A Phase Ⅱa Study of ND-003 Tablets in Patients With Idiopathic Pulmonary Fibrosis

What this study involves

The registry does not currently label this study as recruiting. Ask about its status before planning a screening visit.

Study type

Interventional

Phase

Phase 2

Age range

40 years - Not specified

Sex eligible

All sexes

Healthy volunteers

Not accepted

Participants

10 Estimated

These are starting points, not an eligibility decision. The research team must review the full requirements.

About the research

Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, fibrosing interstitial lung disease that predominantly affects middle-aged and older adults. Progressive replacement of normal lung parenchyma by extracellular matrix and destruction of the alveolar architecture lead to reduced lung compliance and impaired gas exchange. Clinically, IPF is characterized by progressively worsening dyspnea, restrictive ventilatory impairment, impaired gas exchange, hypoxemia, and, in advanced cases, respiratory failure.

Current pharmacological treatment of IPF is primarily based on antifibrotic therapy. Pirfenidone and nintedanib were the first two antifibrotic agents approved for IPF and have been shown to slow the decline in forced vital capacity (FVC) through different mechanisms of action. Pirfenidone is an oral small-molecule agent with antifibrotic, anti-inflammatory, and antioxidant properties. Although its mechanism of action has not been fully elucidated, it is thought to involve inhibition of transforming growth factor-beta (TGF-β)-related signaling and suppression of fibroblast proliferation. Nintedanib is a multitarget tyrosine kinase inhibitor that inhibits several receptors involved in fibrotic pathways, including vascular endothelial growth factor receptors (VEGFRs), fibroblast growth factor receptors (FGFRs), and platelet-derived growth factor receptors (PDGFRs). More recently, nerandomilast, an oral phosphodiesterase 4B (PDE4B) inhibitor with anti-inflammatory and antifibrotic activity, has also been developed for the treatment of IPF.

Despite these therapeutic advances, currently available treatments mainly slow disease progression and do not reverse established pulmonary fibrosis or cure IPF. In addition, treatment may be limited by adverse reactions and tolerability issues. Common adverse reactions associated with pirfenidone include gastrointestinal symptoms, photosensitivity reactions, and rash, while diarrhea is a frequent adverse reaction associated with nintedanib. Therefore, there remains an unmet medical need for novel therapies with improved efficacy and an acceptable safety and tolerability profile.

ND-003, formerly known as ND003, is a novel small-molecule compound jointly developed by Shenzhen Xinyue Biotechnology Co., Ltd. and Shenzhen Small Molecule Innovative Drug Center Co., Ltd. for the treatment of pulmonary fibrosis. ND-003 is a kinase inhibitor targeting discoidin domain receptor 1 (DDR1), colony-stimulating factor 1 receptor (CSF1R), and platelet-derived growth factor receptor beta (PDGFR-β). By selectively interacting with these targets and modulating signaling pathways involved in fibrotic processes, ND-003 is intended to inhibit or delay the progression of tissue fibrosis.

The primary objective of this study is to evaluate the preliminary efficacy of ND-003 tablets in patients with idiopathic pulmonary fibrosis and to provide scientific evidence to support dose selection for subsequent clinical development. The study will also evaluate the safety and tolerability of ND-003 tablets in patients with IPF.

Who may be able to participate?

The list below is the sponsor’s full registry wording. It can include conditions, prior treatment, test results and other requirements. A match in search does not mean you qualify.

Inclusion Criteria:

• Aged ≥40 years (inclusive, based on the date of signing the informed consent form), with no restriction on sex.
• Confirmed diagnosis of idiopathic pulmonary fibrosis (IPF) based on multidisciplinary discussion (MDD), with all of the following criteria met:

1. Based on a comprehensive assessment of detailed medical history, physical examination, and relevant laboratory tests, the investigator must exclude interstitial lung diseases (ILDs) caused by other known factors, such as occupational or environmental exposures, genetic or familial factors, drug-induced lung injury, and connective tissue disease-associated ILD.
2. High-resolution computed tomography (HRCT) must demonstrate a typical usual interstitial pneumonia (UIP) pattern, characterized by subpleural and basal-predominant honeycombing, with or without traction bronchiectasis or bronchiolectasis.

