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AbbVie (ABBV) Highlights Robust Gastroenterology Portfolio with New Data in Crohn's Disease and Ulcerative Colitis at the UEG Week

September 29, 2022 7:02 AM

AbbVie (NYSE: ABBV) today revealed the spectrum of new data from studies of risankizumab (SKYRIZI®) in Crohn's disease and upadacitinib (RINVOQ®) in ulcerative colitis and Crohn's disease that will be presented as live presentations and e-Posters at the United European Gastroenterology (UEG) Week 2022, October 8-11 in Vienna and online. In total, AbbVie is presenting 17 abstracts across a broad range of studies in inflammatory bowel disease (IBD).

"With two decades of world-class science and an unwavering commitment to patients, we continue to advance research within our robust gastro portfolio with the goal of positively impacting the lives of people living with inflammatory bowel disease," said Chiedzo Mpofu, MBChB, Ph.D., vice president, Global Medical Affairs, Immunology, AbbVie. "Our data at UEG Week 2022 reinforce our dedication to innovation and partnership with the gastroenterology community to help address a wide range of patient needs and investigate diverse solutions to help advance standards of care for IBD patients."

Key data to be presented include:

* The use of upadacitinib and risankizumab are investigational in Crohn's disease in the European Union.

AbbVie abstracts in the UEG Week 2022 program include:

Abstract Title

Session Details (All Times CEST)

Risankizumab / Crohn's Disease

Induction and Maintenance Treatment with Risankizumab Leads to Symptomatic Relief in Patients with Moderate to Severe Crohn's Disease

e-Poster Presentation P0437

Sunday, Oct 9

9 a.m.

Fatigue Improvement Correlates with Reductions in Work Productivity Impairment and Related Indirect Cost in Patients with Crohn's disease: Post Hoc Analysis of Two Phase 3 Risankizumab Induction Trials

e-Poster Presentation P0980

Sunday, Oct 9

9 a.m.

Baseline and Early Predictors of Response to Risankizumab Induction and Maintenance Treatment in Patients with Moderate to Severe Crohn's Disease

Live Moderated Poster

MP442

Monday, Oct 10

14:06 – 14:12 p.m.

52-Weeks Risankizumab Subcutaneous Maintenance Dosing is Efficacious and Well Tolerated in Patients with Moderate to Severe Crohn's Disease Who Had Delayed Response to 12-Weeks IV Risankizumab Induction

Live Oral Presentation OP126

Monday, Oct 10

14 – 14:12 p.m.

Clinical and Endoscopic Improvements with Risankizumab Induction and Maintenance Dosing Versus Placebo are Observed Irrespective of Number of Prior Failed Biologics

Live Oral Presentation OP128

Monday, Oct 10

14:24 – 14:36 p.m.

Upadacitinib / Ulcerative Colitis

Efficacy and safety of upadacitinib in patients with moderately to severely active ulcerative colitis receiving 16 weeks' extended induction treatment followed by 52 weeks' maintenance treatment in the U-ACHIEVE/U-ACCOMPLISH trials

e-Poster Session

P0440

Sunday, Oct 9

9 a.m.

Efficacy and safety of upadacitinib maintenance therapy in patients with moderately to severely active ulcerative colitis: Final results from the Phase 3 U-ACHIEVE Maintenance study

Live Oral Presentation

OP001

Sunday, Oct 9

13:55 – 14:07 p.m.

Benefit-risk assessment of upadacitinib treatment in patients with moderately to severely active ulcerative colitis

Live Moderated Poster

MP243

Monday, Oct 10

11:12 – 11:18 a.m.

Matching-Adjusted Indirect Comparison of Upadacitinib Versus Vedolizumabas Induction Therapy in Patients With Moderately to Severely Active Ulcerative Colitis

Live Moderated Poster

MP244

Monday, Oct 10

11:18 – 11:24 a.m.

Benefits of high versus low dose upadacitinib as maintenance treatment in ulcerative colitis patients who were responders to 8-week induction with upadacitinib: Results from the U-ACHIEVE phase 3 maintenance trial

Live Oral Presentation

OP197

Tuesday, Oct 11

11:24 – 11:36 a.m.

Symptoms and Laboratory Values as Proxies for Endoscopic and Histologic Clinical Endpoints in Ulcerative Colitis: A Mediation Analysis Based on Upadacitinib Phase 3 Induction Trials

Live Moderated Poster

MP409

Tuesday, Oct 11

11:48 – 11:54 a.m.

Efficacy of Upadacitinib Dose Escalation in Phase 3 Long-term Extension Ulcerative Colitis Study

Live Oral Presentation

OP199

Tuesday, Oct 11

11:48 – 12:00 p.m.

Impact of Inflammatory Burden on Efficacy of Upadacitinib Maintenance Therapy in Ulcerative Colitis: Results from the Phase 3 U-ACHIEVE Study

Live Moderated Poster

MP441

Tuesday, Oct 11

14 – 14:06 p.m.

Upadacitinib / Crohn's Disease

Efficacy and Safety of Upadacitinib Induction Therapy in Patients with Moderately to Severely Active Crohn's Disease: Results from a Randomized Phase 3 U-EXCEL Study

Live Oral Presentation

OP219

Monday, Oct 10

14:36 – 14:48 p.m.

Disease State Abstracts / Inflammatory Bowel Disease

Steroid use in a high proportion of IBD patients – first results from the German cohort of the IBD-DICE study

e-Poster Presentation

P0436

Sunday, Oct 9

9 a.m.

Patient-reported burden of corticosteroid use in inflammatory bowel disease in the UK: results from the Determinants, Incidence and Consequences of Corticosteroid Excess (DICE) impact questionnaire

Live Oral Presentation

OP107

Monday, Oct 10

11:12 – 11:24 a.m.

Patterns of corticosteroid exposure and excess in inflammatory bowel disease: Results from the Determinants, Incidence and Consequences of Corticosteroid Excess (DICE) online monitoring tool

Live Moderated Poster

MP110

Sunday, Oct 9

15:54 – 16 p.m.

The full scientific program for the UEG Week 2022 is available here.

Risankizumab (SKYRIZI) is part of a collaboration between Boehringer Ingelheim and AbbVie, with AbbVie leading development and commercialization globally.

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