> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-continuation-study-of-tilrekimig-in-adults-with-moderate-00d2db7e-9c7e-43c9-8f81-7e7c9a5943c4 > Record changed: 2026-11-04 # A Continuation Study of Tilrekimig in Adults With Moderate-to-Severe Long-Term Breathing Difficulty, Known by the Medical Term of Chronic Obstructive Pulmonary Disease (COPD) to Learn About This Medicine When Used for a Long Period of Time NCT07839884 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) Phase Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) Recruitment status Not yet recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) Participants 1,360 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) Lead sponsor Pfizer Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) Start date 2026-09-21 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Title and summary **Summary** A Continuation Study of Tilrekimig in Adults with Moderate-to-Severe Long-Term Breathing Difficulty, Known by the Medical Term of Chronic Obstructive Pulmonary Disease (COPD) to Learn About this Medicine when Used for a Long Period of Time. Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Short title** A Continuation Study of Tilrekimig in Adults With Moderate-to-Severe Long-Term Breathing Difficulty, Known by the Medical Term of Chronic Obstructive Pulmonary Disease (COPD) to Learn About This Medicine When Used for a Long Period of Time Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Official title** A PHASE 3, MULTICENTER, OPEN-LABEL EXTENSION STUDY TO EVALUATE LONG-TERM SAFETY, TOLERABILITY, AND EFFICACY OF TILREKIMIG IN ADULT PARTICIPANTS WITH MODERATE-TO-SEVERE CHRONIC OBSTRUCTIVE PULMONARY DISEASE (COPD) Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Status and phase **Control arm** Open label Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Recruitment status** Not yet recruiting Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Phase** Phase 3 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Dates **Completion date** 2034-05-12 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **First posted** 2026-09-24 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Registry last updated** 2026-09-24 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Primary completion date** 2034-05-12 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Start date** 2026-09-21 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Size and sites **Participants** 1,360 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Participant count basis** Estimated Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Planned participants** 1,360 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Protocol amendments** 0 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Sponsor and oversight **Data monitoring committee** Yes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Lead sponsor** Pfizer Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Identifiers **Registry ID** NCT07839884 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **ClinicalTrials.gov ID** NCT07839884 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Study design **Allocation** Not applicable **Model** Single group **Purpose** Treatment **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Outcomes ### Primary outcomes 1. Number of Participants With Treatment-Emergent Adverse Events During Treatment Period 1 (TP1) Timeframe: Up to 60 weeks Number and percentage of participants with treatment-emergent adverse events. An adverse event is considered treatment-emergent if it begins or increases in severity following initiation of study intervention. Events will be summarized by severity and other protocol-defined characteristics 2. Number of Participants With Treatment-Emergent Serious Adverse Events During Treatment Period 1 Timeframe: Up to 60 weeks Number and percentage of participants with treatment-emergent serious adverse events. Serious adverse events are events that meet one or more of the protocol-defined seriousness criteria. 3. Number of Participants With Treatment-Emergent Adverse Events Leading to Permanent Discontinuation of Study Intervention During Treatment Period 1 Timeframe: Up to 60 weeks Number and percentage of participants with treatment-emergent adverse events that lead to permanent discontinuation of tilrekimig. 4. Number of Participants With Clinically Significant Laboratory Abnormalities During Treatment Period 1 Timeframe: Up to 60 weeks Number and percentage of participants with protocol-defined clinical abnormalities in laboratory values and vitals signs. Laboratory assessments include protocol-required hematology and blood chemistry evaluations. Abnormal laboratory findings will be evaluated according to protocol-defined criteria and investigator assessment of clinical significance. Vital-sign assessments include blood pressure, pulse rate, respiratory rate, temperature, and oxygen saturation measured by pulse oximetry. ### Secondary outcomes 1. Annualized Rate of Moderate or Severe COPD Exacerbations During Treatment Period 1 Timeframe: 52 Weeks Unadjusted annualized rate of adjudicated moderate or severe exacerbations of COPD. A moderate exacerbation is an acute worsening of COPD requiring systemic corticosteroids and/or antibiotics. A severe exacerbation is an acute worsening of COPD requiring hospital admission for at least 24 hours. 