A Randomized, Double-blind, Placebo-controlled, Sequential Parallel Group, Single and Multiple Ascending Dose (SAD/MAD) Study in Healthy Subjects To Evaluate The Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Of TLL018 Following Oral Administration And With An Open Label Food Effect Panel
Latest Information Update: 04 Nov 2021
At a glance
- Drugs TLL 018 (Primary)
- Indications Autoimmune disorders; Inflammation; Rheumatoid arthritis
- Focus Adverse reactions; Pharmacokinetics
- Sponsors TLL Pharmaceutical
Most Recent Events
- 29 Mar 2021 Status changed from recruiting to completed.
- 28 Jan 2021 Planned number of patients changed from 84 to 100.
- 28 Jan 2021 Planned End Date changed from 31 Dec 2020 to 31 Jan 2021.