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Good afternoon. We will begin the MacroGenics' 2022 Second Quarter Corporate Progress and Financial Results Conference Call in just a moment. All participants are in a listen-only mode at this moment and we will conduct a question-and-answer session at the conclusion of the call. At this point, I will turn the call over to Chris James, Vice President of Investor Relations and Corporate Communications of MacroGenics.

Thank you, operator. Good afternoon and welcome to MacroGenics’ conference call to discuss our second quarter 2022 financial and operational results. For anyone who has not had the chance to review these results, we issued a press release this afternoon outlining today’s announcement, which is available under the Investors tab on our website at macrogenics.com. You may also listen to this conference call via webcast on our website, where it will be archived for 30 days beginning approximately two hours after the call is completed. I would like to alert listeners that today’s discussion will include statements about the company’s future expectations, plans, and prospects that constitute forward-looking statements for purposes of the Safe Harbor provision under the Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by these forward-looking statements, as a result of various important factors, including those discussed in the Risk Factors section of our annual, quarterly, and current reports filed with the SEC. In addition, any forward-looking statements represent our views only as of today and should not be relied upon as representing our views as of any subsequent date. While we may elect to update these forward-looking statement statements at some point in the future, we specifically disclaim any obligation to do so, even if our views change, except to the extent required by applicable law. And now, I'd like to turn the call over to Dr. Scott Koenig, President and Chief Executive Officer of MacroGenics.

Thank you, Chris. I’d like to welcome everyone participating via conference call and webcast today. This afternoon, I will provide key updates from our clinical programs as well as our restructuring plans headed to extend our cash runway. But before I do so, let me first turn the call to Jim Karrels, our Chief Financial Officer, who will review our financial results.

This afternoon MacroGenics reported financial results for the quarter ended June 30, 2022, which highlighted our financial position as well as our recent progress. As described in our release this afternoon, MacroGenics' total revenue consisting primarily of revenue from collaborative agreements was $26 million for the quarter ended June 30, 2022 compared to total revenue of $30.8 million for the quarter ended June 30, 2021. Revenue for the quarter ended June 30, 2022 included MARGEN

