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Proof of Concept Study of Rilzabrutinib in Adult Participants With Moderate-to-severe Asthma

Phase 2
Completed
Conditions
Asthma
Interventions
Drug: placebo
Registration Number
NCT05104892
Lead Sponsor
Sanofi
Brief Summary

This is a parallel, treatment, Phase 2, double-blind, 2 arm, 12-week Proof of Concept (PoC) study with 2 staggered cohorts (2 arms in each cohort) that is designed to assess the efficacy, safety, and tolerability of rilzabrutinib in adult participants (aged 18-70 years) with moderate-to-severe asthma who are not well controlled on ICS/LABA therapy. Study treatment includes investigational medicinal product (IMP) (rilzabrutinib or placebo) added-on to a background therapy of ICS/LABA (fluticasone/salmeterol \[non-investigational medicinal product\], standardized at screening). Background therapy of ICS/LABA will be withdrawn during the 12week randomized treatment period and resumed at the end of the IMP treatment period, as outlined below:

* Screening period (4 weeks)

* Randomized IMP treatment period (12 weeks ± 3 days)

* Background therapy stabilization phase (4 weeks)

* Background therapy withdrawal phase (4-5 weeks)

* No background therapy phase (3-4 weeks)

* Post IMP treatment safety follow-up period (4 weeks ± 3 days)

