Clinical Burden of Anemia in Inflammatory Bowel Disease: Therapeutic Trial

Summary

Participation Requirements

Description

Anemia is the most common extraintestinal manifestation of inflammatory bowel diseases (IBD). Most cases of anemia in IBD are due to iron deficiency (IDA) and to anemia of inflammation (AI) (Bergamaschi et al, 2010). Guidelines by the European Crohn's and Colitis Organisation (ECCO) suggest that iro...

Anemia is the most common extraintestinal manifestation of inflammatory bowel diseases (IBD). Most cases of anemia in IBD are due to iron deficiency (IDA) and to anemia of inflammation (AI) (Bergamaschi et al, 2010). Guidelines by the European Crohn's and Colitis Organisation (ECCO) suggest that iron supplementation should be started when IDA is present or even in the presence of iron deficiency without anemia (Dignass et al, 2015). However, many IBD patients with IDA are not properly treate, probably due to the belief that mild to moderate degrees of anemia may not have a significant impact on the patient's quality of life, that oral iron supplementation may adversely affect disease activity, and that parenteral iron administration may cause severe side effects. In this study the investigators will compare three iron supplementation regimens (two iv iron formulations and one oral iron integrator) for the treatment of IDA in patients with IBD in terms of both efficacy and safety. Participation to the trial does not involve additional risks for the patients. In fact, the trial does not require additional diagnostic procedures beyond those that are usually performed in IBD patients and the drugs that will be use din the trial are already used in patients with IBD and IDA. According to WHO criteria (WHO scientific groupl, 1968), anemia is defined as Hb <13.0 g/dL in males and Hb <12 g/dL in females (Blanc et al, 1968). A serum ferritin <30 µg/L or a serum ferritin ?100 µg/L with transferrin saturation <20% are required for the diagnosis of isolated IDA and of IDA associated with inflammation, respectively. 300 subjects with IDA and IBD will be recruited in a multicenter trial and randomized 1:1:1 to the three iron replacement arms. Expected duration of subject participation to the trial will be 24 weeks for each patient, consisting of an 8 week treatment period, with follow-up visits at weeks 4, 8, 12 and 24 from treatment start. Study participants can be participating in other research, either observational or interventional, or other drug research concerning the treatment of IBD. Iron gluconate and FCM are licensed for use in Italy and will be used according to AIC. Iron gluconate will be part of the normal hospital stock. FCM will be purchased through an IG-IBD donation to the Fondazione IRCCS Policlinico San Matteo. Microsomial iron is a formulation for oral administration commercially available in Italy as an iron integrator; for the study, however, it will be provided free of charge from Pharmanutra S.r.l. Concomitant therapy No other iron supplementation is allowed during the trial. Vitamin integrators containing folic acid, vitamin B12 and vitamin D or calcium are allowed, as well as any other treatment for IBD and related comorbidities; therefore, study patients can be treated with topic and systemic mesalazine and steroids, or with immunosuppressors (azathioprine, mercaptopurine, cyclosporine, methotrexate) and biologic immunomodulators (infliximab, adalimumab, golimumab) commonly used in IBD patients; pain relievers and antibiotics (the latter for either infection treatment or profilaxis) can be used without restrictions. Procedures and assessments Laboratory assessments can be performed outside the participating Centers, and results faxed or emailed to the Investigators who will register data in the eCRF. Result notification to the trial team must be performed as soon as possible. Safety/Adverse events (AE)/Serious AE (SAE) review as well as treatment compliance review at scheduled time points will be included during every visit. This will be included specifically in the list of assessments. Subject Registration Subjects will be registered locally and assigned a registration number/code. This number, together with the Center code, will constitute the unique patient identification code. Only the patient physicians must be able to identify the patient from the assigned code. Randomization will be performed by the Coordinator Center. Baseline assessments All patients will have a full medical history taken and a clinical examination. The following data points are to be recorded: a) Weight in Kg b) Gender c) Age (year of birth) d) Any significant past medical history e) CDAI and CAI disease activity scores for CD and UC respectively f) Full blood count (including platelets and differential white cell count) g) Biochemical series: including creatinine, serum iron, transferrin, serum ferritin, C reactive protein (PCR), folic acid, vitamin B12 and urine pregnancy test for women of childbearing potential (these are mandatory tests; further biochemical parameters useful for the study are reported in the CRF) h) Tests for HIV, HCV, HBsAg, QuantiFERON TB-2G (QuantiFERON is not necessary in patients previously treated for latent or active TB as per local standard of care) i) IBDQ score, VAS evaluation of fatigue J) Actual treatment k) Chest radiograph l) A blood sample (two 1.5 mL serum vials) will be obtained and stored at -20° C. Timing of assessments Follow-up will be performed at weeks 4, 8, 12 and 24. The following data are to be recorded: Physical examination Adverse Event Review Weight in Kg e) Full blood count f) Biochemical series g) IBDQ score, VAS evaluation of fatigue h) Actual treatment i) One blood sample (two 1.5 mL serum vials) will be obtained at the week 8 follow-up visits and stored at -20° C. Long-Term Follow-up Assessments After the end of the study patients will be followed-up as usual for their conditions. Telephone calls will be used to contact patients if visits or data collection time-points are missed; whenever data collection will be impossible, the patient will be identified