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NCT07839884Not yet recruitingPhase 3

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

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 · Last updated 24 Sept 2026

Brief summary (registry, in English)

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.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
1360 (estimated)
First submitted
18 Sept 2026
Start date
21 Sept 2026
Primary completion date
12 May 2034
Lead sponsor
Pfizer
Diseases
COPD
NCT number
NCT07839884
EU CT number
2026-528166-19-00

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 1360
  • From 21 Sept 2026 to the primary completion date, 12 May 2034
  • No sites listed in no country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Lab values

  • Medical, laboratory, psychiatric, or behavioral condition that increases risk or interferes with study participation.

Other

  • Ongoing safety-significant AE.
  • Parent-study SAE incompatible with continued participation.
  • Pregnancy or breastfeeding.

Who the study is looking for

  • Participants who completed parent study C4531031.
  • Individuals of childbearing potential must be willing to use a highly effective method of contraception.

Age in the registry: 35 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

This page is information, not medical advice. Discuss any trial with your doctor.