AMelioration of Angiotensin Converting Enzyme Inhibitor Induced Angioedema Study

Angioedema Clinical Trial

Official title:

A Multicenter Study, Randomized, Double-blind With 2 Groups as Prove of Concept for the Treatment of ACEI Induced Angioedema With Subcutaneous Icatibant

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01154361
• Other study ID #: AMACE
• Status: Completed
• Phase: Phase 2
• First received: June 29, 2010
• Last updated: December 22, 2011

Study information

• Verified date: December 2011
• Source: Technische Universität München
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Regierung von Oberbayern
• Study type: Interventional

Clinical Trial Summary

This is a multicenter study recruiting patients with angioedema induced by ACEI.

Open-label treatment with subcutaneous Icatibant compared to a historic group of 47 patients with ACE inhibitor induced angioedema which the investigators have been previously treated in the investigators centers with current "standard" therapy (250 mg methylprednisolon and 2 mg clemastine).

In cases with fast progression of edema after application the study-drug, a second application with icatibant could be necessary. Rescue medication and intervention.

Description:

Sudden occurrence of subcutaneous or submucosal non-itchy swelling, so-called angioedema, is a well known side effect of angiotensin-converting enzyme inhibitors (ACEi), which may become life-threatening if the upper airway is involved. To be note, ACEi induced angioedema were always located in the head and neck region.

The pathophysiology of ACE inhibitor (ACEi) induced angioedema most likely resembles that of hereditary angioedema (HAE), i.e. it is mainly mediated by bradykinin induced activation of vascular bradykinin B2 receptors (BKR-2). In contrast to an increased bradykinin generation in HAE, treatment with ACEi decreases the bradykinin degradation in plasma and increases the biological activity of bradykinin.

The current pharmacotherapy of ACEi induced angioedema is not satisfactory. Antihistamines and corticosteroids may be effective in the treatment of urticaria with cutaneous edema and itchy, but are theoretically ineffective and hence superfluous in bradykinin induced angioedema. However, glucocorticoids still belong to the standard treatment of angioedema.

We hypothesized that the BKR-2 antagonist icatibant might be an effective therapy for ACEi-induced angioedema.

Patients with ACEi induced angioedema, located in the upper aero-digestive tract will be randomized and treated either with icatibant and plazebo or cortisone with clemastin and plazebo.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 84 Years

Eligibility

Inclusion Criteria:

• Age >= 18 <85 years

• Patient is currently treated with an ACEI

• Patient must have acute angioedema attack caused by an ACEI

• Treatment should be administrated within 10 hrs after onset by an ACEI

• Patient with angioedema of head and /or neck (face, lips, cheeks, tongue, soft palate/uvula, pharynx and larynx)

• At least one moderate to severe severe angioedema symptom as assessed by the investigator, requiring a medical intervention

• Signed written Informed Consent Form

Exclusion Criteria:

• Diagnosis of angioedema that was not caused by ACEI: e.g. hereditary angioedema (C1-INH deficiency), allergy, anaphylaxis, insect bite, trauma, infection, abscess, tumor, post-radiation or post-operative or processes related to salivary glands and others where it is unlikely that the ACEI is causing the angioedema

• Participation in a clinical trial of another investigational medicinal product (IMP) within 30 days

• Patients with acute urticaria

• Patients with a medical history of any angioedema before taking an ACEI

• Patients with an acute rash or hives in the face or somewhere else

• Unstable angina or acute myocardial infarction

• Acute heart failure

• Serious concomitant illnesses that the physician considers to be a contraindication for participation in the trial

• Pregnancy and/or breast-feeding

• Mental condition rendering the patients, in the opinion of the investigator, unable to understand the nature, scope and possible consequences of the study;

• Unlikely to comply with the protocol, e.g., uncooperative attitude, inability to return for the follow-up visit, or unlikely to complete the study for any reason.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Angioedema

Intervention

Drug:
• Icatibant (subcutaneous) and plazebo (intravenous)

• Cortisone + Clemastin (intravenous) and plazebo (subcutaneous)

Locations

Country	Name	City	State
Germany	Klinikum rechts der Isar Hals-Nasen-Ohrenklinik der TUM	Munich	Bavaria

Sponsors (1)

Lead Sponsor	Collaborator
Technische Universität München

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time to complete resolution of angioedema