Starting soon
Phase 3
A Phase 3 Study of Efficacy and Safety of AK3280 in Patients With Idiopathic Pulmonary Fibrosis
Condition(s) studied
Idiopathic Pulmonary Fibrosis (IPF)
Investigational drug(s) / intervention(s)
AK3280: Participants will receive AK3280 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
Placebo: Participants will receive placebo matching 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
Pirfenidone: Participants will receive pirfenidone three times daily, within 30 minutes after meals. Initial dosing should be titrated gradually under doctor guidance: start with 200 mg each time, increase by 200 mg each time to maintain final dose of 600 mg each time within 2 weeks.
Study summary
This is a phase 3 clinical study conducted in China. The primary objective is to compare the efficacy and safety of AK3280 400 mg versus placebo and active control (pirfenidone) in IPF patients.
Eligibility
Inclusion Criteria:
1. Age ≥ 40 years at enrolment
2. Diagnosis of IPF per ATS/ERS/JRS/ALAT 2022 guidelines
3. HRCT central review completed during screening or within 12 months prior to screening. If participant did not undergo lung surgical biopsy, HRCT imaging must be consistent with usual interstitial pneumonia (UIP) pattern for definitive IPF diagnosis.
4. No prior anti-fibrotic treatment, or discontinued anti-fibrotic therapy for ≥4 weeks or 5 half-lives (whichever is longer) prior to randomization
5. Screening assessments meeting all of the following: 1) Standardized %pFVC ≥ 50% and ≤ 90%;2) Hemoglobin-corrected %pDLco ≥ 30% and ≤ 90%;3) Resting SpO2 ≥ 88%
Exclusion Criteria:
1. History of hypersensitivity to pirfenidone or AK3280
2. Known intolerance to pirfenidone single dose of 200 mg (total daily dose 600 mg)
3. Hospitalization due to acute IPF exacerbation within 8 weeks prior to screening or during screening
4. Within 4 weeks prior to screening or during screening, local or systemic infection requiring: 1) Hospitalization ≥ 24 hours; or 2) Use of systemic antibiotics (IV, IM, oral, or inhaled)
5. History of active tuberculosis within 12 months prior to screening
6. History of other clinically significant lung diseases besides IPF (e.g., asthma, COPD, interstitial pneumonia of known cause, acute severe pulmonary infection, etc.), or planned lung transplantation within 6 months after signing informed consent
7. Post-bronchodilator FEV1/FVC \< 0.7 or positive bronchodilator response (defined as ≥ 12% relative increase in FEV1 and ≥ 200 mL absolute increase in FEV1 after bronchodilator use) during screening
8. History of heart disease meeting NYHA Class III-IV
9. History of liver cirrhosis, severe hepatic impairment, or end-stage liver disease
10. Screening liver function abnormalities meeting any of the following:1) AST ≥ 2× ULN; 2) ALT ≥ 2× ULN; 3) ALP ≥ 2× ULN; 4) Total bilirubin ≥ 1.5× ULN
11. Screening cystatin C-estimated eGFR \< 60 mL/min/1.73m²
12. Screening coagulation test meeting any of the following: 1) INR \> 2; 2) Both PT and APTT prolonged \> 1.5× ULN
13. History of any clinically diagnosed autoimmune disease, including but not limited to scleroderma, polymyositis/dermatomyositis, systemic lupus erythematosus, and rheumatoid arthritis
14. Uncontrolled diabetes during screening (HbA1c \> 10%)
15. History of malignancy or possible malignancy upon evaluation (except treated localized basal cell carcinoma of the skin or cervical carcinoma in situ without recurrence)
16. History of immunodeficiency, including but not limited to HIV infection
17. History of any disease other than IPF with life expectancy \< 18 months; or requiring long-term medical care, or limited self-care ability; or conditions that the investigator believes may affect participant's ability to complete this clinical study, complete study-related assessments, or affect safety or efficacy assessments
18. Use of prohibited medications with potential effects on efficacy endpoints within 4 weeks or 5 half-lives (whichever is longer) prior to randomization
Primary outcome measure(s)
- Absolute change from baseline in FVC at Week 52 — Baseline to Week 52
The FVC indicates the amount of air a person can forcefully and quickly exhale after taking a deep breath.
Trial sites (1)
| Facility | City | Region | Status |
| China-Japan Friendship Hospital |
Beijing |
Beijing Municipality |
|
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