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July 28, 2025 VIKTORIA-1 Pivotal Phase 3 Topline Results from PIK3CA Wild-Type Cohort
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2 Forward-Looking Statements This presentation contains statements that constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. These statements relate to Celcuity’s business, operations, and financial condition, and include but are not limited to our current beliefs, expectations and assumptions regarding the future of our business and our pipeline, including our lead drug candidate gedatolisib and its potential benefits, that involve substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These statements include, but are not limited to, (i) our interpretation of topline clinical trial data; (ii) our expectation regarding regulatory interpretations and assessments of our clinical data; (iii) our expectations regarding the timing of and our ability to obtain regulatory approvals for gedatolisib within and outside the U.S.; (iv) our beliefs with respect to the clinical utility of gedatolisib, its market acceptance and the size of the market, as well as the cost to commercialize and our ability to serve that market; (v) our expectations regarding governmental laws and regulations affecting our operations; (vi) our beliefs about our ability to capitalize on the exclusive global development and commercialization rights obtained from our license agreement with Pfizer Inc. (“Pfizer”) with respect to gedatolisib, and payments due to Pfizer thereunder; (vii) our product pricing, coverage, reimbursement and revenue expectations; (viii) our expectations as to the availability of capital and use of proceeds from our financing activities as well as cash on hand; and (ix) our expectations regarding our ability to obtain and maintain intellectual property protection for gedatolisib. These statements may be affected by underlying assumptions that may prove inaccurate or incomplete and are subject to change. Certain risks, uncertainties and other factors include, but are not limited to: the uncertainties inherent in research and development, including the cost of clinical trials, and the ability to meet anticipated clinical endpoints and commencement and/or completion dates for our clinical trials involving gedatolisib which include our ongoing VIKTORIA-1 and VIKTORIA-2 phase 3 clinical trials, and our ongoing Phase 1b/2 clinical trial; our limited operating history; our potential inability to develop, obtain FDA approval for and commercialize gedatolisib on a timely basis or at all; the reporting of topline results based on a preliminary analysis of key efficacy and safety data prior to a more comprehensive review of the data, and such topline data may not accurately reflect the complete results of a clinical trial; the complexity and difficulty of demonstrating the safety and sufficient magnitude of benefit to support regulatory approval of gedatolisib; the uncertainties and costs associated with commercializing pharmaceuticals; challenges we may face in developing and maintaining relationships with our vendors and partners; the uncertainty regarding market acceptance by physicians, patients, third-party payors and others in the medical community, and with the size of the market opportunity available to us; difficulties we may face in managing growth, such as hiring and retaining a qualified sales force and attracting and retaining key personnel; changes in government regulations; tightening credit markets and limitations on access to capital on favorable terms or at all; the time and expense associated with defending third-party claims of intellectual property infringement, investigations or litigation threatened or initiated against us; and potential changes to economic and trade policy in the U.S. and globally, including tariffs. Actual results may differ materially from past results, future plans and projected future results. As forward-looking statements involve significant risks and uncertainties, caution should be exercised against placing undue reliance on such statements. Additional information regarding these and other factors can be found in Celcuity’s Annual Report on Form 10-K for the fiscal year ended December 31, 2024 and its subsequent Quarterly Reports on Form 10-Q, all of which are filed with the U.S. Securities and Exchange Commission and available at www.sec.gov. The forward-looking statements in this presentation speak only as of the original date of this presentation and we undertake no obligation to update or revise any of these statements, except as required by law. This presentation is intended for the investor community only and is not intended to promote gedatolisib or otherwise influence healthcare prescribing decisions. Definitive conclusions cannot be drawn from cross-trial comparisons or anticipated data as they may be confounded by various factors and should be interpreted with caution. All trademarks in this presentation are the property of their respective owners. This presentation may also contain estimates and other statistical data made by independent parties and by us relating to market size and other data about our industry. This data involves a number of assumptions and limitations, and you are cautioned not to give undue weight to such data and estimates. In addition, projections, assumptions and estimates of our future performance and the future performance of the markets in which we operate are necessarily subject to a high degree of uncertainty and risk. This presentation is intended for the investor community only. It is not intended to promote the products referenced herein or otherwise influence healthcare prescribing decisions. Cross-trial comparisons are not based on head-to-head studies and no direct comparisons can be made.
