Guselkumab History and Updates

240 events · 2013 – present

Synced daily from openFDA and ClinicalTrials.gov. Last sync: .

14
FDA Approvals
1
Label Revisions
321
Trial Milestones
4
Pivotal Publications
Guselkumab — history and updatesFDA approvals, label revisions, recalls, trials, and pivotal publicationsFDA approvalsLabel revisionsRecalls + safetyTrialsPublications20132014201520162017201820192020202120222023202420252026202720282029203020312032Trial: NCT07352566 2026-08-01 → 2030-06-01 (primary completion)Trial: NCT07511647 2026-06-15 → 2027-12-30 (primary completion)Trial: NCT07616687 2026-06-01 → 2029-03-15 (primary completion)Trial: NCT07448402 2026-05-31 → 2031-05-31 (primary completion)Trial: NCT07577856 2026-05-29 → 2028-08-11 (primary completion)Trial: NCT07577843 2026-05-29 → 2028-06-12 (primary completion)Trial: NCT06916390 2026-04-23 → 2028-05-30 (primary completion)Trial: NCT07499232 2026-04-20 → 2028-11-15 (primary completion)Trial: NCT07528040 2026-04-15 → 2028-12-31 (primary completion)Trial: NCT07444060 2026-03-01 → 2028-12-31 (primary completion)Trial: NCT07245394 2026-01-29 → 2027-11-01 (primary completion)Trial: NCT07487311 2026-01-07 → 2027-12-31 (primary completion)Trial: NCT07310095 2025-12-30 → 2027-09-15 (primary completion)Trial: NCT07255781 2025-11-30 → 2025-11-30 (primary completion)Trial: NCT07246460 2025-10-31 → 2027-09-30 (primary completion)Trial: NCT07430319 2025-10-16 → 2026-04-16 (primary completion)Trial: NCT07138898 2025-09-30 → 2027-09-30 (primary completion)Trial: NCT07141004 2025-08-12 → 2027-06-05 (primary completion)Trial: NCT06586281 2025-06-01 → 2027-09-01 (primary completion)Trial: NCT06651489 2025-03-13 → 2026-04-30 (primary completion)Trial: NCT06563323 2025-02-01 → 2027-08-13 (primary completion)Trial: NCT06398106 2024-12-20 → 2028-03-01 (primary completion)Trial: NCT06663332 2024-10-29 → 2031-12-12 (primary completion)Trial: NCT07532486 2024-07-10 → 2027-07-10 (primary completion)Trial: NCT06974474 2024-06-18 → 2025-11-27 (primary completion)Trial: NCT06408935 2024-04-17 → 2027-06-08 (primary completion)Trial: NCT06249555 2024-03-20 → 2026-06-30 (primary completion)Trial: NCT05923073 2024-03-13 → 2027-10-27 (primary completion)Trial: NCT06260163 2024-01-19 → 2028-05-22 (primary completion)Trial: NCT06039189 2023-08-24 → 2025-04-14 (primary completion)Trial: NCT05669833 2023-07-14 → 2026-10-31 (primary completion)Trial: NCT05858632 2023-07-01 → 2028-06-30 (primary completion)Trial: NCT05784129 2023-02-21 → 2023-09-29 (primary completion)Trial: NCT05503875 2023-01-01 → 2027-12-31 (primary completion)Trial: NCT05535738 2022-11-15 → 2027-01-01 (primary completion)Trial: NCT05347095 2022-09-27 → 2027-03-25 (primary completion)Trial: NCT05242484 2022-09-19 → 2025-05-15 (primary completion)Trial: NCT05528510 2022-09-13 → 2024-04-02 (primary completion)Trial: NCT05083182 2022-08-30 → 2026-01-12 (primary completion)Trial: NCT05242471 2022-07-22 → 2025-05-23 (primary completion)Trial: NCT05272150 2022-07-13 → 2025-05-30 (primary completion)Trial: NCT05004727 2022-02-16 → 2026-12-31 (primary completion)Trial: NCT05197049 2022-01-19 → 2023-07-04 (primary completion)Trial: NCT05125679 2021-11-23 → 2023-07-28 (primary completion)Trial: NCT05083078 2021-11-04 → 2022-07-01 (primary completion)Trial: NCT05071664 2021-10-25 → 2024-05-14 (primary completion)Trial: NCT04936308 2021-09-28 → 2024-10-28 (primary completion)Trial: NCT04929210 2021-08-30 → 2026-08-04 (primary completion)Trial: NCT05049798 2021-08-25 → 2027-08-01 (primary completion)Trial: NCT04914429 2021-08-25 → 2023-09-26 (primary completion)Trial: NCT04704843 2021-06-17 → 2021-09-13 (primary completion)Trial: NCT04882098 2021-06-17 → 2024-12-30 (primary completion)Trial: NCT04736966 2021-03-03 → 2024-03-31 (primary completion)Trial: NCT04645355 2021-03-01 → 2025-04-04 (primary completion)Trial: NCT04683029 2021-02-24 → 2023-05-17 (primary completion)Trial: NCT04533737 2020-12-17 → 2022-09-08 (primary completion)Trial: NCT04633447 2020-12-10 → 2024-05-22 (primary completion)Trial: NCT04617691 2020-11-30 → 2021-07-20 (primary completion)Trial: NCT04376827 2020-09-15 → 2023-02-01 (primary completion)Trial: NCT04394936 2020-09-01 → 2023-02-22 (primary completion)Trial: NCT04340076 2020-08-20 → 2025-01-30 (primary completion)Trial: NCT04397263 2020-06-10 → 2024-02-29 (primary completion)Trial: NCT04439526 2020-06-10 → 2023-11-21 (primary completion)Trial: NCT04084665 2020-06-01 → 2020-07-30 (primary completion)Trial: NCT04030533 2019-11-29 → 2020-12-31 (primary completion)Trial: NCT04147338 2019-10-30 → 2021-09-13 (primary completion)Trial: NCT03975153 2019-10-03 → 2022-08-11 (primary completion)Trial: NCT04061395 2019-10-01 → 2021-12-30 (primary completion)Trial: NCT04033445 2019-09-26 → 2023-09-19 (primary completion)Trial: NCT03998683 2019-09-03 → 2021-03-02 (primary completion)Trial: NCT03796858 2019-03-22 → 2020-11-11 (primary completion)Trial: NCT03818035 2019-02-08 → 2022-03-07 (primary completion)Trial: NCT03662542 2018-11-20 → 2020-12-01 (primary completion)Trial: NCT03649971 2018-11-19 → 2021-09-13 (primary completion)Trial: NCT03573323 2018-11-09 → 2019-07-15 (primary completion)Trial: NCT03628924 2018-09-04 → 2020-05-22 (primary completion)Trial: NCT03451851 2018-07-11 → 2023-07-19 (primary completion)Trial: NCT03536325 2018-05-31 → 2018-10-25 (primary completion)Trial: NCT03466411 2018-04-13 → 2023-10-20 (primary completion)Trial: NCT03162796 2017-08-24 → 2019-03-14 (primary completion)Trial: NCT03158285 2017-07-12 → 2019-02-25 (primary completion)Trial: NCT03090100 2017-04-27 → 2018-08-02 (primary completion)Trial: NCT02905331 2017-02-28 → 2018-02-06 (primary completion)Trial: NCT02951533 2016-12-12 → 2017-09-13 (primary completion)Trial: NCT02641730 2015-12-15 → 2017-03-28 (primary completion)Trial: NCT02570373 2015-09-25 → 2016-01-12 (primary completion)Trial: NCT02397382 2015-06-18 → 2016-08-31 (primary completion)Trial: NCT02319759 2015-03-27 → 2016-05-31 (primary completion)Trial: NCT02343744 2015-01-19 → 2015-12-04 (primary completion)Trial: NCT02207231 2014-11-26 → 2015-09-29 (primary completion)Trial: NCT02207244 2014-11-03 → 2015-10-01 (primary completion)Trial: NCT02203032 2014-10-07 → 2015-12-25 (primary completion)Trial: NCT02103361 2013-11-30 → 2030-05-31 (primary completion)Trial: NCT01866007 2013-05-09 → 2013-09-20 (primary completion)FDA approval — 2017-07-13 FDA approved Tremfya (guselkumab) (BLA 761061) Sponsor: JANSSEN BIOTECH. Class: Type 1 - New Molecular Entity.FDA approval (supplemental) — 2019-01-29 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-1) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2019-04-04 FDA approved supplemental application for Tremfya (guselkumab) — Labeling (BLA 761061 