New asthma combo pill for kids shows promise in Late-Stage trial

NCT ID NCT05562466

Disease control Sponsor: Novartis Pharmaceuticals Source: ClinicalTrials.gov ↗

First seen Jun 24, 2026 · Last updated Aug 20, 2026 · Updated 6 times

Summary

This study tests a new once-daily inhaler called QMF149 (a combination of indacaterol and mometasone) against a standard asthma drug, budesonide, in 200 children aged 6 to 12 with asthma. The goal is to see if the new drug works better at improving lung function and controlling asthma symptoms over 12 weeks. Each child will try both treatments in a crossover design, with a washout period in between.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance: QMF149 (indacaterol acetate / mometasone furoate)
What this could lead to: If successful, this could offer a more effective once-daily treatment option for children with asthma, improving lung function and symptom control.
What could go wrong: This is a Phase 3 trial, but results may not show superiority over the existing drug budesonide. Asthma is complex, and individual responses vary.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

May 2023

Expected to finish

May 2028

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

6 to 11 years

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria 1. Male or female children ≥ 6 years and \<12 years in age at randomization. 2. Parents/legal guardian must be willing and able to attend study visits and assist the child with the procedures outlined in the protocol (e.g. compliance with taking study medication and completing the diary) ((≥ 70% during the last 14 days of the Run-in period)). 3. Confirmed/documented diagnosis of asthma, as defined by national or international asthma guidelines for at least 12 months prior to study enrollment. 4. Written and signed informed consent by parent(s)/legal guardian(s) for the pediatric patient and assent by the pediatric patient (depending on local requirements) must be obtained before any study-specific assessment is performed. 5. Patient receiving daily treatment of stable low dose ICS alone (i.e. up to 100ug daily dose of fluticasone propionate DPI or equivalent) without additional controller OR low dose ICS (up to 100ug daily dose of fluticasone propionate DPI or equivalent) with one additional controller prior to starting run-in and eligible after run-in on mono ICS alone (fluticasone 100ug/day) for at least 3 weeks (run-in period) prior to randomization. 6. All patients must be symptomatic at randomization (Visit 30), as defined by ACQ-IA≥1.5. Patients previously on low dose ICS may be included for run-in only if ACQ-IA score ≥1.5 at Visit 20 and will be randomized if ACQ-IA score ≥1.5 at Visit 30. Patients previously on low dose ICS with one controller may do the wash out of the controller before the start of run-in and be included for run-in only if ACQ-IA score ≥ 1 and \<1.5 at Visit 20 and will be randomized if ACQ-IA score ≥1.5 at Visit 30. 7. Pre-Bronchodilator FEV1 ≥50% of predicted normal at start of Run-in (Visit 20) and end of Run-in (Visit 30). Withholding period of bronchodilators prior to spirometry at all time: SABA for ≥ 6 hours. For loose combinations of ICS/LABA\* a wash-out of ≥ 48 hours before Visit 20 is required (14 days for once daily combinations, i.e. indacaterol), short acting anticholinergic (SAMA) for ≥ 8 hours and xanthines ≥7 days. \* In case of combination ICS/LABA at screening, ICS alone should be continued. Wash-out period of each drug should be adhered to as above and should not be longer. If wash-out period is considered to be longer, please contact the Novartis Medical Monitor. A one-time repeat of percent predicted FEV1 (pre-bronchodilator FEV1) within 5 days of the Visit is allowed at Visit 20 as well as Visit 30. That would provide sufficient time to receive confirmation from the spirometry data central reviewer of the validity of the assessment. At Visit 20, the Run-in medication should be dispensed only once the repeat spirometry was qualified, and if all inclusion criteria at Visit 20 are successfully met. If patient fails to meet the pre FEV1 criteria for technical reasons, a rescreen is allowed once and in this circumstance, patients are not required to go back on prior medication (low dose ICS with or without controller) for the full 4 weeks duration and the rescreen can be scheduled at site's convenience. In this case all assessments must be done according to protocol's requirements. 