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3 Overview Brian Sullivan Chief Executive Officer and Co-Founder VIKTORIA-1 Topline Results – PIK3CA WT Igor Gorbatchevsky, M.D. Chief Medical Officer Treatment Landscape Rachel Layman, M.D. Professor, Breast Medical Oncology MD Anderson Cancer Center Commercialization Planning Eldon Mayer Chief Commercial Officer Upcoming Milestones Brian Sullivan Q & A Agenda
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Overview 4 Brian Sullivan Chief Executive Officer and Co-Founder
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5 In patients with HR+/HER2-/PIK3CA wild-type (WT) advanced breast cancer (ABC), ▪ gedatolisib plus fulvestrant and palbociclib (triplet) ▪ gedatolisib plus fulvestrant (doublet) MET THE STUDY’S TWO PRIMARY ENDPOINTS By demonstrating statistically significant and clinically meaningful improvement in progression free survival versus fulvestrant Gedatolisib Triplet ▪ mPFS was 9.3 months vs. 2.0 months for fulvestrant ▪ 7.3-month incremental improvement in mPFS ▪ HR = 0.24 ▪ 4.2x higher likelihood of survival w/o disease progression Gedatolisib Doublet ▪ mPFS was 7.4 months vs. 2.0 months for fulvestrant ▪ 5.4-month incremental improvement in mPFS ▪ HR = 0.33 ▪ 3.0x higher likelihood of survival w/o disease progression Topline VIKTORIA-1 PIK3CA Wild-Type Cohort Data Abbreviations: mPFS - median progression free survival; HR – Hazard Ratio
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Most favorable hazard ratio ever reported by any Phase 3 trial in HR+/HER2- ABC Triplet & Doublet Achieved Unprecedented Efficacy in HR+/HER2- ABC Highest incremental improvement in mPFS ever reported by any Phase 3 trial in 2nd line HR+/HER2- ABC First PI3K/AKT/mTOR (PAM) inhibitor to achieve positive Phase 3 data in PIK3CA WT patients post-CDK4/6 inhibitor Potential to Establish New Standard-of-Care for 2L HR+/HER2- ABC
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Subject Matter Patent Expiration Date Note Composition of Matter (API) (generic and species) Dec 2034 ▪ Includes 209 days of patent term adjustment (PTA), and expected 5 years of patent term extension (PTE) Cyclodextrin Formulations Jan 2041 ▪ Includes 578 days of PTA ▪ Drug product formulation used in current Phase 3 trials ▪ Since Cyclodextrin is a functional excipient, this patent extends patent exclusivity period for gedatolisib Dosage Regimens August 2042 ▪ Patent issued July 8, 2025 ▪ Treatment schedule would be on product label, extending patent exclusivity period for gedatolisib Method of Treatment for Diseases Pending ▪ Filed December 2023 ▪ Covers non-oncology indication Method of Treatment for Cancer Pending ▪ Filed August 2024 ▪ Covers oncology indications 7 Loss of exclusivity now expected to occur in 2042; expect new formulations to extend this period Key Gedatolisib Patents
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VIKTORIA-1 Topline Results - PIK3CA Wild-Type 8 Igor Gorbatchevsky, M.D. Chief Medical Officer
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9 Clinical Background HR+/HER2-/PIK3CA wild-type advanced or metastatic breast cancer (ABC) post-CDK4/6 inhibitor • Current approved regimens are associated with poor mPFS ~2 – 4 months1,2 • 60% of patients with HR+/HER2 ABC have PIK3CA WT tumors • PAM, estrogen receptor (ER) and CDK4/6 pathways are interdependent drivers of HR+/HER2- ABC, independent of PIK3CA status 3-7 • Comprehensive blockade of the PAM pathway offers the potential to: 8-12 • Limits cross-activation of PAM when ER or CDK4/6 is inhibited • Restore or enhance sensitivity to endocrine therapy & CDK4/6 inhibition Sources (1) Bidard et al, JCO 2022; (2) Lindeman et al. Clin Canc Res. 2022; (3) Campbell 2001, J Biol Chem 276(13):9817-24; (4) Yamnik 2009, J Biol Chem 6;284(10):6361-9) (5) Alves, Int J Mol. Sci. 2023; 24, 4522;(6) Simoncini 2000, Nature 407(6803):538–541; (7) Bosch 2015, Sci Transl Med. 7(283):283ra51; (8) Alves 2021, Nature Com, 12:5112; (9) Cai 2022, Sci China Life Sci 65; (10) O’Brien 2020, Breast Cancer Research, 22:89; (11) Karimi 2023, Cancer Communications, 43; (12) Jansen 2017, Cancer Res; 77(9). Abbreviations: mPFS - median progression free survival; ER – estrogen receptor
