Good day, everyone, and welcome to Pfizer's Analyst and Investor Call to review Oncology Business. Today's call is being recorded. At this time, I would like to turn the call over to Mr. Chuck Triano, Senior Vice President of Investor Relations. Please go ahead, sir.
Thank you, operator. Good morning and good afternoon, everyone, and thanks for joining us today to provide An update on our oncology pipeline progress, specifically how we are applying our capabilities to move more quickly and utilize Cutting edge science to key programs. As a note, we plan to conduct a series of these sessions across our therapeutic areas as our pipeline progresses and we have new data and insights to share with you all. We'll be making forward looking statements during this call, and actual results may be different. Additional information regarding forward looking statements is available in our SEC filings on our Forms 10 ks and 10 Q.
Forward looking statements on this call speak only as of the original date of this call, and we undertake no obligation to update or revise any of the statements. With that, I'll now turn the call over to Andy Schmeltz. Andy?
Thanks, Chuck. I'm Andy Schmeltz, and on behalf of my colleagues, Chris Boshoff and Jeff Settlement, we're pleased to have this opportunity to engage with you today. The 3 of us have joint accountability for Pfizer's end to end oncology presence, inclusive of strategy, investments and the full R and D and commercialization continuum. Today, we'll spend about 20 minutes on how we're applying the mindset from Pfizer's recent COVID-nineteen vaccine light speed effort to key clinical programs within oncology. We believe this purposeful, more ambitious approach Can make a significant positive impact both for people afflicted with cancer and for Pfizer.
Then we'll open it up to Q and A. Before jumping into the primary focus of our discussion, let me take a minute to highlight Pfizer Oncology today. We have a broad portfolio of 24 medicines across across 30 types of cancer that brought hope to more than 716,000 people living with cancer in 2020. We continue to see outstanding year over year growth for oncology globally, almost $11,000,000,000 of revenue. Even through a difficult year with the pandemic, we delivered 21% operational growth in 2020.
Ibrance, representing about half the revenue of the portfolio, grew 9%, while our other medicines grew a total of 36% operationally, led by our biosimilars portfolio BRAFTOVI and MEKTOVI and melanoma BRAFTOVI in colorectal cancer and Xtandi in prostate cancer. We also have an incredible amount of activity in clinical development, more than 275 clinical trials currently underway And 6 additional Phase 1 first inpatient clinical program starts since our last discussion with you at Pfizer Investor Day this past September. We've also initiated several new registrational trials in recent months. 2 new trials with BRAFTOVI, BRAKE WATER in first BRAF mutated colorectal cancer, which started in late 2020 and a new Phase III trial that started in February called STARBURGER With BRAFTOVI and MEKTOVI combined with pembrolizumab in first line melanoma. And in prostate cancer, we're expecting data this year from the ongoing Phase 3 Talopro II trial with Xtandi plus Talzena Talazoparib in men with metastatic castrate resistant prostate cancer.
Bottom line, we're proud of our track record and our future prospects for Pfizer Oncology. Let's now shift gears. I cannot understate just how incredibly proud and excited we at Pfizer are about the Lightspeed development in collaboration with BioNTech It delivered the world's 1st breakthrough COVID-nineteen vaccine in less than a year. Our ability to move at such extraordinary speed, While always maintaining our focus on quality and safety was the first powerful display of what the new Pfizer is capable of. Through the vaccine, we found ways to use digital technology to perform tasks in parallel rather than sequentially And to reduce white space between clinical trial cycle times, all of which we're now looking to apply to transform the way we bring breakthrough cancer medicines These light speed learnings and concepts are something that we within oncology have been focusing on to incorporate into our oncology development approach for some time.
Today, we'll walk you through 3 exciting Pfizer discovered programs, Advancing with this light speed mindset, moving at the speed of science. First, a recent example with LORBENA or LORVEQUA internationally In ALK positive non small cell lung cancer, then our BCMA bispecific candidate, elranetimab, in multiple myeloma and how we're taking ambitious steps in what is sure to be a dynamic market. And finally, Jeff Settlement will talk about a collection of early development programs in the breast cancer space, Building on our already strong position here with Ibrance. These examples to be highlighted represent just a small subset of our pipeline portfolio. However, we believe they're indicative of how this new breakthrough mindset is being applied and will propel Pfizer Oncology to continue our growth trajectory and to make a meaningful difference for people with cancer.
