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Asthma controller therapies (incl. prednisone/prednisolone)Wiki

Developed by Shray Alag
Clinical Trial MeSH HPO Drug Gene SNP Protein Mutation


Correlated Drug Terms (4)


Name (Synonyms) Correlation
drug232 Asthma reliever therapies Wiki 1.00
drug796 Dupilumab (SAR231893/REGN668) Wiki 1.00
drug519 Cannabidiol Wiki 1.00
drug1738 PLACEBO Wiki 0.71

Correlated MeSH Terms (1)


Name (Synonyms) Correlation
D001249 Asthma NIH 0.50

Correlated HPO Terms (1)


Name (Synonyms) Correlation
HP:0002099 Asthma HPO 0.50

There is one clinical trial.

Clinical Trials


1 One Year Study to Evaluate the Long-term Safety and Tolerability of Dupilumab in Pediatric Patients With Asthma Who Participated in a Previous Dupilumab Asthma Clinical Study

Primary Objective: To evaluate the long-term safety and tolerability of dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study. Secondary Objectives: - To evaluate the long-term efficacy of dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study. - To evaluate dupilumab in pediatric patients with asthma who participated in a previous dupilumab asthma clinical study with regard to: - Systemic exposure. - Anti-drug antibodies (ADAs). - Biomarkers.

NCT03560466 Asthma Drug: Dupilumab (SAR231893/REGN668) Drug: Asthma controller therapies (incl. prednisone/prednisolone) Drug: Asthma reliever therapies
MeSH:Asthma
HPO:Asthma

Primary Outcomes

Description: The number (n) and percentage (%) of patients experiencing any TEAE

Measure: Treatment-emergent adverse events (TEAEs)

Time: From Day 1 up to Week 64

Secondary Outcomes

Description: Annualized rate of severe asthma exacerbation events, during the treatment period

Measure: Severe asthma exacerbation events

Time: From Day 1 up to Week 52

Description: Change in percentage (%) predicted forced expiratory volume in 1 second (FEV1) - Clinically significant changes from baseline

Measure: Change in % predicted FEV1

Time: From Day 1 up to Week 64

Description: Change in absolute FEV1 - Clinically significant changes from baseline

Measure: Change in absolute FEV1

Time: From Day 1 up to Week 64

Description: Change in forced vital capacity (FVC)

Measure: Change in FVC

Time: From Day 1 up to Week 64

Description: Change in forced expiratory flow (FEF) 25-75%

Measure: Change in FEF

Time: From Day 1 up to Week 64

Description: Serum dupilumab concentrations - Changes from first dupilumab injection

Measure: Assessment of dupilumab concentration

Time: From Day 1 up to Week 64

Description: Titers of Anti-dupilumab antibodies

Measure: Assessment of immunogenicity

Time: From Day 1 up to Week 64

Description: Blood: Eosinophil count

Measure: Assessment of blood Eosinophil count

Time: From Day 1 up to Week 64

Description: Serum: total IgE

Measure: Assessment of total immunoglobulin E (IgE)

Time: From Day 1 up to Week 64


Related HPO nodes (Using clinical trials)