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10 Overview of Gedatolisib Gedatolisib has a highly differentiated mechanism of action ▪ Gedatolisib is a pan-PI3K, mTORC1 and mTORC2 inhibitor ▪ Comprehensively blockades the PAM pathway1, 2 ▪ Limits cross-activation between PAM targets that occurs when only PI3Kα, AKT, or mTORare inhibited 3-11 ▪ Induces anti-tumor cell activity independent of PIK3CA status2 ▪ In live tumor cell proliferation studies, gedatolisib showed 300x higher potency, on average, than PI3Kα, AKT, mTOR12 ▪ Only PAM inhibitor showing comparable activity in PIK3CA wild- type and mutant tumor cells12 Sources: (1) Venkatesan, J Med Chem. 2010;53(6):2636-45; (2) Rossetti, npj Breast Cancer. 2024; (3) Juric, Nature. 2015;518:240-244; (4) Castel, Nat Cancer. 2021;2:587-597; (5) Mao, Nat Commun. 2021;12:5053; (6) Schwartz, Cancer Cell. 2015;27:109-122. (7) Chandarlapaty, Cancer Cell. 2011;19:58-71; (8) Bago, EMBO J. 2016;35:1902-1922; (9) Manning, Cell. 2017;169:381-405; (10) Mukherjee, Mol Cell. 2021;81:708-723 e705 (11) Elkabets, Sci Transl Med. 2013;5(196); (12) Rossetti njp Breast Cancer 2024
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11 Phase 3, global, open-label, randomized study VIKTORIA-1 Study Design for PIK3CA Wild-Type Cohort * Randomization stratified by 1) presence of lung/liver metastases (yes versus no); 2) time of radiological PFS period on immediate prior therapy (<6 months versus >6 months); and 3) Region (North America vs. ROW). Abbreviations: PFS = progression free survival; BICR = blinded independent central review. R 1:1:1* (N=392) • Pre-/post-menopausal women and men • Progression during or after CDK4/6 inhibitor + aromatase inhibitor • < 2 lines of prior endocrine therapy for ABC • No prior mTORi, PI3Ki, or AKTi • No prior chemotherapy for ABC • Measurable disease per RECIST v1.1 Gedatolisib 180 mg IV once weekly, 3 wks on, 1 wk off (day 1, 8, 15) Palbociclib 125 mg daily, 21 days on, 7 days off Fulvestrant 500 mg; cycle 1, day 1 & 15, then every 4 weeks Arm A – Gedatolisib Triplet Gedatolisib 180 mg IV once weekly, 3 wks on, 1 wk off (day 1, 8, 15) Fulvestrant 500 mg; cycle 1, day 1 & 15, then every 4 weeks Arm B – Gedatolisib Doublet Fulvestrant 500 mg; cycle 1, day 1 & 15, then every 4 weeks Arm C PFS (BICR) Arm A vs. Arm C Arm B vs. Arm C Optional Cross-over to Arm A or B upon progressive disease Patients with HR+/HER2-/ PIK3CA-wild-type ABC Primary Endpoints
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12 Achieved statistically significant and clinically meaningful improvement in PFS VIKTORIA-1 PIK3CA WT Cohort Met Primary Endpoint – Triplet Analysis Abbreviations: CI, confidence interval; HR, hazard ratio; m, Median; PFS, Progression-Free Survival. 1. Kaplan Meier method; 2. Stratified Cox regression model; 3. Stratified log-rank test. 100 90 80 70 60 50 40 30 20 10 0 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Months Progression-free Survival (%) Censored 9.3 months mPFS1 (95% CI: 7.2-16.6) HR = 0.24 (95% CI: 0.17-0.35)2 P<0.00013 4.2x increase in likelihood surviving progression-free Arm A: gedatolisib + fulvestrant + palbociclib, n=131 Arm C: fulvestrant, n=131 2.0 months mPFS (95% CI: 1.8-2.3)
