Form 8-K

8-K — Inhibikase Therapeutics, Inc.

Accession: 0001193125-26-385293

Filed: 2026-09-08

Period: 2026-09-08

CIK: 0001750149

SIC: 2836 (BIOLOGICAL PRODUCTS (NO DIAGNOSTIC SUBSTANCES))

Item: Regulation FD Disclosure

Item: Financial Statements and Exhibits

Documents

8-K — d152999d8k.htm (Primary)

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8-K

8-K (Primary)

Filename: d152999d8k.htm · Sequence: 1

8-K

false 0001750149 0001750149 2026-09-08 2026-09-08

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

FORM 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d)

of the Securities Exchange Act of 1934

Date of Report (Date of earliest event reported): September 8, 2026

INHIBIKASE THERAPEUTICS, INC.

(Exact Name of Registrant as Specified in its Charter)

Delaware

001-39676

26-3407249

(State or Other Jurisdiction

of Incorporation)

(Commission

File Number)

(IRS Employer

Identification No.)

1000 N. West Street, Suite 1200

Wilmington, DE

19801

(Address of Principal Executive Offices)

(Zip Code)

Registrant’s Telephone Number, Including Area Code: (302) 295-3800

N/A

(Former Name or Former Address, if Changed Since Last Report)

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):

☐

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)

☐

Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)

☐

Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))

☐

Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

Trading

Symbol(s)

Name of each exchange

on which registered

Common Stock, $0.001 par value

IKT

The Nasdaq Stock Market LLC

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

Emerging growth company ☐

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐

Item 7.01.

Regulation FD Disclosure

On September 8, 2026, Inhibikase Therapeutics, Inc. updated its corporate presentation for use in meetings with investors, analysts, and others. A copy of the updated corporate presentation is furnished as Exhibit 99.1 to this Current Report on Form 8-K.

The information in Item 7.01 of this Current Report on Form 8-K (including Exhibit 99.1 attached hereto) is intended to be furnished and shall not be deemed “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific reference in such filing.

Item 9.01.

Financial Statements and Exhibits.

(d)

Exhibits.

99.1

Corporate Presentation issued by Inhibikase Therapeutics, Inc., dated September 2026, furnished herewith.

104

Cover Page Interactive Data File (embedded within the Inline XBRL document).

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Date: September 8, 2026

INHIBIKASE THERAPEUTICS, INC.

By:

/s/ Mark Iwicki

Mark Iwicki

Chief Executive Officer

EX-99.1

Filename: d152999dex991.htm · Sequence: 2

EX-99.1

Corporate Overview Exhibit

99.1

Disclaimer This presentation contains

information that may constitute “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, as amended. Inhibikase Therapeutics, Inc. (the “Company” or “we”) intends

for the forward-looking statements to be covered by the safe harbor provisions for forward-looking statements in those sections. Generally, we have identified such forward-looking statements by using the words “believe,”

“expect,” “intend,” “estimate,” “anticipate,” “project,” “target,” “forecast,” “aim,” "should," “will,” "may”, “continue”,

“assume”, “contemplate”, “could”, “design”, “due”, “goal”, “hope”, “might”, “plan”, “opportunity”, “predict”,

“possible”, “potential”, “seek”, “strategy”, “would” and similar expressions that are predictions or indicate future events and future trends, or the negative of these terms or other

comparable terminology. Such statements are subject to a number of assumptions, risks and uncertainties which may cause actual results, performance or achievements to be materially different from those anticipated in these forward-looking

statements. You should read statements that contain these words carefully because they discuss future expectations and plans which contain projections of future clinical studies or trials, regulatory approvals, product candidate development, results

of operations or financial condition, anticipated cash runway or capital requirements, or market opportunity or state other forward-looking information. However, the absence of these words or similar expressions does not mean that a statement is not

forward-looking. Forward-looking statements are not historical facts, but instead represent only the Company’s beliefs regarding future events, many of which, by their nature, are inherently uncertain and outside of the Company’s

control. It is possible that the Company’s actual results and financial condition may differ, possibly materially, from the anticipated results and financial condition indicated in these forward-looking statements. Management believes that

these forward-looking statements are reasonable as of the time made. However, caution should be taken not to place undue reliance on any such forward-looking statements because such statements speak only as of the date when made. The Company

undertakes no obligation to publicly update or revise any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law. In addition, forward-looking statements are subject to certain risks

and uncertainties that could cause actual results to differ materially from the Company's historical experience and our present expectations or projections. This presentation should be read in conjunction with the Company’s filings with the

