. We will just have to wait to see how those discussions go, I think.

Thank you. And it’ll be – and if the data supported, it will be a big priority for sure, because we have been encouraged by the limited data that was in the Phase 1, and we are happy that we now have eight of them, but we need to get the 10. We need to analyze the data and reach agreement on an expanded Phase 2 program, and then we will go full out with expanded sites, and trying to move that as quickly as possible, and then in parallel also with the other trials. So, we will keep you updated, though. Thank you.

Understood. Also, just one more question. So, for your CM04S1 candidate, as mentioned with the shifting landscape for COVID-19 and as new variants emerge, does this change in any way the development for this candidate moving forward? And then do you also think it may work equally as well against these newer streams?

Well, we don’t know the latter until we have some testing, and we have evidence of it now. The concept of targeting both the antibody side and T-cells to the spike protein and nucleic acids is done to hopefully achieve a broader, more robust type of protection, and where the antibody alone isn’t sufficient more or less that we can more than compensate for that by incorporating with the T-cells. And so that’s what we are hoping to demonstrate. We did announce recently we had added the rights in terms of related to Omicron, it to be a license agreement that we have. And we will continue to look at the current vaccine, and CM04S1, and also if we decide that we want to do some alternate modifications because of variants that, again, to evolve that they may be significantly different. So, we just have to stay attuned to that. One thing we do know is that the modifications that have been going on with the existing vaccines continue to provide us with the sort of inadequate vaccines for the breadth of populations, and especially, for those individuals with compromised immune system. And as we have discussed before, we are focusing very heavily to differentiate by going after the populations that are underserved or not adequately served by the current authorized vaccines. And that’s the basis behind the structure of CM04S1. And we believe that the initial data we are seeing shows that it is making a much broader difference. So, we will keep you updated as data comes forward.

Got it. Thank you for taking the questions.

Thank you.

Robert LeBoyer with Noble Capital Markets, your line is open.

Thank you. Well, John and Kelly gave a very good answer to my question about the ICI inhibitors and combinations. But the question I still have is about the timing of an announcement for Gedeptin. And based on the earlier comments with the five cycles and looking at the calendar, it looks as if an announcement might come maybe at the end of the year, but more likely first quarter? Is that what you are thinking?

Yes. Robert, depending on, again – obviously, when that 10th patient comes in, etcetera, then we – it’s just like we have always done on trials when you know the length of the evaluation period, you just map that out. So, we are as anxious as everyone to get these last two patients in. But, as Kelly mentioned, as he said, these are patients who have failed everything. There is not anticipated survival from this type of therapy. It is really, can we affect the tumors and improve their quality of life during this terminal period of their lives when they are on palliative care.

Okay. Great. Thank you very much.

Thank you.

There are no further questions at this time. I would like to turn the call back over to David Dodd for closing remarks.

Thank you and thank you everyone for participating in this update call and sharing our achievements progress and outlook. We greatly appreciate your interest. Our biggest focus and greatest challenge is to see an accelerated pace of patient enrollment, getting to data milestones sooner, so we can talk about greater database of results. And we will continue to stay focused on that, that’s what we are focused on, Gedeptin, CM04S1, and the other development programs we have talked about today. Our goal is that by doing this, we will be able to build shareholder value, stakeholder value, and of course, providing a motivating career development opportunities for our team. We want to thank our Board of Directors, our staff, our advisors, and all other parties, including some of you who have been asking questions, who continue to support, advise, and guide us towards achieving success. With that, we wish you all a great evening. Have a great weekend. And again, thank you for your interest in GeoVax.

This concludes today’s GeoVax call. We thank you for your participation. You may now disconnect.