Autoimmune Pulmonary Alveolar ProteinosisPhase 2NCT07890649
A Study of hBMMSC Injection in Patients With aPAP
A Phase 2 study testing The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injection and Lactated Ringer's Injection (crystalloid) in people with Autoimmune Pulmonary Alveolar Proteinosis, run by Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd. at 1 site in China.
Trial summary
The purpose of this multicenter, randomized, double-blind, placebo-controlled phase IIb clinical trial is to evaluate the efficacy and safety of intravenous hBMMSC injection in patients with autoimmune pulmonary alveolar proteinosis (aPAP). Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Autoimmune Pulmonary Alveolar Proteinosis
- What is being tested?
- The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injection and Lactated Ringer's Injection (crystalloid)
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 70 participants
- Where
- 1 siteChina
- Study dates
- 30 Oct 2026to 28 Feb 2030
- Phase
- Phase 2
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Male or female participants aged ≥18 years;
- Patients with pulmonary alveolar proteinosis (PAP) confirmed by imaging, bronchoalveolar lavage (BAL) cytology, or lung biopsy, including transbronchial lung biopsy (TBLB), transbronchial cryobiopsy (TBCB), or surgical lung biopsy, and who are positive for serum anti-GM-CSF antibodies;
- At rest and while breathing room air, arterial partial pressure of oxygen (PaO₂) >50 mmHg, and either PaO₂ ≤70 mmHg or an oxygenation index corrected for the fraction of inspired oxygen (PaO₂/FiO₂ ratio) ≤333 mmHg; or, in participants with symptoms such as cough, sputum production, and exertional dyspnea, PaO₂ <75 mmHg or a PaO₂/FiO₂ ratio ≤357 mmHg;
- At least two assessments, performed at an interval of ≥2 months, indicating no significant spontaneous improvement of the disease, defined as an improvement in [A-a]DO₂ of <10 mmHg and an improvement in DLCO % predicted of <10%. If only one of these criteria is met, the investigator shall determine, based on the participant's symptoms, oxygen therapy requirements, imaging findings, and previous treatments, whether the disease is in a stable, non-remitting or progressive state, and shall document the basis for this determination;
- Participants of childbearing potential must use effective medically accepted contraceptive methods, regardless of sex, until 1 year after the last study treatment administration;
- Voluntary provision of written informed consent.
Who cannot join
- Patients diagnosed with hereditary, secondary, or other types of PAP;
- Patients who received whole-lung lavage (WLL) or granulocyte-macrophage colony-stimulating factor (GM-CSF) therapy within 3 months prior to screening;
- Patients who received treatment as part of another clinical study within 3 months prior to screening;
- Patients who participated in another clinical study involving stem cell therapy within 1 year prior to screening;
- Patients with inflammatory or autoimmune diseases requiring concomitant treatment with immunosuppressive agents, such as prednisolone >10 mg/day;
- Patients with a history of infection requiring systemic antibiotics, antifungal agents, or antiviral agents; active infections (viral, bacterial, fungal, or mycobacterial); or other diseases that may interfere with the assessment of efficacy in the study;
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- History of malignancy;
- Known hypersensitivity or allergic reaction to any component of the investigational product;
- Participants who, in the investigator's judgment, are unsuitable for participation in the study, or who have any condition that, in the investigator's opinion, may increase the participant's risk or interfere with the conduct or assessment of the clinical trial;
- Female participants who are pregnant or breastfeeding, female participants planning to become pregnant, or male or female participants who intend to have children within 3 months after completion of the study.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
China1 site
The First Affiliated Hospital of Guangzhou Medical University
Guangzhou, Guangdong, 510120
Yuan Chen, 86+13671060568, ychen@jztmaker.com
About this study
Official title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IIb Clinical Trial to Evaluate the Efficacy and Safety of Human Bone Marrow-Derived Mesenchymal Stem Cell (hBMMSC) Injection in Patients With Autoimmune Pulmonary Alveolar Proteinosis (aPAP)
The purpose of this multicenter, randomized, double-blind, placebo-controlled phase IIb clinical trial is to evaluate the efficacy and safety of intravenous hBMMSC injection in patients with autoimmune pulmonary alveolar proteinosis (aPAP).
