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NCT Number: NCT05394805

A Study of Subcutaneous HUMIRA (Adalimumab) Injection to Assess Adverse Events and Change in Disease Activity In Adult Participants With Moderate to Severe Active Crohn's Disease (CD)

Crohn's disease (CD) is an incurable chronic inflammatory disorder of the gastrointestinal tract. This study will assess how safe and effective Humira (adalimumab) is in treating moderately to severely active CD in China. Adverse events and change in disease activity will be assessed.

Humira (adalimumab) is a drug approved for the treatment of Crohn's disease (CD).All study participants will receive Humira as prescribed by their study doctor in accordance with approved local label. Approximately 252 participants will be enrolled in China.

Participants will receive subcutaneous HUMIRA (adalimumab) injection as prescribed by their physician according to their routine clinical practice and local label. Participants will be followed for 1 year.

There is expected to be no additional burden for participants in this trial. Participants will attend regular visits during the study at a hospital or clinic according to their routine clinical practice.

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Key information

Conditions

Crohn's Disease Crohn Disease Digestive System Diseases Gastroenteritis Gastrointestinal Diseases Inflammatory Bowel Diseases Intestinal Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Peking University Third Hospital /ID# 242803, Beijing, Beijing Municipality, China

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants meet the diagnosis of moderate to severe Crohn's disease.
  • Participants prescribed with Humira, under investigators' sufficient consideration of benefits/ risks per local label.

Exclusion criteria

  • Participants who have any of the contraindications as per adalimumab (Humira) label in China.
  • Participants who are allergic to any component of adalimumab (Humira).
  • Participants with active hepatitis B diagnosed.
  • Participants with severe active infection, or known history of active or latent tuberculosis (TB), or latent TB infection with inadequate treatment.
  • Participants with cancer diagnosed, excluding also those with non-melanoma skin cancer (NMSC) completely treated, per local label.
  • Participants with moderate to severe heart failure.
  • Participants who are unwilling to participate, or not suitable for participation as judged by the investigator at risk of noncompliance to study procedure.
  • Participants who are enrolled to other interventional studies.
  • Participants who are prescribed with adalimumab but choose Humira bio-similar in China.

Treatment and study plan

Primary outcomes

  1. Number of Participants with Serious Adverse Events (SAEs)

    Time frame: Upto week 52

    An adverse event (AE) is defined as any untoward medical occurrence in a participant or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. The investigator assesses the relationship of each event to the use of study. A serious adverse event (SAE) is an event that results in death, is life-threatening, requires or prolongs hospitalization, results in a congenital anomaly, persistent or significant disability/incapacity or is an important medical event that, based on medical judgment, may jeopardize the participant and may require medical or surgical intervention to prevent any of the outcomes listed above.

Secondary outcomes

  1. Number of Participants With Serious Adverse Drug Reaction (ADR)

    Time frame: Upto week 52

    Adverse drug reactions were defined as adverese events (AEs) of which a causal relationship with adalimumab could not be ruled out.

  2. Number of Participants With Non-Serious Adverse Drug Reaction (ADR)

    Time frame: Upto week 52

    Adverse drug reactions were defined as adverese events (AEs) of which a causal relationship with adalimumab could not be ruled out.

  3. Number of Participants who Achieved Clinical Remission Harvey-Bradshaw index (HBI)

    Time frame: Upto week 52

    The HBI is a simplified version of the Crohn's Disease Activity Index(CDAI). The HBI consists of 5 items encompassing patient-reported (well-being, symptoms)and objective (presence of abdominal mass or complications) variables. The total HBI score is the sum of the values for each of the five items. Higher HBI scores indicate greater disease activity. Scores < 5 indicate clinical remission, 5 - 7 indicate mild disease, 8 - 16 indicate moderate disease, and 16 indicate severe disease.

  4. Number of Participants who Achieved Clinical Response Harvey-Bradshaw index (HBI)

    Time frame: Upto week 52

    The HBI is a simplified version of the Crohn's Disease Activity Index(CDAI). The HBI consists of 5 items encompassing patient-reported (well-being, symptoms)and objective (presence of abdominal mass or complications) variables. The total HBI score is the sum of the values for each of the five items. Higher HBI scores indicate greater disease activity. A reduction of 3 points and above is considered as relevant to define clinical response harvey-bradshaw index (HBI).

Sponsors and collaborators

Lead sponsor

AbbVie

Industry

Registry information

Official study title

A One-year Non-Interventional Registry to Assess Safety and Effectiveness of HUMIRA® (Adalimumab) in Patients With Moderately to Severely Active Crohn's Disease (CD) in China

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
May 27, 2022
Registry last updated
Nov 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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