Safety and Efficacy Study of KAI-1678 to Treat Subjects With Postoperative Pain
A Double-Blind, Randomized, Placebo- and Active-Comparator-Controlled, Single-Dose Study to Assess the Efficacy of KAI-1678 Administered by Subcutaneous Infusion for the Treatment of Postoperative Pain
Sponsor: KAI Pharmaceuticals
Listed as NCT01015235, this PHASE2 trial focuses on Pain, Postoperative and remains completed. Sponsored by KAI Pharmaceuticals, it has been updated 5 times since 2008, reflecting limited change activity. This study adds to the evidence base for this therapeutic area through structured, versioned documentation.
Status Flow
Change History
5 versions recorded-
Sep 2024 — Present [monthly]
Completed PHASE2
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE2
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE2
-
Jun 2018 — Jan 2021 [monthly]
Completed PHASE2
-
Jan 2017 — Jun 2018 [monthly]
Completed PHASE2
First recorded
Dec 2008
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- KAI Pharmaceuticals
- Trident Clinical Research Pty Ltd
For direct contact, visit the study record on ClinicalTrials.gov .