Read the detailed description
Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disease for which there is no specific drug treatment. Currently, the standard treatment strategy for PAP is whole-lung lavage (WLL), which is invasive and has limited therapeutic efficacy. The purpose of this study is to evaluate the efficacy and safety of hBMMSC intravenous treatment in patients with aPAP. The clinical trial intends to involve 10 participants. The trial is expected to last approximately 3 years.
- Being tested
- The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injection, Lactated Ringer's Injection (crystalloid)
- Medical subject headings
- Pulmonary Alveolar Proteinosis, Acquired
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injectionDrug
The hBMMSC injection will be administered by intravenous infusion at a dose of 2.0 × 10⁶ cells/kg per administration. A total of 2 doses will be administered, with a 2-week interval between doses.
Lactated Ringer's Injection (crystalloid)Drug
Lactated Ringer's Injection will be used as the comparator and administered by intravenous infusion at a volume of 2 mL/kg per administration. A total of 2 doses will be administered, with a 2-week interval between doses.
| Study group | Role | What they receive |
|---|---|---|
| hBMMSC injection: 2.0×10^6 cells/kg | Experimental | The hBMMSC injection will be administered by intravenous infusion. Receives: Drug: The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injection |
| Lactated Ringer's Injection | Placebo comparator | Lactated Ringer's Injection will be used as the comparator and administered by intravenous infusion. Receives: Drug: Lactated Ringer's Injection (crystalloid) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Alveolar-arterial difference in oxygen tension (A-aDO2)
The between-group difference in the change from baseline in the alveolar-arterial oxygen tension gradient ([A-a]DO₂) at Week 24, comparing the hBMMSC injection group with the placebo group.
Measured: 24 weeks
Secondary outcomes (32)
Diffusing capacity of the lungs for carbon monoxide (DLCO, % predicted)
The between-group differences in the efficacy of hBMMSC injection versus placebo on the diffusing capacity of the lungs for carbon monoxide (DLCO, % predicted) at Weeks 24 and 48 after treatment
Measured: 24 weeks/48 weeks
PaO₂
The between-group differences in PaO₂ at Weeks 24 and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 24 weeks/48 weeks
Oxygenation index
The between-group differences in oxygenation indexat Weeks 24 and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 24 weeks/48 weeks
Oxygen therapy requirements
The between-group difference in oxygen therapy requirements at Weeks 24 and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 24 weeks/48 weeks
Disease severity score (DSS)
The between-group differences in disease severity score (DSS) at Weeks 24 and 48 after treatment, comparing the hBMMSC injection group with the placebo group.Disease Severity Score (DSS) is a scoring system used to evaluate disease severity based on predefined clinical signs, symptoms, or pathological changes. a higher DSS indicates more severe disease, whereas a lower DSS indicates milder disease, with 0 typically representing no detectable disease.
