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6-K

Argenx SE (ARGX)

6-K 2022-01-10 For: 2022-01-10
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Added on April 10, 2026

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 6-K


REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO RULE 13a-16 OR 15d-16

UNDER THE SECURITIES EXCHANGE ACT OF 1934

For the Month of January 2022

Commission File Number: 001-38097

ARGENX SE

(Translation of registrant’s name into English)

Willemstraat5****4811 AH, Breda, the Netherlands

(Address of principal executive offices)

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

Form 20-F  x     Form 40-F  o

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1): o

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7): o

argenx SE

On January 10, 2022, argenx SE (the “Company”) posted a corporate presentation to its website. The Company intends to use the presentation at the 40^th^ Annual J.P. Morgan Healthcare Conference being held from January 10 to 13, 2022. A copy of the presentation is filed herewith as Exhibit 99.1 and is incorporated by reference herein.

The information contained in this Current Report on Form 6-K,including Exhibit 99.1, is incorporated by reference into the Company’s Registration Statements on Forms F-3 (File No. 333-258251)and S-8 (File Nos. 333-225375 and 333-258253).

Exhibit Description
99.1 Corporate Presentation
2

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, thereunto duly authorized.

ARGENX SE
Date: January 10, 2022 By: /s/ Pieter Spuijbroek
Pieter Spuijbroek
Corporate Secretary
3

