Adalimumab for the Management of Post-operative Crohn's Disease (CD)

NCT01629628 | Unknown Phase 3

• 1 other identifier: TASMC-10-ES-0446-TLV-CTIL
• Study Type: interventional
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

This study will be a prospective, open label, randomized, comparative study. Comparing the efficacy of adalimumab with immunomodulator therapy (i.e. 6-mercaptopurine, 6-MP), in maintaining remission of post-operative CD patients, with a high risk of disease recurrence. Patient assessment for efficacy will be conducted through interval endoscopic surveillance at 24 and 52 weeks. Patients in the adalimumab arm, showing endoscopic remission at 52 weeks of therapy, will be re-randomized to either maintain adalimumab therapy for an additional 52 weeks or conclude therapy. A third endoscopic assessment for these patients will be conducted at 104 weeks. The investigators expect a substantial increase in both endoscopic, as well as clinical remission rate in patients on adalimumab therapy.

Conditions

Crohn Disease

Keywords

Crohn Disease; Colitis Granulomatous; Crohn's Disease; Enteritis Regional; Ileitis Regional; Ileitis Terminal; Ileocolitis

Outcome Measures

Primary Outcomes (1)

• The proportion of patients with endoscopic recurrence at 12 months, as evaluated by the Rutgeerts endoscopic scoring system.

  Primay outcome measure will assess the efficacy of adalimumab, compared to immunomodulator therapy in maintaining mucosal healing after 52 weeks (1 year).

  52 weeks

Secondary Outcomes (1)

• Proportion of patients in clinical remission at 12 months as assessed by the CDAI score.

  52 weeks

Study Arms (2)

Adalimumab

EXPERIMENTAL

Drug: Adalimumab

6-mercaptopurine

ACTIVE COMPARATOR

Drug: 6 Mercaptopurine

Interventions

Adalimumab DRUG

Subcutaneous adalimumab injections, loading dose of 160 mg and 80 mg on 0 and 2 weeks and maintenance of 40 mg every other week for the duration of the study.

Also known as: Humira

Adalimumab

6 Mercaptopurine DRUG

6MP will be administered orally starting at a dose of 6MP of 50mg/day with escalating doses every 1-2 weeks as tolerated, to a target dose of 1-1.5 mg/kg. \--------------------------------------------------------------------------------

Also known as: Purinethol

6-mercaptopurine

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• years old at the time of screening
• Male or female
• Firs ileocolonic surgical resection (
• Evidence of both macroscopic as well an microscopic evidence of Crohn's disease in the resected intestinal segment
• Patient able to undergo pre randomization screening no earlier then 14 days and no later then 45 days post operatively.
• Patients may receive anti-TNF-agents (i.g. infliximab or adalimumab)previously
• Patients may receive corticosteroids, 6MP/AZA, methotrexate, or mesalamine prior to surgery.
• Antibiotics, or mesalamine, must be discontinued within the screening/baseline 4 week period. Patients on steroids may be enrolled as long as steroids are tapered off.
• Remission as defined by a CDAI ≤ 150.
• Women of childbearing potential, and men, must use medically acceptable methods of contraception \[surgical sterilization, IUD, hormonal preparations, or double barrier method (e.g. condom or diaphragm, and spermicide)\] throughout the study and for a period of 6 months after receiving the last injection.
• Screening lab results must be within prespecified limits: Hemoglobin ≥ 8.8 g/dl; SGOT/SGPT \< 3 X the upper limit of normal; Neutrophil count ≥ 1.0 X 109/L \& lymphocyte cont of ≥ 0.5 X 109/L
• Must have a documented PPD ≤ 5 mm, in patients taking steroids, within the month before randomization, or taking immunomodulators 2 months prior to randomization. Other patients must have documented PPD ≤ 10 mm prior to randomization. PPD must be preformed and documented by an appointed member of the investigatory stuff. Patients must have a normal chest radiograph (both posterior-anterior and lateral views), read by a certified radiologist, within 3 months prior to randomization.
• Commitment to adhere to study protocol requirements
• Negative stool cultures for enteric pathogens (Salmonella, Shigella, Campylobacter, Ova \& parasites), and negative clostridium difficile toxin assay in stool.
• Patients are able to self-inject or have a designee or healthcare professional who can inject the study medication at the appropriate intervals.