8. FEV1 bronchodilator responsiveness testing using up to 4 puffs of SABA (up to 400μg salbutamol or 360μg albuterol) at Run-in Visit (Visit 20): increase \> and/or = 12% (performed according to ATS/ERS 2019 guidelines). All patients must perform a bronchodilator responsiveness test at start of Run-in. If responsiveness is not demonstrated at Run-in, it may be repeated once on the same day. If responsiveness is still not demonstrated after repeat, documentation of historical reversibility is accepted. If not available patients must be screen failed. Spacers may be used for bronchodilator responsiveness testing. 9. Demonstrate acceptable inhaler use technique with Breezhaler® at randomization, as well as acceptable use of other study devices and be able to complete spirometry procedures. 10. A parent/legal guardian is to complete all e-Diary entries and attend all clinic visits with the patient. It is recommended, if possible, to have the same parent/legal guardian to complete the e-diary entries and attend clinic visits with the patient. 11. Have a documented negative COVID-19 test (validated PCR or antigenic test)) within 3 days prior to randomization visit. 12. For optional Pharmacokinetics (PK) analysis: Participants willing to participate in the optional PK analysis will need to weigh at least 25 kg at screening. Exclusion Criteria Participants meeting any of the following criteria are not eligible for inclusion in this study. 1. Prior intubation for asthma. 2. Patients who have had a severe asthma exacerbation requiring in the previous month either systemic steroids or hospitalization due to asthma (\>24h) or emergency room visit (≤24 hours). 3. Subjects receiving any medications in the classes specified in Table 6 6 unless they undergo the required washout period prior to Treatment Visit (Day 1) and follow the adjustment through the treatment period. 4. Use of other investigational drugs within 5 half-lives of enrollment, or within 30 days, whichever is longer. 5. History of malignancy of any organ system (other than localized basal cell carcinoma of the skin or in situ cervical cancer), treated or untreated, within the past 5 years prior to screening, regardless of whether there is evidence of local recurrence or metastases. 6. History or presence of impaired renal function as indicated by clinically significant abnormal creatinine or blood urea nitrogen (BUN) and/or urea values, or abnormal urinary constituents (e.g. albuminuria) according to investigator's judgement. * Evidence of urinary obstruction, or difficulty in voiding * Evidence of congenital renal abnormalities with an established effect on renal function * Calculated eGFR \<60 mL/min/1.73m2 using the Bedside Schwartz formula. 7. Patients who have had a respiratory tract infection as determined by the investigator within 4 weeks prior to Visit 1, or between Visit 1 and Visit 30. Patients may be re-screened once, 4 weeks after recovery from their respiratory tract infection. 8. Any chronic condition of the respiratory tract which in the opinion of the investigator may interfere with study evaluation or optimal participation in the study. 9. Patient with evidence upon visual inspection (laboratory culture not required) of clinically significant (upon the opinion of the investigator) oropharyngeal candidiasis at Visit 30 or earlier, with or without treatment, Patients may be rescreened once their candidiasis has been treated and has resolved. 10. History of chronic lung disease other than asthma such as and not limited to, sarcoidosis interstitial lung disease, cystic fibrosis, mycobacterial or other infection (including active tuberculosis or atypical mycobacterial disease), chronic obstructive pulmonary disease (COPD) and asthma/COPD overlap syndrome (ACOS). 11. Patients with a history of long QT syndrome or whose corrected QT interval (QTc) measured at start of Run-in or Baseline (Fridericia method) is prolonged (≥ 450 msec for boys and girls) and confirmed by a central assessor (these patients should not be rescreened). 