S-2) Sponsor: JANSSEN BIOTECH. Class: Labeling.FDA approval (supplemental) — 2019-11-22 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-4) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2020-06-01 FDA approved supplemental application for Tremfya (guselkumab) — Labeling (BLA 761061 S-9) Sponsor: JANSSEN BIOTECH. Class: Labeling.FDA approval (supplemental) — 2020-07-13 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-7) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2023-06-29 FDA approved supplemental application for Tremfya (guselkumab) — Labeling (BLA 761061 S-15) Sponsor: JANSSEN BIOTECH. Class: Labeling.FDA approval (supplemental) — 2024-09-11 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-21) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2025-03-20 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-24) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2025-03-25 FDA approved supplemental application for Tremfya (guselkumab) — Manufacturing (CMC) (BLA 761061 S-27) Sponsor: JANSSEN BIOTECH. Class: Manufacturing (CMC).FDA approval (supplemental) — 2025-06-17 FDA approved supplemental application for Tremfya (guselkumab) — Labeling (BLA 761061 S-30) Sponsor: JANSSEN BIOTECH. Class: Labeling.FDA approval (supplemental) — 2025-09-19 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-26) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2025-09-26 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-29) Sponsor: JANSSEN BIOTECH. Class: Efficacy.FDA approval (supplemental) — 2025-09-26 FDA approved supplemental application for Tremfya (guselkumab) — Efficacy (BLA 761061 S-28) Sponsor: JANSSEN BIOTECH. Class: Efficacy.Label revision — 2026-06-04 Indication and usage updated on TREMFYA label (effective 2026-06-04) 1 INDICATIONS AND USAGE TREMFYA is an interleukin-23 antagonist indicated for the treatment of: adults and pediatric patients 6 years of age and older who also weigh at least 40 kg with moderate-to-severe plaque psoriasis and who are candidRecall — 2021-03-09 TREMFYA recall — Class III: Temperature Abuse Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by: Janssen Biotech, Inc., Horsham, PA 19044; NDC 57894-640-01.Results posted — 2017-07-17 Trial results posted: NCT02203032 A Study of Guselkumab in Participants With Moderate to Severe Plaque-type Psoriasis and an Inadequate Response to UstekinumabResults posted — 2017-10-19 Trial results posted: NCT02207231 A Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type PsoriasisResults posted — 2017-11-06 Trial results posted: NCT02207244 A Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type Psoriasis With Randomized Withdrawal and RetreatmResults posted — 2018-09-06 Trial results posted: NCT02905331 Efficacy and Safety Study of Guselkumab in the Treatment of Participants With Moderate to Severe Plaque-Type PsoriasisResults posted — 2019-02-15 Trial results posted: NCT02951533 A Study to Compare the Efficacy of Guselkumab to Fumaric Acid Esters for the Treatment of Participants With Moderate to Severe Plaque PsoriaResults posted — 2019-02-21 Trial results posted: NCT02641730 An Efficacy and Safety of Guselkumab in Participants With Palmoplantar PustulosisResults posted — 2019-10-01 Trial results posted: NCT03090100 A Study to Evaluate the Comparative Efficacy of CNTO 1959 (Guselkumab) and Secukinumab for the