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13 Achieved statistically significant and clinically meaningful improvement in PFS VIKTORIA-1 PIK3CA WT Cohort Achieved Primary Endpoint – Doublet Analysis 100 90 80 70 60 50 40 30 20 10 0 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Months 25 26 Progression-free Survival (%) Abbreviations: CI, confidence interval; HR, hazard ratio; m, Median; PFS, Progression-Free Survival. 1. Kaplan Meier method; 2. Stratified Cox regression model; 3. Stratified log-rank test. Censored 7.4 months mPFS1 (95% CI: 5.5-9.9) HR = 0.33 (95% CI: 0.24-0.48)2 P<0.00013 3.0x increase in likelihood surviving progression-free Arm B: gedatolisib + fulvestrant, n=130 Arm C: fulvestrant, n=131 2.0 months mPFS (95% CI: 1.8-2.3)
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14 Additional Findings and Next Steps Discontinuation rates and safety profile better than observed in Phase 1b study Additional Findings ▪ The treatment discontinuation rates due to a TRAE for the gedatolisib triplet and doublet were lower than observed in Arm D of the Phase 1b trial in ABC patients ▪ Additionally, they were lower than was observed in any Phase 3 trials for currently approved drug combinations in HR+/HER2- ABC. ▪ The safety profile of the gedatolisib triplet and gedatolisib doublet was better than observed in the Phase 1b trial in ABC patients, including lower rates of hyperglycemia and stomatitis ▪ Favorable overall survival trend for both the gedatolisib triplet and the gedatolisib doublet, although the data is immature Next Steps ▪ Full results for VIKTORIA-1 PIK3CA Wild-Type cohort will be presented at an upcoming medical conference later in 2025 ▪ Anticipate filing NDA submission in Q4 2025
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Treatment Landscape 15 Rachel Layman, M.D. Professor, Breast Medical Oncology MD Anderson Cancer Center Prof. Rachel Layman, MD MD Anderson Cancer Center
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16 Therapy after Progression on a CDK4/6 Inhibitor –SERD’s (1) Bidard F, JCO 2022; (2) Campone M, NEJM 2025; (3) Jhaveri KL, NEJM supplement 2024; (4) Neven P, ESMO Breast Poster FPN-306P, 2025 Note: Vepdegestrant and Imlunestrant are investigational therapies and do not have FDA approval. Abbreviations: SERD – selective endocrine receptor degrader; ET – endocrine therapy; WT – wild-type; MT – mutant. Note: To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable Positive readouts in Phase 3 studies limited to patients with ESR1 mutations Therapies (Study) Prior CDK4/6i 2nd/3rd Line PI3K Status ESR1 Status Results Elacestrant vs ET (EMERALD)1 100% 100% WT/MT MT 3.8 vs 1.9 months HR = 0.55 Vepdegestrant vs. ET (VERITAC-2)2 100% 100% WT/MT MT 5.0 vs 2.1 months HR = 0.58 Imlunestrant vs. ET (EMBER-3)3,4 70% 79% WT/MT MT 5.5 vs 3.8 months HR = 0.62 Prof. Rachel Layman, MD MD Anderson Cancer Center
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17 Therapy after Progression on a CDK4/6 Inhibitor – CDK4/6i + ET (1) Kalinsky K, ASCO Presentation, 2024; (2) Jhaveri KL, NEJM 2024; (3) Neven P, ESMO Breast Poster FPN-306P, 2025 Note: Abemaciclib + imlunestrant is an investigational therapeutic regime and does not have FDA approval. Abbreviations: ET – endocrine therapy; WT – wild-type; MT – mutant. Note: To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable Other positive Phase 3 studies report incremental mPFS benefit of 0.7 – 3.9 months Therapies (Study) Prior CDK4/6i 2nd/3rd Line PI3K Status ESR1 Status Results Abemaciclib + Fulvestrant vs. Fulvestrant (postMONARCH)1 100% 100% WT/MT WT/MT 6.0 vs 5.3 months (HR = 0.73) Abemaciclib + Imlunestrant vs. Imlunestrant (EMBER-3)2,3 65% 68% WT/MT WT/MT 9.4 vs 5.5 months (HR = 0.57) Prof. Rachel Layman, MD MD Anderson Cancer Center