Thank you, Jim. We made important progress in the second quarter with regard to multiple investigational molecules. Before I walked through the progress we made on our pipeline, let me update you on MacroGenics restructuring plan that we are announcing today. Listeners will recall that over the past several quarters, we have prioritized our pipeline of product candidates and discontinued certain studies to reduce our spending. We have initiated additional cost saving measures to extend our cash runway with a goal of delivering value creating data with our existing and anticipated financial resources. The additional decisive actions we have announced today should put MacroGenics macrobiotics in a stronger position to execute on our prioritized programs. The cost saving measures include an approximate 15% workforce reduction in full time employees and closure of two of our satellite facilities, including a Brisbane, California-based research site at a smaller scale non-commercial GMP manufacturing site in Rockville, Maryland. We believe these measures will provide resources to advance our pipeline of innovative product candidates. Reduction in workforce announced today will be implemented immediately in some areas and completed over time and certain projects are wound down and sites are closed. The decision to reduce our workforce and close two sites was not taken lightly and we are grateful to every MacroGenics employee who has helped advance our company. With these actions, we believe our updated cash runway should enable the delivery of interim data from the Phase 2 portion of the MGC018 prostate cancer study by the end of 2024. Data from the Phase 1 dose expansion of lorigerlimab by early 2023. And data from the dose escalation of MGD024 in AML patients as well as execution of our other ongoing clinical and preclinical studies. In terms of our pipeline, since our last quarterly update, we completed enrollment of the Phase 1/2 dose expansion study lorigerlimab, a bispecific DART molecule targeting PD-1 and CTLA-4 in advanced solid tumors. Also in July, we dosed the first patient in the Phase 1 study of MGD024, our next generation CD-123X CD-3 DART molecule in patients with CD-123 positive hemolytic malignancies. In addition, we continue to dose patients in the dose escalation combination study of MGC018, or B7-H3 directed antibody drug with lorigerlimab in patients with advanced solid tumors. Also, I'm happy to announce that our planned Phase 2/3 study of MGC018 and patients with metastatic castration resistant prostate cancer has a name which is TAMARACK. We continue to expect to start the TAMARACK study by year end. In addition to these programs, we and our partners continued to progress our other clinical and preclinical candidates and expect to provide further updates as the data matures. With that backdrop, let me use our remaining time to walk through our updates on our portfolio of investigational clinical molecules, starting with MGC018, our ADC designed to deliver DNA-alkylating duocarmycin cytotoxic payload to tumors expressing B7-H3. B7-H3, the member of the B7 family molecules involved in immune regulation. MGC018 was designed to take advantage of this antigen's broad expression across multiple cellular tumor types. We continue to make progress as we operationalize the TAMARACK study. After constructive interactions with the FDA and EMA, we provided key details about the design of the TAMARACK study during the first quarter conference call. As a reminder, during the Phase 2 portion of the study, approximately 150 patients will be randomized one-to-one-to-one to receive either 2 mg per kg or 2.7 mgs per kg of MGC018 every four weeks in the experimental groups are physicians choice of an antigen receptor access target or ARAT agent, such as abiraterone, enzalutamide, not previously received in the controlled group. Following completion of the Phase 2 portion the study and interim analysis of the data will be performed to further inform the Phase 3 portion in which we plan to randomize additional patients one-to-one to receive either MGC018 at the recommended dose, or ARAT agent for the controlled group. We continue to expect to start the TAMARACK study by year end and anticipate the delivery of interim data from the study by the end of 2024. Next, let me update you on lorigerlimab. We continue to dose patients in the Phase 1 dose escalation combination study of MGC018 with lorigerlimab in patients with advanced solid tumors included including renal cell carcinoma, pancreatic cancer, ovarian cancer, hepatocellular carcinoma, metastatic castration resistant prostate cancer, and melanoma. Based on data from our preclinical studies, anti-tumor activity with MGC018 may be enhanced by combination therapy with an anti-PD-1 agent without significant incremental toxicities. During the second quarter, we completed enrollment in a Phase 1/2 dose expansion study with large lorigerlimab as monotherapy and cohorts of patients with microsatellite stable colorectal cancer, mCRPC, melanoma, and checkpoint-naive non-small cell lung cancer. We expect to provide a data update from this study by early 2023. Next up, I'll discuss our efforts to advance treatment of patients with CD123 positive hematological malignancies. MGF024 is our next-generation bispecific CD123/CD3 DART molecule that incorporates a CD3 component designed to minimize cytokine release syndrome, while maintaining anti-tumor cytolytic activity and permitting intermittent dosing to a longer half-life. We recently dosed the first patient in a Phase 1 study of MGD024 in CD123 positive relapsed or refractory hematologic malignancies, including patients with acute myeloid leukemia and myelodysplastic syndromes. enoblituzumab, an investigational FC-engineered B7-H3 monoclonal antibody created using our FC optimization platform being evaluated in solid tumors. In July, we issued a press release, announcing the closure of the Phase 2 study evaluating the investigational regimen of enoblituzumab in combination with retifanlimab, an anti-PD-1 monoclonal antibody or tebotelimab, our PD-1 x LAG-3 bispecific DART molecule in the first line treatment of patients with recurrent or metastatic squamous cell carcinoma of the head and neck. The decision to discontinue the study was based on an internal review of safety data and a risk benefit analysis in frontline patient of squamous cell carcinoma of the head and neck. We don't believe that decision has any impact on our other B7-H3 directed programs, or our ability to develop enoblituzumab in other indications. At ASCO in June, investigators from Johns Hopkins presented a poster with encouraging clinical activity from an ongoing Phase 2 study of enoblituzumab in patients with localized prostate cancer in the neoadjuvant setting. enoblituzumab showed encouraging clinical activity with 66% of patients have a PSA zero at one year post, which correlated with peripheral expansion of tumor-associated T cell clones. The published data from the ongoing investigator sponsored trial to-date provide rationale for further evaluation of enoblituzumab in prostate cancer. Next, I will provide an update of our product candidates being developed by our collaboration partners for watching retain certain economic rights. Our second investigational ADC IMGC936, which targets at ADAM9, a cell surface protein overexpressed in several solid tumor types is being advanced under a co-development agreement with ImmunoGen. Under our 50/50 collaboration, ImmunoGen is leading clinical development and as indicated, our plan to complete dose escalation in the Phase 1 study evaluating IMDC936 in multiple solid tumors with initial data anticipated before year end. teplizumab is an anti-CD3 monoclonal antibodies that Provention Bio acquired from us under an asset purchase agreement in 2018. Provention is developing teplizumab for the treatment of type 1 diabetes. On June 30th, Provention announced the FDA has extended its review period by three months for the BLA for teplizumab -- that we exclusively licensed Incyte Corporation. MacroGenics is eligible to receive royalties on net sales of retifanlimab, if approved, in addition to milestone payments. In July 2022, MacroGenics received $30 million in milestone payments from Incyte as part of its a collaboration agreement. retifanlimab is currently being studied as monotherapy or in combination with other agents across multiple studies. In conclusion, we continue to believe 2022 will be another important year for MacroGenics. During the first half of the year, we initiated two clinical studies and we expect to start TAMARACK, a registration-directed study of MGC018 in mCRPC by year end. We remain committed to developing and delivering life changing medicines to cancer patients. We would be now happy to open the call for questions operator.