12. Subjects who have a clinically significant ECG abnormality reported before Visit 30 (End of Run-in). 13. Subjects who have a clinically significant abnormal laboratory values as per investigator judgement or abnormal liver chemistry results (i.e. ALT, AST, total bilirubin, alkaline phosphatase, GGT and albumin above the upper limit of normal) reported before Visit 30 (End of Run-in). 14. Any surgical or medical condition which might significantly alter the absorption, distribution, metabolism, or excretion of drugs, or which may jeopardize the subject in case of participation in the study. 15. Subjects who, in the opinion of the investigator, are not able to be compliant with study treatment or who have any medical or mental disorder, situation, or diagnosis which could interfere with the proper completion of the protocol requirements or risk the subject's safety while participating in the study. 16. Subject is an immediate family member of the participating investigator, sub-investigator, study coordinator, or employee of the participating investigator. 17. Patients who have been treated with long-acting theophylline preparations within four weeks prior to Screening and/or during the screening period or who have been treated with short-acting theophylline preparations within two weeks prior to Screening. 18. Patients who have been treated with non-approved and according to international guidelines not recommended experimental drugs for routine asthma therapy within four weeks prior to Visit 1 and/or during the screening period. 19. Use of Long-Acting Muscarinic Antagonist (LAMA) as maintenance treatment within 3 months prior to Screening. 20. Evidence of unstable disease within 4 weeks prior to Screening (Visit 1) that in the opinion of the investigator would put the safety of the subject at risk through study participation or would confound the interpretation of the results if the condition/disease exacerbated during the study. 21. History of hypersensitivity to any ingredients of the study drugs including fluticasone propionate, indacaterol acetate, mometasone furoate, budesonide and salmeterol/albuterol or drug of similar chemical classes. This includes any known hypersensitivity or intolerance to the excipients, including lactose. 22. Patients with Type I diabetes or uncontrolled Type II diabetes either by HBA1c\>8 or as per judgement of investigator prior to End of Run-In (Visit 30) 23. Patients receiving any asthma-related or non asthma-related prohibited medications as specified in the protocol. 24. Immunotherapy or desensitization for allergies started within 3 months prior to Visit 20, or where the maintenance dose is expected to change during the study. 25. Female patients of childbearing potential defined as all females physiologically capable of becoming pregnant (including female pediatric patients who are menarchal or who become menarchal during the study)) who do not agree to abstinence or, if sexually active, do not agree to the use of contraception as defined in the exclusion criteria. Effective contraception methods include: * Total abstinence (when this is in line with the preferred and usual lifestyle of the subject. Periodic abstinence (e.g., calendar, ovulation, symptothermal, post-ovulation methods) and withdrawal are not acceptable methods of contraception * Barrier methods of contraception: Condom or Occlusive cap (diaphragm or cervical/vault caps). For UK: with spermicidal foam/gel/film/cream/ vaginal suppository * Use of oral, (estrogen and progesterone), injected or implanted hormonal methods of contraception or other forms of hormonal contraception that have comparable efficacy (failure rate \<1%), for example hormone vaginal ring or transdermal hormone contraception or placement of an intrauterine device (IUD) or intrauterine system (IUS) If using oral contraception females should have been stable on the same pill for a minimum of 3 months before taking investigational drug. The decision on the contraceptive method should be reviewed at least every 3 months to evaluate the individual need and compatibility of the method chosen.

