Skip to main content
OpenTrials
Not Yet Recruiting

NCT Number: NCT06989333

Local Spraying of GM-CSF Via Bronchoscopy in the Treatment of Autoimmune Pulmonary Alveolar Proteinosis

This study aims to explore a new therapeutic approach: the feasibility, safety and preliminary efficacy of directly spraying GM-CSF into the airway through bronchoscopy for the treatment of aPAP.

Not Yet Recruiting

Trial opening soon.

Get Notified

Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age: 18 to 60 years old;
  • A clear diagnosis of aPAP must meet at least one of the following diagnostic criteria:
  • BALF appears "milky white"; Or cytological examination reveals a large amount of PAS-positive protein deposition; 2) HRCT shows typical "paving stone-like changes"; 3) Positive for serum GM-CSF antibody. 3. There are more than one of the following treatment indications: Symptoms such as progressive breathing difficulties, coughing, and shortness of breath after activity occur; 2) Without oxygen inhalation, PaO2 > 65 mmHg 3) Pulmonary function DLCO accounts for % of the predicted value, ranging from 60% to 80%, including the critical value.
  • No other PAP specific treatments (such as WLL, inhaled GM-CSF, biological agents, etc.) have been received recently (for more than 4 weeks).
  • Agree to participate in this study and sign the informed consent form.

Exclusion criteria

  • Secondary PAP (such as secondary to blood diseases, etc.);
  • Patients with obvious pulmonary fibrosis, emphysema or irreversible lung function impairment;
  • Patients in the acute exacerbation stage;
  • Patients with other lung diseases (such as active pulmonary tuberculosis, bronchiectasis with purulent infection or other chronic infections; Have severe asthma, chronic bronchospasm, etc.
  • Have a history of allergy to GM-CSF antibodies or related drug components;
  • Patients who have participated in other clinical drug trials within the past three months;
  • Patients who have experienced severe complications related to bronchoscopy or are intolerant to bronchoscopy;
  • Concurrent with other serious cardiovascular and cerebrovascular diseases, hematological disorders, malignant tumors, etc.
  • Pregnant or lactating women.

Treatment and study plan

GM-CSF (granulocyte-macrophage colony-stimulating factor)

Drug

Bronchoscopy under general anesthesia or sedation; The predetermined dose of recombinant GM-CSF was dissolved in normal saline. The diseased lung segments were located through bronchoscopy and the liquid medicine was sprayed.

Primary outcomes

  1. Chest HRCT

    Time frame: 12 weeks

Study contacts

Contact information is provided by the study sponsor or research team.

Jiu-Wu Bai Doctor

CONTACT

[email protected]

13651602925

Sponsors and collaborators

Lead sponsor

Jiuwu Bai

Other

Registry information

Official study title

A Single-arm Clinical Study of Local Spraying of GM-CSF Via Bronchoscopy in the Treatment of Autoimmune Pulmonary Alveolar Proteinosis

Acronym: aPAP and GMCSF

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
May 25, 2025
Registry last updated
May 25, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.