Exhibit 99.1

Together<br>We Discover<br>J.P. Morgan Healthcare Conference<br>January 10, 2022<br>Reaching Patients Through<br>Immunology Innovation
Forward Looking Statements<br>This presentation has been prepared by argenx se (“argenx” or the “company”) for informational purposes only and not for any other purpose. Nothing<br>contained in this presentation is, or should be construed as, a recommendation, promise or representation by the presenter or the company or any director,<br>employee, agent, or adviser of the company. This presentation does not purport to be all-inclusive or to contain all of the information you may desire. This<br>presentation also contains estimates and other statistical data made by independent parties and by us relating to market size and growth and other data<br>about our industry. This data involves a number of assumptions and limitations, and you are cautioned not to give undue weight to such estimates.<br>Safe Harbor: Certain statements contained in this presentation, other than present and historical facts and conditions independently verifiable at the<br>date hereof, may constitute forward-looking statements. Examples of such forward-looking statements include those regarding expectations with respect<br>to potential commercial franchise launches; its plans for global commercialization launch of VYVGART across three continents; expectation of Japan’s<br>MAA approval of VYVGART during the first quarter of 2022 and expected approval by European Medicines Agency of MAA in the second half of 2022;<br>plans for Medison to file for approval in Israel in second quarter of 2022, and Zai Lab to file for approval in greater China by mid-2022; focus on<br>expansion and acceleration of clinical development of its efgartigimod portfolio; the timing and its expectations with respect to reporting data from<br>registrational trials and initiate trials in new indications; its statements related to its goal to develop a global multifranchise autoimmune portfolio and<br>leading immunology company; the intended results of its strategy including global launch preparation; development of the efgartigimod portfolio for<br>additional indications; and its clinical development and regulatory plans, including the timing, design and outcome of ongoing and planned clinical trials<br>and preclinical activities and the timing and outcome of regulatory filings and approvals. A further list and description of these risks, uncertainties and<br>other risks can be found in argenx’s U.S. Securities and Exchange Commission (SEC) filings and reports, including in argenx’s most recent annual report on<br>Form 20-F filed with the SEC as well as subsequent filings and reports filed by argenx with the SEC. Given these uncertainties, the reader is advised not to<br>place any undue reliance on such forward-looking statements. These forward-looking statements speak only as of the date of publication of this<br>document. argenx undertakes no obligation to publicly update or revise the information in this press release, including any forward-looking statements,<br>except as may be required by law.<br>!<br>2
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3<br>VYVGART is indicated for the treatment of generalized myasthenia<br>gravis (gMG) in adult patients who are anti-acetylcholine receptor<br>(AchR) antibody positive<br>Please see Important Safety Information and the full Prescribing Information for VYVGART at https://vyvgart.com
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Challenging the gMG Treatment Paradigm<br>4<br>Best-in-Class<br>Patient<br>Support<br>Rapid HCP<br>Adoption of<br>VYVGART<br>Enable<br>Appropriate<br>Access<br>Meeting our stakeholders where they are<br>Empower Patients<br>to Demand Better
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Infrastructure to Bring VYVGART to<br>Physicians and Patients<br>5<br>Infusion Sites<br>of Care<br>Home Infusion<br>Nurses<br>Access in all 50<br>States<br>VYVGART Field Teams<br> • 71 Territory Business<br>Managers<br> • 10 Thought Leader Liaisons<br> • 16 Medical Research<br>Liaisons<br> • 10 Nurse Case Managers<br> • 13 Market Access<br>Professionals<br> • 10 Field Reimbursement Managers<br>National Specialty<br>Pharmacies<br>7.7K* Neurologists treat 97% of gMG patients *<br>*Information from argenx market research
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Global gMG Launch Underway<br>6<br>VYVGART Approved<br>December 17, 2021<br>United States Global Japan<br>Anticipated decision in 1Q 2022<br>Europe<br>Anticipated decision in 2H 2022<br>China (Zai Lab)<br>Anticipated filing by mid-2022<br>Israel (Medison)<br>Anticipated filing in 2Q 2022
