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Study of RSS0343 Tablets in Patients With Non-cystic Fibrosis Bronchiectasis

Study of RSS0343 Tablets in Patients With Non-cystic Fibrosis Bronchiectasis

Recruiting
18-75 years
All
Phase 2

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Overview

Studies to evaluate the safety, tolerability, pharmacodynamics, and efficacy of RSS0343 tablets in patients with non-cystic fibrosis bronchiectasis

Eligibility

Inclusion Criteria:

  1. Age 18-75 years old (including boundary values), male and female.
  2. Female subjects weigh ≥45 kg and male subjects weigh ≥50 kg.
  3. HRCT shows bronchiectasis affecting one or more lobes of the lung and is confirmed by the clinician as NCFB.
  4. The expected survival is greater than 12 months.
  5. Informed consent was signed before the trial.
  6. Potentially fertile subjects voluntarily take appropriate contraceptive measures.

Exclusion Criteria:

  1. Patients with pulmonary hypertension or chronic obstructive pulmonary disease (COPD) or asthma as determined by the investigators were the primary diagnosis were screened.
  2. An active, symptomatic infection caused by respiratory viruses, including COVID-19, influenza viruses, etc.
  3. Have psoriasis or lichen planus.
  4. Have Wright's disease/keratosis or hemorrhagic keratosis, or reactive arthritis.
  5. Have chlorine acne, large common warts, or keratodermatitis.
  6. Has diabetic foot.
  7. Have periodontal disease, oral infection, or loose teeth.
  8. History of malignant tumor within 5 years prior to screening.
  9. Screening subjects with a history of liver disease or currently receiving treatment for liver disease, including but not limited to acute or chronic hepatitis, cirrhosis, or liver failure.
  10. Researchers consider any other unstable clinical disease.
  11. Oral or inhaled antibiotics were received 4 weeks prior to first administration.
  12. Immunosuppressants were administered 4 weeks before the first dose.
  13. Received drugs within 4 weeks prior to screening that may cause hyperkeratosis of the skin.
  14. Received live attenuated vaccine within 30 days prior to initial administration.
  15. Participated in clinical trials of any medical device within 3 months prior to screening.
  16. Active hepatitis B virus infection, active hepatitis C virus infection, or known HIV infection or known syphilis infection.
  17. Drug abusers.
  18. Current smoker or former smoker for less than 3 months.
  19. Suspected allergy to the investigational product or any component of the investigational product, or severe allergy to any drug, food, toxin or other exposure.
  20. Pregnant or lactating women.
  21. The subjects were unable to complete the questionnaires due to their limited educational level, or neither the subjects themselves nor their families could fill in the subject log card.
  22. The researchers determined that there were other circumstances that were not suitable for participation in this study.

Study details
    Adolescent Asthma

NCT06775340

Jiangsu HengRui Medicine Co., Ltd.

16 October 2025

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FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
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