Now I'd like to turn it over to Chris Boshoff to discuss LORBRANA in more detail. Chris?
Thank you very much, Andy. Thank you. As you all know, ALK positive lung cancer accounts for 3% to 5% of all lung cancer. Almost a decade ago, we pioneered the field with the development of CellCore. Rolatinib was discovered And developed in house by Pfizer Chemists and it has a unique macrocyclic structure as illustrated in the center of the slide.
Up to 40% of patients with ALK positive non small cell lung cancer present with BRAIN metastases. LORBRAINA is a next generation ALK inhibitor targeting most of the known resistant mutations and also covering brain metastases. On the right side is the list of the most common mutations Developing to other ALK inhibitors demonstrating the coverage of lorlatinib to these. We're very proud of the flawless execution And accelerated development of flurlatinib. From 1st patient dose to 1st regulatory approval was less than 5 years.
Our PROM and first line Phase 3 study from top line report to FDA approval was just over 6 months. We utilized the latest regulatory tools, including real time oncology review pilot and project Orbis, allowing simultaneous reviews In the participating countries and all submissions are now complete. The FDA approval in first on small cell lung cancer is based on the combined results from the CROWN trial, which demonstrated a 72% reduction in the risk of This study also showed in patients presenting with intracranial disease, a 78% complete remission, which is the highest ever demonstrated for any ALK inhibitor. For those presenting without any intracranial metastases, The CROWN study also demonstrated a hazard ratio of 0.06 for progression in the brain versus LKORE. We believe that the CROWN results will position Lorena to be highly competitive with 2nd generation ALK inhibitors in the first line setting, Especially in those 40% of patients presenting with brain metastases.
Furthermore, LORBENA will continue to be a standard of Care of the 2nd generation ALK inhibitors in the second line setting. We are also pleased to still have 27 patients on treatment more than 5 years after starting LORBRAINA on our Phase 1 dose escalation and Moving now to investigational BCMA bispecific, arenatumab, Which we recently announced the initiation of the 1st pivotal trial in relapsedrefractorymultiple myeloma. Multiple myeloma remains a significant unmet need with only 50% of patients surviving Past 5 years with current standard of care, as multiple myeloma progresses, tumors become resistant to the 3 main classes of therapies, The I MIDS, including lenalidomide, the proteasome inhibitors and the anti CD38 antibodies. We believe that the next major pillar of treatment for multiple myeloma will be medicines targeting BCMA, Which is highly expressed in multiple myeloma cells. And among the BCMA targeted therapies, we believe the bispecific molecules We'll become the next standard of care backbone across the treatment paradigm because of efficacy, their safety profile, Combination opportunities and convenience.
Arolonatumab is a full length humanized bispecific antibody optimized for binding affinity To both BCMA and to CD3, enabling more potent T cell mediated tumors out training. Orenatumab is being developed as a subcutaneous injection with the aim of reducing the incidence and grade of cytokine release syndrome or CRS, which is a dose limiting toxicity, particularly for CAR T cells. The development program for aldronetimab is called magnetism. Shown are data from Phase 1 trial Presented at ASH in December 2020, updates of these data will be presented at an upcoming medical conference. In patients with relapsedrefractory multiple myeloma, 83% of patients achieved a clinical response at a recommended Phase 2 dose.
Overall, 30% of patients treated achieved complete response or stringent complete response. This was also the first study with a BCMA bispecific to show responses in patients who had received Prior BCMA target therapy, including ADC or CAR T. Note, 3 out of 4 responses, including a stringent complete remission, We're observed in patients with multiple myeloma progressing on BCMA Tylenolus therapy. Based on these data, We initiated the pivotal Phase 2 study, magnetism 3, earlier this year. This study is now recruiting patients with triple class refractory Multiple myeloma globally.
MAPSYSM III is enrolling 2 cohorts of participants, 1 with And was that prior treatment with the BCMA directed ADC or CAR T therapy? The primary endpoint is objective response rate as assessed by Glanet Independent Central Review. The study's estimated primary completion date is June 2022. Oronatumab is one of the key medicines we are prioritizing at Pfizer to apply light speed concepts from the COVID-nineteen vaccine To accelerate the clinical development program, we are doing this in a variety of ways, including real time monitoring of blinded independent central review, Acceleration of commercial ready product supply by leveraging internal resources, data review and analysis powered by machine learning technologies. As an illustration, from final proof protocol for this study to first subject dose for mechanism 3 was achieved within 30 days In addition to magnetism 3, We are initiating a comprehensive development program building a wall of clinical studies.