[Operator Instructions] Our first question comes from Jon Miller from Evercore. Please go ahead.

Hi, guys. Thanks so much for asking the question and congrats on restructuring and biting the bullet a little bit and extending the runway a little further. I'd love to get a sense of exactly what the new guidance is, though, precisely because it seems like there were two different languages being used in 2024, I think was mentioned in the press release. But then it also, Scott you mentioned having runway through year end 2024 where the TAMARACK data was expected? So, can you just provide me with the exact guidance is [indiscernible]?

Yes, thanks Jon. I'll start and I think Scott will probably finish. So, the exact guidance is that our cash runway, which reflects not only the $134 million that we had at June 30, but the additional $34.5 million that we received subsequently in the month of July, plus product revenues and other anticipated payments from partners pushes our cash runway into 2024.

Yes, and just, first of all, John obviously, we can get more precision on this when the study starts, and how quickly the patients get enrolled. But given where we are right now, in that process, we are confident that we'll be able to start the study before the end of the year getting enrolled during 2023 and have the readout by the end of the year. So, we think that without exact precision right now, because in addition to milestone payments, which obviously, we can never guarantee, we have considerable amount of BD activity ongoing, which could obviously extend runway further, we should be able to provide further precision in the future with regard to how far to 2024 that goes.

Thanks very much. And one -- maybe one or two more, if I may. I'm curious now at this point about enobli versus 018 overlap, and I think maybe it made sense to have them separate before. But I'd love in light of the prioritization for you to tell me a little bit about how you're feeling about having both of these -- having studies ongoing both these programs, are they differentiated enough to justify keeping both active especially as 018 sort of advances to later stage trials. And then not exactly the same, obviously, but a little bit related. Should we expect similar dynamics for 024 as we had from flotetuzumab, so should we be looking for the same sorts of signals in terms of patients and subpopulations, refractory versus relapsed patients? That sort of thing as we look forward to early data there. Thanks.

Great questions. So, we were very excited about the update that the Johns Hopkins group was able to provide at ASCO as you know that received a lot of positive feedback in a neoadjuvant setting, which as you know, is either not or very little efforts are being conducted there and then fairly early setting, despite the fact of the head and neck set setback with regard to the stopping the study, for enoblituzumab, the safety profile for enoblituzumab in the early neoadjuvant prostate setting was excellent. And based on both the encouraging data, the biomarker data and the patient's responses, the group that conducted that study is an expanded group is are very enthusiastic to look at it very early settings for prostate cancer and enoblituzumab. As you know our current efforts right now with regard to MGC018 is in the later line metastatic setting and so we're again focused on both patients that had been experienced with ARAT agents as well as taxane agents still opportunities to move up the line. But given that we need to have a very clean drug for treating patients with localized disease, we think enoblituzumab is better set up for pursuing that indication. Now, I should also indicate that we are looking at other possibilities of enoblituzumab beyond that of early stage prostate cancer and of course, as you know, we have the ongoing combination studies of MGC018 and lorigerlimab in seven different tumor types. And based on the results of those studies, can guide us in other solid tumor indications going forward with MGC018. Now with regard to the question you had about the MGD024 with respect to flotetuzumab, and it's use in refractory disease, as we've outlined that the last ash meeting, we are very encouraged that the use of MGD024, both based on the better profiled and reducing cytokine release, as well as intermittent dosing will allow a much broader application of MGD024 beyond what we were able to do with flotetuzumab, both in late line refractory patients, as well as patients with early disease. In particular, we are extremely encouraged by the combination studies we had with MGD024 and other standard therapies and look to using this quite broadly after we initially do the dose escalation studies in patients with relapsed refractory disease. We're also looking at the opportunity of MGD024 beyond AML using is in tumor settings, where CD123 is over expressed, including model dysplastic syndrome and other indication. So, there is certainly a differentiation and expansion of our intended use for MGD024 provided some of the rationale of why we stopped them further pursuing refractory the mass development.

