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Low-dose Methotrexate for Change in Global Initiative for Asthma Step 5 Medications in Chronic Severe Asthma

Low-dose Methotrexate for Change in Global Initiative for Asthma Step 5 Medications in Chronic Severe Asthma: a Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02124226
Enrollment
102
Registered
2014-04-28
Start date
2021-12-31
Completion date
2022-07-31
Last updated
2021-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Dose Methotrexate in Severe Chronic Asthma

Keywords

Chronic severe asthma, immunomodulation, methotrexate, steroids, omalizumab

Brief summary

Patients with chronic severe asthma (CSA) have a crippling disease and current available treatments are not satisfactory. Thus, management of CSA remains a major unmet need. Although the evidence from existing randomized controlled trials fails to support a definite role for immunomodulatory drugs in these patients due to major methodologic drawbacks, findings with low-dose methotrexate (MTX) are encouraging. However, larger and well designed clinical trials are required to establish the beneficial role of MTX in CSA and for the detection of the key characteristics of those who are going to respond to this drug. This study will be the first multi-centre RCT investigating the role of an add-on immunological modifier as a clinically useful therapeutic strategy in patients with well-phenotyped chronic severe asthma. As such, this study does not overlap with any other research currently ongoing.

Detailed description

Patients will be recruited from the accessible asthmatic patients lists of tertiary referral centers. All patients will meet the stringent diagnostic criteria for CSA, including the requirement for the regular use of Step 5 medications (i.e. oral prednisone and/or omalizumab). The experimental design of the proposed study will take the form of a double-blind parallel-randomized placebo-controlled trial consisting of a total of eight visits including run-in and run-out periods. Patients will be randomly allocated to receive either MTX or matched placebo once a week as add-on therapy to their existing medication after run-in. Physiological, laboratory and clinical assessments will be measured regularly throughout the study and compared with baseline assessments. We expect that MTX will reduce Step 5 medications dosage in patients with CSA without compromising the overall disease control. Improvement in several indicators of asthma severity and control will be also investigated

Interventions

DRUGMethotrexate

7.5 mg/week + folic acid the day after

DRUGPlacebo

matched placebo

Sponsors

Universita degli Studi di Catania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Caregiver)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. patients with a diagnosis of CSA taking GINA Step 5 medications (i.e. regular OCS and/or omalizumab for a minimum of 6 months); 2. failure in weaning patients completely from Step 5 medications during run-in; 3. male and female individuals age 18 - 75 years; 4. patients must be able to provide consent;

Exclusion criteria

1. use of immunomodulatory therapies in the preceding 3 months; 2. recent or current history of alcoholism; 3. high liver enzyme levels (greater than 2.5 times the upper limit of the normal range); 4. serum creatinine levels greater than 2.0 mg/dL 5. acute illness within 15 days of study medication administration; 6. leucopenia (below 3.0x109/L) and/or thrombocytopenia (below 100x109/L). 7. pregnancy or planning to become pregnant;

Design outcomes

Primary

MeasureTime frame
At least 50% reduction in total dosage of GINA step 5 medications80 weeks

Secondary

MeasureTime frame
clinically significant changes in clinimetric scores80 weeks

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026