Clinical trial
A Phase I/II, Randomized, Double-blind, Comparator-controlled, Dose-escalation Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of TLC590 for Postsurgical Pain Management Following Inguinal Hernia Repair
NCT03591146 is registered in ClinicalTrials.gov with Taiwan Liposome Company as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase I/II, Randomized, Double-blind, Comparator-controlled, Dose-escalation Study to Evaluate the Safety, Pharmacokinetics, and Efficacy of TLC590 for Postsurgical Pain Management Following Inguinal Hernia Repair
- Lead sponsor
- Taiwan Liposome Company
- Phase
- Phase 1/2
- Overall status
- Completed
- Start date
- July 31, 2018
- Completion date
- January 14, 2019
- Enrollment
- 65 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
inguinal hernia