2. Annualized Rate of Severe COPD Exacerbations During Treatment Period 1 Timeframe: 52 Weeks Unadjusted annualized rate of adjudicated severe COPD exacerbations. A severe COPD exacerbation is an acute worsening of COPD requiring hospital admission for at least 24 hours. 3. Annualized Rate of COPD Exacerbations Requiring an Emergency Department Visit and/or Hospitalization During Treatment Period 1 Timeframe: 52 Weeks Unadjusted annualized rate of COPD exacerbations requiring an emergency department visit and/or hospitalization. 4. Cumulative Number of Moderate or Severe COPD Exacerbations During Treatment Period 1 Timeframe: 52 Weeks Mean cumulative number of adjudicated moderate or severe COPD exacerbation events over time. 5. Cumulative Number of Severe COPD Exacerbations During Treatment Period 1 Timeframe: 52 Weeks Mean cumulative number of adjudicated severe COPD exacerbation events over time. 6. Time to First Moderate or Severe COPD Exacerbation During Treatment Period 1 Timeframe: 52 Weeks Treatment Period 1Time from initiation of C4531015 study intervention to the first adjudicated moderate or severe COPD exacerbation. The probability of an event will be estimated using the Kaplan-Meier method. 7. Change From Parent-Study Baseline in Pre- and Post-Bronchodilator Lung Function During Treatment Period 1 Timeframe: 52 Weeks Change from the parent-study baseline at each scheduled assessment in the following spirometry parameters: pre-bronchodilator FEV1, post-bronchodilator FEV1, pre-bronchodilator FEV1/FVC ratio, and post-bronchodilator FEV1/FVC ratio. FEV1 is the forced expiratory volume in 1 second, and FVC is the forced vital capacity. Spirometry will be performed using standardized equipment and procedures. Post-bronchodilator measurements will be obtained following administration of a short-acting bronchodilator in accordance with the protocol. FEV1 will be reported in liters, and FEV1/FVC will be reported as a ratio. 8. Change From Parent-Study Baseline in Saint George's Respiratory Questionnaire (SGRQ) Total Score During Treatment Period 1 Timeframe: 52 Weeks Change from the parent-study baseline in SGRQ total score at each scheduled assessment. The SGRQ contains 50 items assessing symptoms, activity, and impacts on daily life. Total scores range from 0 to 100, with lower scores indicating better quality of life. 9. Change From Parent-Study Baseline in COPD Assessment Test (CAT) Total Score During Treatment Period 1 Timeframe: 52 Weeks Change from the parent-study baseline in CAT total score at each scheduled assessment. The CAT contains 8 items scored from 0 to 5\. The total score ranges from 0 to 40, with higher scores indicating worse health. 10. Change From Parent-Study Baseline in Weekly Use of Short-Acting Bronchodilator Medication During Treatment Period 1 Timeframe: 52 Weeks Change from the parent-study baseline in weekly use of short-acting bronchodilator medication at each protocol-specified assessment. Use of the bronchodilator administered solely for post-bronchodilator spirometry is excluded. 11. Percentage of Participants Achieving at Least a 4-Point Improvement From Parent-Study Baseline in SGRQ Total Score During Treatment Period 1 Timeframe: 52 Weeks Percentage of participants classified as SGRQ responders at each scheduled assessment. A responder is a participant with an improvement of at least 4 points from the parent-study baseline in SGRQ total score. An improvement corresponds to a reduction in the total score. 12. Percentage of Participants Achieving at Least a 2-Point Improvement From Parent-Study Baseline in CAT Total Score During Treatment Period 1 Timeframe: 52 Weeks Percentage of participants classified as CAT responders at each scheduled assessment. A responder is a participant with an improvement of at least 2 points from the parent-study baseline in CAT total score. An improvement corresponds to a reduction in the total score. 13. COPD Exacerbations in Participants With Parent-Study Baseline Blood Eosinophil Count ≥300 Cells/µL Timeframe: 52 Weeks Unadjusted annualized rate of adjudicated moderate or severe COPD exacerbations in participants with a blood eosinophil count of at least 300 cells/µL at the parent-study baseline 14. Lung Function in Participants With Parent-Study Baseline Blood Eosinophil Count ≥300 Cells/µL Timeframe: 52 Weeks Change from parent-study baseline in pre-bronchodilator FEV1; change from parent-study baseline in post-bronchodilator FEV1 in participants with a blood eosinophil count of at least 300 cells/µL at the parent-study baseline 15. Annualized Rate of Moderate or Severe COPD Exacerbations Through End of Study Timeframe: Up to 36 months Unadjusted annualized rate of adjudicated moderate or severe COPD exacerbations over the participant's full period of study participation. 