Placebo-controlled Study to Determine the Safety and Tolerability of Subcutaneous Doses of Sevuparin

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

February 6, 2019

Primary Completion Date

May 6, 2019

Study Completion Date

May 6, 2019

Conditions
Safety and Tolerability
Interventions
DRUG

Sevuparin

The study will consist of three dose cohorts (3, 6 and 9 mg/kg sevuparin). Subjects in each cohort will receive a single dose of sevuparin or placebo subcutaneously on Day 1.

Trial Locations (1)

33014

Clinical Pharmacology of Miami (CPMI), Miami

Sponsors
All Listed Sponsors
lead

Modus Therapeutics AB

INDUSTRY

NCT03853421 - Placebo-controlled Study to Determine the Safety and Tolerability of Subcutaneous Doses of Sevuparin | Biotech Hunter | Biotech Hunter