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Full Name:Argenx Se Industry:biological products (diagnostic and non diagnostic) CIK:1697862 Fiscal Year End:12-31 State/Country:BELGIUM

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US clinical trial status

Size of symbol reflects the phase of clinical trial. E.g. Phase 3 trial has the largest size.
Shape definition
Up-triangle: study first submitted.
Square: study completion(actual/anticipated).
Circle: result first posted.
Color definition
Green: study is ongoing.
Blue: recruitment completed.
Red: study aborted/terminated/withdrawn.
Pink: study in abnormal state.

US FDA submission

Size of symbol reflects the type of submission. E.g. Type 1 drug has the largest size.
: Approved.
: Tentative Approval.

Drug marketing & current status

Circle bubble denotes new drug marketing. Size is determined by drug type and market(i.e. population) size. E.g. Type 1 drug marketed in US has the largest size. Drug marketed in CA has the smallest size due to small population size.
Color definition
Blue circle: drug marketed (EU,CA), FDA submission approved (US).
Cyan circle: drug approved (CA), tentative approval (US), received positive opinion (EU)
Red circle: drug marketed/approved on the corresponding day but was later withdrawn, discontinued, cancelled, or received negative opinion.

Drug marketing status change

Square bubble denotes marketing status change. Size is determined by drug type and market(i.e. population) size.
Color definition
Blue square: change from other status to marketed.
Cyan square: change from other status to tentative status.
Red square: change from other status to abnormal or withdrawn status.

US Clinical Trials

Clinical Trials Summary Statistics

Year Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
ALL 1 1 9
2024
2023 1 1
2022 1
Year Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
ALL 6 4 1 4
2024 1
2023 4 1
2022 2 1
Year Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
ALL 3 1
2024
2023
2022 2 1
Year Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
ALL 5 4 6 1 1
2024 3
2023 1
2022 1
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 1 6 3 5
2024 3
2023 4 1
2022 1 2 2 1
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 1 4 1 4
2024
2023 1 1
2022 1 1
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 1
2024 1
2023
2022
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 9 4 6
2024
2023 1
2022
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 1
2024
2023
2022
Year Phase 1 Phase 2 Phase 2|Phase 3 Phase 3
ALL 1
2024
2023
2022
Phase Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
Phase 1 1 1 9
Phase 2 6 4 1 4
Phase 2|Phase 3 3 1
Phase 3 5 4 6 1 1
Phase Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
Phase 1
Phase 2 1
Phase 2|Phase 3
Phase 3 3
Phase Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
Phase 1 1 1
Phase 2 4 1
Phase 2|Phase 3
Phase 3 1
Phase Recruiting Active, Not Recruiting Not Yet Recruiting Completed Terminated Withdrawn
Phase 1 1
Phase 2 2 1
Phase 2|Phase 3 2 1
Phase 3 1

Note: "Year" represents clinical trail start year determined by study first submit date.
Three grouping strategies present the same statistical data from different angles, choose any one you are comfortable with.
at least one study with latest update posted within 7 days.  at least one study with latest update posted within 30 days.  at least one study with latest update posted within 90 days. 

Clinical Trials Records

Sponsor Overall Status Phase Brief Title Disease Condition Intervention Name Study First Submit Date Last Update Post Date Results First Post Date Completion Date Completion Date Type Enrollment Count
argenx Recruiting Phase 3 A Study of Efgartigimod PH20 SC Given by Prefilled Syringe in Adults With Thyroid Eye Disease. Thyroid Eye Disease Efgartigimod PH20 SC|Placebo PH20 SC 2024-03-06 2024-04-04 2027-10-01 Anticipated 108
argenx Recruiting Phase 3 A Study of Efgartigimod PH20 SC Given by Prefilled Syringe in Adults With Thyroid Eye Disease Thyroid Eye Disease Efgartigimod PH20 SC|Placebo PH20 SC 2024-03-06 2024-04-04 2027-10-01 Anticipated 108
argenx Recruiting Phase 3 A Phase 3 Study to Evaluate the Efficacy and Safety of Efgartigimod IV in Patients With Acetylcholine Receptor Binding Antibody Seronegative Generalized Myasthenia Gravis Generalized Myasthenia Gravis Efgartigimod IV|Placebo IV 2024-03-01 2024-04-23 2027-07-23 Anticipated 110
argenx Recruiting Phase 3 A Study to Assess the Long-term Safety and Efficacy of a Subcutaneous Formulation of Efgartigimod in Adults With Active Idiopathic Inflammatory Myopathy Myositis|Active Idiopathic Inflammatory Myopathy|Dermatomyositis|Polymyositis|Immune-Mediated Necrotizing Myopathy|Antisynthetase Syndrome EFG PH20 SC 2023-07-28 2024-04-08 2027-09-01 Anticipated 240
argenx Recruiting Phase 3 A Phase 3 Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid Bullous Pemphigoid efgartigimod PH20 SC|Prednisone 2022-12-08 2024-04-09 2026-03-06 Anticipated 160
argenx Recruiting Phase 2|Phase 3 A Study to Investigate the Efficacy and Safety of Efgartigimod PH20 SC in Adult Participants With Active Idiopathic Inflammatory Myopathy. Active Idiopathic Inflammatory Myopathy|Myositis|Dermatomyositis|Polymyositis|Immune-Mediated Necrotizing Myopathy|Antisynthetase Syndrome EFG PH20 SC|PBO 2022-08-30 2024-04-08 2027-02-01 Anticipated 240
argenx Recruiting Phase 2|Phase 3 Evaluating Long-term Safety of Efgartigimod Administered Intravenously and Efgartigimod PH20 Administered Subcutaneously in Children With Generalized Myasthenia Gravis Generalized Myasthenia Gravis Efgartigimod IV or Efgartigimod PH20 SC 2022-04-01 2024-04-11 2028-09-01 Anticipated 12
argenx Active, not recruiting Phase 2|Phase 3 A Phase 2/3 Study of Efgartigimod PH20 SC in Adult Participants With Bullous Pemphigoid (BALLAD) Bullous Pemphigoid efgartigimod PH20 SC|placebo|Prednisone 2022-02-14 2024-01-17 2025-03-28 Anticipated 98