This includes other Phase III studies and earlier lines of therapy, Magnetism 5, 6 and 7 expected to initiate over the coming 12 months. We also initiated MAPFITIZEN 4, exploring the potential role of novel combinations through an umbrella study with both internal and external molecules. In the future, the appropriate sequencing and rational combinations of aldronetimab with other medicines Has the potential to transform the outcome of patients with multiple myeloma. I'll now hand it over to Jeff to talk to you about our next generation breast cancer franchise.
Thanks, Chris. So as you just heard from Andy and Chris, we're now applying the learnings of the COVID vaccine development experience to our oncology programs. And I'll briefly describe how we're applying these principles as we explore potential new therapies for estrogen receptor positive breast cancer patients. As you know, the approval of palbociclib, Ibrance in 2017 established Pfizer as a leader in the treatment of ER positive breast cancer. And we've maintained a strong commitment to these patients.
One of the most significant challenges still facing ER positive breast cancer patients is that there's no clear Standard of care in the post CDK4six inhibitor setting. So to address that important unmet need, We've been focused intensively on the development of additional therapies that can overcome drug resistance and potentially provide these patients with more We've been taking a multi pronged approach to targeting ER positive breast cancer, Not only targeting the cell cycle, but also targeting estrogen receptor activity, disrupting signaling pathways that drive breast cancer cell survival And through immuno oncology approaches that promote engagement of immune cells with breast cancer cells. Here, I'll briefly highlight 4 of these programs, including 3 which all entered the clinic at nearly the same time last year. First, I'll describe Our 3 most advanced next generation CDK inhibitor programs, which each enable disruption of the critical G1 cell cycle checkpoint. On the left is our CDK-two forty six inhibitor, which differentiates from our CDK-four forty six inhibitor palbociclib With the ability to additionally target CDK2 and since CDK2 activation seems to drive palbociclib resistance in some breast cancers, This molecule has the potential to overcome such resistance.
We also see opportunities to develop this inhibitor in other tumor types, including triple negative breast cancer and ovarian cancer. This molecule is currently in Phase 1 clinical development And combination studies with endocrine therapy are now underway. And it's worth noting that we've been very encouraged by the early responses we're Thus far with this inhibitor even as monotherapy, especially considering that we're treating patients who have previously progressed on CDK4six inhibitors, which is consistent with our hypothesis that CDK2 contributes to resistance to current standard care treatments and that a CDK2, foursix inhibitor And potentially mitigate such resistance. Next is our CDK4 selective inhibitor, which has been shown preclinically to target CDK4 with more than 10 times the potency of topociclib and without the neutropenia sometimes seen with CDK4six inhibition. And that improved TI potentially provides more opportunity for safer combination treatments and additional cancer types, including lung, colorectal and prostate cancers.
To the right of CDK4 is our CDK2 selective inhibitor, which has been shown in preclinical models to combine with palbociclib or with our CDK4 selective inhibitor to overcome resistance in ER positive breast cancer and has the potential to drive efficacy in a variety of tumors exhibiting CDK2 activation, especially in combination with standard care therapies. Following the successful acceleration of preclinical timelines for these programs, we were able to Move both the CDK2 and CDK4 molecules into the clinic within 8 days of each other in October of 2020. And it's worth noting that each of these next generation CDK inhibitors resulted from innovative structure guided medicinal chemistry efforts From Pfizer Sciences that yielded candidates with selectivity profiles that many had predicted would not be possible to achieve. Now in addition to our robust CDK franchise, we're very excited about the potential for our novel cat6 small molecule inhibitor, A potential first in class agent that blocks the enzymatic activity of the histone acetyltransferase, CAT6A, An epigenetic regulator that's amplified and overexpressed in breast cancer. Cat6a is required for expression of the gene encoding the estrogen receptor And we've observed that this inhibitor can overcome endocrine therapy resistance associated with in preclinical models of ER positive breast cancer and show synergistic activity with CDK inhibition in combination studies.
