60 Participants NeededMy employer runs this trial

Mirikizumab for Crohn's Disease

(MIRIAD Trial)

Recruiting at 4 trial locations
SA
AC
JE
Overseen ByJennifer Earle
Age: 18+
Sex: Any
Trial Phase: Phase 4
Sponsor: Alimentiv Inc.
Must be taking: Oral corticosteroids
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Prior Safety DataThis treatment has passed at least one previous human trial

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to test the safety and effectiveness of mirikizumab, a treatment for Crohn's disease, specifically for people with strictures (narrowed sections) in the intestines. Participants will receive mirikizumab through a series of injections to determine if it helps manage their symptoms and improves their condition. It suits adults who have had Crohn's disease affecting their ileum (part of the small intestine) for at least three months, experience abdominal pain after eating, and have certain types of intestinal narrowing. As a Phase 4 trial, this research seeks to understand how this already FDA-approved and effective treatment can benefit more patients.

Do I have to stop taking my current medications for the trial?

Participants can continue taking certain medications for Crohn's Disease, like oral 5-ASA drugs, sulfasalazine, AZA, 6-MP, MTX, rectal therapies, antidiarrheal drugs, and bile acid sequestrants, as long as they have been stable for a specified period before the trial. However, some medications like cyclosporine, tacrolimus, and certain biologics must be stopped before the trial. Participants on corticosteroids must be willing to taper off after 8 weeks.

What is the safety track record for this treatment?

Research has shown that mirikizumab is generally safe for people with Crohn's disease. Studies have found that patients can use mirikizumab safely for extended periods, with many experiencing significant improvements. Specifically, using mirikizumab for up to 104 weeks helped heal the gut and control symptoms effectively. Safety data over several years indicate that patients often remain in remission without needing steroids, which supports its safety. Overall, mirikizumab has a positive safety record for treating moderate-to-severe Crohn's disease, with no major safety issues reported in the studies.12345

Why are researchers enthusiastic about this study treatment?

Mirikizumab is unique because it targets the p19 subunit of interleukin-23, a protein involved in inflammation, which is different from many existing Crohn's disease treatments that target other inflammatory pathways, like TNF inhibitors. Researchers are excited about Mirikizumab because it offers a new mechanism of action, potentially providing relief for patients who do not respond well to current therapies. Additionally, its administration starts with an intravenous dose and transitions to a subcutaneous form, which can offer both rapid initial relief and convenient ongoing treatment.

What is the effectiveness track record for mirikizumab in treating Crohn's disease?

Research has shown that mirikizumab can help treat Crohn's disease. In some studies, up to 96% of patients experienced significant symptom improvement, and about 87% saw their symptoms become minimal or disappear. Another study found that 60.5% to 67.1% of patients showed improvement in intestinal inflammation. These findings suggest that mirikizumab could be a promising option for effectively managing Crohn's disease symptoms.12367

Are You a Good Fit for This Trial?

This trial is for adults (18+) with Crohn's disease who have a narrowing in their small intestine causing some blockage symptoms, but do not need urgent surgery or hospitalization. Participants must be stable on certain medications and able to eat enough food, even if they need to modify their diet.

Inclusion Criteria

My symptoms are manageable, and I have maintained my weight for the past 4 weeks.
I am at least 18 years old and not pregnant or breastfeeding.
My bowel has a narrowed area that is 50% or less of the normal width.
See 7 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

5 weeks
Includes MRE and ileocolonoscopy

Treatment

Participants receive 900 mg mirikizumab IV Q4W to Week 12 and then 300 mg mirikizumab SC Q4W to Week 24

24 weeks
Routine safety assessments at clinic visits

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks
Safety Follow-up Visit can be performed by telephone

What Are the Treatments Tested in This Trial?

Interventions

  • Mirikizumab

Trial Overview

The study tests mirikizumab, a medication given to about 60 people with Crohn's-related intestinal strictures. All participants receive the drug; there is no comparison group. The main goal is to see how safe and effective mirikizumab is for this condition.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: MirikizumabExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Alimentiv Inc.

Lead Sponsor

Trials
15
Recruited
3,300+

Citations

1.

pubmed.ncbi.nlm.nih.gov

pubmed.ncbi.nlm.nih.gov/41794217/

Mirikizumab Long-Term Efficacy and Safety in Patients with ...

Results: In the efficacy population, 60.5%(mNRI)/67.1%(OC) achieved endoscopic response, 37.9%/41.7% achieved endoscopic remission, and 73.4%/ ...

Mirikizumab Long-Term Efficacy and Safety in Patients ...

In the efficacy population, 60.5% (mNRI) and 67.1% (OC) achieved endoscopic response, 37.9% and 41.7% achieved endoscopic remission, and 73.4% ...

DOP046 Effectiveness and Safety of Mirikizumab after ...

Mirikizumab (Miri), an interleukin-23p19 inhibitor, has shown strong efficacy and was well-tolerated in patients with moderately-to-severely active Crohn's ...

Lilly's mirikizumab is first and only IL23p19 antagonist to ...

96% of patients had clinical response as measured by the Crohn's Disease Activity Index (CDAI); 87% were in clinical remission as measured by ...

Mirikizumab is Safe and Effective for Moderate-to-Severe ...

Results: Both co-primary endpoints were met for mirikizumab versus placebo: endoscopic response-composite 38.0% vs 9.0% (P <0.01) and CDAI ...

Study Details | NCT07059130 | Evaluating the Efficacy and ...

Evaluating the Efficacy and Safety of Mirikizumab in Adults Over 60 With Moderate to Severe Crohn's Disease and Ulcerative Colitis.

S1446 Efficacy and Safety of Long-Term Mirikizumab...

Mirikizumab (miri), an anti-IL-23p19 antibody, was efficacious and safe as a treatment for moderately-to-severely active Crohn's disease (CD) over 104 weeks ...