You may not qualify if:

• evidence of macroscopic inflammatory disease at the surgical margins or else ware, according to the surgeon
• Patients who discontinued anti TNF-alpha agents due to loss of efficacy or tolerability issues.
• Patients with temporary ileostomy.
• Patients with longstanding quiescent CD undergoing surgery for the treatment of a fibrostenotic lesion, without an active inflammatory disease process in the resected segment.
• Any of the following medications taken within 3 months prior to randomization: cyclosporine, tacrollimus, mycophenolate mofetil, or other investigational anti-inflammatory agents. Medication targeting the reduction of TNF-alpha (infliximab, golimumab, cetrolizumb pegol, etanercept), natalizumab, or other FDA approved biological agents may be administered up until to index surgery.
• Patient who have an ongoing active infection within the baseline period: intra-abdominal abscess, enteric infection as determined by stool cultures for bacteria, parasites and clostridium difficile toxin, other serious systemic bacterial infection within 3 months before randomization (e.g. Pneumonia; pyelonephritis; meningitis).
• Patients with active TB, patients in close contact to individuals with active TB, patients with latent TB whether receiving or not receiving prophylaxis.
• Patient that have or had an opportunistic infection within the last 6 months
• Patients seropositive to HIV, HBV, or HCV. Patients will be actively screened for HBV vaccination, and will be required to undergo vaccination according to international guidelines.
• Patients having current signs/symptoms of severe or progressive systemic disease: any progressive/uncontrolled renal, hepatic, hematologic, gastrointestinal, endocrine, pulmonary, cardiac, neurologic, or psychiatric illness.
• Patients after organ transplantation
• Any current or known malignancies
• Use of any investigational drug within 60 days prior to randomization
• Current/frequent use of NSAIDS (i.e. regular use of NSAIDS for more than 3 times a week for longer than 7 consecutive days during the trial period).
• Pregnant or lactating women

Sponsors & Collaborators

• Tel-Aviv Sourasky Medical Center: lead
• Abbott: collaborator

Study Sites (1)

Department of Gastroenterology and Liver Diseases, Tel-Aviv Soursky Medical Center

Tel Aviv, 64239, Israel

Location

Related Publications (2)

• Regueiro M, Schraut W, Baidoo L, Kip KE, Sepulveda AR, Pesci M, Harrison J, Plevy SE. Infliximab prevents Crohn's disease recurrence after ileal resection. Gastroenterology. 2009 Feb;136(2):441-50.e1; quiz 716. doi: 10.1053/j.gastro.2008.10.051. Epub 2008 Oct 31.

  PMID: 19109962 BACKGROUND

• Hirsch A, Scapa E, Fliss-Isakov N, Tulchinsky H, Itzkowitz E, Kariv Y, Ron Y, Yanai H, White I, Yassin S, Cohen NA, Brazovski E, Dotan I, Maharshak N. Early Initiation of Adalimumab Significantly Diminishes Postoperative Crohn's Disease Endoscopic Recurrence and Is Superior to 6-Mercaptopurine Therapy: An Open-Label, Randomized Controlled Study. J Clin Med. 2023 Dec 10;12(24):7600. doi: 10.3390/jcm12247600.

  PMID: 38137669 DERIVED

MeSH Terms

Conditions

Crohn Disease

Interventions

Adalimumab; Mercaptopurine

Condition Hierarchy (Ancestors)

Inflammatory Bowel Diseases; Gastroenteritis; Gastrointestinal Diseases; Digestive System Diseases; Intestinal Diseases

Intervention Hierarchy (Ancestors)

Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal; Antibodies; Immunoglobulins; Immunoproteins; Blood Proteins; Proteins; Amino Acids, Peptides, and Proteins; Serum Globulins; Globulins; Sulfhydryl Compounds; Sulfur Compounds; Organic Chemicals; Purines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds

Study Officials

• Erez F Scapa, M.D.

  Tel-Aviv Sourasky Medical Center, Affiliated to Tel-Aviv University

  PRINCIPAL INVESTIGATOR

• Iris Dotan, M.D.

  Tel-Aviv Sourasky Medical Center, Affiliated to Tel-Aviv University

  STUDY DIRECTOR

Central Study Contacts

Erez F Scapa, M.D.

CONTACT

972-52-4266345; erezs@tasmc.health.gov.il

Sara Pel, MPH

CONTACT

972-3-6973011; sarap@tasmc.health.gov.il

Study Design

• Study Type: interventional
• Phase: phase 3
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: PREVENTION
• Intervention Model: PARALLEL
• Sponsor Type: OTHER GOV
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: director, R&D Division

Study Record Dates

• First Submitted: June 19, 2012
• First Posted: June 27, 2012
• Study Start: July 1, 2012
• Primary Completion: July 1, 2016
• Study Completion: July 1, 2016
• Last Updated: June 27, 2012

Record last verified: 2012-06

Locations

IL (1)