And this program also moved into the clinic in late 2020. Now it's important to emphasize that we've applied light speed principles to Discovery and development of each of these assets that I just described. Our work on both the cell cycle and cat6 inhibitors has yielded both Complementary and overlapping opportunities with multiple spots on goal to deliver clinical benefit for patients And with strategic optimization of resources across programs, we took the approach of developing the parallel And we were able to deliver 3 new programs to the clinic within a month and a half of each other in 2020. Going forward, we also plan to efficiently drive Acceleration or deprioritization if appropriate of individual assets via umbrella studies and by employing specifically predefined Go no go criteria. This is a paradigm that will continue to guide our oncology research enterprise as we work to bring additional breakthrough therapies to cancer patients in the future.
So with that, I'll pass it back to Andy to wrap up the presentation.
Thanks, Jeff. As you've just heard, we're moving at light speed to advance these programs using enhanced processes, efficiency and technology. Each of the programs highlighted by Chris and Jeff respectively represents a compelling opportunity for patients and for our business. Here, we're depicting the opportunity for the G7 markets. For LORBRANA, the first indication will allow us to expand our share of the ALK positive non small cell lung cancer market, which we anticipate to peak in the range of 25% to 30% share overall.
For elrenodimab, the multiple myeloma market is large and is expected to reach $3,000,000,000 $4,000,000,000 by 2,030 due to multi drug combinations and increasing Within BCMA, we believe the bispecifics will become the standard of care, Being preferred over the antibody drug conjugates and CAR Ts, offering the potential for the efficacy of a CAR T with compelling safety and convenience advantages. While it's still early days, we believe eliranadamab truly has a right to win, Not only in the initial triple refractory indication, but also over time in the double relapsed and newly diagnosed multiple myeloma settings. We anticipate 15% to 20% peak share across multiple myeloma lines of therapy. And for our next generation breast cancer portfolio, we have a strong scientific rationale for our CDT programs as well as for our CAP6A program. We believe there's potential for breakthrough efficacy in the Pope CDK4six setting where no clear standard of care exists and also in the first line metastatic setting to prevent the emergence of CDK resistance.
Leveraging our leadership in HR positive HER2 negative breast cancer, we believe this multiple shot bundle approach will lead to tremendous opportunity and leadership as a follow on to Ibrance. So there you have it. Hopefully, our enthusiasm and conviction regarding our future prospects and our light speed mindset have shown through. Thanks for your time. We now like to take questions.
Chuck,
over to you.
Thanks, Andy, and thanks to Chris and Jeff for the Operator, can we please poll the audience for questions? Thank you.
Your first question comes from the line of Louise Chen from Cantor.
Hi, thanks for taking my questions here. So first question I had for you is, if it's approved, where do you see your next gen CDK inhibitors fitting into the You have 3. So what's your go to market strategy? Second question I have for you is how important is your heme malignancy franchise to you going forward? And if it's important, how do you plan to build this franchise out?
What type of targets and type of drugs are you most interested in? And then last question is just on your early stage Oncology pipeline, which you didn't talk as much about today, what gets you most excited? I know you have a lot of compounds in development. Thank you.
Thanks, Louise, for your three questions. We'll try to take them 1 at a time. I'll talk about the next gen CDK go to market strategy and the heme build out. Maybe Chris, you can chime in and then Jeff, certainly over to you for the Early pipeline. So with our next gen CDK franchise, We see clear opportunity here.
Well, CDK inhibitors led by Ibrance have really established themselves as the modality And standard of care for metastatic HR positive HER2 negative breast cancer That there's clear unmet need. 70% of first line metastatic patients are on a CDK inhibitor. And so they're going to need options Eventually, when the cancer wins out. And so clearly, we're designing this portfolio of early compounds to be able to be Effective after prior CDK therapy, but then also, as a next generation, we envision them having Address, as Jeff kind of commented on, some of the toxicities of the current CDKs. And so they certainly Could have a strong role in first line as well.
So we see quite broad opportunity there for the Next gen CDKs. And as Jeff also mentioned, there's the possibility with some of these that breast cancer is not the only tumor area that could be applicable, That by having a larger therapeutic window, a broader therapeutic window that there'll be a potential in other tumor areas. Maybe before we go on to the Heme question, Chris or Jeff, do you want to add anything there?
