A Randomized, Double-Blind, Placebo-controlled, Parallel Arm, 52-week Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of Two Doses of EXPD-101 in Participants with COPD

Trial details

Who runs it

Expedition Therapeutics Inc.

Trial code

EU 2026-525216-34-00

Record updated

2026. október 5.

Original description

To evaluate the effect of EXPD-101 compared with placebo on annualized rate of moderate and severe COPD exacerbations over 52 weeks of treatment.Read full original descriptionShow less

To evaluate the effect of EXPD-101 compared with placebo on annualized rate of moderate and severe COPD exacerbations over 52 weeks of treatment.

To assess the safety and tolerability of EXPD-101 compared with placebo.

Inclusion: Capable and willing to provide written informed consent for the study prior to any study activities and is willing to comply with all requirements of the protocol; If participant is of childbearing potential, must commit to practicing highly effective methods of birth control and not donating eggs during the study and at least 14 days after the last dose. A highly effective contraception method is defined as a method resulting in a failure rate of less than 1% per year when used consistently and correctly. See for complete details of study contraception requirements and highly effective methods; Male participants commit to the following during the study and for at least 14 days after the last dose: • Practice true sexual abstinence (refrain from heterosexual intercourse) • Use a condom with any female partner of childbearing potential and ensure that the partner uses a highly effective contraceptive method (eg, IUD/IUS, combined hormonal contraception, progestogen-only contraception, or bilateral tubal occlusion). • Be vasectomized (≥ 3 months prior to screening) • Refrain from donating sperm during the Treatment Period and for at least 14 days after the last dose of the IP; Body mass index (BMI) ≥ 18.5 kg/m² and < 35 kg/m² at screening (weight ≥ 50 kg for males and ≥ 45 kg for females); Diagnosis of COPD for at least 1 year according to Global Initiative for Chronic Obstructive Lung Disease (GOLD) criteria; or with a COPD history of ≥ 12 months at Screening supported by medical records; COPD with physician-confirmed diagnosis of chronic bronchitis (persistent, productive cough and sputum for at least 3 months in the past year); At least 2 moderate or > 1 severe exacerbation within 12 months prior to screening; Current or ex-tobacco smokers with history of ≥ 10 pack-years (1 pack year = 20 cigarettes smoked per day for 1 year); • Never tobacco smokers are not eligible for study entry; Stable maintenance therapy with either dual or triple inhaled therapy for ≥ 3 months prior to enrollment per below: a. Dual therapy: long-acting beta-2 agonist/muscarinic antagonist (LABA/LAMA) or inhaled corticosteroids (ICS)/LAMA, or ICS/LABA OR b. Triple therapy: ICS/LAMA/LABA; Post–BD FEV1/FVC < 0.7 and post-BD FEV1(% predicted) ≥ 40% at Screening; COPD Assessment Test (CAT) score ≥ 10 at Screening.

Exclusion: COPD exacerbation within the 4 weeks prior to randomization; Known history of allergy or reaction to any component of the investigational product formulation; Current treatment with biologic drugs for COPD (eg, dupilumab, mepolizumab) or use of Therapeutics, biologics within 5 half-lives or 4 months, whichever is longer, from randomization; Current long-term treatment with oxygen therapy > 12 hours per day; Newly initiated chronic therapy for COPD in the previous 3 months; Use of immunoglobulin or blood products in 30 days prior to Screening; Received a live attenuated vaccine within 30 days prior to Screening; Participants who are participating in the acute phase of a pulmonary rehabilitation program, i.e. who started rehabilitation < 4 weeks prior to screening (Note: participants in the maintenance phase of a rehabilitation program can be included); Pneumonia requiring antibiotics or antiviral medication within 28 days prior to Visit 1, based on the last day of antibiotics or hospitalization date, whichever occurred later if this occurs during screening); History of clinically significant infection (excluding pneumonia), acute upper or lower respiratory infection, requiring antibiotics or antiviral medication within 14 days prior to Visit 1 based on the last day of antibiotic/antiviral treatment or hospitalization date, whichever occurred later; Use of allergy immunotherapy. Participants can only be in the stable phase for at least 1 month, but not in the induction phase; Have any tooth that can potentially cause pain or infection as noted in the oral exam unless they are corrected before the study; Clinically important pulmonary disease other than COPD (eg, asthma, active lung infection, clinically significant bronchiectasis (per investigator judgement by Screening CT scan), pulmonary fibrosis, cystic fibrosis, lung cancer, alpha-1 antitrypsin deficiency, tuberculosis); Has active periodontal disease and are either: a. Currently treated by a dentist for this condition or b. Expected to have periodontal disease-related procedures within the study period; Significant immunodeficiency and/or positive serological tests for hepatitis B, hepatitis C, or known human immunodeficiency virus (HIV) infection; Evidence of active liver disease (with or without ongoing treatment); History of cancer except: a. Participants who have had basal cell carcinoma, localized squamous cell carcinoma of the skin or in situ carcinoma of the cervix are eligible to participate in the study provided that curative therapy was completed at least 12 months prior to Visit 1 b. Participants who have had other malignancies are eligible provided that curative therapy was completed at least 5 years prior to Visit 1; Participants with a QT interval, from the ECG conducted at Screening Visit 1, corrected with Fridericia’s formula (QTcF) > 450 msec (or QTcF > 480 msec in participants with bundle branch block); Any clinically significant abnormal findings in physical examination, vital signs, hematology, clinical chemistry, or urinalysis during Screening Period, which in the opinion of the investigator, may put the participant at risk because of his/her participation in the study, or may influence the results of the study, or the participant’s ability to complete the entire duration of the study; Are scheduled to have tooth extraction that will occur during the study period; Current or history, within the past year of Visit 1, of substance and/or alcohol abuse.

EU CTIS 2026-525216-34-00