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7<br>Our Mission is<br>Innovation<br>Where critical patient need meets breakthrough science<br>That is where we redefine immunology
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Molecule Design:<br>Immunology Innovation<br>Program<br>My Real<br>World™ MG<br>DISCOVERY<br>We Innovate At Every Step<br>Clinical Development:<br>Individualized Dosing<br>Strategic Indication Selection<br>Adapt<br>DEVELOPMENT<br>Commercial Approach:<br>Aligning Stakeholder<br>Interests<br>REACHING PATIENTS<br>Molecule<br>Image
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ANTIBODY ENGINEERING<br>CLINICAL DEVELOPMENT<br>FIRST IN CLASS UNIQUE DESIGN MULTIPLE INDICATIONS<br>Efgartigimod ARGX-119 ARGX-117<br>Internal Value Creation Strategy<br>LEADING<br>TRANSLATIONAL<br>BIOLOGY LABS<br>External Value Creation Strategy<br>Cusatuzumab LEO<br>(ARGX-112)<br>Genor<br>(ARGX-109)<br>AbbVie<br>(ARGX-115)<br>ARGX-118 AgoMAb<br>(ARGX-114)<br>Staten<br>(ARGX-116) Dualyx<br>Pipeline Growth Driven By Immunology Innovation<br>Program
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Efgartigimod Blocks FcRn Leading to<br>IgG Elimination<br>IgG Antibody FcRn Efgartigimod<br>Fc fragment uniquely modulates FcRn<br>No observed impact on IgM, IgA or human<br>serum albumin<br>No observed effect on IgG production<br>(i.e. vaccine response)
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NEURO HEME SKIN KIDNEY Key:<br>gMG ITP Pemphigus CIDP<br>11<br>gMG is Just the Beginning<br>BP Myositis<br>Four New Launches Anticipated By End of 2024<br>Q1 2022 (SC) Q2 2022 (IV)<br>Q1 2023 (SC)<br>Q4 2022 Q1 2023<br>New POC indications Registrational trials ongoing<br>Membranous<br>Nephropathy<br>Lupus<br>Nephritis<br>COVID-19-<br>mediated<br>POTS<br>Sjogren’s<br>Syndrome<br>70k US pts 45k US pts 500k US pts 300k US pts
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IgG<br>IgG IgG<br>IgG Myositis<br>Autoimmune<br>Encephalitis<br>Bullous<br>Pemphigoid<br>Thyroid<br>Eye Disease<br>Membranous<br>Nephropathy<br>ITP<br>Sjogren’s<br>Syndrome<br>GBS AMR Pemphigus POTS CIDP<br>Myasthenia<br>Gravis<br>Lupus<br>Nephritis<br>RA<br>MOGAD<br>NMO<br>HDFN SLE wAIHA<br>APS<br>Anca<br>Vasculitis<br>Precision Tool<br>Designed to<br>Revolutionize<br>Autoimmunity<br>Indications where biology is believed to be IgG-mediated
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C5<br>C5-C9<br>(MAC)<br>C1<br>qrs<br>C4<br>C2<br>C3a C3b<br>C5a<br>C3 convertase<br>C5 convertase<br>C3<br>Mannose sugar<br>MBL MAS<br>Ps<br>IgG IgM<br>ARGX-117 Blocks C2<br>Targeting C2:<br> • Leaves alternative pathway intact against infection<br> • Blocks all complement effector functions<br>Classical Lectin<br>ARGX-117: Sweeping Antibody<br>Designed to Target Unique<br>Intervention in Complement<br>Multifocal Motor Neuropathy;<br>Phase 2 trial started<br>Delayed Graft Function in Kidney<br>Transplant
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ARGX-119: MuSK<br>Agonist with Broad<br>Potential<br>in Neuromuscular<br>Disease<br>ARGX-119 ( ) induces AChR clustering, NMJ maturation and stabilization<br>Oury, J., Zhang, W., Leloup, N. et al. Mechanism of disease and therapeutic<br>rescue of Dok7 congenital myasthenia. Nature 595, 404–408 (2021).<br>https://doi.org/10.1038/s41586-021-03672-3
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Neuro<br>Heme<br>Skin<br>Kidney<br>Global Multifranchise<br>Autoimmune Portfolio<br>ROW<br>China<br>Europe<br>Japan<br>US<br>INDICATIONS<br>THERAPEUTIC<br>FRANCHISES<br>GLOBAL<br>MARKETS<br>Israel<br>Canada<br>MOLECULES<br>Efgartigimod<br>ARGX-117<br>ARGX-119<br>gMG<br>ITP<br>PV<br>CIDP<br>IIM<br>BP<br>LN<br>MN<br>Sjogren’s<br>Long COVID-19 POTS<br>MMN<br>DGF<br>Congenital MG<br>ALS<br>MuSK MG<br>SMA<br>gMG: generalized myasthenia gravis; ITP: immune thrombocytopenia; PV: pemphigus vulgaris; CIDP: chronic inflammatory demyelinating polyneuropathy; MN: membranous nephropathy; IIM: idiopathic inflammatory neuropathies; LN: lupus nephritis;<br>BP: bullous pemphigoid; DGF: delayed graft function; MMN: multifocal motor neuropathy; POTS; postural orthostatic tachycardia syndrome; MusK: muscle specific kinase; SMA: spinal muscular atrophy; ALS: amyotrophic lateral sclerosis;