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18 Therapy after Progression on a CDK4/6 Inhibitor – Inhibitors of PAM Targets Source: Turner N, NEJM 2023; (2) US FDA Center for Drug Evaluation and Research, Mutli-Discipline Review, Capivasertib, 2023. Note: Abemaciclib + imlunestrant is an investigational therapeutic regime and does not have FDA approval. Abbreviations: ET – endocrine therapy; WT – wild-type; MT – mutant. Note: To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable No PAM pathway inhibitor has shown improvement in PIK3CA WT patients who received prior CDK4/6 Therapies (Study) Prior CDK4/6i 2nd/3rd Line PI3K Status ESR1 Status Results Capivasertib + Fulvestrant vs. Fulvestrant1,2 (CAPItello-291) 100% 100% WT WT/MT 3.8 vs 3.5 months HR = NS Alpelisib + Fulvestrant No prospective data available Everolimus + exemestane No prospective data available Prof. Rachel Layman, MD MD Anderson Cancer Center
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Gedatolisib and approved regimens with Phase 3 data for 2L HR+/HER2-/PIK3CA WT post-CDK4/6i How Does the Gedatolisib Regimen Potentially Fit in the 2L Landscape? Gedatolisib + Fulvestrant + Palbociclib 9.3 months Gedatolisib + Fulvestrant Elacestrant 1 Median Progression-Free Survival 7.4 months 1.8x 3.9 months Prof. Rachel Layman, MD MD Anderson Cancer Center (1) Bidard F, JCO 2022; (2) Campone M, NEJM 2025; (3) Jhaveri KL, NEJM 2024; (4) Neven P, ESMO Breast Poster FPN-306P , 2025 (5) Kalinsky K, ASCO Presentation, 2024. Note: Vepdegestrant and Imlunestrant are investigational therapies and do not have FDA approval. Abemaciclib + imlunestrant is an investigational therapeutic regime and does not have FDA approval. Abbreviations: ET – endocrine therapy; WT – wild-type; MT – mutant. To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable 19 Fulvestrant 1 2.0 months 2L 2L 2L ESR1 MT 2L Patient Population
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Gedatolisib regimens showed highest incremental mPFS improvement versus endocrine therapy How Does the Gedatolisib Regimen Potentially Fit in the 2L Landscape? Patient Population 2L 2L 1L/2L 2L ESR1 MT 2L ESRI MT 1L/2L ESR1 MT 2L Gedatolisib + Fulvestrant + Palbociclib Imlunestrant + Abemaciclib 3 Gedatolisib + Fulvestrant Vepdegestrant 2 Elacestrant 1 Imlunestrant 3,4 Abema + Fulv5 Δ 7.3 months Δ 1.9 months Δ 0.7 months Δ 1.7 months Δ 3.9 months Δ 5.4 months Δ 2.9 months Incremental mPFS improvement relative to endocrine therapy Prof. Rachel Layman, MD MD Anderson Cancer Center (1) Bidard F, JCO 2022; (2) Campone M, NEJM 2025; (3) Jhaveri KL, NEJM 2024; (4) Neven P, ESMO Breast Poster FPN-306P , 2025 (5) Kalinsky K, ASCO Presentation, 2024. Note: Vepdegestrant and Imlunestrant are investigational therapies and do not have FDA approval. Abemaciclib + imlunestrant is an investigational therapeutic regime and does not have FDA approval. Abbreviations: ET – endocrine therapy; WT – wild-type; MT – mutant. To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable 20 Not FDA approved Not FDA approved Not FDA approved