Measured: 24 weeks/48 weeks
6-minute walk test (6MWT)
The between-group differences in the 6-minute walk test (6MWT) results at Weeks 12, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 12/24/48 weeks
Cardiopulmonary exercise testing (CPET)
The between-group differences in the cardiopulmonary exercise testing (CPET) results at Weeks 12, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 12/24/48 weeks
Forced vital capacity (FVC)
The between-group differences in forced vital capacity (FVC) at Weeks 4, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 4/24/48 weeks
Forced expiratory volume in 1 second (FEV₁)
The between-group differences in forced expiratory volume in 1 second (FEV₁) at Weeks 4, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 4/24/48 weeks
Pulmonary lesions assessed by imaging
The between-group difference in changes in pulmonary lesions assessed by imaging at Weeks 24 and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 24/48 weeks
Proportion of patients whose disease progressed to requiring whole-lung lavage (WLL) during the study period and the interval to WLL
The between-group difference in the proportion of patients whose disease progressed to requiring whole-lung lavage (WLL) during the study period and the interval to WLL, comparing the hBMMSC injection group with the placebo group
Measured: 96 weeks
Medical Research Council (mMRC) dyspnea scores
The between-group differences in modified Medical Research Council (mMRC) dyspnea scores at Weeks 4, 12, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group. Modified Medical Research Council (mMRC) Dyspnea Scale is a questionnaire used to assess the severity of breathlessness and its impact on daily activities, particularly in patients with chronic obstructive pulmonary disease (COPD). The score ranges from 0 to 4, with Grade 0 indicating breathlessness only during strenuous exercise and Grade 4 indicating severe breathlessness that limits leaving the house or dressing. A higher mMRC score indicates more severe dyspnea and greater activity limitation
Measured: 4/12/24 weeks
St. George's Respiratory Questionnaire (SGRQ) scores
The between-group differences in St. George's Respiratory Questionnaire (SGRQ) scores at Weeks 4, 12, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group. The St. George's Respiratory Questionnaire (SGRQ) is a disease-specific questionnaire used to assess health-related quality of life in patients with respiratory diseases. The total score ranges from 0 to 100, where higher scores represent worse respiratory health status and greater impairment of quality of life.
Measured: 4/12/24/48 weeks
The safety of hBMMSC injection
The safety of hBMMSC injection compared with placebo during Weeks 24 and 48, as assessed by the incidence of adverse events (AEs), serious adverse events (SAEs), adverse drug reactions (ADRs), important adverse events, and discontinuations due to AEs.
Measured: 24/48 weeks
The proportion of patients with an improvement from baseline in [A-a]DO₂
The proportion of patients with an improvement from baseline in [A-a]DO₂ at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The proportion of patients with an improvement from baseline in DLCO
The proportion of patients with an improvement from baseline in DLCO at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The incidence of AEs and SAEs
The incidence of AEs and SAEs through Week 48 after treatment
Measured: 48 weeks
The proportion of patients with improvements from baseline in PaO₂
The proportion of patients with improvements from baseline in PaO₂ at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The proportion of patients with improvements from baseline in oxygenation index
The proportion of patients with improvements from baseline in oxygenation index at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The proportion of patients with improvements from baseline in disease severity score (DSS)
The proportion of patients with improvements from baseline in disease severity score (DSS) at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The proportion of patients with improvement in pulmonary lesions
The proportion of patients with improvement in pulmonary lesions as assessed by imaging at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The between-group differences in peripheral capillary oxygen saturation (SpO₂)
The between-group differences in peripheral capillary oxygen saturation (SpO₂) at Weeks 4, 12, 24, and 48 after treatment, comparing the hBMMSC injection group with the placebo group
Measured: 4/12/24/48 weeks
The proportion of patients with improvements in the 6-minute walk test (6MWT)
The proportion of patients with improvements in the 6-minute walk test (6MWT) results at Weeks 12, 24, and 48 after treatment
Measured: 12/24/48 weeks
The proportion of patients with improvements in the cardiopulmonary exercise testing (CPET)
The proportion of patients with improvements in the cardiopulmonary exercise testing (CPET) results at Weeks 12, 24, and 48 after treatment
Measured: 12/24/48 weeks
The change in serum anti-GM-CSF antibody levels
The between-group difference in the change from baseline in serum anti-GM-CSF antibody levels at Weeks 24 and 48 after treatment
Measured: 24/48 weeks
The changes in body weight in the hBMMSC injection group compared to the placebo group
Measured: 4/12/24/48 weeks
The changes in height in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
The changes in blood pressure in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
The changes in pulse rate in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
The changes in body temperature in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
The changes in complete blood count in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
The changes in urinalysis in the hBMMSC injection group compared with the placebo group
Measured: 4/12/24/48 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Oct 2026
- Study start30 Oct 2026 (estimated)
- Primary completion30 Oct 2029 (estimated)
- Study completion28 Feb 2030 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Autoimmune Pulmonary Alveolar ProteinosisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 70 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd.