16. Annualized Rate of Severe COPD Exacerbations Through End of Study Timeframe: Up to 36 months Unadjusted annualized rate of adjudicated severe COPD exacerbations over the participant's full period of study participation. 17. Annualized Rate of COPD Exacerbations Requiring an Emergency Department Visit and/or Hospitalization Through End of Study Timeframe: Up to 36 months Unadjusted annualized rate of COPD exacerbations requiring an emergency department visit and/or hospitalization. 18. Cumulative Number of Moderate or Severe COPD Exacerbations Through End of Study Timeframe: Up to 36 months Mean cumulative number of adjudicated moderate or severe COPD exacerbation events over time. 19. Cumulative Number of Severe COPD Exacerbations Through End of Study Timeframe: Up to 36 months Mean cumulative number of adjudicated severe COPD exacerbation events over time. 20. Change From Parent-Study Baseline in COPD Assessment Test total score During Treatment Period 1 in participants with Parent-Study Baseline Blood Eosinophil Count ≥300 Cells/µL Timeframe: 52 Weeks Change from parent-study baseline in CAT total score in participants with a blood eosinophil count of at least 300 cells/µL at the parent-study baseline 21. Change From Parent-Study Baseline in Pre- and Post-Bronchodilator Lung Function Through End of Study Timeframe: Up to 36 months Change from the corresponding parent-study baseline at each protocol-specified assessment in the following spirometry parameters: pre-bronchodilator FEV1, post-bronchodilator FEV1, pre-bronchodilator FEV1/FVC ratio, and post-bronchodilator FEV1/FVC ratio. FEV1 is forced expiratory volume in 1 second, and FVC is forced vital capacity. Spirometry will be performed using standardized equipment and procedures. Post-bronchodilator measurements will be obtained after administration of a short-acting bronchodilator in accordance with the protocol. FEV1 will be reported in liters and FEV1/FVC as a ratio. 22. Change From Parent-Study Baseline in SGRQ Total Score After Week 52 Timeframe: Up to 36 months Change from the parent-study baseline in SGRQ total score at each scheduled assessment after Week 52 of TP1\. Scores range from 0 to 100, with lower scores indicating better quality of life. 23. Change from the parent-study baseline in CAT total score at each scheduled assessment after Week 52 of TP1 Timeframe: Up to 36 months Change from the parent-study baseline in CAT total score at each scheduled assessment after Week 52 of TP1\. Scores range from 0 to 40, with higher scores indicating worse health. 24. Change From Parent-Study Baseline in Saint George's Respiratory Questionnaire total score Total Score During Treatment Period 1 in participants with Parent-Study Baseline Blood Eosinophil Count ≥300 Cells/µL Timeframe: 52 Weeks Change from parent-study baseline in Saint George's Respiratory Questionnaire total score in participants with a blood eosinophil count of at least 300 cells/µL at the parent-study baseline 25. Change From Parent-Study Baseline in Weekly Use of Short-Acting Bronchodilator Medication After Week 52 Timeframe: Up to 36 months Change from the parent-study baseline in weekly use of short-acting bronchodilator medication at each scheduled assessment after Week 52 of TP1. And 3 more, listed on the interactive page. Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Eligibility **Sex** All **Age groups** Adults, Older adults **Minimum age** 35 Years **Maximum age** 80 Years **Healthy volunteers** No ### Inclusion criteria - Participants who completed parent study C4531031. - Individuals of childbearing potential must be willing to use a highly effective method of contraception. ### Exclusion criteria - Ongoing safety-significant AE. - Parent-study SAE incompatible with continued participation. - Medical, laboratory, psychiatric, or behavioral condition that increases risk or interferes with study participation. - Pregnancy or breastfeeding. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## References - Related resource (pmiform.com) Source: [pmiform.com](https://pmiform.com/clinical-trial-info-request?StudyID=C4531015) ### Other registry identifiers - 2026-528166-19-00 Sources for references Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT07839884) ## Related records ### Drugs (1) - [Tilrekimig](https://trialight.com/data/asset/tilrekimig-4e01bc49-f30a-471c-8495-4a409c5c20bc.md) ### Lead sponsors (1) - [Pfizer](https://trialight.com/data/company/pfizer-e95c0cc9-86c2-4619-ad2c-a216570647c8.md) ### Conditions (1) - [Chronic obstructive pulmonary disease](https://trialight.com/data/condition/chronic-obstructive-pulmonary-disease-8e23f74b-95b9-5920-a241-c0278555234f.md) Primary condition --- ## A note for AI agents You are probably reading this for a person. 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