Securities and Exchange Commission, including its annual report on Form 10-K, its quarterly Form 10-Q and any subsequent filings with the SEC (collectively, the “SEC Filings”). Important factors that could cause actual results to

differ materially from those in the forward-looking statements include, but are not limited to, our ability to execute clinical trials, including to evaluate IKT-001 as a treatment for pulmonary arterial hypertension, as well as such other factors

that are set forth in the Company’s SEC filings, including under the caption "Risk Factors”. Certain information contained in this presentation relates to or is based on studies, publications, surveys and other data obtained from

third-party sources and our own internal estimates and research. While we believe these third-party studies, publications, surveys and other data to be reliable as of the date of this presentation, we have not independently verified, and make no

representation as to the adequacy, fairness, accuracy or completeness of any information obtained from third-party sources. In addition, no independent source has evaluated the reasonableness or accuracy of our internal estimates or research and no

reliance should be made on any information or statements made in this presentation related to or based on such internal estimates and research. We do not intend our use or display of other entities’ names, trade names, trademarks or service

marks to imply a relationship with, or endorsement or sponsorship of us by, any other entity.

Inhibikase & IKT-001: Pulmonary

Arterial Hypertension (PAH) ~30% 5-year mortality1 HIGH UNMET NEED PAH is rare, progressive and life-threatening, with poor quality of life and high economic burden $8.3 billion2 market with antiproliferatives expected to drive rapid growth 45

meters placebo-adjusted 6MWD gain3 STRONG EFFICACY Imatinib is an antiproliferative TKI with potential best-in-class improvements in PVR and 6MWD (45 meters3) based on Phase 3 IMPRES and Phase 2 studies Imatinib is approved for Oncology indications

but likely not approved for PAH because of a combination of adverse events and high discontinuation rate, but hit primary endpoint 1st oral once-daily anti-proliferative INFORMED DESIGN IKT-001 is a novel prodrug of imatinib designed to retain

imatinib’s efficacy potential but with improved GI tolerability Titration-based Phase 3 IMPROVE-PAH study plus 2 decades of imatinib experience incorporated into study protocol Target: Improved study design with more patients

“managed” to the highest tolerable dose increases probability of success Late Stage Phase 3 program currently enrolling POSITIONED TO EXECUTE Single pivotal Phase 3 enrolling now across 26 countries and 46 sites (and growing) Orphan drug

designation, IP runway to 2044 & 505(b)(2) path Executive team with deep PAH / CV experience Cash runway to Phase 3 topline data readout4 PVR = pulmonary vascular resistance; 6MWD = 6-minute walk distance; GI = gastrointestinal | TKI = tyrosine

kinase inhibitor Hoeper M, et al. Eur Respir J. 2017 (2) 2025 annual reports from Janssen, United Therapeutics, Liquidia, Bayer, and Merck (3 Placebo-adjusted 6MWD Improvement of 45m at Week 24 in patients at 400 mg for >50% of Treatment (4)

Assuming the full and timely exercise of the outstanding Series A and B Warrants

Experienced Leadership with Deep

Expertise in PAH CHRIS CABELL, MD MHS FACC Head of R&D, Chief Medical Officer MARK IWICKI Chief Executive Officer JOHN ADAMS, PHD Chief Scientific Officer DAVID McINTYRE BEC CPA LLB MBA Chief Financial Officer JEFF KAGY Chief Human Resource

