Mode
Text Size
Log in / Sign up
Phase 2 N=118 Randomized Quadruple-blind Treatment

Study to Assess the Efficacy and Safety of CJM112 in Patients With Inadequately Controlled Severe Asthma

Asthma

Enrolled (actual)
118
Serious AEs
4.2%
Results posted
Aug 2020
Primary outcome: Primary: Change From Baseline in Forced Expiratory Volume in One Second (FEV1) — 0.043; 0.016 Liters — p=0.7374

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
CJM112 (Drug); Placebo to CJM112 (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Novartis Pharmaceuticals
Primary completion
Apr 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Forced Expiratory Volume in One Second (FEV1)
0.043; 0.016 0.7374
SECONDARY
Change From Baseline in Forced Expiratory Volume 1 (FEV1) % of Predicted
1.064; 0.151 0.263
SECONDARY
Change From Baseline in Asthma Control Questionnaire 6 (ACQ6) Score
-0.93; -0.71 0.061
SECONDARY
Change From Baseline in Asthma Control Questionnaire 7 (ACQ7) Score
-0.83; -0.60 0.040 sig
SECONDARY
Percentage of Patients With at Least 0.5 Decrease in ACQ7 Score
38; 19
SECONDARY
Percentage of Patients With Adverse Events (AEs) Leading to Discontinuation of Study Treatment
8; 4

Summary

An unmet medical need exists for patients with moderate and severe asthma who continue to demonstrate symptoms despite being on standard of care medications, and are not eligible for other biologic therapies developed or in development for T2-high(allergic/eosinophilic) asthma. The purpose of this study was to determine if CJM112, an anti-IL-17A antibody, displayed the clinical efficacy and safety profile to support further development in patients with inadequately controlled moderate to severe asthma with low IgE and low circulating eosinophil levels.

Eligibility Criteria

Inclusion Criteria

  • Patients with a physician-diagnosed history of moderate to severe asthma for a period of at least one year prior to screening.
  • Patients on a stable therapy regimen of asthma for at least 3 months prior to screening with at least medium dose inhaled glucocorticoid and at least one additional asthma controller medication (such as inhaled long-acting bronchodilator, leukotriene antagonist, theophylline, stable low dose glucocorticoid, etc).
  • Acceptable and reproducible spirometry with FEV1 ≥ 40 and ≤ 90% of predicted at screening and baseline (re-testing is allowed once).
  • ACQ score ≥ 1.5 at screening and baseline (re-testing is allowed once).
  • Total serum IgE < 150 IU/mL
  • Peripheral blood eosinophils <300/μL

Exclusion Criteria

  • Previous use of biologics or other concomitant medications within the time periods specified in the SOM/protocol.
  • History of ongoing, chronic, or recurrent moderate or severe infectious disease.
  • Patients who have smoked or inhaled nicotine or tobacco products within the 6 month period prior to Visit 1 or who have a smoking history of greater than 10 pack years.
  • Patients who have had an asthma attack/exacerbation requiring systemic corticosteroids for at least 3 continuous days within 4 weeks prior to screening.
  • Patients who have had a respiratory tract infection or asthma worsening within 4 weeks prior to Visit 1 or during the screening period.
  • Women of child-bearing potential unless they use highly effective methods of contraception during dosing and for 13 weeks after stopping of investigational drug.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03299686). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search