Triple vs High Dose Inhaled CORticosteroids

Last updated: June 16, 2023
Sponsor: Galaxia Empírica
Overall Status: Active - Recruiting

Phase

4

Condition

Asthma

Treatment

To compare in both treatment arms the percentage of patients controlled at week 52.

Clinical Study ID

NCT05919394
TRICORDA
  • Ages 18-80
  • All Genders

Study Summary

Increase in inhaled corticosteroid dose vs triple therapy in T2-high asthma patients who remain uncontrolled with medium dose inhaled corticosteroids/long-acting β2 adrenergic combination: a real-life study.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Patients between 18 and 80 years of age diagnosed of uncontrolled asthma.
  • T2 high asthma: > 300 cels/mm3 blood Eos (current value) or 150 cels/mm3 blood Eos (current value) and a historical value ≥ 300 cels/mm3 or FENO ≥ 25 ppb (currentvalue).
  • Uncontrolled asthma, this is, ACT <20 and/or > 1 of an exacerbation in the last 12months, despite treatment with ICS/LABA at medium dose.
  • Written informed consent.

Exclusion

Exclusion Criteria:

  • Patients who refuse to sign the informed consent form.
  • Medical situation that prevents the collection of study information.
  • Diagnosis of severe uncontrolled asthma established with criteria other than thoseestablished (ACT <20 and/or > 1 exacerbation in the last 12 months, despite treatmentwith ICS / LABA at medium dose).
  • Medical or administrative situation that prevents the patient from following up to aminimum of 52 weeks.
  • Treatment with high dose ICS/LABA, LAMA, systemic corticosteroid, azithromycin,monoclonal antibody.

Study Design

Total Participants: 620
Treatment Group(s): 1
Primary Treatment: To compare in both treatment arms the percentage of patients controlled at week 52.
Phase: 4
Study Start date:
June 01, 2023
Estimated Completion Date:
September 30, 2024

Study Description

It remains to be clarified whether triple therapy is better than high dose inhaled corticosteroids and long-acting beta2-agonists combination (ICS/LABA) in patients with uncontrolled asthma despite the use of medium dose ICS/LABA combinations, particularly in cases with high T2 biomarkers´ values. The aim of this study is to evaluate, in a real-world setting, which is the best therapeutic strategy in this clinical scenario.

This study will be a randomized, open-label, two-arm, prospective, 12-month trial to be conducted in 53 hospital asthma units. Participants will be allocated to receive one of two therapeutic strategies: same ICS/LABA combination at highest doses or the same maintenance therapy plus a long-acting anticholinergic (LAMA). Follow up visits will be scheduled at 12-16, 24-28 and 52 weeks after the baseline visit. The investigators can optimise therapy according to their clinical opinion if the patient remains uncontrolled. Demographic, clinical and lung function information will be collected at each visit.

The primary endpoint will be the percentage of patients controlled at week 52, with both an ACT score of 20 or greater and no severe exacerbations). 620 patients (282 patients per treatment group, considering 10% drop-out) will be required for the study to have 80% power to detect non-inferiority limit of 10% in the rate of controlled patients between the high dose ICS/LABA arm and the triple therapy arm. All effectiveness analyses will be done according to the intention-to-treat principle. Secondary endpoints: percentage of patients controlled at week 24, ACT at weeks 12, 24 and 52, AIRQ at weeks 12, 24 and 52, quality of life (Mini-AQLQ) at weeks 12, 24 and 52, postbronchodilator FEV1 at weeks 12, 24 and 52, severe exacerbations at week 24 and 52. Differences between groups in 8 AM serum cortisol at week 52. Adherence at week 52 in the two study arms. Factors related to triple and high-dose ICS/LABA failure and success (control) at week 52.

The results of this study will help physicians to decide the most appropriate therapeutic strategy for a large number of asthma patients: those who do not gain control with medium dose ICS/LABA. If non-inferiority of triple therapy vs high dose ICS/LABA is demonstrated, it could lead to a modification of the current guidelines.

Connect with a study center

  • Hospital Comarcal de Inca - Tramuntana

    Inca, Baleares 07300
    Spain

    Active - Recruiting

  • Hospital Universitario Son Espases

    Palma De Mallorca, Baleares 07120
    Spain

    Active - Recruiting

  • Hospital Universitario de Cruces

    Barakaldo, Bizkaia 48903
    Spain

    Active - Recruiting

  • Hospital Universitario Galdakao-Usansolo

    Galdakao, Bizkaia 48960
    Spain

    Active - Recruiting

  • Hospital Universitario De Jerez

    Jerez De La Frontera, Cádiz 11407
    Spain

    Active - Recruiting

  • Hospital Universitario de Navarra

    Pamplona, Navarra 31008
    Spain

    Active - Recruiting

  • Hospital de Sagunto

    Sagunto, Valencia 46520
    Spain

    Active - Recruiting

  • Hospital Costa del Sol

    Marbella, Álaga 29603
    Spain

    Active - Recruiting

  • Hospital Universitario de A Coruña

    A Coruña, 15006
    Spain

    Active - Recruiting

  • Hospital General Universitario Dr. Balmis de Alicante

    Alicante, 03010
    Spain

    Active - Recruiting

  • Hospital de la Santa Creu i Sant Pau

    Barcelona, 08025
    Spain

    Active - Recruiting

  • Hospital Universitario Clínico San Cecilio

    Granada, 18016
    Spain

    Active - Recruiting

  • Hospital Universitario Virgen de las Nieves

    Granada, 18014
    Spain

    Active - Recruiting

  • Hospital Universitario Lucus Augusti

    Lugo, 27003
    Spain

    Active - Recruiting

  • Hospital Universitario Ramón y Cajal

    Madrid, 28034
    Spain

    Active - Recruiting

  • Hospital Clínico Universitario de Salamanca

    Salamanca, 37007
    Spain

    Active - Recruiting

  • Hospital Universitario Doctor Peset

    Valencia, 46017
    Spain

    Active - Recruiting

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