I'll just quickly add first And Jeff, this is also for Jeff to expand on. Remember in our PALOMA studies, we show that one of the mechanisms of resistance That was demonstrated was the those tumors that mainly express or over express cyclin E. We know cyclin E binds to CDK2. So that propelled the development of the next generation CDK2 inhibitors. So the CDK2 4six could either be to prevent or to Manage and treat resistance to the current therapies.
And Jeff, perhaps you can also expand on why we're specifically interested in the CDK4.
Sure. Yes. So the CDK4 selective inhibitor, we see opportunities, as I mentioned, not only in ER positive Breast cancer as potentially safer molecule than the 4six inhibitors, but also a molecule that more potently hit CDK4 And therefore, could be more effective in the early line setting, It's especially when combined with CDK2, as Chris mentioned, to prevent resistance. That's one scenario for a 2, 4 combination. We also see opportunities as I mentioned in other indications outside of your positive breast cancer where clinically that more potent Coverage of CDK4 has yielded efficacy and preclinical models that we don't see with palbociclib.
Thanks. Let me tackle the hematology .:] Clearly, we're very excited by the prospects of elranonumab in multiple myeloma. But we should note that we have an existing actually fast growing hematology portfolio with 4 medicines. We've got bosalithin in CML, Vesponsa in ALL and then we have 2 medicines In AML and collectively, we're approaching $1,000,000,000 in revenue with this portfolio. We've got infrastructure globally.
And most importantly, we understand the dynamics in the blood cancer space. So very excited to bring on and see our enab progress quickly and to tap into this infrastructure. But certainly, if there are other opportunities to further expand our hematology portfolio, we'll be primed to do so. Maybe to touch on the early pipeline, the last question, Jeff, anything you want to add about the early pipeline?
Sure. Yes, we're very excited about our early programs and maybe I can comment on a couple of areas that are particularly a high priority. In the IO space, so in addition to our approved PD L1 antibody avelumab and our E1 antibody cesamlimab, Phase 3 development in early bladder cancer. We have several enemies in Phase 1 now including 2 different T cell redirecting bispecific antibodies. You heard about BCMA, we also have a bispecific T cell redirecting antibody targeting UG2C, an antigen that's highly expressed in GI malignancies.
We have 2 different programs targeting the immunosuppressive TGF beta pathway And we have recently introduced into the clinic a PD-one antibody conjugated to A modified version of an IL-fifteen cytokine, we're really excited about that one. Also from our Boulder site, we have a small molecule inhibitor of the TAM kinases. So We have a robust early pipeline in immuno oncology. We also have several promising earlier stage programs that are focused on the PDX I O space, a few of which we're expecting to bring into the clinic in the second half of this year, including an oncolytic Virus that looks very promising in preclinical studies. Another area of scientific emphasis has been on Regulators of chromatin, epigenetic modulators, I mentioned CAB6, we also have an EZH2 program that we're excited about And our PRNT5 inhibitor, which is differentiated from some of the other programs in the clinic With some very high potency and a unique mechanism of target engagement.
So those are a few of the areas that we're especially excited about with respect to our early pipeline.
Thanks, Jeff.
Thanks, folks. Thanks, Louise, for the question. Operator, please let's move to the
Your next question comes from the line of Terence Flynn with Goldman Sachs.
Hi, good morning. Thanks for taking the questions. I appreciate you walking through all this today. I guess a couple for me. The BCMA market, you mentioned differentiation versus the ADCs and the CAR Ts.
But if you look at the various bi Specific antibodies, what do you see as kind of the key differentiated features there for your asset and what's going to really drive market share shift Among those various agents. And then the second one I had is on your CDK-two forty six in hip, are we going to Any data there at ASCO this year or potentially maybe another conference later this year? And what is the bar? What are you guys looking for in Just can you remind us if you ever saw any activity for Palbo in other tumor types beyond breast cancer? Thank you.
Thanks for your questions. I'll start and then we'll tag team with Chris and Jeff on these others Regarding CDK-two forty six and PALBO activity. So for elranonumab, Role and differentiation within relative to other BCMA modalities. So first, again, BCMA relative To CAR Ts relative to antibody drug conjugates, we believe that the bispecifics are going to be the winners in the long run here. The efficacy of the CAR Ts combined with safety and convenience advantages.