Detailed Description

The total study duration per participant is expected to be up to 20 weeks: up to 4 weeks screening, 12 weeks on-treatment double-blind period, and 4-week post-IMP treatment follow up.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
196
Inclusion Criteria
  • A physician diagnosis of asthma for at least 12 months based on the Global Initiative for Asthma (GINA) 2018,2019, 2020 Guidelines.
  • Participants with existing treatment with at least moderate to high doses of ICS therapy in combination with a LABA as second controller for at least 3 months with a stable dose ≥1 month prior to Visit 1.
  • Participants with prebronchodilator FEV1 >40% of predicted normal at Visit 1/Screening. Prebronchodilator FEV1 ≥50% of predicted normal at Visit 2/Baseline.
  • Participants with reversibility of at least 12% and 200 mL in FEV1 15 to 30 minutes after administration of 2 to 4 puffs (200-400 mcg) of albuterol/salbutamol or levalbuterol/levosalbutamol during screening or documented history of a reversibility test that meets this criterion within 5 years prior to Visit 1 or documented positive response to methacholine challenge (a decrease in FEV by 20% [PC20] of <8mg/mL) within 5 years prior to Visit 1/Screening is considered acceptable to meet this inclusion criterion.
  • Participants must have experienced, within 2 years prior to Visit 1, any of the following asthma exacerbation events at least once: Treatment with a systemic steroid (oral or parenteral) for worsening asthma OR Hospitalization or emergency medical care visit for worsening asthma.
  • Body mass index (BMI) ≥17.5 and ≤40 kg/m2
  • All Contraceptive use by men and women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
  • Participants must have completed COVID-19 vaccination per current regional health authority recommendations prior to screening.
Exclusion Criteria
  • History of serious infections requiring intravenous therapy with the potential for recurrence (as judged by Site Investigator), with less than 4 weeks interval between resolution of serious infection and first dose of study drug, or currently active moderate-to-severe infection at Screening (Grade 2 or higher).
  • Chronic lung disease (for example, chronic obstructive pulmonary disease [COPD], or idiopathic pulmonary fibrosis [IPF]) which may impair lung function, or another diagnosed pulmonary or systemic disease associated with elevated peripheral eosinophil counts, for e.g. eosinophilic granulomatosis with polyangiitis.
  • History of life-threatening asthma (i.e., severe exacerbation that requires intubation).
  • Participants with any of the following events within the 4 weeks prior to their Screening Visit 1 or during the screening period: Treatment with 1 or more systemic (oral and/or parenteral) steroid bursts for worsening asthma OR Hospitalization or emergency medical care visit for worsening asthma
  • Asthma Control Questionnaire 5-question version (ACQ-5) score <1.25 or >3.0 at V2/randomization. During the screening period an ACQ-5 of up to ≤4 is acceptable.
  • Current smoker or cessation of smoking within the 6 months prior to Visit 1.
  • Previous smoker with a smoking history >10 pack-years.
  • Current or chronic history of liver disease.
  • Known hepatic or biliary abnormalities, e.g. moderate or severe hepatic impairment, such as Child Pugh B or C
  • Symptomatic herpes zoster within 3 months prior to screening.
  • Refractory nausea and vomiting, malabsorption, external biliary shunt, or significant bowel resection that would preclude adequate rilzabrutinib/placebo absorption.
  • Conditions that may predispose the participant to excessive bleeding
  • History of solid organ transplant.
  • A history of malignancy of any type within 5 years before Day 1, other than surgically excised non-melanoma skin cancers or in situ cervical cancer.
  • Is not up-to-date with recommended vaccinations per local guidelines.
  • Anti-immunoglobulin E (IgE) therapy (e.g., omalizumab [Xolair®]) within 130 days prior to Visit 1 or any other biologic therapy (including anti-IL4/4R or IL-5/5R monoclonal antibodies [mAb]) or systemic immunosuppressant (e.g., methotrexate) to treat inflammatory disease or autoimmune disease (e.g., rheumatoid arthritis, inflammatory bowel disease, primary biliary cirrhosis, systemic lupus erythematosus, multiple sclerosis) and other diseases, within 2 months or 5 half-lives prior to Visit 1, whichever is longer.
  • Use of inhalers other than ICSs, LABAs, and short-acting beta agonists (no long-acting muscarinic antagonists (LAMAs) or mucolytics) and leukotriene receptor antagonists (montelukast, zafirkulast) during the study period.
  • Participants who have received bronchial thermoplasty within 2 years prior to Visit 1 or plan to begin therapy during the screening period or the randomized treatment period.
  • Use of proton pump inhibitor drugs such as omeprazole and esomeprazole within 3 days of Day 1.
  • Use of known systemic strong-to-moderate inducers or inhibitors of CYP3A within 14 days or 5 half-lives (whichever is longer) of Study Day 1 and until the end of the active treatment period.
  • Live vaccine except Bacille Calmette Guerinn-vaccination within 28 days prior to Day 1 or plans to receive one during the trial; Calmette Guerin-vaccination within 12 months prior to Screening.
  • COVID-19 vaccine within 14 days prior to Study Day 1.
  • Previous use of a Bruton tyrosine kinase (BTK) inhibitor.
  • Has received any investigational drug (or is currently using an investigational device) within the 30 days before Day 1, or at least 5 times the respective elimination half-life time (whichever is longer).
  • Electrocardiogram (ECG) findings of QT corrected for heart rate (QTc) >450 msec (males) or >470 msec (females), poorly controlled atrial fibrillation (i.e., symptomatic patients or a ventricular rate above 100 beats/min on ECG), or other clinically significant cardiovascular abnormalities.
  • Active COVID-19 infection as documented by a positive COVID-19 molecular test.

The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
RilzabrutinibRilzabrutinibRilzabrutinib BID or TID and ICS/LABA
PlaceboplaceboPlacebo and ICS/LABA
Primary Outcome Measures
NameTimeMethod
Proportion of participants with an LOAC event during the treatment periodUntil Week 12

Loss of Asthma Control (LOAC) event is defined as any of the following:

* A 30% or greater reduction from baseline in morning peak expiratory flow (PEF) on 2 consecutive days

* ≥6 additional reliever puffs of salbutamol/albuterol or levosalbutamol/levalbuterol in a 24-hour period (compared to baseline) on 2 consecutive days

* Increase in ICS ≥4 times the last prescribed ICS dose (or ≥50% of the prescribed ICS dose at V2 if background therapy withdrawal completed)

