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Advancing Clinical Research in Gastroenterology and Liver Disease Pioneering Innovative Studies to Improve Digestive and Liver Health Outcomes Globally
Specialized Research in Gastroenterology and Hepatology From IBD to NAFLD, Our Studies target Critical Needs in Digestive and Liver Disorders
About Integrity Advanced Therapeutics (cibra)
Advancing Research in Gastroenterology and Liver Disease

At CIBRA, the clinical research arm of Continental Hospitals, Hyderabad, we lead transformative studies focused on Gastroenterology, Hepatology, and Liver Transplantation. Our trials are built on global best practices and designed to generate real-world patient outcomes.

Scientific Excellence

We follow global standards such as ICH-GCP and FDA protocols to ensure precision-driven, ethical clinical trials.

Patient-Centered Approach

Our research places patients at the core—ensuring clarity, safety, and compassionate care from consent to follow-up.

Driving Innovation in Liver and Digestive Research with Compassionate Care

At CIBRA, every study is guided by compassion and clinical excellence. Our board-certified investigators and research professionals work together to accelerate discoveries in digestive and liver health. We bridge science and empathy to bring tomorrow’s treatments to today’s patients—safely, ethically, and effectively.

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Why choose us?
Clinical Research Backed by Science, Built Around Patients

At CIBRA, we blend scientific precision with a patient-first mindset to deliver meaningful clinical outcomes across digestive and liver health.

Expert Investigators

Led by experienced, board-certified clinical researchers in hepatology, oncology, and gastroenterology.

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Regulatory Compliance

Our trials strictly follow FDA, DCGI, and ICH-GCP standards for safety, ethics, and transparency.

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Trusted Partnerships

Collaborating with leading CROs, pharma sponsors, and academic institutions globally.

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Patient-Centered Design

We prioritize comfort, clarity, and care—from informed consent to post-trial follow-up.

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Rapid Study Start-Up

Agile processes for fast site activation and efficient patient onboarding.

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On-Site Pharmacy & Infusion Support

Seamless delivery and administration of investigational therapies through integrated facilities.

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  • Clinical Research Excellence
  • Patient-Centered Innovation
  • Gastroenterology & Liver Studies
  • FDA-Compliant Trials
  • Advancing Healthcare Outcomes
  • Precision-Driven Clinical Trials
  • Clinical Research Excellence
  • Patient-Centered Innovation
  • Gastroenterology & Liver Studies
  • FDA-Compliant Trials
  • Advancing Healthcare Outcomes
  • Precision-Driven Clinical Trials
How We Work
A Smarter, Patient-Centered Approach to Clinical Research
01

Strategic Study Design

We create scientifically sound, FDA- and ICH-GCP-compliant protocols tailored to patient needs and trial objectives. Each study is crafted for maximum regulatory success, clinical impact, and translational value.

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02

Seamless Patient Experience

From informed consent to follow-up, every touchpoint is built for comfort, clarity, and trust. We ensure patients feel supported and informed at every phase of their clinical journey.

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03

Precise Execution & Compliance

With rigorous oversight and operational excellence, we ensure high-quality data, ethical standards, and full regulatory adherence. Our team consistently meets FDA, DCGI, and GCP standards—without compromising efficiency.

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  • Clinical Research Excellence
  • Patient-Centered Innovation
  • Gastroenterology & Liver Studies
  • FDA-Compliant Trials
  • Advancing Healthcare Outcomes
  • Precision-Driven Clinical Trials
  • Clinical Research Excellence
  • Patient-Centered Innovation
  • Gastroenterology & Liver Studies
  • FDA-Compliant Trials
  • Advancing Healthcare Outcomes
  • Precision-Driven Clinical Trials

Get in Touch With Us

    What to Consider Before Participating in a Clinical Trial?

    You should know as much as possible about the clinical trial and feel comfortable asking members of the study team questions about it, the care expected while in a trial and the cost of the trial.  To make the right decision for yourself, it helps to know what questions to ask.  You want to be well-informed and feel safe with your decision about joining a clinical trial. Some of the answers to these questions will be found in the informed consent form and process, but there are other questions to consider asking and discussing with the study team:

    • What is the purpose of the study?
    • Who is going to be in the study?
    • Does the study involve a placebo or a treatment already on the market?
    • Why do researchers believe the new treatment being tested may be effective? Has it been tested before and have the results been published?
    • What kinds of tests and treatments are involved?
    • How do the possible risks, side effects, and benefits in the study compare with my current treatment?
    • How might this trial affect my daily life?
    • How long with the trial last, and what will I be asked to do as a participant?
    • Will hospitalization be required?
    • Can anyone find out if I’m participating?
    • Who will pay for the treatment? Will my insurance cover the costs?
    • Will I be reimbursed for other expenses like travel or childcare?
    • What type of long-term follow-up care is part of this study?
    • How will I know that the treatment is working? Will results of the trials be provided to me?
    • If the treatment works for me, will I be able to continue using it once the trial is over?
    • Who will be in charge of my care? Will I be able to see my own doctor?
    • What are the credentials and research experience of the physician and study staff?
    • Does the physician/investigator have any financial or special interest in the clinical study?
    • What will happen to my medical care if I stop participating?

    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