Note: Use 'Search' box on top right cornor to narrow down search results. E.g. type in "phase 3" (case insensitive, with double quote) to show Phase 3 trials.
latest update posted within 7 days.  latest update posted within 30 days.  latest update posted within 90 days. 

US FDA Submissions

US FDA Submission Summary Statistics*

Year TYPE 1 UNKNOWN
ALL 1 1
2024
2023 1
2022

Note: "Year" determined by submission status date.
* Original submissions only. Supplementary records not counted.
at least one submission within 7 days.  at least one submission within 30 days.  at least one submission within 90 days. 

US FDA Submission Records

Sponsor Application Type Drug Name Active Ingredient Submission Code Submission Type Submission Status Status Date Application Number
Argenx Bv BLA Vyvgart Hytrulo Efgartigimod Alfa And Hyaluronidase Qvfc Unknown Orig Approval 2023-06-20 761304

Note: Use 'Search' box on top right cornor to narrow down search results. E.g. type in "NDA" (case insensitive) to show records with "NDA" (New Drug Applications) tag.
submission status date within 7 days.  submission status date within 30 days.  submission status date within 90 days. 

US Drug Marketing Status
Category Sponsor Marketing Date Current Marketing Status Drug Name Active Ingredient Submission Status Date Submission Code Submission Status Marketing Status Change Date
Human Non-Bioproduct Argenx Bv 2023-06-20 Prescription Vyvgart Hytrulo Efgartigimod Alfa And Hyaluronidase Qvfc 2023-06-20 Unknown Approval 2023-11-30

Note: This table contains human and animal drugs regulated by US FDA, and biological products regulated by CBER (Center for Biologics Evaluation and Research).
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "discontinued" (case insensitive) to show discontinued drug products.
For human non-bioproduct, marketing date was set to submission approval date.
Possible marketing statuses: Marketed, Prescription, Over-the-counter, Discontinued, None (Tentative Approval).
any of (marketing/submission/status change) within 7 days.  any of (marketing/submission/status change) within 30 days.  any of (marketing/submission/status change) within 90 days. 

EU Drug Marketing Status
Category Sponsor Authorization Date Current Marketing Status Latest Status Update Drug Name Active Ingredient Withdraw Date Opinion Date Summary of Opinion
Human Argenx 2022-08-10 Authorised 2022-09-12 Vyvgart Efgartigimod Alfa

Note: This table contains human and animal drugs regulated by EMA (European Medicines Agency), and summary of opinion published by EMA based on the CHMP's or CVMP's positive or negative recommendation.
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "withdrawn" (case insensitive) to show drugs withdrawn.
Possible marketing statuses: Authorised, Refused, Withdrawn, Summary of Opinion.
Summary of Opinion: published by European Medicines Agency (EMA) based on the CHMP's or CVMP's positive or negative recommendation. Further marketing authorization is partially based on this opinion.
any of (authorization/withdrawn/opinion/status change) date within 7 days.  any of (authorization/withdrawn/opinion/status change) date within 30 days.  any of (authorization/withdrawn/opinion/status change) date within 90 days. 

CA Drug Marketing Status
Category Sponsor Authorization Date Current Marketing Status Status Date Drug Name Active Ingredient
Human Argenx Bv 2023-09-19 Marketed 2023-11-06 Vyvgart Efgartigimod Alfa (20 Mg)

Note: This table contains human, animal drugs, radiopharmaceutical and disinfectant regulated by CFIA(Canadian Food Inspection Agency) and Health Canada.
Use 'Search' box on top right cornor to narrow down search results. E.g. type in "marketed" (case insensitive) to show drugs marketed.
Possible marketing statuses: Marketed, Approved, Dormant, Cancelled Pre Market, Cancelled Post Market, Cancelled (Safety Issue), Cancelled (Unreturned Annual).
any of (authorization/status change) date within 7 days.  any of (authorization/status change) date within 30 days.  any of (authorization/status change) date within 90 days.