* Requiring use of systemic (oral and/or parenteral) steroid treatment

* Requiring hospitalization or emergency room visit for asthma exacerbation

Secondary Outcome Measures
NameTimeMethod
Pre-bronchodilator FEV1 (Forced expiratory volume in one second) change from baseline to EOT (end of treatment)From baseline to Week 12
Post-bronchodilator FEV1 change from baseline to EOTFrom baseline to Week 12
The absolute change in the percent predicted FEV1 from baseline to EOT (pre- and post-bronchodilator)From baseline to Week 12
Change from baseline in pre- and post-bronchodilator FEV1 and forced vital capacity [FVC] at each spirometry endpointFrom baseline until Week 12
Change from baseline in peak expiratory flow [PEF] and forced expiratory flow [FEF] 25-75% at each spirometry endpointFrom baseline until Week 12
Asthma Control Questionnaire-5 (ACQ-5) score change from baseline at EOT and at each assessment time pointFrom baseline until Week 12

The ACQ-5 is a questionnaire that measures the adequacy of asthma control and any changes in asthma control that may occur spontaneously or as a result of treatment. The ACQ-5 has five questions on the asthma symptoms and patients are asked to recall how their asthma has been during the previous week and to respond on a 7-point scale for each question (0 = no impairment, 6 = maximum impairment). The ACQ-5 score is the mean of the 5 questions and, therefore, between 0 (totally controlled) and 6 (severely uncontrolled). A high score indicates low asthma control.

Asthma Quality of Life Questionnaire with Standardized Activities (AQLQ[S]) Self-administered score change from baseline at EOT and at each assessment time pointFrom baseline until Week 12

The AQLQ(S) was designed as a self-administered patient reported outcome to measure the functional impairments that are most troublesome to adolescents and adults ≥12 years of age as a result of their asthma. The instrument is comprised of 32 items, each rated on a 7-point Likert scales from 1 to 7. Higher scores indicate better quality of life.

Change in Asthma Daytime Symptom Diary (ADSD) and Asthma Nighttime Symptom Diary (ANSD) scores from baseline to EOT and each weekFrom baseline until Week 12

ADSD and ANSD assess asthma severity based on patient self-report of asthma core symptoms, i.e., difficulty of breathing; wheezing; shortness of breath; chest tightness; chest pain; and cough. Both the ADSD and ANSD are composed of 6 items rated using an 11-point numerical rating scale (NRS) that ranges from 0 = None to 10 = As bad as you can imagine. The participants will record their daytime and nighttime asthma symptoms in an electronic diary, once in the evening and once in the morning, respectively.

Plasma pharmacokinetic (PK) concentrations of rilzabrutinib in participants with asthmaUntil Week 16
Change in numbers of inhalations/day of albuterol or levalbuterol for symptom relief from baseline to EOT and each weekFrom baseline until Week 12
Participants with Treatment Emergent Adverse EventsUntil Week 16

Trial Locations

Locations (51)