Elinotumab from day 1 designed to be subcutaneous administration. Many of the other bispecifics started out as Many of the other bispecifics started out as infusion molecules and they're trying to make them more convenient into subcutaneous. Certainly, it's early days in terms of differentiation amongst the bispecifics. We're very excited about the early efficacy results And safety results that we have in our trials, and we'll have to see how this plays out. But given the our intent to move quickly And to generate robust data across different patient segments, we're quite confident that Then we're going to be primed and have a right to win over time.
Chris, anything to add there?
I'll add just 2 other points of differentiation is the molecule The molecule was designed for optimal affinity to both BCMA And CD3, which resulted in a very favorable PK profile for us. So as Andy pointed out, we're starting in the trial with And then 2 weekly subcutaneous dosing, but we also now started to test in methadism-nine, 4 weekly subcutaneous Dosing, which of course could be differentiated. The overall risk benefit profile, as mentioned, the safety, we so far only have Grade 1 or Grade 2 cytokine release syndrome and specifically we were the first to notice or observe Responses including a stringent complete remission in patients previously exposed to either ADC, BCMA ADC For BCMA CAR T. So we certainly believe we will be in the first wave with olanatumab. Jeff, over to you for CDKs.
Yes, I think there was a question about the path for CDK246. I think while we don't have a specific plan for the presentation of the data, as I mentioned, What we're especially encouraged by is seeing responses with the monotherapy treatment In patients who have progressed on CDK4six. So again, this does seem to support our hypothesis around the role of CDK2 In driving resistance, as I mentioned, we're also exploring the endocrine therapy combination, which is already underway. I think as far as where the bar is, I don't have specific metric to point to at this time, but I would say that We do see the CDK246 on therapy if there is transformational efficacy as our first path to And approval with our next generation CEK molecules. I think there was also a question about, albociclib and other Tumor types and maybe Chris, I'll hand back to you for that one.
Thank you. So we did observe a number of Some of the rarer tumors, some of the rarer lymphomas and sarcomas, soft tissue sarcomas, where we did observe single agent activity with palbociclib. One of the challenges have been in combinations apart from hormonal therapy has been either DDIs or and the therapeutic index, Especially with cytotoxic therapy, although we've noticed in some of the Phase 1 study significant activity with avacyclin combination with cytotoxic therapy, That has always been hampered by hematological toxicity and we hope that that can be overcome with the CDK4 specific inhibitor. Having said that, we still have ongoing pediatric stays in human sarcomas and other types of sarcomas with a combination of palbarkocytotoxic therapy, which
Operator, can we move to our next questioner, please?
Your next question comes from Vamil Divan from Mizuho Securities.
Great. Thanks so much for taking my questions. So one maybe I may have missed it, but just on the earlier stage assets, Your HER2 ADC, we get questions on that periodically. I'm wondering if you can just give any update on when we might see some more data on that product for 103. And then maybe just you talked a lot about encouragingly on the learning from the COVID situation, how you're transferring over.
I'm wondering if you can just talk more specifically around So mRNA technology and how you sort of need to see that, any further development you look to doing on that in terms of Oncology vaccines or otherwise would be helpful. Thanks.
Steph, I think both of these are squarely in your shot.
Sure. Yes. So for our HER2 ADC, and we've recently stopped that program, we had seen robust clinical responses, but We just felt that the therapeutic index wouldn't quite be adequate to move into earlier line indications when considering the competitive landscape. And so we decided to prioritize other programs where we see greater potential. Also worth mentioning that from our Boulder site, we have a small molecule program that targets HER2 exon 20 mutations.
As far as the RNA technology in cancer vaccines, absolutely, this is something we're looking at very carefully. We do have an interest in cancer vaccines. We've seen how the power of RNA As producing immunogens that seem to be quite effective in the preventive vaccine setting, we think that that Technology may very well translate into therapeutic cancer vaccines and we're excited about that possibility. So that is something that we're actively investigating.
Right. Thank you, Jeff, for those responses. Let's move to our next question, please.
Your next question comes from Geoffrey Porges from SVB Leerink.
Thank you very much for taking the question and Chuck, I hope they let you out of the witness protection program soon. It looks like the last year where you are. So two questions, both related about earlier lines of treatment. First, on the CDK4six, Do you have any insight yet as to why Ibrance was not successful in the adjuvant setting? And then secondly, which of the CDKs that you outlined You believe has the best opportunity to move into the adjuvant setting and related to that, are there any principles from Lightspeed That you think can accelerate the path to either first line or to adjuvant short of showing an overall survival benefit.