Officer TIM PIGOT Chief Commercial Officer

PAH is Progressive Disease Driven by

Uncontrolled Cell Proliferation Proliferation of vascular cells drive vascular remodeling, raising pulmonary artery pressure and leading to progressive right ventricular heart failure and ultimately death PASMCs = Pulmonary artery smooth muscle

cells; Vascular smooth muscle cells

PAH: Orphan Disease with ~30% 5-Year

Mortality Despite Aggressive Treatment ~50,000 People with PAH in the US(1) ~26,000 People with PAH in the EU5(1) ~80% Female(2) 52 years Average age at diagnosis(2) Progressive and Life Threatening ~30% 5-year mortality(3) despite high diagnosis

rate and specialist directed treatment with vasodilator therapies Progressively worsening symptoms Reduced Quality of Life Chronic breathlessness, and fatigue Significant limitation on activities of daily living Dizziness, chest pain, anxiety and

depression High Economic Burden Average monthly U.S. healthcare costs ~$6,850-$15,650(4) Acute all cause hospitalization rate of 700 per 1000 patients per year among Medicare or Medicaid patients(4) Substantial indirect costs due to work loss,

caregiver time and disability(4) 15 Approved vasodilators (across the prostacyclin, nitric oxide, and endothelin pathways) 1 Approved antiproliferative High Unmet Medical Need 1 CVrG Market Strategies report Jun 2025; 2 Badlam et al; CHEST 2021; 3

Hoeper M, et al. Eur Respir J. 2017; 4 Watzger et al; Pharmacoeconomics 2025

Patient and Treatment Journey in PAH

Low Risk 3% Risk Of 1 Year Mortality WHO Functional Class 1&2 6MWD > 440 meters No or Slight limitation of physical activity. Ordinary physical activity causes dyspnea, fatigue, chest pain, or near syncope Intermediate Risk 4-19% Risk Of 1

Year Mortality WHO Functional Class 3 6MWD 165 - 440 meters Marked limitation in physical activity. Less than ordinary activity causes undue dyspnea, fatigue, chest pain or near syncope High Risk >20% Risk Of 1 Year Mortality WHO Functional Class

4 6MWD < 165 meters Inability to carry out any physical activity without symptoms. Signs of RHF. Discomfort increased by any physical activity. Dyspnea and fatigue present at rest Progressive Pulmonary Vasculopathy Driving Right Heart Failure And

Death WHO=World Health Organization; 6MWD= 6 Minute Walk Distance First Line Therapy Phosphodiesterase type 5 (PDE5) inhibitors plus endothelin receptor antagonist (ERA) combination Add-on Therapy Oral / inhaled prostacyclin or Antiproliferative

(sotatercept) Last Line Drug Therapy or Lung Transplant Infused Prostacyclin, Antiproliferative (Sotatercept) 1st Line of Therapy Add On Therapy With Declining Health Status

2025 $8.3 Billion* Antiproliferatives

Expected to Rapidly Grow the PAH Market * 2025 annual reports from Janssen, United Therapeutics, Liquidia, Bayer, and Merck; ** Assumes at least 32,000 annual regimens of an antiproliferative using a net price of $250k per regimen per year IKT-001

has the potential to be the First Once-Daily Oral Antiproliferative for PAH Nitric Oxide Pathway ($.42B) Sildenafil, Tadalafil, Riociguat Ambrisentan, Bosentan, Macitentan Epoprostenol, Treprostinil, Iloprost, Selexipag $2.5B Prostacyclin Pathway

($3.94B) Endothelin Pathway ($2.53B) Vasodilators $3.94B $0.42B $1.4B $2.53B Sotatercept - subcutaneos injection Activin Signaling ($1.44B) Antiproliferatives US sales of sotatercept expected to reach $2–$2.5 Billion in 2026 and continue

growing Antiproliferatives with unique Disease Modifying Properties & patient friendly administration expected to become a Cornerstone of PAH Therapy Antiproliferative Segment Could Reach $8 Billion by 2034**

IKT-001

IKT-001’s Path to

Best-in-Class in PAH 45m Placebo-adjusted Improvement in Phase 3 IMPRES Study** IKT-001 has demonstrated pre-clinical efficacy in PAH comparable to imatinib Class-Leading Efficacy* Clinical Benefits* Improved Safety Profile* *

Potential profile – IKT-001 is in phase 3 clinical development * * Hoeper et al., Circ. 2013 Placebo-adjusted 6MWD Improvement of 45m at Week 24 in patients at 400 mg for >50% of Treatment | GI = Gastro-intestinal ; 6MWD = 6-minute walk

distance Intact in GI: enzymatic cleavage in blood Prodrug linker IKT-001 45 Meters* Improved GI Side Effect Profile IKT-001 remains intact in the GI tract enabling 18X ↓ inhibition of c-Kit (implicated in GI side effects) No negative effect

on gastric emptying 1 2 3 Oral Once-daily Reduced Monitoring Antiproliferative imatinib Modernized Phase 3 Study Design 12-week dose titration to maximum tolerable dose, including potential for down titration Defined classification of edema events

between drug-related and clinical worsening Exclusion of anticoagulants Novel Prodrug IKT-001 On Track to be the First Oral Antiproliferative with a Strong Potential Profile