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Hazard ratios for gedatolisib regimens are unprecedented How Does the Gedatolisib Regimen Potentially Fit in the 2L Landscape? Patient Population 2L 2L 2L ESR1 MT 1L/2L 2L ESR1 MT 1L/2L ESR1 MT 2L Geda + Fulv+ Palbo 0.24 Gedatolisib + Fulvestrant Elacestrant 1 Vepdegestrant 2 Imlunestrant + Abemaciclib 3 Imlunestrant 3,4 Abemaciclib + Fulv 5 Hazard Ratio (lower is better) 0.33 0.55 0.58 0.62 0.73 Prof. Rachel Layman, MD MD Anderson Cancer Center (1) Bidard F, JCO 2022; (2) Campone M, NEJM 2025; (3) Jhaveri KL, NEJM 2024; (4) Neven P, ESMO Breast Poster FPN-306P, 2025 (5) Kalinsky K, ASCO Presentation, 2024. Note: Vepdegestrant and Imlunestrant are investigational therapies and do not have FDA approval. Abemaciclib + imlunestrant is an investigational therapeutic regime and does not have FDA approval. Abbreviations: ET – endocrine therapy; WT – wild-type; MT – mutant. To-date, no head-to-head comparisons of any other products to any of our product candidates in any clinical trial have been completed; results have been obtained from different trials with different designs, endpoints and patient populations; results may not be comparable 21 Not FDA approved Not FDA approved Not FDA approved 0.57
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22 Data Support Potential for Gedatolisib to Become the SOC drug for 2L HR+/HER2-/PIK3CA-wild-type ABC Key Takeaways 1 2 3 ▪ IV administration was not a barrier to usage 4 Prof. Rachel Layman, MD MD Anderson Cancer Center ▪ Highest incremental improvements in median PFS over ET ever reported in 2L HR+/HER2- ABC ▪ HR for triplet of 0.24 and 0.33 for doublet are the most favorable reported for any study in HR+/HER2- ABC ▪ Patients tolerated both gedatolisib regimens well with very low discontinuation rates ▪ Safety profile for triplet and doublet was more favorable than reported in Phase 1b ABC study
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Commercialization Planning 23 Eldon Mayer Chief Commercial Officer
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24 Favorable Potential Market Landscape in HR+/HER2- ABC 2nd Line Setting PFS benefit is limited with current 2L standards of care Clearly differentiated efficacy relative to currently available therapies Streamlined reimbursement for infused oncology drugs Can build rapid awareness and adoption UNMET NEED WELL DIFFERENTIATED POSITIVE MARKET DYNAMICS LARGE POPULATION 34,000 patients1 with HR+/HER2- ABC receive 2L Rx post- CDK4/6i 60% are PIK3CA WT $5 billion served market revenue potential1 (1) Internal estimates using data from American Cancer Society, Breast Cancer Statistics 2022; American Cancer Society Facts and Figures 2019-2020; Dowsett, M JCO 2009; Salvo, E. M. et al.The Breast 2021; Abbreviations: HR, hormone receptor; ABC, advanced breast cancer, cancer; WT, wild-type, 2L, second line, PFS, progression free survival
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25 Experienced Teams at Celcuity Actively Preparing for Potential Launch Market Preparation Priorities Engage health systems, payers, pathway decision makers, GPOs, and patient advocacy Build awareness about importance of multi-target PAM inhibition Build-out distribution, reimbursement, and patient support systems Gain feedback and insights from Key Opinion Leaders 1 2 3 4
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26 Experienced Teams at Celcuity Actively Preparing for Potential Launch Planning & Infrastructure Development 1 2 3 4 Continuing to build launch team Conducting market research and engaging KOLs Create supply chain, IT systems, data/analytics, field support Strategic and tactical plans developed
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Upcoming Milestones 27 Brian Sullivan Chief Executive Officer and Co-Founder
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Present full data at a major medical conference later this year 28 Upcoming Milestones Submit New Drug Application for VICTORIA-1 PIK3CA wild-type cohort indication in Q4 2025 Report topline data for VIKTORIA-1 PIK3CA mutation cohort by end of 2025
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29 Q & A