- Sponsor type
- University, hospital or other
- Collaborators
- The First Affiliated Hospital of Guangzhou Medical University
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07890649
- Sponsor's protocol ID
- MKMSC-CT-201
- Status last verified
- Oct 2026
- First submitted
- 28 Sep 2026
- Last updated
- 22 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
Study at a glance
From the registry record, last updated by the sponsor on 22 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Multicenter, Randomized, Double-Blind, Placebo-Controlled Phase IIb Clinical Trial to Evaluate the Efficacy and Safety of Human Bone Marrow-Derived Mesenchymal Stem Cell (hBMMSC) Injection in Patients With Autoimmune Pulmonary Alveolar Proteinosis (aPAP)
- ClinicalTrials.gov ID
- NCT07890649
- Acronym / sponsor ID
- MKMSC-CT-201
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 70 participants (estimated)
- Lead sponsor
- Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd.University, hospital or other
- Collaborators
- The First Affiliated Hospital of Guangzhou Medical University
- Study start
- 30 Oct 2026 (estimated)
- Primary completion
- 30 Oct 2029 (estimated)
- Study completion
- 28 Feb 2030 (estimated)
- First posted
- 22 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this multicenter, randomized, double-blind, placebo-controlled phase IIb clinical trial is to evaluate the efficacy and safety of intravenous hBMMSC injection in patients with autoimmune pulmonary alveolar proteinosis (aPAP).
Detailed description
Autoimmune pulmonary alveolar proteinosis (aPAP) is a rare lung disease for which there is no specific drug treatment. Currently, the standard treatment strategy for PAP is whole-lung lavage (WLL), which is invasive and has limited therapeutic efficacy. The purpose of this study is to evaluate the efficacy and safety of hBMMSC intravenous treatment in patients with aPAP. The clinical trial intends to involve 10 participants. The trial is expected to last approximately 3 years.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| hBMMSC injection: 2.0×10^6 cells/kg | Experimental | Drug: The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injectionThe hBMMSC injection will be administered by intravenous infusion. |
| Lactated Ringer's Injection | Placebo comparator | Drug: Lactated Ringer's Injection (crystalloid)Lactated Ringer's Injection will be used as the comparator and administered by intravenous infusion. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Male or female participants aged ≥18 years;
- Patients with pulmonary alveolar proteinosis (PAP) confirmed by imaging, bronchoalveolar lavage (BAL) cytology, or lung biopsy, including transbronchial lung biopsy (TBLB), transbronchial cryobiopsy (TBCB), or surgical lung biopsy, and who are positive for serum anti-GM-CSF antibodies;
- At rest and while breathing room air, arterial partial pressure of oxygen (PaO₂) >50 mmHg, and either PaO₂ ≤70 mmHg or an oxygenation index corrected for the fraction of inspired oxygen (PaO₂/FiO₂ ratio) ≤333 mmHg; or, in participants with symptoms such as cough, sputum production, and exertional dyspnea, PaO₂ <75 mmHg or a PaO₂/FiO₂ ratio ≤357 mmHg;
- At least two assessments, performed at an interval of ≥2 months, indicating no significant spontaneous improvement of the disease, defined as an improvement in [A-a]DO₂ of <10 mmHg and an improvement in DLCO % predicted of <10%. If only one of these criteria is met, the investigator shall determine, based on the participant's symptoms, oxygen therapy requirements, imaging findings, and previous treatments, whether the disease is in a stable, non-remitting or progressive state, and shall document the basis for this determination;
- Participants of childbearing potential must use effective medically accepted contraceptive methods, regardless of sex, until 1 year after the last study treatment administration;
Key exclusion criteria (10 listed)
- Patients diagnosed with hereditary, secondary, or other types of PAP;
- Patients who received whole-lung lavage (WLL) or granulocyte-macrophage colony-stimulating factor (GM-CSF) therapy within 3 months prior to screening;
- Patients who received treatment as part of another clinical study within 3 months prior to screening;
- Patients who participated in another clinical study involving stem cell therapy within 1 year prior to screening;
- Patients with inflammatory or autoimmune diseases requiring concomitant treatment with immunosuppressive agents, such as prednisolone >10 mg/day;
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injectionThe hBMMSC injection will be administered by intravenous infusion at a dose of 2.0 × 10⁶ cells/kg per administration. A total of 2 doses will be administered, with a 2-week interval between doses. | Drug | hBMMSC injection: 2.0×10^6 cells/kg |
| Lactated Ringer's Injection (crystalloid)Lactated Ringer's Injection will be used as the comparator and administered by intravenous infusion at a volume of 2 mL/kg per administration. A total of 2 doses will be administered, with a 2-week interval between doses. | Drug | Lactated Ringer's Injection |
Primary outcome
Alveolar-arterial difference in oxygen tension (A-aDO2)
Time frame: 24 weeks
The between-group difference in the change from baseline in the alveolar-arterial oxygen tension gradient ([A-a]DO₂) at Week 24, comparing the hBMMSC injection group with the placebo group.