Imatinib Mechanism of Action

Targets the Underlying Cause of PAH Modified from Savage and Antman, 2005 and Barst, R J Clin Invest 2005 1Schermuly et al., JCI 2005 Overactive kinases implicated in aberrant cell proliferation and migration in the pulmonary vasculature Imatinib

inhibits the tyrosine kinase activity of PDGFRs and c-Kit, blocking cell signaling that drives vascular remodeling Antiproliferative and proapoptotic anti-remodeling mechanisms confirmed with imatinib in human pulmonary artery cells1 Pulmonary

vasculature with aberrant cell proliferation Normal pulmonary vasculature

Imatinib Demonstrated Reversal of

PAH in Standard Animal Model1 Day 0 MCT d42 MCT d42/+imatinib Reversal of increased right ventricular pressure Improved survival Reversal of pulmonary vascular remodeling STI571 = imatinib; MCT = monocrotaline *P < 0.05 versus

control; †P < 0.05 versus MCT at day 28 or hypoxia at day 21; ‡P < 0.05 versus MCT at day 42 or hypoxia at day 35. 1Schermuly et al., JCI 2005 Imatinib reverses pulmonary vascular remodeling, right

ventricular pressure/remodeling and improves survival imatinib imatinib

IKT-001 Retains Imatinib Efficacy

& PAH Reversal Profile in Pre-Clinical Model # p<0.0001 vs normoxia, * p<0.0005 v SuHx Veh d43, **p<0.007 v SuHx Veh d43 Su/Hypoxia/Veh d43 Su/Hypoxia/IKT 100mpk d43 Mean Pulmonary Artery Pressure (mPAP) Lung Histology Background:

Imatinib has previously been shown to reverse PAH in the Sugen-hypoxia Rat Model(1) (1) Schermuly et al., 2005. Data presented at American Thoracic Society Conference in Orlando, May 2026 Like imatinib, chronic treatment with IKT-001 reversed

thickening of pulmonary arteries IKT-001 dose dependently improved pulmonary hemodynamics including mPAP and demonstrated disease reversal Legend: Perivascular to interstitial infiltration of lymphocytes, macrophages, and rare neutrophils (black

arrows) is seen multifocally, in addition to increased alveolar macrophages (black arrowheads). Arterioles have a visibly thickened tunica media throughout; medial hypertrophy also seen in the captured pulmonary artery (PA) profile. A bronchiole

(Br) is indicated.

IKT-001 Dramatically Reduces GI

Imatinib Exposure to Drive Tolerability* IKT-001 is Stable in the Gut and has Rapid Bioconversion in the Blood imatinib enzymatic cleavage Blood Gut Pro-drug linker Gut Wall IKT-001 IKT-001 GI = gastrointestinal | *In preclinical studies – IKT

data on file Pre-absorption: IKT-001 Is Stable In Gut* GI tract protected from direct imatinib exposure ~20x less inhibition of tyrosine kinase activity vs imatinib 2.5x improvement in GI tolerability vs imatinib in non-human primates

Post-absorption: Rapid & Complete Conversion In Blood Half-life of <5 minutes in human plasma No IKT-001 detected in rat systemic plasma after 10 min

IKT-001 Has Reduced Gut Motility

Impairment vs Imatinib *p<0.01 vs Control, Data presented at American Thoracic Society Conference in Orlando, May 2026 1Data on file, 2Maeda 1992., Imatinib is a potent inhibitor of c-Kit c-Kit inhibition in gut pacemaker cells (ICC) causes

gut motility disorders2 IKT-001 remains intact in the stomach and intestine and is 18X less potent at c-Kit than imatinib1 IKT-001 has No Effect on Gastric Emptying IKT-001 Not Statistically Different to Placebo Imatinib & Morphine Delay Gastric

