drugset / Trial / NCT03542435

Randomized, Double-Blind, Placebo-Controlled, MAD Study to Assess the Safety, Tolerability, and Pharmacokinetics of SXC 2023

NCT03542435 ↗

Phase 1 Completed 40 enrolled Promentis Pharmaceuticals, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This is a randomized, double-blind, placebo-controlled, multiple ascending dose study conducted at one study center in the United States. Safety and tolerability will be assessed throughout the study and serial blood samples and urine samples will be collected for the safety and pharmacokinetic assessment of SXC-2023.

Timeline

Start
2018-04-26
Primary completion
2018-08-08
Completion
2018-09-10

Drugs

EvaluationDrugModalityDoseRoute
Subject SXC-2023 Unknown — Oral

Indications

No indication recorded.