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At Labstica, we are dedicated to innovation, collaboration, and seamless growth.

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Clinical Trials (Phase I–IV) - Our Scientific & Research Expertise

At our center, we are committed to advancing gastrointestinal care through research. Our Phase I–IV clinical trials offer eligible patients early access to innovative therapies for Ulcerative Colitis (UC) and Crohn’s Disease (CD) – conditions that impact quality of life and often require long-term management. Whether you’re newly diagnosed or haven’t responded to current medications, a clinical trial could provide new options while contributing to medical advancements.

What Are Clinical Trials?

Clinical trials are research studies that evaluate the safety, effectiveness, and side effects of new medications or therapies. Trials are conducted in phases:

  • Phase I – Safety and dosage
  • Phase II – Effectiveness and side effects
  • Phase III – Comparison with current standard treatments
  • Phase IV – Post-marketing surveillance and long-term data
Current Focus Areas

We are actively enrolling patients for research in the following areas:

  • Moderate to Severe Ulcerative Colitis
  • Moderate to Severe Crohn’s Disease
  • Biologic therapies (e.g., anti-TNF, JAK inhibitors, IL-12/23 blockers)
  • Novel small molecules and monoclonal antibodies
  • Drug comparisons for patients naive to targeted therapies

Each study is sponsored by leading pharmaceutical or biotech companies, including AbbVie, Roche-Genentech, and Mirador Therapeutics.

Benefits of Participation
  • No-cost access to investigational treatment
  • Thorough medical evaluations and diagnostics
  • Regular monitoring by IBD specialists
  • Travel support (if eligible)
  • Contribution to future therapies
Who Can Participate?

Eligibility depends on each study. In general, you may qualify if:

  • You are aged 18–80
  • You have a confirmed diagnosis of Ulcerative Colitis or Crohn’s Disease
  • You’ve had an inadequate response or intolerance to standard medications
  • You are not currently on conflicting investigational drugs
  • You do not have severe comorbidities or active infections

To check your eligibility, contact our clinical trial coordinator or use the form below.

Who Can Participate?

Eligibility depends on each study. In general, you may qualify if:

  • You are aged 18–80
  • You have a confirmed diagnosis of Ulcerative Colitis or Crohn’s Disease
  • You’ve had an inadequate response or intolerance to standard medications
  • You are not currently on conflicting investigational drugs
  • You do not have severe comorbidities or active infections

To check your eligibility, contact our clinical trial coordinator or use the form below.

What to Expect
  • Pre-Screening: Medical history review and initial eligibility check
  • Screening Visit: Lab tests, endoscopy (if needed), and informed consent
  • Trial Participation: Regular visits, medication administration, and progress monitoring
  • Follow-Up: Post-treatment observation and care

Every participant receives personalized care throughout the trial under a dedicated medical team.

Why Choose Us?
  • Internationally recognized IBD research site
  • State-of-the-art endoscopy and lab facilities
  • Experienced principal investigators and IBD specialists
  • Strong partnerships with global sponsors and CROs
  • Compassionate support and clear communication

Get in Touch With Us

    Common Questions About Clinical Trials

    What is a clinical trial?
    A clinical trial is a research study designed to learn how our bodies respond to medicines or other treatments.
    Who can take part in clinical trials?
    Eligibility depends on the trial. Some trials recruit patients with a specific disease or condition, while others enroll healthy volunteers.
    Where do the ideas for clinical trials come from?
    Ideas usually come from researchers who test treatments in labs. Promising ones are moved into trials for human testing.
    What are different types of clinical trials?
    Types include:
    • Treatment Trials: Test new treatments or drug combinations.
    • Prevention Trials: Study ways to prevent disease.
    • Diagnostic Trials: Improve testing methods.
    • Screening Trials: Test ways to detect diseases.
    • Quality of Life Trials: Focus on patient comfort during illness.
    Who pays for clinical trials?
    Sponsors may include doctors, institutions, charities, pharmaceutical companies, or government bodies like the NIH.
    Where do clinical trials take place?
    Trials may be conducted in hospitals, universities, community clinics, or doctor’s offices.
    What is a control group?
    A control group receives a standard treatment or placebo to compare outcomes with the investigational group.
    What are side effects and adverse events?
    Side effects are additional effects of treatment. Adverse events are medical problems that may or may not be caused by the trial treatment.
    How is my safety protected if I take part in a clinical trial?
    Every trial is reviewed by an IRB and follows a detailed protocol to ensure participant safety. Issues can halt or pause the trial if needed.
    Will I keep working with my doctor while I'm in a clinical trial?
    Yes, your doctor will coordinate with the trial team to ensure your overall care continues smoothly.
    Can I leave a clinical trial after it has started?
    Yes, you can leave any time. Inform the trial team for a safe exit and proper support.
    Can I get the trial treatment if I don't qualify to take part?
    You may be eligible for “expanded access” if your condition is serious and other treatments aren’t effective. This must be approved by regulatory authorities.
    How should I prepare for a meeting with the trial coordinator or doctor?
    • Write down questions in advance
    • Bring someone along
    • Record the meeting if permitted
    • Ask to take home the Informed Consent Form to review