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Study to Evaluate the Efficacy and Safety of Ruxolitinib Cream in

Trial
Focused scale · updates evenly spaced
65%53.8%42.5%31.3%20%Aug 23Aug 24Aug 24Oct 6Aug 23 • YES 54.0%Aug 24 00:00 UTC • YES 28.1%Aug 24 19:12 UTC • YES 52.5%Aug 24 19:13 UTC • YES 47.3%Aug 24 19:13 UTC • YES 44.6%Aug 24 19:13 UTC • YES 37.5%Aug 24 19:14 UTC • YES 39.0%Aug 24 19:14 UTC • YES 33.8%Aug 24 19:14 UTC • YES 28.1%Oct 6 00:00 UTC • YES 29.9%Oct 6 17:05 UTC • YES 27.8%Oct 6 17:06 UTC • YES 29.0%Oct 6 17:07 UTC • YES 29.9%
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Will this trial show a positive result on proportion of participants who achieve Hidradenitis Suppurativa (HS) Clinical Response 75 (HiSCR75) from baseline?

YES30¢
NO70¢

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INCY

Incyte Announces 24-Week Long-Term Data from Phase 3 TRuE-AD4 Trial of Opzelura® (ruxolitinib) Cream in Adults with Moderate Atopic Dermatitis

First presentation of Week 24 results from TRuE-AD4 study in adults with moderate atopic dermatitis (AD) who had an inadequate response, intolerance or contraindication to topical corticosteroids (TCSs) and topical calcineurin inhibitors (TCIs) at the 2026 EADV Symposium The vast majority of

Trial Results • Phase 3Matched evaluate, efficacy, safety, ruxolitinib, cream
INCY

Incyte Data at the European Academy of Dermatology and Venereology (EADV) Congress Underscore the Breadth of Incyte’s Inflammation and Autoimmunity Portfolio

WILMINGTON, Del. --(BUSINESS WIRE)--Sep. 22, 2026-- Incyte (Nasdaq:INCY) today announced that data from across its Inflammation and Autoimmunity (IAI) portfolio will be presented at the European Academy of Dermatology and Venereology (EADV) 2026, held September 30 - October 3, 2026, in Vienna,

Presentation / Abstract • Phase 3EADV poster presentations Wed, Sep 30, 2026, 1:00 AM ETMatched efficacy, safety, ruxolitinib, cream, hidradenitis
INCY

Mirum Pharmaceuticals and Incyte Announce Positive Pivotal Phase 2 Results from PROGRESS Study of Zilurgisertib in Fibrodysplasia Ossificans Progressiva

- Cohort 1 results presented at ENDO 2026 demonstrate meaningful reductions in total heterotopic ossification (HO) lesion volume, new HO lesions and flare activity in adolescents and adults with FOP - U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for zilurgisertib

Trial Results • Phase 2ENDO 2026 presentation Sun, Jun 14, 2026, 4:35 PM EDTMatched evaluate, efficacy, safety, drug
INCY

Incyte Presents Phase 1/2 Multidose Data for VGA039 (Latarcibart) at ISTH 2026, Showing Substantial Bleed Reductions in Patients with all Von Willebrand Disease Types

- Treatment with latarcibart led to an 81% median reduction in annualized bleeding rate (ABR) across all bleeding categories and patient types with von Willebrand disease (VWD) - Latarcibart, administered via a once monthly subcutaneous dosing regimen, was shown to be safe and well tolerated over

Presentation / Abstract • Phase 1/2ISTH oral presentation Mon, Jul 13, 2026, EDTMatched efficacy, safety, participants, drug
INCY

Incyte Announces New Positive Data at EHA 2026 Showed INCA033989 Achieved Rapid, Robust and Sustained Clinical and Molecular Responses and Was Well Tolerated in Patients with Myelofibrosis and Essential Thrombocythemia

In myelofibrosis (MF), INCA033989 delivered rapid and durable clinical benefits including meaningful spleen volume reductions, symptom improvement and anemia responses, both as a monotherapy and in combination with ruxolitinib In essential thrombocythemia (ET), 87% of patients achieved a

Presentation / Abstract • Phase 1EHA 2026 oral presentation Sat, Jun 13, 2026, 11:15 AM EDTMatched evaluate, efficacy, safety, ruxolitinib
INCY

Mirum Pharmaceuticals and Incyte Announce Pivotal Late-Breaking Results for Zilurgisertib in Fibrodysplasia Ossificans Progressiva Accepted for Presentation at ENDO 2026

- Late-breaking rapid-fire presentation to include results from Cohort 1 of the placebo-controlled PROGRESS study evaluating zilurgisertib in fibrodysplasia ossificans progressiva (FOP) FOSTER CITY, Calif. & WILMINGTON, Del. --(BUSINESS WIRE)--Jun. 4, 2026-- Mirum Pharmaceuticals, Inc.

Presentation / Abstract • Phase 2Late-breaking rapid-fire presentation Sun, Jun 14, 2026, 3:30 PM CTMatched evaluate, efficacy, safety, drug
INCY

Incyte Announces More Than 20 Abstracts Accepted for Presentation at the European Hematology Association (EHA) 2026 Congress

Data from pivotal Phase 3 frontMIND trial evaluating tafasitamab (Monjuvi ® /Minjuvi ®) in first-line diffuse large b-cell lymphoma (DLBCL) selected for prestigious Plenary Abstracts Session Oral and poster presentations to feature new data for INCA033989, an anti-mutant calreticulin

Presentation / Abstract • Phase 3EHA Plenary Abstract Session Sat, Jun 13, 2026, 6:00 AM ETMatched efficacy, safety, ruxolitinib, drug
INCY

Incyte Highlights New Phase 3 Tafasitamab Data at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting

- Data from pivotal frontMIND study of tafasitamab (Monjuvi®/Minjuvi®) in first-line diffuse large b-cell lymphoma (DLBCL) featured in oral presentation at ASCO; results support global regulatory submissions WILMINGTON, Del. --(BUSINESS WIRE)--Apr. 21, 2026-- Incyte (Nasdaq:INCY) today announced

Presentation / Abstract • Phase 3Matched efficacy, safety, drug