as 'lost to follow-up'. Patients will be expected to return to normal standard of care following their participation in the trial. Trial restrictions Women of childbearing potential participating in the trial are required to use adequate contraception for the duration of the trial and for 3 months after the completion of the trial/last treatment. This includes: Intrauterine Device (IUD) Hormonal based contraception (pill, contraceptive injection or implant etc) Barrier contraception (condom and occlusive cap e.g. diaphragm or cervical cap with spermicide) True abstinence (where this is in accordance with the patients preferred and usual lifestyle) Men are not required to use contraception and do not need to refrain from donating sperm for the duration of the trial and any period thereafter. Assessment of efficacy will be performed at 4, 8, 12 and 24 weeks after the start of treatment and will be based on determination of complete blood counts. Other informations concerning laboratory parameters, quality of life, clinical course, serum hepcidin and inflammatory cytokine concentrations will be gathered at the scheduled follow-up visits. Data analysis Primary endpoint: the rate of response will be compared between groups with the Fisher exact test. The combined iv regimens will be compared to the oral regimen at the 5.0% significance level. Difference in response rate (iv regimens - oral regimen) and 95% confidence interval will be computed. If the lower limit of the confidence interval for the difference in rates is above 15%, the non-inferiority limit, non-inferiority will be claimed. If non inferiority is shown overall, 97.5% confidence intervals will be computed for the difference of oral vs each i.v. regimen and non-inferiority will be assessed as above. Finally if non inferiority against the combined iv regimen is shown, superiority will be tested at the same 5% level. Further paired comparisons will be performed using the Bonferroni correction and will be considered descriptive only. The primary endpoint will be analyzed both in the intention to treat and in the per-protocol (PP) population. In a non inferiority setting. The PP population represents the primary population. Data handling and record keeping All data will be transferred into an electronic Case Report Form (eCRF) identified by a patient code. All trial data in the eCRF will be extracted from and be consistent with the relevant source documents. The eCRFs will be completed, dated and electronically signed by the investigator or designee in a timely manner. It remains the responsibility of the investigator for the timing, completeness and accuracy of the eCRF pages. The eCRF will be accessible to trial coordinators, data managers, the investigators, Clinical Trial Monitors, Auditors and Inspectors as required. The investigator will maintain a logbook with patients identification and the allocated codes in the investigator study file. Remote data-entry will be performed through the RedCap platform by each investigator. A paper copy of the eCRF will be provided with the investigator study file. Remote monitoring of the eCRF completeness and incongruences will be performed at the clinical trial center of the coordinating center and queries will be submitted to the investigators as appropriate. The investigator will also supply the trial coordination Center with any required, background information from the medical records as required. Data should be entered into the database within 2 months of the patient visit being completed. The investigators may retain copies of the eCRF in the relevant sections of their Investigator Site File with any required coded background information from the medical records as required. Source Data The investigators agree to keep records of all participating patients: sufficient information to link eCRFs, hospital records and samples, all original signed informed consent forms and copies of the CRFs, Patient Medical Records, On-line test results, sample logs. Data Safety Monitoring Board/Trial Steering Committee The study has been planned in Pavia by Prof. A. Di Sabatino, Dr. G. Bergamaschi and Prof. G.R. Corazza, from the Department of Internal Medicine, and DR. C. Klersy, Servizio di Biometria, all from Fondazione IRCCS Policlinico San Matteo; they represent the Trial Steering Committee. Consent The Informed Consent is in compliance with GCP, local regulatory requirements and legal requirements. Informed consent from each patient or the patient's legally acceptable representative will be obtained before any trial-specific activity is performed. The informed consent form used and any change made during the course of this trial, will be submitted to the REC. The investigator will retain the original of each patients signed informed consent form. Should a patient require a verbal translation of the trial documentation by a locally approved interpreter/translator, it is the responsibility of the individual investigator to use locally approved translators. Any new information which becomes available, which might affect the patient's willingness to continue participating in the trial, will be communicated to the patient as soon as possible. This may occur either verbally over the telephone, or at their next visit (if visits are close together). Regulatory Compliance The trial started after approval by the National Competent Authority and by the Ethics Committees of the participating Centers. The protocol and trial conduct will comply with the Medicines for Human Use (Clinical Trials) Regulations 2004. The trial will be performed in accordance with the spirit and the letter of the declaration of Helsinki, the conditions and principles of Good Clinical Practice, the protocol and applicable local regulatory requirements and laws. Sponsorship, Financial and Insurance The trial has obtained financial support from IG-IBD for patients' insurance, FCM procurement and FCM and microsomial iron shipment to participating Centers. Microsomial iron will be provided for free from Pharmanutra S.r.l.

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