32 secondary outcomes
Diffusing capacity of the lungs for carbon monoxide (DLCO, % predicted)
Time frame: 24 weeks/48 weeks
PaO₂
Time frame: 24 weeks/48 weeks
Oxygenation index
Time frame: 24 weeks/48 weeks
Oxygen therapy requirements
Time frame: 24 weeks/48 weeks
Disease severity score (DSS)
Time frame: 24 weeks/48 weeks
6-minute walk test (6MWT)
Time frame: 12/24/48 weeks
Cardiopulmonary exercise testing (CPET)
Time frame: 12/24/48 weeks
Forced vital capacity (FVC)
Time frame: 4/24/48 weeks
Forced expiratory volume in 1 second (FEV₁)
Time frame: 4/24/48 weeks
Pulmonary lesions assessed by imaging
Time frame: 24/48 weeks
Proportion of patients whose disease progressed to requiring whole-lung lavage (WLL) during the study period and the interval to WLL
Time frame: 96 weeks
Medical Research Council (mMRC) dyspnea scores
Time frame: 4/12/24 weeks
St. George's Respiratory Questionnaire (SGRQ) scores
Time frame: 4/12/24/48 weeks
The safety of hBMMSC injection
Time frame: 24/48 weeks
The proportion of patients with an improvement from baseline in [A-a]DO₂
Time frame: 24/48 weeks
The proportion of patients with an improvement from baseline in DLCO
Time frame: 24/48 weeks
The incidence of AEs and SAEs
Time frame: 48 weeks
The proportion of patients with improvements from baseline in PaO₂
Time frame: 24/48 weeks
The proportion of patients with improvements from baseline in oxygenation index
Time frame: 24/48 weeks
The proportion of patients with improvements from baseline in disease severity score (DSS)
Time frame: 24/48 weeks
The proportion of patients with improvement in pulmonary lesions
Time frame: 24/48 weeks
The between-group differences in peripheral capillary oxygen saturation (SpO₂)
Time frame: 4/12/24/48 weeks
The proportion of patients with improvements in the 6-minute walk test (6MWT)
Time frame: 12/24/48 weeks
The proportion of patients with improvements in the cardiopulmonary exercise testing (CPET)
Time frame: 12/24/48 weeks
The change in serum anti-GM-CSF antibody levels
Time frame: 24/48 weeks
The changes in body weight in the hBMMSC injection group compared to the placebo group
Time frame: 4/12/24/48 weeks
The changes in height in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
The changes in blood pressure in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
The changes in pulse rate in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
The changes in body temperature in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
The changes in complete blood count in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
The changes in urinalysis in the hBMMSC injection group compared with the placebo group
Time frame: 4/12/24/48 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Oct 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing The human Bone Marrow Mesenchymal Stem Cell (hBMMSC) injection and Lactated Ringer's Injection (crystalloid) in people with Autoimmune Pulmonary Alveolar Proteinosis, run by Jiuzhitang Maker (Beijing) Cell Technology Co.,Ltd. at 1 site in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 10 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: opening soon, as of the sponsor's last update on 22 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Yuan Chen (+86 13671060568, ychen@jztmaker.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Alveolar-arterial difference in oxygen tension (A-aDO2) (time frame: 24 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Oct 2026.