Treatment of Moderate to Severe Plaque-type PResults posted — 2020-07-28 Trial results posted: NCT03573323 A Study of Ixekizumab (LY2439821) Compared to Guselkumab in Participants With Moderate-to-Severe Plaque PsoriasisResults posted — 2020-10-14 Trial results posted: NCT03162796 A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis IncludiResults posted — 2020-10-14 Trial results posted: NCT02319759 Efficacy and Safety Study of Guselkumab in the Treatment of Participants With Active Psoriatic Arthritis (PsA)Results posted — 2020-11-05 Trial results posted: NCT03158285 A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic ArthritisResults posted — 2021-06-14 Trial results posted: NCT03628924 A Study to Evaluate the Efficacy, Safety, and Tolerability of Guselkumab for the Treatment of Participants With Moderate to Severe HidradeniResults posted — 2023-05-10 Trial results posted: NCT03818035 A Study to Evaluate Further Therapeutic Strategies With Guselkumab in Participants With Moderate-to-Severe Plaque-Type PsoriasisResults posted — 2023-12-12 Trial results posted: NCT03662542 A Study of Efficacy and Safety of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active UlcerResults posted — 2024-01-09 Trial results posted: NCT04533737 Efficacy and Safety of Brodalumab Compared With Guselkumab in the Treatment of Plaque Psoriasis After Inadequate Response to UstekinumabResults posted — 2024-04-16 Trial results posted: NCT04376827 A Study of Guselkumab in Participants With Active Lupus NephritisResults posted — 2024-05-24 Trial results posted: NCT03975153 Guselkumab in the Treatment of Pityriasis Rubra Pilaris (PRP)Results posted — 2024-10-09 Trial results posted: NCT04683029 A Study of Guselkumab in Participants With Systemic SclerosisResults posted — 2024-10-28 Trial results posted: NCT05784129 A Study of Guselkumab for the Treatment of Participants With Crohn's Disease After Surgical ResectionResults posted — 2024-11-18 Trial results posted: NCT04033445 A Study of Guselkumab in Participants With Moderately to Severely Active Ulcerative ColitisResults posted — 2025-01-27 Trial results posted: NCT05125679 Effect of Guselkumab on Cardiovascular Risk Surrogate Markers in Participants With Moderate to Severe Plaque PsoriasisResults posted — 2025-02-21 Trial results posted: NCT05197049 A Study of Guselkumab Subcutaneous Therapy in Participants With Moderately to Severely Active Crohn's DiseaseResults posted — 2025-03-28 Trial results posted: NCT03451851 A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Guselkumab for the Treatment of Chronic PlaqueResults posted — 2025-05-07 Trial results posted: NCT03466411 A Study of the Efficacy and Safety of Guselkumab in Participants With Moderately to Severely Active Crohn's DiseaseResults posted — 2025-05-20 Trial results posted: NCT04397263 A Study of Guselkumab in Participants With Moderately to Severely Active Crohn's DiseaseResults posted — 2025-07-01 Trial results posted: NCT04633447 A Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell ArteritisResults posted — 2025-12-08 Trial results posted: NCT04936308 Guselkumab in Active Psoriatic Arthritis Participants With Inadequate Response/Intolerance to One Prior Anti-TNF Alpha AgentResults posted — 2025-12-09 Trial results posted: NCT05528510 A Study of Guselkumab Therapy in Participants With Moderately to Severely