For participants with a typical UIP pattern on HRCT, a diagnosis of IPF can be established without lung biopsy. For participants with a probable UIP pattern on HRCT and corresponding clinical features (e.g., age 60 years, male sex, and a history of smoking), the diagnosis of IPF may be established following MDD evaluation. For participants with a probable UIP pattern on HRCT but without corresponding clinical features, an indeterminate UIP pattern, or findings suggestive of an alternative diagnosis, further examinations, such as bronchoalveolar lavage (BAL), transbronchial lung biopsy (TBLB), or surgical lung biopsy (SLB), may be considered. The final diagnosis should be determined through a comprehensive MDD assessment.\[Reference: 2022 American Thoracic Society/European Respiratory Society/Japanese Respiratory Society/Latin American Thoracic Association (ATS/ERS/JRS/ALAT) Clinical Practice Guideline for the Diagnosis of Idiopathic Pulmonary Fibrosis.

• Participants must meet either of the following conditions:

1. Have not received treatment with nintedanib, pirfenidone, or nerandomilast for at least 8 weeks prior to screening and throughout the screening period, and do not plan to initiate or reinitiate antifibrotic therapy; or
2. Have received a single stable treatment regimen of nintedanib, pirfenidone, or nerandomilast for at least 8 weeks prior to screening and throughout the screening period. Stable treatment is defined as the participant being able to generally tolerate pirfenidone ≥400 mg TID, nintedanib ≥100 mg BID, or nerandomilast 18 mg BID, or the prescribed dose, with no dose changes for at least 8 consecutive weeks.
* Percent predicted forced vital capacity (FVCpp) ≥45% during the screening period.
* Hemoglobin-corrected percent predicted diffusing capacity of the lungs for carbon monoxide (DLCOpp) ≥25% during the screening period.
* Female participants of childbearing potential (excluding women who have undergone surgical sterilization and women who have been postmenopausal for at least 1 year) must have a negative serum pregnancy test within 72 hours prior to the first administration of the investigational product. Female participants of childbearing potential must agree to remain abstinent or use a highly effective method of contraception from the time of signing the informed consent form until 6 months after the last administration of the investigational product.
* Male participants of reproductive potential must agree to use effective contraception from the time of signing the informed consent form until at least 6 months after the last administration of the investigational product and must not donate sperm during this period.
* Participants must fully understand the study prior to participation and voluntarily sign a written informed consent form.

Exclusion Criteria:

• Known hypersensitivity to any component of ND-003 tablets.
• Acute exacerbation of pulmonary fibrosis within 3 months prior to screening.
• Presence during the screening period of any clinically significant major pulmonary disease or condition other than IPF, including but not limited to: active lung cancer; uncontrolled persistent asthma; acute exacerbation of chronic obstructive pulmonary disease; severe pneumonia requiring hospitalization or intravenous anti-infective therapy within 4 weeks prior to screening; or any other major pulmonary disease that, in the investigator's judgment, may significantly interfere with assessment of study endpoints, increase the risk to the participant, or affect pulmonary function or imaging assessments, such as active pulmonary tuberculosis, diffuse alveolar hemorrhage, pulmonary vasculitis, clinically significant pulmonary hypertension, or other respiratory failure requiring long-term oxygen therapy or mechanical ventilation.
• Major surgery within 4 weeks prior to the first dose, or planned surgery during the study period.
• Planned lung transplantation within 12 months after the first dose.
• Active pulmonary tuberculosis within 12 months prior to screening, or any active bacterial, viral, parasitic, or fungal infection requiring systemic treatment during the screening period.
• Receipt of a live vaccine within 4 weeks prior to the first dose, or planned receipt of a live vaccine during the study period. Live vaccines include, but are not limited to, vaccines against measles, mumps, rubella, varicella, yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid.
• Use of systemic glucocorticoids, either orally or by injection, for any reason within 4 weeks prior to the first dose at a dose exceeding prednisone 15 mg/day or an equivalent dose, for more than 7 consecutive days. Dose equivalence shall be calculated with oral prednisone as the reference, where intravenous methylprednisolone 4 mg is equivalent to oral prednisone 5 mg, and dexamethasone 0.75 mg is equivalent to oral prednisone 5 mg. The following is excluded from this criterion: routine use of inhaled glucocorticoids in participants with stable disease where, in the investigator's judgment, such treatment does not affect participant safety or study assessments, such as maintenance treatment for concomitant chronic obstructive pulmonary disease or asthma.
• Use, for respiratory or pulmonary indications, of immunomodulatory agents other than glucocorticoids within 4 weeks or 5 half-lives prior to the first dose, whichever is longer, including but not limited to cyclophosphamide, mycophenolate mofetil, azathioprine, cyclosporine, tacrolimus, rituximab, and JAK inhibitors, regardless of dose or treatment duration.
• Use within 7 days prior to the first dose of concomitant medications known to prolong the QT interval and/or strong inhibitors and/or inducers of CYP2C8 or CYP3A, or anticipated need for continued use of any of the above medications during the study.
• History of malignancy within the past 5 years, except for malignancies considered to be at very low risk after curative treatment, such as cervical carcinoma in situ, non-melanoma skin cancer, localized prostate cancer, and ductal carcinoma in situ.
• Laboratory test results at screening or baseline exceeding any of the following thresholds:

1. Liver function: total bilirubin \>1.5 × ULN, or AST or ALT \>2 × ULN, or serum CK \>1.5 × ULN;
2. Hematology: hemoglobin \<9 g/dL, platelet count \<90 × 10\^9/L, or white blood cell count \<4.0 × 10\^9/L;
3. Renal function: eGFR \<60 mL/min/1.73 m², calculated using the CKD-EPI equation.
* History of unstable or worsening cardiac disease within 6 months prior to screening, including but not limited to any of the following:

1. Unstable angina;
2. Myocardial infarction;
3. Congestive heart failure requiring hospitalization or New York Heart Association (NYHA) Class III or IV heart failure;
4. Uncontrolled severe arrhythmia, such as symptomatic ventricular tachycardia or atrial fibrillation that cannot be adequately controlled with medication.
* History of pancreatitis associated with prior use of tyrosine kinase inhibitors, or current evidence of mild to moderate pancreatitis.
* Family history of long QT syndrome or sudden death, or clinically significant electrocardiographic abnormalities at screening or baseline, including but not limited to: QTcF interval \>470 ms in females or \>450 ms in males, atrial fibrillation or atrial flutter, second- or third-degree atrioventricular block, or left bundle branch block.
* Echocardiographic evidence of a left ventricular ejection fraction (LVEF) \<50% or below the lower limit of normal, whichever threshold is higher.
* Systolic blood pressure \>160 mmHg or diastolic blood pressure \>100 mmHg at screening or baseline, measured after at least 5 minutes of rest and confirmed by one repeat measurement.
* Inability to swallow oral medication; presence of clinically significant gastrointestinal abnormalities, such as status post gastrointestinal resection, status post gastrointestinal anastomosis, chronic diarrhea, or intestinal obstruction; or any condition that, in the investigator's judgment, may severely impair gastrointestinal absorption.
* History of smoking within 3 months prior to screening, or unwillingness to abstain from smoking during the study.
* Known alcohol or drug dependence.
* Positive human immunodeficiency virus (HIV) antibody test; active syphilis; positive hepatitis C virus antibody with a positive hepatitis C virus (HCV) RNA result; or active hepatitis B, defined as positive hepatitis B surface antigen (HBsAg) with HBV DNA ≥ the upper limit of normal.
* Female participants who are pregnant or breastfeeding, or who plan to become pregnant during the study.
* Participation in any clinical study within 4 weeks prior to the first dose.
* Any other condition that, in the investigator's judgment, may affect participant compliance or render the participant unsuitable for participation in this study.

Treatment, groups and participation

The registry may describe treatments and study duration without a complete visit calendar. Ask the study team for the exact schedule, procedures, risks, costs and alternatives. Keep your usual care plan unless your treating clinician tells you otherwise.

Assignment

Random assignment

Masking

No masking

What researchers are measuring

Outcome measures describe what is being studied. They are not proof that a treatment works.

Primary measures

Secondary measures

Research locations (1)

The overall study status and a local site’s status can differ. Confirm that location’s availability before traveling.

1 locations

Study team and timeline

Lead sponsor

Shenzhen NewDEL Biotech, Co., Ltd

Study start

Aug 18, 2026 Actual

Primary completion

Jun 30, 2028 Estimated

Study completion

Dec 31, 2028 Estimated

First posted

Nov 10, 2026 Actual

Last updated

Nov 10, 2026 Actual

Official study contacts

No central contact is listed. Check the locations and the official record.