Effects of TNX-832 (Sunol cH36) in Subjects With Acute Lung Injury/Acute Respiratory Distress Syndrome
The Safety, Pharmacokinetics, and Pharmacodynamic Effects of TNX-832 (Sunol cH36) in Subjects With Acute Lung Injury/Acute Respiratory Distress Syndrome
Sponsor: Altor BioScience
Listed as NCT01438853, this PHASE1 trial focuses on Acute Lung Injury and Acute Respiratory Distress Syndrome and remains completed. Sponsored by Altor BioScience, it has been updated 9 times since 2004, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
9 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE1
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Feb 2025 — Sep 2025 [monthly]
Completed PHASE1
-
Sep 2024 — Feb 2025 [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE1
▶ Show 4 earlier versions
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE1
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Sep 2017 — Jun 2018 [monthly]
Completed PHASE1
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Feb 2017 — Sep 2017 [monthly]
Completed PHASE1
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE1
First recorded
Dec 2004
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Altor BioScience
- Genentech, Inc.
- Tanox
For direct contact, visit the study record on ClinicalTrials.gov .