If you could address that for both the CDKs and for the BCMA because as you allude to, The first line indication and or the adjuvant indications for both these diseases are by far the majority of the revenue opportunity. Thanks.
Thanks for the questions. Chris, I think that you're probably best positioned to speak to our early breast cancer experience with Ibrance And how we would apply learnings to next gen CDKs perhaps for early breast cancer as well as our light speed approach with Elrin Altman?
Thank you very much, Andy. We're obviously very disappointed in the data from our early breast cancer studies, Especially Pallas. Overall, it's very difficult to compare the various studies in early breast cancer because of obviously demographics. Need to point out as well that these were not Pfizer sponsored studies. So we're working with the sponsors of those 12, so The cooperative groups who conducted those studies, and as you would have noticed in the public in the presentations last year, there was High number of a high percentage of patients that discontinued palvaciclib during the study that was also disappointing to us.
Having said that, we have collected both tissue samples as well as plasma samples during that study And that is starting to reveal a lot of interesting data for us and data that could be applied to our future studies, specifically for our silicate 4 and our silicate And 246 programs as we could potentially developing them into earlier settings. So early breast cancer, we believe, will become Molecularly fractionated between different risk groups, not everyone will benefit from adding a silicate 2, foursix or silicate 4 or silicate 4six. So using those translational data, I think, is going to be enormously helpful to us. I do want to point out quickly another study we just initiated was And that's been led by Yale University as CRC or Collaborative Research study is in the early setting called M0. So what this study is doing is a very novel study in breast Stanson patients very early on, we sequence all their samples, then determine the genetic drivers of their specific disease.
Those genetic drivers are then detected in plasma with circulating tumor DNA. And as soon as they become detectable, patients are randomized to either continue their standard of care hormonal therapy ought to be randomized to be added as CDK4six. So that study, which has just opened, a randomized trial, We also believe we'll give significant insight how to develop the base combination and at what time
do you want to comment on applying light speed to our elinonumab?
Yes. So I think as you've seen from the slides we've Sharon, with the 9 studies that's now in initiation and some of them already started, it's mechanism 129, A lot of things are done in parallel. We're using the latest digital tools, virtual tools for virtual site initiation, Getting data in from sites using artificial intelligence and machine learning, pattern recognition to see if there's any regarding AEs or any other Information we're collecting from the sites, particularly also the acceleration of our CMC commercial ready product will be ready Should be launched. As you've seen, the current primary completion date is June 2022 for our first study. We're very excited to do things in parallel and apply the latest digital technologies in that program.
Great. Thanks for that, Chris. Operator, let's take our next question, please.
Your next question comes from Steve Scala from Cowen.
Thank you. Two questions. I think CDK4six inhibitors overall have been studied unsuccessfully in lung, pancreatic and prostate cancer. I think you mentioned interest in triple negative breast and ovarian as targets now. Is that the totality of the other tumors that you plan to pursue?
And secondly, why did Pfizer outlicense the PI3K mTOR given its promising clinical response post CDK4six inhibitor failure? Thank you.
Thanks, Steve, for those questions. Jeff, let me hand it to you first for other opportunities for our CDK Franchise.
Right. So based on preclinical data, we've been exploring each of these next generation CDK inhibitors in a broad panel of preclinical models across many indications. There are for the CDK II and 2 forty six programs, there are clearly settings where CDK2 activity is driven by, for example, increased cyclin T expression or amplification, Loss of RB such as seen frequently in small cell lung cancer, so that would be 1 triple negative breast cancer, endometrial cancer, Ovarian cancer, these are places where CDK2 activation seems to play an important role. In terms of CDK4 activity, As I mentioned briefly there with the greater potency we can achieve in the absence of the CDK6 associated neutropenia, We can push the coverage of CDK4 and at least based on preclinical modeling, we can see activity in settings like lung cancer, Colorectal and prostate cancer, where with palbociclib had similar concentrations that is lower Exposures of CDK4, we're not seeing that kind of efficacy. So that gives you some sense as to how we're thinking about Positioning each of these molecules in other indications beyond ER positive breast cancer.
Thanks, Jeff. And I don't know, Chris, you want to take the out licensing of Genentasa?
