Clinical Trial to Evaluate the Safety and Efficacy of DWN12088 in Patients With IPF

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age40+
SponsorDaewoong Pharmaceutical Co. LTD.

About this trial

This is a randomized, double-blinded, placebo-controlled multicenter study to evaluate the safety and efficacy of DWN12088 in patients with Idiopathic Pulmonary Fibrosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male or female patients aged ≥40 years based on the date of the written informed consent form

Diagnosis of IPF as defined by American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association guidelines

In a stable condition and suitable for study participation based on the results of medical history, physical examination, vital signs, 12-lead ECG, and laboratory evaluation

Patients receiving local standard-of-care for IPF, defined as either pirfenidone or nintedanib, at a stable dose for at least 3 months prior to screening, or neither pirfenidone nor nintedanib. If the patients were on pirfenidone or nintedanib previously and have been off for at least 3 months prior to screening, they will be considered as not on any treatment for IPF

Disqualifiers

Acute IPF exacerbation within 6 months prior to screening and/or during the screening period

Patients who are unwilling to refrain from smoking within 3 months prior to screening and until the end of the study

Female patients who are pregnant or nursing

Abnormal ECG findings

Trial design

Design model

Parallel

Treatments tested in this trial

  • DWN12088

    Drug

    DWN12088 Xmg Tablet (BID)

  • Placebo

    Drug

    Placebo 0mg Tablet (BID)

Treatment groups

102 Participants
are divided into 2 treatment groups
Group A: DWN12088 Xmg Tablet (BID)Experimental treatment 1 intervention
Group B: Placebo 0mg Tablet (BID)Placebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Rate of decline of FVC

To investigate the efficacy of DWN12088 on pulmonary function

Time frame
From Day 1 through Week 24
2

Incidents of treatment-emergent adverse events

To evaluate the safety and tolerability of DWN12088 compared with placebo

Time frame
From Day 1 through Week 24

Secondary outcomes

1

Time to progression of IPF

To evaluate the efficacy of DWN12088 on time to progression of IPF

Time frame
From Day 1 through Week 24
2

Quantitative high-resolution computed tomography

To evaluate the efficacy of DWN12088 as measured by quantitative high-resolution computed tomography

Time frame
From Day 1 through Week 24
3

Functional exercise capacity, assessed by the 6-minute walk test (6MWT) distance

To evaluate the efficacy of DWN12088 on functional exercise capacity, assessed by 6MWT distance

Time frame
From Day 1 through Week 24
4

Diffusing capacity of lung for carbon monoxide (DLCO) corrected for Hgb

To evaluate the efficacy of DWN12088 on pulmonary diffusion function

Time frame
From Day 1 through Week 24

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.