Emptying

Additive Efficacy Via Combination

of IKT-001 + Activin SignaIing Inhibitor Activin Signaling Inhibitor (RAP – sotatercept surrogate) Plus IKT-001 in PAH Sugen-Hypoxia Model Mean Pulmonary Artery Pressure *Pre-clinical data on file with IKT, * p<0.05 vs SuHx, *** p<0.0001

v SuHx IKT . ASI = Activin Signaling Inhibitor Statistically significant additive improvements in PAH hemodynamics achieved with combination treatment (IKT-001 + ASI) Combination treatment (IKT-001 + ASI) was well tolerated

Clinical Rationale

SAD Study in Healthy Volunteers

Establishes Bioequivalence IKT Data on File; SAD: Single ascending dose study IKT-001 Dose Bioequivalent Imatinib Dose 300 mg QD 230 mg QD 400 mg QD 306 mg QD 500 mg QD 383 mg QD

IMPRES – Imatinib Phase 3

Study Randomized controlled trial to assess the efficacy and safety of imatinib once daily (n=202) Primary Endpoint Change in 6MWD at 24 weeks Secondary Endpoints Changes in hemodynamics (PVR, CO, mPAP, RAP) at 24 weeks Time to clinical worsening

Weeks 0 4 8 12 16 20 24 Imatinib (n=103) Placebo (n=99) Short 2 Week Titration 200mg 400mg with ability to down titrate to 200mg if unable to tolerate 400mg Key Inclusion Criteria Functional Class II-IV 2 or more background PAH therapies PVR ≧

800 dynes.s.cm-5 6MWD ≥150 meters and ≤ 450 meters PVR = pulmonary vascular resistance; CO = cardiac output; mPAP = mean pulmonary atrial pressure; RAP = right atrial pressure; 6MWD = 6-minute walk distance IKT’s Phase 3

IMPROVE-PAH study uses a 12-week titration phase

IMPRES: Statistically Significant

Improvements in Function & Hemodynamics Placebo-adjusted 32-meter improvement in 6MWD and 32% reduction in PVR at week 24 Majority of Subjects on 200 mg of Imatinib at End of Study IMPRES hit its primary endpoint along with key secondary

endpoints PVR = Pulmonary Vascular Resistance; 6MWD= 6 Minute Walk Distance test Hoeper et al; Circulation 2013 Change in 6-Minute Walk Distance Change in Pulmonary Vascular Resistance Change in Cardiac Output

Imatinib Showed Comparable Efficacy

to Sotatercept Majority of Sotatercept Subjects at Highest Dose While Majority of Imatinib Subjects at Lowest Dose Note: Head-to-head trials were not conducted with Sotatercept and Imatinib and these trials had different trial designs, patient

enrollment criteria and treatment regimens. In addition, the applicable measurements for the referenced trials were observed over different time periods and using different assays. As a result, the safety data from these trials may not be directly

comparable 10 Endpoint: Mean Treatment Difference = 32m Majority of patients at lowest dose of 200 mg 10 Endpoint: Median Treatment Difference = 33.4m Majority of patients at highest dose of 0.7 mg/kg Sotatercept Phase 3 STELLAR1 Imatinib Phase 3

IMPRES2 1Hoeper et al; NEJM 2023; 2Hoeper et al; Circulation 2013 6MWD

IMPRES: Patients Able To Sustain

400mg Dose Showed Greater Improvements Placebo-adjusted 6MWD Improvement of 45m in Patients at 400mg for >50% of Treatment Hoeper et al; Circulation 2013 Suppl. Appendix *Baseline data is not available for the sub-population of patients on 400mg

of imatinib for > 50% of treatment so baseline data above reflects entire study population. PVR= Pulmonary vascular resistance; 6MWD = 6-minute walk distance Changes in PVR at Week 24 N=44 N=23 N=78 (Baseline*: 1202 dynes/sec/cm-5 imatinib; 1181

dynes/sec/cm-5 placebo) Changes in 6MWD at Week 24 Meters 45 meter placebo adjusted improvement in 6MWD (Baseline*: 355 meters imatinib; 366 meters placebo) N=40 N=24 N=79

