- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07719023
A Phase 3 Study of Efficacy and Safety of AK3280 in Patients With Idiopathic Pulmonary Fibrosis
A Multicenter, Randomized, Double-Blind, Placebo-Controlled and Open-Label Active-Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of AK3280 in Patients With Idiopathic Pulmonary Fibrosis (IPF)
Studieoversigt
Status
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This is a multicenter, randomized, double-blind, placebo-controlled and open-label active-controlled phase 3 clinical study conducted in China. This study plans to enroll 263 IPF participants. After completing screening assessments and meeting all enrollment criteria, IPF participants will be randomized in a 4:2:1 ratio to: AK3280 400 mg BID group (double-blind); Placebo BID group (double-blind); Pirfenidone 600 mg TID group (open-label).
The doctors regularly test participants' lung function. The results of the lung function tests are compared between the groups. The doctors also regularly check participants' health and record any adverse medical events.
Participants are in the study for up to one and a half years. Subjects who complete the Week 52 visit of randomized controlled treatment study may be offered the opportunity to enter an open-label extension (OLE) study.
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 3
Kontakter og lokationer
Studiekontakt
- Navn: Jayson Zhou
- Telefonnummer: +8618796252099
- E-mail: jayson.zhou@arkbiosciences.com
Studiesteder
-
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Beijing Municipality
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Beijing, Beijing Municipality, Kina, 100029
- China-Japan Friendship Hospital
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Kontakt:
- Huaping Dai
- Telefonnummer: +861084205566
- E-mail: daihuaping@ccmu.edu.cn
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Ledende efterforsker:
- Huaping Dai
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
- Ældre voksen
Tager imod sunde frivillige
Beskrivelse
Inclusion Criteria:
- Age ≥ 40 years at enrolment
- Diagnosis of IPF per ATS/ERS/JRS/ALAT 2022 guidelines
- 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.
- No prior anti-fibrotic treatment, or discontinued anti-fibrotic therapy for ≥4 weeks or 5 half-lives (whichever is longer) prior to randomization
- 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:
- History of hypersensitivity to pirfenidone or AK3280
- Known intolerance to pirfenidone single dose of 200 mg (total daily dose 600 mg)
- Hospitalization due to acute IPF exacerbation within 8 weeks prior to screening or during screening
- 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)
- History of active tuberculosis within 12 months prior to screening
- 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
- 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
- History of heart disease meeting NYHA Class III-IV
- History of liver cirrhosis, severe hepatic impairment, or end-stage liver disease
- 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
- Screening cystatin C-estimated eGFR < 60 mL/min/1.73m²
- Screening coagulation test meeting any of the following: 1) INR > 2; 2) Both PT and APTT prolonged > 1.5× ULN
- History of any clinically diagnosed autoimmune disease, including but not limited to scleroderma, polymyositis/dermatomyositis, systemic lupus erythematosus, and rheumatoid arthritis
- Uncontrolled diabetes during screening (HbA1c > 10%)
- History of malignancy or possible malignancy upon evaluation (except treated localized basal cell carcinoma of the skin or cervical carcinoma in situ without recurrence)
- History of immunodeficiency, including but not limited to HIV infection
- 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
- Use of prohibited medications with potential effects on efficacy endpoints within 4 weeks or 5 half-lives (whichever is longer) prior to randomization
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: AK3280 400 mg BID
During the randomized controlled treatment study, participants will receive AK3280 400 mg twice daily in a masked manner.
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Participants will receive AK3280 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
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Placebo komparator: Placebo
During the randomized controlled treatment study, participants will receive placebo matching 400 mg twice daily in a masked manner.
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Participants will receive placebo matching 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
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Aktiv komparator: Pirfenidone 600 mg TID
During the randomized controlled treatment study, participants will receive pirfenidone titrated gradually to 600 mg three times daily in an open-label manner.
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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.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Absolute change from baseline in FVC at Week 52
Tidsramme: Baseline to Week 52
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The FVC indicates the amount of air a person can forcefully and quickly exhale after taking a deep breath.
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Baseline to Week 52
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Absolute change from baseline in FVC at Week 12, 24, and 42
Tidsramme: Baseline to Week 12, 24, and 42
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The FVC indicates the amount of air a person can forcefully and quickly exhale after taking a deep breath.
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Baseline to Week 12, 24, and 42
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Proportion of participants with relative decline from baseline in FVC ≥10%, ≥15%, and ≥20% at Week 12, 24, 42, and 52
Tidsramme: At Week 12, 24, 42, and 52
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Relative decline from baseline in FVC ≥10%, ≥15%, and ≥20% indicates varying degrees of disease progression.
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At Week 12, 24, 42, and 52
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Absolute change from baseline in standardized %pFVC at Week12, 24, 42, and 52
Tidsramme: Baseline to Week 12, 24, 42, and 52
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Standardized %pFVC is calculated as the ratio of measured FVC to predicted FVC.
The predicted FVC is derived using a standardized formula.
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Baseline to Week 12, 24, 42, and 52
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Proportion of participants with absolute decline from baseline in standardized %pFVC ≥10% at Week 12, 24, 42, and 52
Tidsramme: At Week 12, 24, 42, and 52
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Absolute decline from baseline in standardized %pFVC ≥10% indicates rapid disease progression.
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At Week 12, 24, 42, and 52
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Absolute change from baseline in hemoglobin-corrected %pDLco at Week 12, 24, 42, and 52
Tidsramme: At Week 12, 24, 42, and 52
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The hemoglobin-corrected %pDLco measures the ability of oxygen moves from alveoli to blood.
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At Week 12, 24, 42, and 52
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Change from baseline in L-PF score at Week 12, 24, 42, and 52
Tidsramme: At Week 12, 24, 42, and 52
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The L-PF is a self-administered, quality of life questionnaire validated for patients with progressive fibrosing interstitial lung disease (ILD), including IPF.
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At Week 12, 24, 42, and 52
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Change from baseline in 6MWT distance at Week 12, 24, 42, and 52
Tidsramme: At Week 12, 24, 42, and 52
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At Week 12, 24, 42, and 52
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Time to first acute exacerbation of IPF within 52 weeks
Tidsramme: Baseline to Week 52
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An exacerbation of IPF is defined as an acute, clinically significant, respiratory deterioration characterized by evidence of new widespread alveolar abnormality in HRCT.
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Baseline to Week 52
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Progression-free survival (PFS), defined as the time from randomization to disease progression or death, whichever occurs first.
Tidsramme: Baseline to Week 52
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IPF disease progression is defined as the occurrence of any of the following events:
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Baseline to Week 52
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Incidence and severity of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) within 52 weeks
Tidsramme: Baseline to Week 52
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TEAEs and SAEs will be assessed via patient-reported symptoms, vital signs, physical examination, 12-lead ECG, HRCT, and laboratory assessments.
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Baseline to Week 52
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Samarbejdspartnere og efterforskere
Efterforskere
- Studieleder: Zhen Fu, Medical Director
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- AK3280-2005
Plan for individuelle deltagerdata (IPD)
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