Clinical trial

Prospective Open-Label Trial of Rituximab for Primary Pulmonary Alveolar Proteinosis

Name
U2990s
Description
The purpose of this study is to determine whether the use of rituximab is effective in treating pulmonary alveolar proteinosis by leading to an improvement in lung function and disease status.
Trial arms
Trial start
2007-01-01
Estimated PCD
2009-07-01
Trial end
2011-12-01
Status
Completed
Phase
Early phase I
Treatment
rituximab
IV, 1000 mg, two weeks, 2 times
Arms:
1
Other names:
Rituxan, MabThera
Size
10
Primary endpoint
Evaluate symptomatic, physiologic and radiographic effects of therapy
6-months
Eligibility criteria
Inclusion Criteria: * Diagnosis of primary PAP (new or chronic) with presence of anti-GM-CSF antibody * Moderately symptomatic disease with PaO2 \<70 on room air and on less than 6 L/min oxygen * Able to give written informed consent and comply with the requirements of the study * Adequate renal and liver function * Negative serum pregnancy test (for women of child bearing age) and on acceptable birth control during and after study completion Exclusion Criteria: * Severe PAP and requires in-patient care and more urgent therapy with bilateral whole lung lavage * Treatment with any investigational agent within 4 weeks of screening * History of severe allergic or anaphylactic reactions to humanized or murine monoclonal antibodies * History of HIV, recurrent significant infection or recurrent bacterial infections * Known active bacterial, viral, fungal, mycobacterial, or other infection * Ongoing use of high dose steroids (\>10mg/day) or unstable steroid dose * Significant cardiac or pulmonary disease or blood disorder
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 10, 'type': 'ACTUAL'}}
Updated at
2023-09-28

1 organization

1 drug

2 indications

Indication
Primary Disease