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A Phase 3 Study of Efficacy and Safety of AK3280 in Patients With Idiopathic Pulmonary Fibrosis

17 luglio 2026 aggiornato da: Shanghai Ark Biopharmaceutical Co., Ltd.

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)

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.

Panoramica dello studio

Stato

Non ancora reclutamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

263

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Cina, 100029
        • China-Japan Friendship Hospital
        • Contatto:
        • Investigatore principale:
          • Huaping Dai

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: AK3280 400 mg BID
During the randomized controlled treatment study, participants will receive AK3280 400 mg twice daily in a masked manner.
Participants will receive AK3280 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
Comparatore placebo: Placebo
During the randomized controlled treatment study, participants will receive placebo matching 400 mg twice daily in a masked manner.
Participants will receive placebo matching 400 mg twice daily, within 30 minutes after breakfast and dinner, with breakfast and dinner approximately 12 hours apart.
Comparatore attivo: 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.
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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Absolute change from baseline in FVC at Week 52
Lasso di tempo: Baseline to Week 52
The FVC indicates the amount of air a person can forcefully and quickly exhale after taking a deep breath.
Baseline to Week 52

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Absolute change from baseline in FVC at Week 12, 24, and 42
Lasso di tempo: Baseline to Week 12, 24, and 42
The FVC indicates the amount of air a person can forcefully and quickly exhale after taking a deep breath.
Baseline to Week 12, 24, and 42
Proportion of participants with relative decline from baseline in FVC ≥10%, ≥15%, and ≥20% at Week 12, 24, 42, and 52
Lasso di tempo: At Week 12, 24, 42, and 52
Relative decline from baseline in FVC ≥10%, ≥15%, and ≥20% indicates varying degrees of disease progression.
At Week 12, 24, 42, and 52
Absolute change from baseline in standardized %pFVC at Week12, 24, 42, and 52
Lasso di tempo: Baseline to Week 12, 24, 42, and 52
Standardized %pFVC is calculated as the ratio of measured FVC to predicted FVC. The predicted FVC is derived using a standardized formula.
Baseline to Week 12, 24, 42, and 52
Proportion of participants with absolute decline from baseline in standardized %pFVC ≥10% at Week 12, 24, 42, and 52
Lasso di tempo: At Week 12, 24, 42, and 52
Absolute decline from baseline in standardized %pFVC ≥10% indicates rapid disease progression.
At Week 12, 24, 42, and 52
Absolute change from baseline in hemoglobin-corrected %pDLco at Week 12, 24, 42, and 52
Lasso di tempo: At Week 12, 24, 42, and 52
The hemoglobin-corrected %pDLco measures the ability of oxygen moves from alveoli to blood.
At Week 12, 24, 42, and 52
Change from baseline in L-PF score at Week 12, 24, 42, and 52
Lasso di tempo: At Week 12, 24, 42, and 52
The L-PF is a self-administered, quality of life questionnaire validated for patients with progressive fibrosing interstitial lung disease (ILD), including IPF.
At Week 12, 24, 42, and 52
Change from baseline in 6MWT distance at Week 12, 24, 42, and 52
Lasso di tempo: At Week 12, 24, 42, and 52
At Week 12, 24, 42, and 52
Time to first acute exacerbation of IPF within 52 weeks
Lasso di tempo: Baseline to Week 52
An exacerbation of IPF is defined as an acute, clinically significant, respiratory deterioration characterized by evidence of new widespread alveolar abnormality in HRCT.
Baseline to Week 52
Progression-free survival (PFS), defined as the time from randomization to disease progression or death, whichever occurs first.
Lasso di tempo: Baseline to Week 52

IPF disease progression is defined as the occurrence of any of the following events:

  1. ≥ 10% absolute decline from baseline in standardized %pFVC
  2. ≥ 15% absolute decline from baseline in hemoglobin-corrected %pDLco
  3. Unscheduled hospitalization due to respiratory events
Baseline to Week 52
Incidence and severity of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) within 52 weeks
Lasso di tempo: Baseline to Week 52
TEAEs and SAEs will be assessed via patient-reported symptoms, vital signs, physical examination, 12-lead ECG, HRCT, and laboratory assessments.
Baseline to Week 52

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Zhen Fu, Medical Director

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

31 agosto 2026

Completamento primario (Stimato)

30 settembre 2028

Completamento dello studio (Stimato)

31 marzo 2029

Date di iscrizione allo studio

Primo inviato

17 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

17 luglio 2026

Primo Inserito (Effettivo)

22 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Parole chiave

Altri numeri di identificazione dello studio

  • AK3280-2005

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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