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Efgartigimod in 15 indications (commercial and development)<br>Global autoimmune market has surpassed $150B<br>Vibrant neuromuscular, hematology, skin and kidney franchises<br>New asset each year from IIP<br>Reaching patients globally<br>ARGX-117 in multiple late-stage trials<br>Our Plan to Build a Leading Immunology Company<br>Committed to<br>our Patients and<br>their<br>Communities<br>Proof-of-concept demonstrated with ARGX-119<br>We believe the future belongs to those who collaborate best<br>Enviable<br>Immunology<br>Pipeline<br>Rooted in<br>Science through<br>our IIP<br>ar<br>genx<br>2025
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17<br>Like the Argonauts,<br>we’re on a bold mission:<br>Engineer potentially<br>life-changing immunology<br>therapies for patients.<br>argenx<br>One Plan<br>One Team<br>Determined to Achieve the<br>Unthinkable
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CONFIDENTIAL. FOR INTERNAL USE ONLY.<br>Appendix
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Immune Thrombocytopenia ADVANCE Trials:<br>Two Run in Parallel<br>24 weeks 1000mg SC efgartigimod<br>Durable response:<br>sustained platelet<br>count (≥50×109/L)<br>in 4/6 visits<br>between weeks 19<br>and 24<br>Phase 3, multicenter, randomized, double-blind, placebo-controlled trial<br>24 weeks 10mg/kg IV efgartigimod Primary<br>objective<br>Patients with<br>primary ITP<br>with platelet<br>counts<br> ≤30x109/L<br>N=156<br>Fixed weekly<br>or q2w dosing<br>Determined<br>at week 16<br>Weekly or q2w dosing adjusted<br>according to platelet count<br>thresholds<br>Weeks 5-16<br>Fixed weekly<br>dosing<br>Weeks 1-4<br>N=156<br>Topline IV data expected 2Q 2022; topline SC data expected 1Q 2023
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Topline data expected 1Q 2023<br> • Worsening of disease within<br>12 weeks after drug<br>withdrawal (INCAT, I-RODS,<br>grip strength)<br> • Newly diagnosed/ treatment<br>naïve skip run-in period<br> • Confirmation<br>of diagnosis by<br>independent<br>committee<br>Chronic Inflammatory Demyelinating<br>Polyneuropathy ADHERE Trial<br>Treatment period<br>Open-label Placebo-controlled Identify patients with active CIDP<br>Confirm IgG autoantibody<br>involvement<br>Assess efficacy & safety<br>efgartigimod vs placebo<br>Run-in period Stage A Stage B<br>(Stage A responders only) Screening<br>Efficacy analysis<br>based on relapse<br>(adjusted INCAT)<br>Study endpoint<br>with 88 relapse<br>events in stage B<br>N=sample size<br>estimation<br>~120-130<br>Followed by<br>Open Label<br>Extension study ≤13weeks<br> ≤4weeks<br>Efgartigimod weekly SC<br>Placebo weekly SC<br>Efgartigimod weekly SC<br>Up to 12 weeks, until<br>clinical improvement<br>(ECI)<br>Up to 48 weeks
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Topline data expected 4Q 2022<br>Pemphigus ADDRESS Trial:<br>Focus on Fast Onset and Steroid-sparing<br>1-3 weeks<br>Screening<br>Efgartigimod weekly SC<br>Placebo weekly SC<br>Pemphigus vulgaris<br>(PV) and foliaceus (PF)<br>Moderate-to-Severe<br>Disease (PDAI activity<br>score ≥ 15)<br>Newly Diagnosed<br>and Relapsing<br>Prednisone starting<br>dose 0.5 mg/kg/day<br>with ability to adjust<br>Active tapering to<br>start from sustained<br>CR or EoC<br>Concomitant<br>prednisone Randomization (2x1)<br>30 weeks<br>Primary endpoint is<br>proportion of PV<br>patients achieving<br>CRmin* within 30<br>weeks<br>N=sample size<br>estimation<br> ≤150 patients (PV<br>and PF) with PF<br>patients capped<br>Followed by<br>Open Label<br>Extension study<br>CR=complete clinical remission; CRmin=complete remission on minimal therapy; EoC=end of consolidation; SC=subcutaneous.
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Trial to initiate in 1Q 2022<br>Myositis: Adaptive Phase 2/3 Trial Design<br>1000mg efgartigimod SC (+ SOC)<br>Placebo SC (+ SOC)<br>Total Duration: 52 weeks<br>Independent<br>adjudication committee<br>Stratified for<br> • IMNM<br> • ASyS<br> • DM<br> • Severity of muscle<br>weakness (MMT)<br>Eligibility criteria<br> • Muscle weakness<br> • No malignancies<br>Interim Analysis of First 30 Patients of Each Subtype<br>Independent DSMB<br>Subtype selection Sample size re-estimation<br>IMNM<br>ASyS<br>DM<br>Primary<br>Mean Total Improvement Score (TIS)<br>Change (ACR/EULAR endorsed)<br>Key Secondary<br> • Response based on TIS, time to reach<br>TIS, TIS duration<br> • Quality of Life<br> • Individual Core Set Measures TIS<br> • MMT-8 score<br> • Physician Global Assessment<br> • Patient Global Assessment<br> • HAQ-Disability Index score<br> • Extramuscular Global<br>Assessment<br> • Muscle enzyme serum level<br>1000mg efgartigimod SC (+ SOC)<br>Placebo SC (+ SOC)<br>1000mg efgartigimod SC (+ SOC)<br>Placebo SC (+ SOC)<br>180 patients Proposed Endpoints<br>Adults