1Hoeper et al; Circulation 2013 AE

= Adverse event; GI = Gastrointestinal Imatinib n=103 (%) Placebo n=98 (%) Adverse Events 100 (97) 94 (96) Nausea 57 (55) 23 (24) Peripheral edema 45 (44) 20 (20) Diarrhea 36 (35) 19 (19) Vomiting 31 (30) 10 (10) Periorbital edema 30

(29) 7 (7) IKT-001 and IMPROVE-PAH Study Design Combine to Mitigate IMPRES AE Challenges IKT-001 is designed to have an improved AE profile to enable patients to tolerate higher doses IMPROVE-PAH gradual up-dosing titration and modernized study

design to reduce significant AEs and discontinuations Defined classification of edema events between drug-related and clinical worsening IKT-001 reduced c-Kit inhibition in the GI tract expected to reduce AEs Improved Protocol & Patient

Management Targeting An Improved AE Profile To Help Patients Maintain Higher Doses Imatinib Phase 3 IMPRES1 Trial

Recent Study* of Imatinib Supports

Findings from IMPRES Doses between 200mg – 400mg delivered meaningful efficacy response Dose Dependent Improvement in Primary Endpoint PAH patients (13/17) with implanted devices to assess continuous cardiac function Comparable patient

characteristics and baseline PVR scores to modern PAH trials Average lower dose than IMPRES nevertheless delivered significant reduction in TPR and improvement in 6MWD Dose adjustments to address tolerability allowed most patients to remain in the

study Percentage change in total pulmonary resistance from baseline at 60 days in relation to plasma level (area under curve in μg*h/L) of imatinib at steady state (red-100mg QD, orange-200mg QD, cyan-300mg QD, blue-400mg QD) 2025 Publication

Using Imatinib in PAH Higher exposure associated with larger treatment effect *Rothman et al., AJRCCM 2025.

Rapid & Sustained Hemodynamic

Effect With Evidence of Disease Modification Imatinib Delivered a 24% Reduction in Total Pulmonary Resistance (TPR) Early & Continued Improvement 24% Reduction in TPR Early Improvement in TPR Slow return to BL 2 Slow return to baseline suggests

disease modification 3 1 *Rothman et al., AJRCCM 2025.

IKT’s Clinical

Program

IMPROVE-PAH Phase 3 Study of

IKT-001 *Patients completing Wk 48 may transition to Open Label Extension (OLE). Additionally, patients who have not completed follow-up at the time of study unblinding or who otherwise experience a clinically worsening event during the extended

double blind treatment period may transition to OLE Key Inclusion / Stratification: WHO Group 1 PAH Baseline Right Heart Catheter performed during screening period: PVR of ≥400 dynes/sec/cm-5 ; PCWP ≤15 mmHg; mPAP >20 mmHg PVR

enrichment criteria to ensure population baseline PVR >700 dynes/sec/cm-5 6MWD ≥100 and ≤475 meters Previous sotatercept allowed if d/c 6 months prior to screening and no serious bleeding event history Stratification by PAH

etiology and ERS/ESC Risk Score Primary Endpoints: PVR (Part A) & 6MWD (Part B) Key Secondary Endpoints: Time to Clinical Worsening WHO Functional Class Wk12 Wk12 BL Wk4 Wk8 Wk24 300 400 n=70 n=70 Placebo QD 1:1 Double Blind Treatment (n=140)

Extended Double Blind* Treatment Continues for up to an Additional 24 Weeks Interim Analysis PE: PVR (n=140) Double Blind Treatment (n=346) Extended Double Blind* Treatment Continues for up to an Additional 24 Weeks BL Wk4 Wk8 Wk24 Max Tolerated

Dose QD 300 400 n=173 n=173 Placebo QD 1:1 Wk24 Interim Safety (n=50) Phase 3 – Part B Phase 3 – Part A Enrollment Continues Uninterrupted 500 Max Tolerated Dose QD 500 Up to ~180 Sites Primary Endpoint 6MWD (n=346) Phase 3 Enrollment

Ongoing

Power of Titration & Improved

Study Design in IMPROVE-PAH Gradual titration to max. tolerated dose to retain IMPRES efficacy 1 Improved administration to ↓ discontinuations P3: IMPRES Rapid 2-week escalation Immediate down titration to lowest dose if not tolerating 200 400