Active Ulcerative ColitisResults posted — 2026-02-04 Trial results posted: NCT04882098 A Study of Guselkumab in Participants With Active Psoriatic ArthritisResults posted — 2026-05-01 Trial results posted: NCT06039189 Study of Guselkumab Versus Placebo for the Treatment of Low Body Surface Area Moderate Plaque PsoriasisPivotal publication — 2020-01-01 Guselkumab in patients with active psoriatic arthritis who were biologic-naive or had previously received TNFα inhibitor treatment (DISCOVER-1): a double-blind, (Lancet) Discover-1 — A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis Including Those Previously Treated With Biologic Anti -Tumor NecrosPivotal publication — 2020-01-01 Guselkumab in biologic-naive patients with active psoriatic arthritis (DISCOVER-2): a double-blind, randomised, placebo-controlled phase 3 trial. (Lancet) A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic ArthritisPivotal publication — 2025-01-01 Efficacy and safety of intravenous induction and subcutaneous maintenance therapy with guselkumab for patients with Crohn's disease (GALAXI-2 and GALAXI-3): 48- (Lancet) GALAXI — A Study of the Efficacy and Safety of Guselkumab in Participants With Moderately to Severely Active Crohn's DiseasePivotal publication — 2025-01-01 Guselkumab in patients with moderately to severely active ulcerative colitis (QUASAR): phase 3 double-blind, randomised, placebo-controlled induction and mainte (Lancet) QUASAR — A Study of Guselkumab in Participants With Moderately to Severely Active Ulcerative Colitistoday (2026-06-18)FDA approvalLabel revisionRecall or safetyTrial activityPivotal publication

Source: openFDA, ClinicalTrials.gov via AACT, PubMed · Hipa.ai, 2026-06-18Download chart as PNG

This page tracks every FDA action, clinical trial milestone, and major publication for Guselkumab since 2013, drawn from openFDA, ClinicalTrials.gov, and PubMed.

All published updates (27)

2025

Upcoming & expected milestones

Primary completion· ClinicalTrials.gov
VOICE-Early Response to Vedolizumab and IL-23 Antagonists in Participants With Crohn's Disease: A Prospective Observational Study
Primary completion· ClinicalTrials.gov
A Study of Guselkumab Administered Subcutaneously in Bio-naive Participants With Active Psoriatic Arthritis Axial Disease
Primary completion· ClinicalTrials.gov
Elucidating Shared Mechanisms Contributing to NAFLD and PsA Disease Severity With Guselkumab Therapy
Primary completion· ClinicalTrials.gov
A Study of Guselkumab Administered Subcutaneously in Treatment of Indian Participants With Psoriatic Arthritis (PsA)
Primary completion· ClinicalTrials.gov
A Study to Evaluate Comparative Efficacy and Safety of Guselkumab in High-dose and Extended-interval Versus Standard-dose in Chinese Partici
Primary completion· ClinicalTrials.gov
A Study of Guselkumab and Interleukin-17 (IL-17) Inhibitor Therapies in Participants With Psoriatic Arthritis in Routine Clinical Practice
Primary completion· ClinicalTrials.gov
A Study to Assess Concentration of TREMFYA in Breast Milk of Lactating Women Who Are Receiving TREMFYA Therapeutically
Primary completion· ClinicalTrials.gov
Elucidating Shared Mechanisms Contributing to NAFLD and PsA Disease Severity With Guselkumab Therapy
Primary completion· ClinicalTrials.gov
Ultrasound and Proteomics for Guselkumab Response Assessment in Crohn's Disease (UPGRADE).
