Evaluating the Efficacy and Safety of of HSK44459 in People With Progressive Pulmonary Fibrosis

Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorHaisco Pharmaceutical Group Co., Ltd.

About this trial

This study is open to adults with PPF . The main objective is to evaluate of the efficacy and the secondary objective is to evaluate the safety and pharmacokinetic.

Eligibility criteria

Qualifiers

Adults aged ≥18 year.

Diagnosis of PPF other than IPF prior to screening or during the screening period.

Disqualifiers

Clinically significant airways obstruction (Forced Expiratory Volume in One Second (FEV1)/Forced Vital Capacity (FVC) < 0.7) at screening.

In the opinion of the Investigator, other clinically significant pulmonary abnormalities.

Acute ILD exacerbation within 3 months prior to screening and/or during the screening period.

History of malignancy within 5 years prior to screening.

Trial design

Treatments tested in this trial

  • HSK44459
  • Placebo

Treatment groups

378 Participants
are divided into 2 treatment groups

Locations

This trial has no locations