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Trial resultsH2 2027a window, not a day

UNITY registrational topline: efgartigimod in Sjogren's disease

argenx expects to report results from its Registrational (UNITY) study of Efgartigimod (Vyvgart) for Sjogren's disease in the second half of 2027 (no exact date yet). Registrational (UNITY) is a study designed to support approval.

Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary

DetailsClinical trial results · also called: readout / topline data
Company
argenx SE ARGX
Drug
Efgartigimod (Vyvgart)
For
Sjogren's disease
Stage
Registrational (UNITY) · a study designed to support approval
When
H2 2027 · the company gave a window, not a day; the calendar never invents one
Source note
H1 2026 results PR: 'Topline results from registrational UNITY study (Sjogren's disease) expected in second half of 2027.'
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MilestoneARGXargenx2026

Adimanebart (ARGX-119) registrational study start in congenital myasthenic syndromes, expected during 2026 (no exact date yet). A company milestone for argenx (adimanebart (ARGX-119) for congenital myasthenic syndromes): a step in the program rather than a decision or a data readout.

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Entry
Adimanebart (ARGX-119) registrational study start in congenital myasthenic syndromes · Company milestone
Drug
adimanebart (ARGX-119)
For
congenital myasthenic syndromes
Stage
Registrational · a study designed to support approval
When
2026 · the company gave a window, not a day
Source note
Q2 2026 PR (Jul 23, 2026) guides 2026 start; the Q1 2026 PR had said 'CMS registrational study on track to start in third quarter of 2026'. Using the less precise, more recent guidance.
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page

MilestoneARGXargenx2026

ARGX-121 (anti-IgA) Phase 2 start in IgA nephropathy, expected during 2026 (no exact date yet). A company milestone for argenx (ARGX-121 for IgA nephropathy): a step in the program rather than a decision or a data readout.

More details
Entry
ARGX-121 (anti-IgA) Phase 2 start in IgA nephropathy · Company milestone
Drug
ARGX-121
For
IgA nephropathy
Stage
Phase 2 · the stage that tests whether the drug actually works
When
2026 · the company gave a window, not a day
Source note
argenx H1 2026 results (Jul 23, 2026) reiterated 2026 Phase 2 start for ARGX-121 in IgAN.
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page

MilestoneARGXargenx2026

ARGX-118 and ARGX-125 to enter Phase 1 in 2026, expected during 2026 (no exact date yet). A company milestone for argenx (ARGX-118 / ARGX-125 for undisclosed): a step in the program rather than a decision or a data readout.

More details
Entry
ARGX-118 and ARGX-125 to enter Phase 1 in 2026 · Company milestone
Drug
ARGX-118 / ARGX-125
For
undisclosed
Stage
Phase 1 · an early safety study in a small group of people
When
2026 · the company gave a window, not a day
Source note
argenx H1 2026 results (Jul 23, 2026): two new first-in-class molecules on track for Phase 1 entry in 2026 (TSP-101 Phase 1 already ongoing).
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page

Trial resultsARGXargenxQ4 2026

argenx expects to report results from its Registrational (EMPASSION) study of Empasiprubart (ARGX-117) for Multifocal motor neuropathy (MMN) in Q4 2026 (Oct–Dec) (no exact date yet). Registrational (EMPASSION) is a study designed to support approval.

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Entry
EMPASSION registrational topline: empasiprubart in multifocal motor neuropathy · Clinical trial results (readout / topline data)
Drug
Empasiprubart (ARGX-117)
For
Multifocal motor neuropathy (MMN)
Stage
Registrational (EMPASSION) · a study designed to support approval
When
Q4 2026 · the company gave a window, not a day
Source note
H1 2026 results PR: 'Topline results from registrational EMPASSION study (MMN) expected in fourth quarter of 2026.'
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MilestoneARGXargenxQ4 2026

ARGX-124 (next-gen FcRn) to complete Phase 1 evaluation by end of 2026, expected in Q4 2026 (Oct–Dec) (no exact date yet). A company milestone for argenx (ARGX-124 for FcRn (undisclosed autoimmune)): a step in the program rather than a decision or a data readout.

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Entry
ARGX-124 (next-gen FcRn) to complete Phase 1 evaluation by end of 2026 · Company milestone
Drug
ARGX-124
For
FcRn (undisclosed autoimmune)
Stage
Phase 1 · an early safety study in a small group of people
When
Q4 2026 · the company gave a window, not a day
Source note
argenx H1 2026 results PR (Jul 23, 2026) guides ARGX-124 Phase 1 completion by year-end 2026; ARGX-213 described as Phase 3 ready. Dated Q4 per 'by end of 2026'.
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page

Trial resultsARGXargenxH1 2027

argenx expects to report results from its Registrational (ADVANCE-NEXT) study of Efgartigimod (Vyvgart) for Primary immune thrombocytopenia in the first half of 2027 (no exact date yet). Registrational (ADVANCE-NEXT) is a study designed to support approval.

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Entry
ADVANCE-NEXT registrational topline: efgartigimod in primary ITP · Clinical trial results (readout / topline data)
Drug
Efgartigimod (Vyvgart)
For
Primary immune thrombocytopenia
Stage
Registrational (ADVANCE-NEXT) · a study designed to support approval
When
H1 2027 · the company gave a window, not a day
Source note
H1 2026 results PR: 'Topline results from registrational ADVANCE-NEXT study (primary ITP) expected in first half of 2027.'
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Plain-English summary generated from this entry’s own fields (drug, condition, stage, date). Glossary · Open this catalyst’s page