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Conditions

The condition(s) this trial relates to.

asthma

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Asthma

How to take part

Only the study team decides who joins. These are the ways to reach them.

The places running it

51 sites in 15 countries. The list below names each one and where it is.
The official record

ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

Open the record ↗
A doctor treating you

A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

Novartis Investigative Site
RECRUITING

CABA, Buenos Aires, C1122AAK, Argentina
Novartis Investigative Site
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CABA, Buenos Aires, C1414AIF, Argentina
Novartis Investigative Site
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CABA, Buenos Aires, C1425BEN, Argentina
Novartis Investigative Site
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Mendoza, Mendoza Province, 5500, Argentina
Novartis Investigative Site
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Rosario, Santa Fe Province, 2000, Argentina
Novartis Investigative Site
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Rosario, Santa Fe Province, S2000JKR, Argentina
Novartis Investigative Site
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Graz, 8036, Austria
Novartis Investigative Site
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Salzburg, 5020, Austria
Novartis Investigative Site
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Sankt Pölten, 3100, Austria
Novartis Investigative Site
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Porto Alegre, Rio Grande do Sul, 90160-093, Brazil
Novartis Investigative Site
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Sorocaba, São Paulo, 18040-425, Brazil
Novartis Investigative Site
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Rousse, 7002, Bulgaria
Novartis Investigative Site
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Sevlievo, 5400, Bulgaria
Novartis Investigative Site
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Bucaramanga, Santander Department, 680001, Colombia
Novartis Investigative Site
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Ibague, Tolima Department, 730006, Colombia
Novartis Investigative Site
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Cali, Valle del Cauca Department, 760001, Colombia
Novartis Investigative Site
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Plzen Bory, 301 00, Czechia
Novartis Investigative Site
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Prague, 128 08, Czechia
Novartis Investigative Site
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Athens, 115 27, Greece
Novartis Investigative Site
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Chaïdári, 124 62, Greece
Novartis Investigative Site
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Heraklion Crete., 715 00, Greece
Novartis Investigative Site
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Pátrai, 265 04, Greece
Novartis Investigative Site
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Thessaloniki, 546 42, Greece
Novartis Investigative Site
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Guatemala City, GTM, 01011, Guatemala
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Guatemala City, 01010, Guatemala
Novartis Investigative Site
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Budapest, 1033, Hungary
Novartis Investigative Site
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Gödöllő, 2100, Hungary
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Szeged, 6720, Hungary
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Szigetvár, 7900, Hungary
Novartis Investigative Site
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Brescia, BS, 25123, Italy
Novartis Investigative Site
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Catania, CT, 95123, Italy
Novartis Investigative Site
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Florence, FI, 50139, Italy
Novartis Investigative Site
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Pavia, PV, 27100, Italy
Novartis Investigative Site
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Roma, RM, 00161, Italy
Novartis Investigative Site
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Naples, 80138, Italy
Novartis Investigative Site
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Guadalajara, Jalisco, 44100, Mexico
Novartis Investigative Site
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Guadalajara, Jalisco, 44130, Mexico
Novartis Investigative Site
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San Juan del Río, Querétaro, 76800, Mexico
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Villahermosa, Tabasco, 86035, Mexico
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Querétaro, 76000, Mexico
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Panama City, Provincia de Panamá, 8185, Panama
Novartis Investigative Site
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Lisbon, 1649-035, Portugal
Novartis Investigative Site
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Lisbon, 1998-018, Portugal
Novartis Investigative Site
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Porto, 4099-001, Portugal
Novartis Investigative Site
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Porto, 4100-180, Portugal
Novartis Investigative Site
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Timișoara, Timiș County, 300723, Romania
Novartis Investigative Site
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Bucharest, 050152, Romania
Novartis Investigative Site
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Bloemfontein, Free State, 9301, South Africa
Novartis Investigative Site
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Pretoria, Gauteng, 0181, South Africa
Novartis Investigative Site
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Raslouw Centurion, Gauteng, 0157, South Africa
Novartis Investigative Site
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Cape Town, Western Cape, 7130, South Africa
Novartis Investigative Site
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George, Western Cape, 6529, South Africa
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Cape Town, Western Province, 7700, South Africa
Novartis Investigative Site
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Cape Town, 7531, South Africa
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Centurion, 0157, South Africa
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Esplugues, Barcelona, 08950, Spain
Novartis Investigative Site
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Sabadell, Barcelona, 08208, Spain
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Barcelona, 08035, Spain
Novartis Investigative Site
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Córdoba, 14004, Spain
Novartis Investigative Site
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Madrid, 28034, Spain
Novartis Investigative Site
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Málaga, 29011, Spain
Novartis Investigative Site
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Haiphong, 180000, Vietnam
Novartis Investigative Site
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Hanoi, 100000, Vietnam
Novartis Investigative Site
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Ho Chi Minh City, 700000, Vietnam

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