Our next question comes from David Dai from SMBC.

Hey great. Thanks for taking my questions. So, I have a couple of questions as well. So, first question is just around MGC018. So, when we look at the Phase 1 dose expansion study that was presented at ESMO last year, we saw that about 30% of patients were those reduced and 55% of the mCRPC patients were dose interrupted. So, could you provide some color on what was lowest dose level that was dose reduced? And how long were the duration of the dose interruption for these patients? And then how should we think about the potential read through to the reduced dose regimen for the TAMARACK trial -- the Phase 2/3 TAMARACK trial?

David, thank you very much for that question. And, obviously, we've been spent a lot of time of analyzing the data that we extracted from the study not only in patients with prostate cancer, but those that we tested in other solid tumor indication. Again, just to refresh everyone's memory, the expansion cohorts for the studies have started out with a 3 mg per kg dosing to three-week level. It turns out the majority of patients had either dose reductions or holding doses with longer periods before the patients were restarting dosing, largely due to side effect profiles. We took this into account, we looked at the full data set from all patients treated with MGC018 and identified the ultimate dose that every patient was ultimately treated with during the course of therapy, and came out with average amount of drug that was delivered to those patients. We sized up that results with their clinical responses, both in terms of side effect profiles, as well as responsiveness. And by doing this, we were highlighting particular side effects that seemed most problematic to the continued treatment of patients. Ones that we highlighted before was hand-foot syndrome, where while the majority of patients had only Grade 1, or Grade 2 side effect profiles, very few Grade 3s, it turned out a significant number of patients were had Grade 2S, which was manifested by the appearance of pain in those patients, caused many those patients who stopped continuing treatment. And so when we did an analysis of the actual dose that was both effective in inducing responsiveness, as well as reducing the incidence and severity of side effects, we saw a difference that fell in that range that we ultimately decided on treating these patients, 2 mgs per kg on a Q4 weekly basis, up to 2.7 mgs per kg a Q4 weekly basis. So, we've boxed in that dosing range to ultimately move forward in this now Phase 2 -- components of the Phase 2/3 study.

Our next question comes from Stephen Willey from Stifel.

Yes, good afternoon. Thanks for taking the questions. Maybe just with respect 024, is there anything that you can say about, I guess, how you're dosing this drug during cycle one? Is it just a flat dose that you're administering? Is there going to be some attempt to migrate over to some kind of titration regimen? And then if you could speak to the pre-medication that you're using as well, that'd be helpful. And then just had a quick follow-up on TAMARACK?

Yes. Steve, based on interactions with the FDA, we started out with MABEL dosing of this drug this was a requirement. And as you know, we spent a lot of time with flotetuzumab ultimately getting a dose escalation and a increase, particularly on the flotetuzumab in the first week. We ultimately believe on the dosing, that this can be based on either weight or body weight, or on a flat dosing regimen going forward. So, we'll have to see how that goes. But if particularly, it's a lower doses, we expect those to move up quite quickly, but we'll have to see as we move up the line.

Okay, and then, just with respect to TAMARACK, can you I guess, speak to the number of sites that you're hoping to enroll the these 150 patients across? And should be just expect that interim analysis of -- I guess the efficacy data, what is the trigger for the presentation of that interim data on the efficacy side? Is it going to be based upon some threshold number of radiographic progression events, if there's, I guess, anything that you can say to that that would be helpful?

So with regard to number of sites, we haven't come up with a final number. We're obviously starting given the regulatory timing of things in US sites. Our plan is to have this as a worldwide study in US, Europe and Asia. So the – I can't come up with a specific number that we will ultimately end up with. Obviously, it will be a large number of double digit initially as we do the Phase 2 study, then we'll expand – the intent would be to expand as we move over from Phase 2 to Phase 3. And we hope by the time we start the enrollment at the end of the year, we'll be able to give a little bit more precision on site engagement and plans for expansion, especially when we get the feedback from the European sites. With regard to the analysis of the data we have, predefined analysis, defined in our protocol that is being given to the DSMB. Again, we're not at liberty right now to disclose what those specific – which will include, obviously, response rates going forward. We obviously have also had the ability to amend that at any particular time during that course of that Phase 2 study. There will be a futility analysis that is incorporated in this during the course of enrollment. Again, the plan is to enroll 150 patients in those three groups to two experimental groups and one control group.