Yes, I'll be quick. Thanks, Andy. As Jeff mentioned earlier, And by the end of 2021, we'll have 21 steemolecular entities in the clinic. In 2020 alone, we had 5 FIHS First in humans and already 3 achieved in 2021. So we really have to prioritize across our portfolio.
We agree that's an Medicine is an intravenous PI3K and inhibitor and mTOR inhibitor and we're very pleased that There's a home now with Celcuity and they will take it on and develop it further, but it's clearly an active molecule, you're correct.
Great. Thanks, Chris. And operator, if we could take our last question now, please.
Your final question comes from the line of Seamus Fernandez from Guggenheim.
Great. Thanks for the question. So just a couple of questions here. First off, in terms of the interest in other mechanisms on the breast cancer side, I was just wondering if you guys could update us if you're doing work on oral surge or if you're watching that space relatively closely. And if not, What are the issues that you see with regard to the oral SERD class?
Is it just sort of the hurdle of stepping above fulvestrant Or other dynamics in that regard. The second question, just in terms of protein degrader technology, You guys mind updating us on the work that Pfizer is doing in this space, whether it be through the Our Venus collaboration or otherwise and when might we see some more products from Pfizer on the protein degrader side of things? And then the last question, in terms of feedback that we've gotten so far, can you just update us on when we might know The sort of ultimate dosing regimen for your BCMA, I believe you'll start with kind of a once a week dosing Profile follow that with expansion to kind of every 2 week and then pursue every 3 weeks. But just wondering when we might have Good visibility on the treatment duration. Thanks so much.
Thanks for your questions. We'll try to tick them off one at a time. So in breast cancer, Sir, you asked about additional mechanisms of action, specifically oral SERDS. Clearly, this is an interesting space Where it looks like if they can actually have significant improvement upon fulvestrant that they'll have Utility in the breast cancer setting and we're actually working with many of the companies that have oral service today because it's about combination studies And Ibrance palacyclab is the combination agent of choice. So we're closely monitoring the space to see How it plays out and if there's really a true winner that can establish a new standard of care for hormone therapy.
Chris, do you want to answer that?
I think you said it. And importantly, those companies that You're all very well aware of. That's now got in pivotal studies starting or started with the search. Those in the earlier lines have been combined with Ibrance and we're partnering with them with Ibrance for those at least 3.
Okay. The next question was about protein degrader technology and how that's playing out. Jeff,
do you want
to take that or maybe Chris?
Yes. Thanks, Andy. Yes. No, as was mentioned, we Have an active collaboration with Arvinis on protein degraders. It's a research collaboration.
We have several programs that are Part of that collaboration, we haven't disclosed targets that we're working on, but just fair to say that we've been very thoughtful about Choosing targets for which we think that ProTac type technology is especially relevant And we're excited about how that collaboration is going. We also have internal programs focused on similar technology. We've developed that capability in house And we have a few complementary programs that we're driving internally that we're very excited about. So that's what I can say about It's a greater technology. It's really opening up the difficult to drug space and so we're excited about what we're doing there.
Great. And Chris, on to you for dosing with alarinaumab.
Thank you. You're absolutely correct. Current study is that's the Phase 1 study is weekly. All our PK modeling has indicated that we can move to 2 weekly. The pivotal trial that is now ongoing, MATTHISM 3, therefore, has a regimen of weekly with to further reduce any cytokine release syndrome and then after a couple of months moving to 2 weekly.
We've also just initiated magnetism 9 And again from PK modeling, inferring that this molecule can be moved to 4 weekly. So later probably More on the same 2022, you'll see data emerging with moving from 2 weekly to 4 weekly. Do you ask about duration of response? As I mentioned, we'll update later this year. You'll see updated data from our Phase 1 study.
Just to point out that the data I've Shown, of all those patients that's responding, there's only one that has progressed and that was at the lowest dose during dose So all the other responses are currently ongoing. This is highly encouraging for us. Thank you.
Terrific. So as you can all hear, a lot going on in the oncology portfolio and broadly at Pfizer. So We will look forward to periodically hosting similar sessions like this to highlight other parts of our portfolio. So I'd like to thank everyone for their attention this morning and to Andy, Chris and Jeff for their insights. Have a great day.
Ladies and gentlemen, this concludes today's conference. Thank you for your participation. You may now all disconnect.