CompletedPhase 1NCT01438853
Effects of TNX-832 (Sunol cH36) in Subjects With Acute Lung Injury/Acute Respiratory Distress Syndrome
Studying Acute lung injury
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Altor BioScience
- Principal Investigator
- Hing Wong, PhDAltor BioScience
- Intervention
- TNX-832(biological)
- Enrollment
- 18 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2004 – 2008
Study locations (7)
- University of Miami, Miami, Florida, United States
- Beth Israel Deconess Medical Center, Boston, Massachusetts, United States
- Washington University, St Louis, Missouri, United States
- Wake Forest University, Winston-Salem, North Carolina, United States
- Akron General Medical Center, Akron, Ohio, United States
- Baylor School of Medicine, Houston, Texas, United States
- Capital Health, Halifax, Nova Scotia, Canada
Collaborators
Genentech, Inc. · Tanox
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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