Vedolizumab + Adalimumab/Ustekinumab for Crohn's Disease
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores the effectiveness of a combination of medications for individuals with moderate to severe Crohn's disease, which causes inflammation in the digestive tract. Participants will initially receive a mix of vedolizumab (Entyvio) with either adalimumab (Humira) or ustekinumab (Stelara) to determine if these combinations can manage symptoms. Those who benefit will then continue with vedolizumab alone to maintain improvement. Ideal participants are those who have tried other treatments for Crohn's but found them ineffective or intolerable. As a Phase 4 trial, the treatment is already FDA-approved and proven effective, with research helping to understand how it benefits more patients.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
What is the safety track record for these treatments?
Research has shown that vedolizumab, adalimumab, and ustekinumab are generally safe for treating Crohn's Disease. Vedolizumab has demonstrated a strong safety record across various studies, with some patients experiencing minor reactions at the injection site. Long-term use of vedolizumab has been positive for many patients, with few serious side effects reported.
When combined with adalimumab, studies indicate that this treatment is effective and maintains a good safety record. Some patients have reported mild side effects, which are usually easy to manage.
Similarly, combining vedolizumab with ustekinumab yields similar safety results. Research indicates both drugs generally have a low rate of serious side effects. Ustekinumab users reported a few adverse events, but these were not significantly different from those seen with vedolizumab.
Overall, these treatments are well-tolerated by most patients, with a low chance of serious side effects. Participants in clinical trials often report minor and manageable side effects, reflecting the treatments' established safety profiles.12345Why are researchers enthusiastic about this study treatment?
Unlike the standard treatments for Crohn's Disease, which often rely on single biologic agents, the investigational approach of combining Vedolizumab with either Adalimumab or Ustekinumab offers a novel synergy. Vedolizumab specifically targets the gut, potentially minimizing systemic side effects, while Adalimumab and Ustekinumab work through different immune pathways, offering a multi-faceted attack on inflammation. This combination therapy could provide enhanced efficacy for patients who do not respond adequately to conventional single-agent therapies. Researchers are hopeful that this dual-targeted approach will lead to better disease control and improved quality of life for patients.
What evidence suggests that this trial's treatments could be effective for Crohn's Disease?
Research shows that vedolizumab effectively treats Crohn's disease. One study found that 48% of people taking vedolizumab were symptom-free after one year. In this trial, participants in Part A, Cohort 1 will receive a combination of vedolizumab and adalimumab, which previous studies have shown resulted in 54.5% of patients being symptom-free after 26 weeks. Meanwhile, participants in Part A, Cohort 2 will receive a combination of vedolizumab and ustekinumab, which also seems promising for people with more difficult cases of Crohn's disease. These findings suggest that these treatments can help manage symptoms and improve the quality of life for those with moderate to severe Crohn's disease.46789
Who Is on the Research Team?
Study Director
Principal Investigator
Takeda
Are You a Good Fit for This Trial?
Adults with moderate to severe Crohn's Disease who have had an inadequate response, lost response, or intolerance to certain treatments. They must have a confirmed diagnosis for at least 3 months and meet specific disease severity scores. Not eligible if they've had extensive colon resections, certain infections like TB or HIV, previous nonresponse to multiple treatments, or any immunodeficiency.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment Part A
Participants receive dual targeted treatment with vedolizumab and either adalimumab or ustekinumab
Treatment Part B
Participants who achieve clinical remission in Part A receive vedolizumab monotherapy
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Adalimumab
- Ustekinumab
- Vedolizumab
Adalimumab is already approved in European Union, United States, Canada, Japan for the following indications:
- Rheumatoid arthritis
- Psoriatic arthritis
- Ankylosing spondylitis
- Crohn's disease
- Ulcerative colitis
- Plaque psoriasis
- Juvenile idiopathic arthritis
- Rheumatoid arthritis
- Psoriatic arthritis
- Ankylosing spondylitis
- Crohn's disease
- Ulcerative colitis
- Plaque psoriasis
- Juvenile idiopathic arthritis
- Hidradenitis suppurativa
- Rheumatoid arthritis
- Psoriatic arthritis
- Ankylosing spondylitis
- Crohn's disease
- Ulcerative colitis
- Plaque psoriasis
- Juvenile idiopathic arthritis
- Rheumatoid arthritis
- Psoriatic arthritis
- Ankylosing spondylitis
- Crohn's disease
- Ulcerative colitis
- Plaque psoriasis
- Juvenile idiopathic arthritis
Find a Clinic Near You
Who Is Running the Clinical Trial?
Takeda
Lead Sponsor
Dr. Naoyoshi Hirota
Takeda
Chief Medical Officer since 2020
MD from University of Tokyo
Christophe Weber
Takeda
Chief Executive Officer since 2015
PhD in Molecular Biology from Université de Montpellier