Investigational Site Number : 7240004

🇪🇸

Santander, Cantabria, Spain

Investigational Site Number : 1000004

🇧🇬

Kozloduy, Bulgaria

Investigational Site Number : 1000003

🇧🇬

Sevlievo, Bulgaria

Investigational Site Number : 6160002

🇵🇱

Krakow, Poland

Investigational Site Number : 4840003

🇲🇽

Durango, Mexico

Investigational Site Number : 4840004

🇲🇽

Veracruz, Mexico

Investigational Site Number : 6160007

🇵🇱

Lublin, Lubuskie, Poland

Investigational Site Number : 0320004

🇦🇷

Berazategui, Buenos Aires, Argentina

Investigational Site Number : 1520005

🇨🇱

Curicó, Maule, Chile

Investigational Site Number : 0320001

🇦🇷

Buenos Aires, Argentina

Investigational Site Number : 0320005

🇦🇷

Ciudad Autonoma Buenos Aires, Argentina

Investigational Site Number : 0320006

🇦🇷

Caba, Buenos Aires, Argentina

Investigational Site Number : 0320002

🇦🇷

Ciudad Autonoma Buenos Aires, Argentina

Investigational Site Number : 1520007

🇨🇱

Santaigo, Reg Metropolitana De Santiago, Chile

Investigational Site Number : 1520002

🇨🇱

Talca, Maule, Chile

Investigational Site Number : 1000001

🇧🇬

Ruse, Bulgaria

Investigational Site Number : 1000002

🇧🇬

Sofia, Bulgaria

Investigational Site Number : 1240006

🇨🇦

Vancouver, British Columbia, Canada

Investigational Site Number : 3480003

🇭🇺

Pécs, Hungary

Investigational Site Number : 4100004

🇰🇷

Seoul, Seoul-teukbyeolsi, Korea, Republic of

Investigational Site Number : 4100001

🇰🇷

Seoul, Korea, Republic of

Investigational Site Number : 6160003

🇵🇱

Bialystok, Podlaskie, Poland

Investigational Site Number : 6160006

🇵🇱

Gdansk, Pomorskie, Poland

Investigational Site Number : 6160008

🇵🇱

Ostrowiec Swietokrzyski, Swietokrzyskie, Poland

Investigational Site Number : 6160010

🇵🇱

Lodz, Poland

Investigational Site Number : 8260002

🇬🇧

Cambridge, Cambridgeshire, United Kingdom

Investigational Site Number : 8260001

🇬🇧

Bradford, United Kingdom

Investigational Site Number : 1520001

🇨🇱

Santiago, Reg Metropolitana De Santiago, Chile

Investigational Site Number : 1240005

🇨🇦

Waterloo, Ontario, Canada

Investigational Site Number : 6420001

🇩🇪

Dusseldorf, Germany

Investigational Site Number : 4100007

🇰🇷

Daegu, Daegu-gwangyeoksi, Korea, Republic of

Investigational Site Number : 4100002

🇰🇷

Seoul, Seoul-teukbyeolsi, Korea, Republic of

Investigational Site Number : 4100006

🇰🇷

Seoul, Seoul-teukbyeolsi, Korea, Republic of

Investigational Site Number : 4100005

🇰🇷

Seoul, Seoul-teukbyeolsi, Korea, Republic of

Investigational Site Number : 6160005

🇵🇱

Bialystok, Poland

Investigational Site Number : 6160009

🇵🇱

Poznan, Wielkopolskie, Poland

Investigational Site Number : 7240003

🇪🇸

Madrid / Madrid, Madrid, Comunidad De, Spain

Investigational Site Number : 6420002

🇷🇴

Cluj-Napoca, Romania

Investigational Site Number : 6160001

🇵🇱

Lodz, Poland

Investigational Site Number : 7240001

🇪🇸

Málaga, Spain

Investigational Site Number : 7920002

🇹🇷

Istanbul, Turkey

Investigational Site Number : 7920001

🇹🇷

Mersin, Turkey

Investigational Site Number : 0320003

🇦🇷

Caba, Buenos Aires, Argentina

Investigational Site Number : 1520004

🇨🇱

Santiago, Reg Metropolitana De Santiago, Chile

Investigational Site Number : 1520003

🇨🇱

Santiago, Reg Metropolitana De Santiago, Chile

Investigational Site Number : 3480001

🇭🇺

Edelény, Hungary

Investigational Site Number : 3480004

🇭🇺

Hajdunánás, Hungary

Investigational Site Number : 4840005

🇲🇽

San Juan del Rio, Querétaro, Mexico

Investigational Site Number : 1520006

🇨🇱

Quillota, Valparaíso, Chile

Investigational Site Number : 4840002

🇲🇽

Monterrey, Nuevo León, Mexico

Investigational Site Number : 4840001

🇲🇽

Guadalajara, Jalisco, Mexico

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