Okay. Thanks for taking the questions.

Thanks, Steve.

Our next question comes from Etzer Darout from BMO Capital Markets.

Great. Thanks for taking the question. Just again on MGC018. Just wondered if you could speak to a little bit about perhaps the population of patients that you'll look at in the metastatic castration-resistant prostate cancer cohort? Should we think about it similar to what you looked at in the Phase 1/2? And then maybe if you can, again, speak to any appropriate benchmarks we should think about now for that study in terms of how to kind of compare responses that we'll see at interim analysis?

So, thanks so much for that question or sets of questions with regards to TAMARACK. So again, very similar to what we had enrolled in the expansion cohort of the 40 patients. These will be metastatic castration-resistant prostate patients that had one prior androgen-receptor targeting agent. They can have -- they will have on prior docetaxel regimen. And we will also allow up to one prior cabazitaxel regimen, obviously, in optional but no other prior chemotherapy. The patients will be stratified based on visceral disease, whether they've had cabazitaxel and also regional analysis of the drug. Again, I think the benchmarks differ depending on lines of therapy. And I mean, you're very well aware that, that has a wide range of baseline responses of overall response rates in the two to three months to up to four months baseline depending on the previous lines of therapy. So for that reason and obviously, the changing landscape of what these patients are now receiving and obviously, introduction of new agents into the metastatic market, we have included a control group. So we'd be able to do a very good job of benchmarking to the current status of patients.

Our next question comes from Kim Masaga [ph] from FactSet. Your line is open. Please go ahead.

We can skip to the next one.

Our next question comes from Jonathan Chang from SVB Securities.

Hi, guys. Thanks for taking question. This is Faisal Khurshid on for Jonathan. I wanted to ask for the MGC018 plus lorigerlimab combination. Can you remind us the study design here, in particular, what dose of MGC018 is being used? And then also, when we might be able to see data for that combination?

Yeah. Thanks very much. So the starting dose for MGC018 is one mgs per kg on I think it's Q4 weekly basis now. And lorigerlimab is at 6 mgs per kg on the same dosing regimen. The plan would be to dose escalate the MGC018. We're going to -- the expected next dose would be 2 mgs per kg, and we have other interval dosing. There can be modifications based on side effect profiles, etcetera. But right now, we're targeting the lorigerlimab dose we like to take forward both as monotherapy in combination and slowly titrate up the MGC018 dosing.

Our next question comes from Charles

This is Edward on for Charles. Maybe regarding MGC018 and apologies if I missed this, but are you planning to present some of the expansion data that you had on the old dosing regimen? I think you talked about last time about maybe later this year, having some prostate and melanoma data.

Yeah. So thanks very much for the question. At the time, we discussed this, we were intending to add an expansion cohort for melanoma. And as you've heard today, with regard to the prioritization program, one of the things we said we're going to hold off on was adding additional patients to the melanoma cohort at this time, despite encouraging data that we had seen. So our plans right now on updates on this program, it will depend on when we are going to initiate additional studies with other indications. And at that time, we've got to update everyone regarding our experience with these other indications. So for the prostate, we have our feedback from the key experts, from the regulators and the plan going forward with regard to the TAMARACK study. So right now, further updates on this will come in some sort of scientific publication at a future date.

Our final question comes from Peter Lawson from Barclays.

This is Shay on for Peter Lawson. Thanks for taking the question. With the restructuring, could you help us -- how we should be thinking about the OpEx for the remainder of 2022 and through 2023? Thank you

Yeah. We're not providing specific guidance today, Shay, with regard to the expenses. What we are providing, as you've heard us say, is the cash runway. I'll note that the anticipated savings from headcount on a steady-state basis should be approximately $10 million annually. Now that's not -- this year, obviously, because we're more than halfway through the year but in full -- the full amount of the savings from the approximate 15% of reduction in force.

Thank you.

We do have a final question from Jim Masaga from FactSet. At this time, I would now like to turn the call over to Dr. Scott Koenig for closing remarks.

Thank you, everyone, for joining our call today. We look forward to updating you on the progress of our various programs in the near future. We hope you have a good evening.