Primary completion· ClinicalTrials.gov
Switching to the IL-23 Inhibitor Guselkumab for People With Active IBD Who Previously Used Ustekinumab (SHIFT-IBD)
Primary completion· ClinicalTrials.gov
A Prospective Cohort Study Evaluating the Efficacy and Safety of Guselkumab (GUS) With JAK Inhibitors in Patients With Difficult-To-Treat In
Primary completion· ClinicalTrials.gov
A Study of Guselkumab Versus Risankizumab in Participants With Moderately to Severely Active Crohn's Disease
Primary completion· ClinicalTrials.gov
An Observational, Multicenter Study to Evaluate the Effectiveness of Guselkumab for the Treatment of Participants With Crohn's Disease After
Primary completion· ClinicalTrials.gov
Optimal Care With Guselkumab in Crohn's Disease / OPTIM Study A Prospective Open Label Interventional, Multicenter Study
Primary completion· ClinicalTrials.gov
Stelara and Tremfya Pregnancy Exposure Registry OTIS Autoimmune Diseases in Pregnancy Project

Past events

2026
Trial started· ClinicalTrials.gov
Optimal Care With Guselkumab in Crohn's Disease / OPTIM Study A Prospective Open Label Interventional, Multicenter Study
Trial started· ClinicalTrials.gov
Costa Rican Registry of IL-23 Inhibitors in Psoriatic Disease
Trial started· ClinicalTrials.gov
A Study of JNJ-78934804 in Participants With Moderately to Severely Active Ulcerative Colitis
Trial started· ClinicalTrials.gov
A Study of JNJ-78934804 in Participants With Moderately to Severely Active Crohn's Disease
Results posted· ClinicalTrials.gov
Study of Guselkumab Versus Placebo for the Treatment of Low Body Surface Area Moderate Plaque Psoriasis
Trial started· ClinicalTrials.gov
A Study of Guselkumab Versus Risankizumab in Participants With Moderately to Severely Active Crohn's Disease
Trial started· ClinicalTrials.gov
An Observational, Multicenter Study to Evaluate the Effectiveness of Guselkumab for the Treatment of Participants With Crohn's Disease After
Trial started· ClinicalTrials.gov
Switching to the IL-23 Inhibitor Guselkumab for People With Active IBD Who Previously Used Ustekinumab (SHIFT-IBD)
Trial started· ClinicalTrials.gov
A Prospective Cohort Study Evaluating the Efficacy and Safety of Guselkumab (GUS) With JAK Inhibitors in Patients With Difficult-To-Treat In
2025
Trial started· ClinicalTrials.gov
A Study to Evaluate the Efficacy of Guselkumab in Chinese Participants With Crohn's Disease (CD)
Results posted· ClinicalTrials.gov
A Study of Guselkumab Therapy in Participants With Moderately to Severely Active Ulcerative Colitis
Results posted· ClinicalTrials.gov
Guselkumab in Active Psoriatic Arthritis Participants With Inadequate Response/Intolerance to One Prior Anti-TNF Alpha Agent
Trial started· ClinicalTrials.gov
Shared Pathways Between Non-Alcoholic Fatty Liver Disease and Psoriatic Disease With Guselekumab Therapy
Primary completion· ClinicalTrials.gov
Shared Pathways Between Non-Alcoholic Fatty Liver Disease and Psoriatic Disease With Guselekumab Therapy
Primary completion· ClinicalTrials.gov
Potential Role of Guselkumab in Modulating PAIN Perception and Related Gene Pathways: a Proof-of-concept Study.
Trial started· ClinicalTrials.gov
Ultrasound and Proteomics for Guselkumab Response Assessment in Crohn's Disease (UPGRADE).
Trial started· ClinicalTrials.gov
Real-Life Evaluation of Guselkumab Dosing Interval Adjustments
Trial started· ClinicalTrials.gov
Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty
Trial started· ClinicalTrials.gov
A Study of Guselkumab Administered Subcutaneously in Treatment of Indian Participants With Psoriatic Arthritis (PsA)
Results posted· ClinicalTrials.gov
A Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell Arteritis
Trial started· ClinicalTrials.gov
Elucidating Shared Mechanisms Contributing to NAFLD and PsA Disease Severity With Guselkumab Therapy
Primary completion· ClinicalTrials.gov
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Crohn's Disease
Results posted· ClinicalTrials.gov
A Study of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease
Primary completion· ClinicalTrials.gov
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcerative Colitis
Results posted· ClinicalTrials.gov
A Study of the Efficacy and Safety of Guselkumab in Participants With Moderately to Severely Active Crohn's Disease
Results posted· ClinicalTrials.gov
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Guselkumab for the Treatment of Chronic Plaque
Results posted· ClinicalTrials.gov
A Study of Guselkumab Subcutaneous Therapy in Participants With Moderately to Severely Active Crohn's Disease
Results posted· ClinicalTrials.gov
Effect of Guselkumab on Cardiovascular Risk Surrogate Markers in Participants With Moderate to Severe Plaque Psoriasis
2024
Results posted· ClinicalTrials.gov
A Study of Guselkumab in Participants With Moderately to Severely Active Ulcerative Colitis
Results posted· ClinicalTrials.gov
A Study of Guselkumab for the Treatment of Participants With Crohn's Disease After Surgical Resection
Primary completion· ClinicalTrials.gov
Guselkumab in Active Psoriatic Arthritis Participants With Inadequate Response/Intolerance to One Prior Anti-TNF Alpha Agent
Trial started· ClinicalTrials.gov
A Study to Evaluate Comparative Efficacy and Safety of Guselkumab in High-dose and Extended-interval Versus Standard-dose in Chinese Partici
Trial started· ClinicalTrials.gov
Potential Role of Guselkumab in Modulating PAIN Perception and Related Gene Pathways: a Proof-of-concept Study.