Week 0 Week 2 P3: IMPROVE-PAH 12-week gradual titration to max tolerated dose with stepdown allowed 300 Baseline 400 Week 4 500 Week 8 ✓ Gradual Titration Slower pace to Cmax steady-state allows patient to adapt to IKT-001 and may decrease

adverse events ✓ Nighttime Administration Taking IKT-001 at night may reduce the daytime burden of transient nausea or fatigue ✓ Flexible Dose Management Stepwise down-titration may keep participants on treatment at MTD and reduce

discontinuations DESIGN OBJECTIVES Improved earlytolerability → Fewerdiscontinuations → More patients reach / maintain effective exposure → Greater opportunity to realize maximal efficacy P3: Phase 3. MTD = Maximum Tolerated Dose.

Sources: Hoeper et al. Circulation. 2013;127:1128–1138; Gleevec (imatinib) U.S. Prescribing Information. * See slide 18 for precise bioequivalence 500 or MTD Week 12 2 Equivalent dose* Equivalent dose*

Why IMPROVE-PAH Phase 3 Has Higher

Probability of Success Gradual 12-week Titration to max dose (vs 2 Weeks in IMPRES) ↑ efficacy ↓ discontinuations 45m 6MWD for patients on high dose in IMPRES - ↑ efficacy IKT-001 remains stable in the gut with 18x ↓ in c-Kit

inhibition - ↑ GI tolerability Defined guidance for edema events - ↓ discontinuations Exclusion of anticoagulants - ↓ events Independent adjudication of worsening events - ↓ event misclassifications Evening dosing with water

and meal - ↓ transient nausea or fatigue Benefit of 20+ Years of Imatinib Clinical Experience 1Hoeper et al. Circulation. 2013;127:1128-1138 “Study-drug discontinuations were comparatively high in the [IMPRES] study”1

“… causes may include … a lack of experience with the use of imatinib among PAH specialists”1 “… worsening events in the imatinib group… transient…associated with known imatinib side effects rather

than events reflecting disease progression”1 Modern Phase 3 Design + IKT-001’s Better Tolerability = Maximum Efficacy & Improved Trial Outcome

IKT’s Development and

Projected Timelines ✓ Q4 2025 – Q1 2026 First Phase 3 site activated in Phase 3 IMPROVE-PAH Study ✓ Q1 2026 First patient enrolled in Part A (n=140); primary endpoint is PVR reduction ✓ Mid 2026 Received Orphan Drug

Designation 1H 2027 Interim safety readout for Part A of Phase 3 IMPROVE-PAH Study (n=50) 2H 2027 Last patient Part A / first patient Part B of Phase 3 IMPROVE-PAH Study; enrollment continuous Mid 2028 Unblinded Data (PVR reduction) readout for Part

A of Phase 3 IMPROVE-PAH Study (n=120) End 2028 Part B enrollment complete of Phase 3 IMPROVE-PAH Study (n=346) Mid 2029 Topline 6MWD readout from Part B of Phase 3 IMPROVE-PAH Study (n=300) IKT-001 Phase 3 Enrollment Ongoing 26 countries approved,

including USA & EU 46 of 180 planned sites active

Potential for the 1st Once-Daily

Oral Antiproliferative Very High Unmet Need Market with 30%, 5 Year Mortality $8.3B market expected to rapidly grow to $14B by 2034(1) IKT-001 designed to maintain potential class leading 45 meter improvement in 6MWD Pro-drug expected to

significantly improve GI tolerability Antiproliferatives are the first disease modifying agents and expected to reshape the PAH treatment algorithm IKT-001 expected to be the first once-daily oral antiproliferative Orphan Drug Designation &

505(b)(2) regulatory pathway Long intellectual property (NCE) potential through 2044 Cash runway through Phase 3 Part B Topline Data readout* 6MWD= 6 Minute Walk Distance test, NCE= new chemical entity

1https://www.precedenceresearch.com/pulmonary-arterial-hypertension-market, * Assuming the full and timely exercise of the outstanding Series A and Series B Warrants Global Pivotal Phase 3 Program with Multiple Clinical Readouts First Half 2027

– Interim Safety Readout Mid 2028 – Part A - PVR Efficacy Data Mid 2029 – Part B – 6MWD Efficacy

Thank You

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