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Bullous Pemphigoid Registrational Trial Underway<br>Total Duration: 36 weeks<br>Bullous Pemphigoid<br>Moderate-to-severe<br>disease (Investigator<br>Global Assessment<br>Score (IGA))<br>Newly diagnosed and<br>relapsing<br>Proposed primary endpoint<br> • Proportion of participants in complete<br>remission while on minimal OCS<br>(≤0.1mg/kg/day) for ≥8 weeks at week<br>26<br>Secondary endpoints<br> • Cumulative dose of OCS<br> • Proportion of participants who achieve<br>IGA BP score of 0 or 1 while off OCS for<br>for ≥8 weeks at week 36<br> • Proportion of participants who are in<br>CR while off OCS for ≥8 weeks at week<br>36<br> • Changes from baseline to week 36 in<br>24-hour average itch<br> • Proportion of participants with CDA<br>and remain free of relapse<br> • Quality of life<br>Followed by Open Label Extension study<br>160 patients Endpoints<br>Adults<br>Randomization (1:1)<br>Efgartigimod weekly SC<br>Placebo weekly SC<br>Concomitant Oral Corticosteroids (OCS)<br>OCS starting dose 0.5 mg/kg/day with ability to adjust<br>Active tapering to start from sustained control of disease activity (CDA)<br>Interim Analysis of First 40 Patients
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Multifocal Motor Neuropathy Phase 2 Trial Underway<br>Total Duration: 16 weeks Patient Population Key Outcome Measures<br>Adults<br>Trial to enroll<br>approximately 45 MMN<br>patients<br> • Probable or definite<br>MMN (per EFNS/PNS<br>2010)<br> •Independent<br>adjudication<br>committee<br> • Stable IVIg regimen<br> • IVIg treatment<br>dependent<br>Safety and tolerability<br>Time to IVIg re-treatment<br>Measures of peripheral muscle<br>strength: grip strength, mMRC sum<br>score, 9-HPT, MMN-RODS<br>Patient-reported outcomes<br>PK, PD, biomarkers<br>ARGX-117 Dose<br>Regimen 1 (N=15)<br>ARGX-117 Dose<br>Regimen 2 (N=15)<br>Placebo (N=15)<br>ARGX-117<br>Open-label<br>Extension<br>R<br>a<br>n<br>d<br>o<br>m<br>i<br>z<br>a<br>t<br>i<br>o<br>n<br>(1:1:1)<br>IVIg<br>Monitoring<br>Period
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Membranous Nephropathy (MN):<br>Most Common Cause of Nephrotic Syndrome<br>No Current FDA-Approved Therapies<br>~70,000 patients in the U.S.<br>Mean age of diagnosis is 50-60<br>years<br>More predominant in men<br>No approved therapies; all<br>used off-label<br>Currently used therapies<br>include cyclophosphamide,<br>rituximab and calcineurin<br>inhibitors<br>Nephrotic syndrome,<br>characterized by proteinuria<br>and decreased serum albumin,<br>presents in 80% of patients<br>70% of MN patients have IgG4<br>autoantibodies against PLA2R<br>PLA2R-negative patients can<br>have anti- THSd7A or anti-<br>NELL1 antibodies<br>Thickening of the glomerular<br>capillary walls due to immune<br>complex deposition<br>20-30% progress to end-stage<br>renal disease<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br>Ronco, P., Beck, L., Debiec, H. et al. Membranous nephropathy. Nat Rev Dis Primers 7, 69 (2021)
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Lupus Nephritis (LN):<br>Severe Organ Manifestation of Systemic Lupus Erythematosus<br>Need for new therapies with better tolerability profile<br>~45,000 patients in the U.S.<br>60% of adult patients with SLE<br>develop renal symptoms<br>Oral corticosteroids and broad<br>immunosuppressants are<br>current standard of care<br>Therapies not uniformly<br>effective<br>Substantial cause of morbidity<br>and death among patients with<br>SLE<br>LN can be presenting<br>manifestation for diagnosis of<br>SLE<br>Presence of anti-DNA<br>antibodies and related anti-<br>nuclear antibodie; some<br>closely associated with<br>different histological classes<br>Form of glomerulonephritis<br>5-20% of LN patients progress<br>to end-stage renal disease<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br>Anders HJ, Saxena R, Zhao MH, Parodis I, Salmon JE, Mohan C. Lupus nephritis. Nat Rev Dis Primers. 2020 Jan 23;6(1):7. doi: 10.1038/s41572-019-0141-9. PMID: 31974366.
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Sjogren’s Syndrome:<br>Systemic Autoimmune Disorder of Exocrine Glands<br>~300,000 patients in the U.S.<br>9:1 female to male<br>Men less likely to have systemic<br>manifestations<br>Age of typical onset: 40-50 years<br>IVIg treatment used to treat severe<br>cases<br>Mild to moderate patients typically<br>treated with secretagogues or<br>sialagogues (e.g., eye drops,<br>Biotene products)<br>Oral corticosteroids can be used for<br>flare-ups<br>Delayed diagnosis, often due to<br>multifactorial nature of disease<br>Can take multiple years for correct<br>diagnosis, typically by<br>rheumatologist<br>Antibody presence (% of patients):<br> >80% ANA ; 70% anti-Ro/SSA; 50 %<br>anti-La/SSB<br>Inflammation of exocrine glands<br>results in the development of sicca<br>symptoms, such as dryness of the<br>eyes and mouth<br>Some patients present with extra-<br>glandular manifestations, including<br>neuropathy, cutaneous, and<br>pulmonary manifestations<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br>Brito-Zerón P, Baldini C, Bootsma H, Bowman SJ, Jonsson R, Mariette X, Sivils K, Theander E, Tzioufas A, Ramos-Casals M. Sjögren syndrome. Nat Rev Dis Primers. 2016 Jul 7;2:16047. doi:<br>10.1038/nrdp.2016.47. PMID: 27383445.<br>No Current FDA-Approved Therapies