Primary completion· ClinicalTrials.gov
A Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell Arteritis
Trial started· ClinicalTrials.gov
VOICE-Early Response to Vedolizumab and IL-23 Antagonists in Participants With Crohn's Disease: A Prospective Observational Study
Trial started· ClinicalTrials.gov
A Study of Guselkumab in Pediatric Participants With Moderately to Severely Active Crohn's Disease
Trial started· ClinicalTrials.gov
A Study of Guselkumab in Pediatric Participants With Moderately to Severely Active Ulcerative Colitis
Results posted· ClinicalTrials.gov
Efficacy and Safety of Brodalumab Compared With Guselkumab in the Treatment of Plaque Psoriasis After Inadequate Response to Ustekinumab
2023
Results posted· ClinicalTrials.gov
A Study of Efficacy and Safety of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcer
Primary completion· ClinicalTrials.gov
A Study of Guselkumab in Naive or Bio-experienced Participants With Regional (Facial and Genital) Psoriasis
Trial started· ClinicalTrials.gov
Study of Guselkumab Versus Placebo for the Treatment of Low Body Surface Area Moderate Plaque Psoriasis
Primary completion· ClinicalTrials.gov
Effect of Guselkumab on Cardiovascular Risk Surrogate Markers in Participants With Moderate to Severe Plaque Psoriasis
Primary completion· ClinicalTrials.gov
A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Subcutaneously Administered Guselkumab for the Treatment of Chronic Plaque
Primary completion· ClinicalTrials.gov
A Study of Guselkumab Subcutaneous Therapy in Participants With Moderately to Severely Active Crohn's Disease
Results posted· ClinicalTrials.gov
A Study to Evaluate Further Therapeutic Strategies With Guselkumab in Participants With Moderate-to-Severe Plaque-Type Psoriasis
Trial started· ClinicalTrials.gov
A Study of Guselkumab for the Treatment of Participants With Crohn's Disease After Surgical Resection
2022
Trial started· ClinicalTrials.gov
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcerative Colitis
Trial started· ClinicalTrials.gov
A Study of Guselkumab Therapy in Participants With Moderately to Severely Active Ulcerative Colitis
Primary completion· ClinicalTrials.gov
Efficacy and Safety of Brodalumab Compared With Guselkumab in the Treatment of Plaque Psoriasis After Inadequate Response to Ustekinumab
Trial started· ClinicalTrials.gov
A Study of Ustekinumab or Guselkumab in Pediatric Participants With Active Juvenile Psoriatic Arthritis
Trial started· ClinicalTrials.gov
A Study of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Crohn's Disease
Trial started· ClinicalTrials.gov
Study of Guselkumab in Skin of Color Participants With Moderate-to-severe Plaque and/or Scalp Psoriasis
Primary completion· ClinicalTrials.gov
A Study to Evaluate Further Therapeutic Strategies With Guselkumab in Participants With Moderate-to-Severe Plaque-Type Psoriasis
Trial started· ClinicalTrials.gov
A Study of Guselkumab Subcutaneous Therapy in Participants With Moderately to Severely Active Crohn's Disease
2021
Trial started· ClinicalTrials.gov
Effect of Guselkumab on Cardiovascular Risk Surrogate Markers in Participants With Moderate to Severe Plaque Psoriasis
Trial started· ClinicalTrials.gov
A Study of Guselkumab and Risankizumab in Healthy Participants and Participants With Psoriatic Arthritis
Trial started· ClinicalTrials.gov
A Study of Guselkumab and Golimumab Combination Therapy in Participants With Active Psoriatic Arthritis
Trial started· ClinicalTrials.gov
Guselkumab in Active Psoriatic Arthritis Participants With Inadequate Response/Intolerance to One Prior Anti-TNF Alpha Agent
Primary completion· ClinicalTrials.gov
A Study of Subcutaneously-administered Guselkumab Delivered by 3 Different Devices in Healthy Participants
Trial started· ClinicalTrials.gov
A Study of Guselkumab Administered Subcutaneously in Bio-naive Participants With Active Psoriatic Arthritis Axial Disease
Trial started· ClinicalTrials.gov
A Study of Guselkumab and Interleukin-17 (IL-17) Inhibitor Therapies in Participants With Psoriatic Arthritis in Routine Clinical Practice
Trial started· ClinicalTrials.gov
A Study of Guselkumab (TREMFYA) in Chinese Participants With Moderate to Severe Plaque Psoriasis
Primary completion· ClinicalTrials.gov
A Study of Intravenous Formulation of Guselkumab Using Prefilled Syringes and Final Vialed Product in Healthy Participants
Results posted· ClinicalTrials.gov
A Study to Evaluate the Efficacy, Safety, and Tolerability of Guselkumab for the Treatment of Participants With Moderate to Severe Hidradeni
Recall· FDA
Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by: Janssen Biotech, Inc., Horsham, PA 19044; NDC 57894-640-01.
2020
Primary completion· ClinicalTrials.gov
Study of Guselkumab and Ustekinumab Following a Single Intravenous or Subcutaneous Administration in Healthy Chinese Participants
Trial started· ClinicalTrials.gov
Efficacy and Safety of Brodalumab Compared With Guselkumab in the Treatment of Plaque Psoriasis After Inadequate Response to Ustekinumab
Trial started· ClinicalTrials.gov
A Study to Evaluate Guselkumab for the Treatment of Participants With New-onset or Relapsing Giant Cell Arteritis
Primary completion· ClinicalTrials.gov
A Study of Efficacy and Safety of Combination Therapy With Guselkumab and Golimumab in Participants With Moderately to Severely Active Ulcer
Trial started· ClinicalTrials.gov
A Study of Intravenous Formulation of Guselkumab Using Prefilled Syringes and Final Vialed Product in Healthy Participants
Primary completion· ClinicalTrials.gov
A Study of Guselkumab in Participants With Active Psoriatic Arthritis and an Inadequate Response to Anti-Tumor Necrosis Factor Alpha (Anti-T
Results posted· ClinicalTrials.gov
A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis
Results posted· ClinicalTrials.gov
A Study Evaluating the Efficacy and Safety of Guselkumab Administered Subcutaneously in Participants With Active Psoriatic Arthritis Includi
Results posted· ClinicalTrials.gov
Efficacy and Safety Study of Guselkumab in the Treatment of Participants With Active Psoriatic Arthritis (PsA)
Results posted· ClinicalTrials.gov
A Study of Ixekizumab (LY2439821) Compared to Guselkumab in Participants With Moderate-to-Severe Plaque Psoriasis

Sources

FDA approvals, label revisions, and recalls come from the public openFDA APIs (Drugs@FDA, Drug Label, Drug Enforcement). Drug-safety communications come from the FDA RSS feed. Trial milestones come from ClinicalTrials.gov via the AACT pg dump. Pivotal-publication events come from PubMed, filtered to high-impact journals linked to a Phase 3 trial in our inventory.