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COVID-19 Mediated Postural Orthostatic Tachycardia<br>Syndrome: Emerging Data Linking IgG Autoimmunity to Long COVID<br>No Current FDA-Approved Therapies<br>~500,000 – 1,000,000 POTS<br>patients in the U.S. before COVID<br>~80% of patients are women<br>between 15-50 years of age<br>No approved therapies<br>Symptomatic treatments focus on<br>blood volume, kidney sodium<br>levels, heart rate reduction and<br>vessel constriction<br>POTS is associated with significant<br>employment and economic loss<br>Despite well-defined diagnostic<br>criteria, diagnosis can be<br>challenging due to non-specific and<br>multi-organ nature of symptoms<br>Excessive heart rate increase in an<br>upright or standing position<br>Can prevent a person from being<br>upright for more than a couple of<br>minutes<br>Shortness of breath, headache,<br>fatigue, poor concentration, heart<br>palpitations, weakness, anxiety<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br>Rodriguez B, Hoepner R, Salmen A, Kamber N, Z'Graggen WJ. Immunomodulatory treatment in postural tachycardia syndrome: A case series. Eur J Neurol. 2021 May;28(5):1692-1697. doi: 10.1111/ene.14711. Epub 2021 Jan 19.<br>PMID: 33382525; Li H, Yu X, Liles C, et al. Autoimmune basis for postural tachycardia syndrome. J Am Heart Assoc. 2014;3(1):e000755. Published 2014 Feb 26. doi:10.1161/JAHA.113.000755; argenx market research
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Multifocal Motor Neuropathy:<br>Serious, Debilitating Neuromuscular Disease<br>Need for new therapies that slow progression of disease and reduce reliance on IVIg<br>~13,000 patients in the U.S. –<br>increasing<br>Often underdiagnosed<br>Predominantly men<br>Median age 40 years<br>Steroids ineffective<br>First line and only approved<br>therapy is frequent, high doses of<br>IVIg over 2-5 days<br>Often misdiagnosed as ALS<br>Takes ~1.5 years for correct<br>diagnosis<br>Nerve conduction blocks<br>Anti-GM1 IgM antibody presence<br>Slowly progressive muscle<br>weakness due to motor neuron<br>degeneration<br>Mainly affects hands and forearms<br>- patients become dependent<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br> >$0.5B IVIg sales and growing<br>Kevin Budding, Lill Eva Johansen, Inge Van de Walle, Kim Dijkxhoorn, Elisabeth de Zeeuw, Lauri M. Bloemenkamp, Jeroen W. Bos, Marc D. Jansen, Chantall A.D. Curial, Karen Silence, Hans de Haard, Christophe<br>Blanchetot, Liesbeth Van de Ven, Jeanette H.W. Leusen, R. Jeroen Pasterkamp, Leonard H. van den Berg, C. Erik Hack, Peter Boross, W. Ludo van der Pol Neurol Neuroimmunol Neuroinflamm Jan 2022, 9 (1) e1107; DOI:<br>10.1212/NXI.0000000000001107; argenx market research
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Delayed Graft Function After Kidney Transplant<br>Complication Leading to Negative Graft Outcome<br>Need for new therapies that prevent graft loss and shortens hospitalization<br>Occurs in up to 40% of kidney<br>transplant recipients<br>Over 2 million people worldwide<br>currently receive dialysis treatment<br>or are recipients of a kidney<br>transplant<br>No current FDA-approved therapies<br>to prevent DGF<br>DGF is associated with higher<br>prolonged hospitalization<br>Delayed graft function (DGF),<br>commonly defined as the need for<br>dialysis within the first week post-<br>transplantation<br>Increased serum creatinine levels<br>Ischemia reperfusion injury (IRI) is<br>a prime contributor to<br>development of DGF<br>Negatively affects short and long-<br>term graft outcome<br>MBL/C4d co-staining is observed in<br>kidney biopsies<br>PREVALENCE UNMET NEED DIAGNOSIS HALLMARK<br>Growing market due to expanded criteria donor kidneys<br>Pascual J ,et al. Am J Kidney Dis. 2008; Biglarnia et al, Nat Rev Nephrol, 2018; Yarlagadda SG et al,. Nephrol Dial Transplant . 2009<br>Castellano, Am J Pathol 2010, 176:1648 –1659
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