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

Phase 1

Completed

• Conditions: Safety and Tolerability
• Interventions: Drug: Sevuparin

• Registration Number: NCT03853421
• Lead Sponsor: Modus Therapeutics AB

Brief Summary

A Double-blind, Placebo-controlled study in Healthy Volunteers to Determine the Safety and Tolerability of Single, Ascending Subcutaneous Doses of Sevuparin

Detailed Description

This is a randomized, double-blind, placebo-controlled, sequential cohort, single escalating dose study to explore the safety, tolerability, pharmacokinetics and pharmacodynamics of sevuparin in healthy volunteer adult male and female subjects. The study will consist of three subcutaneous dose cohorts (3, 6 and 9 mg/kg sevuparin). Each dosing cohort will consist of 8 subjects who will be randomized to receive either a single dose of sevuparin or matching placebo in a 3:1 ratio (6 active/2 placebo).

Study Timeline

• Status Verified: 2019-02
• Study Start: 2019-02-06
• Study First Submitted: 2019-02-15
• Study First Submitted QC: 2019-02-22
• Study First Posted: 2019-02-25
• Primary Completion: 2019-05-06
• Study Completion: 2019-05-06
• Last Update Submitted: 2019-07-15
• Last Update Posted: 2019-07-16

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 24

Inclusion Criteria

• Informed consent form is signed and dated
• Adult male or female subjects, aged ≥18 to ≤65 years of age inclusive;
• Body mass index ≥19.0 to ≤29.0 kg/m2 and a body weight 50.0-100.0 kg
• Subjects must have a negative pregnancy test and subjects of childbearing potential must either be surgically sterile or be willing to practice a highly effective method of contraception
• Subjects must be in good health, as determined by a medical history, physical examination
• Subjects with no clinically significant and relevant history that could affect the conduct of the study.

Exclusion Criteria

• Recent trauma or injury or history of clinically significant bleeding.
• Clinical evidence of significant or unstable medical illness
• Subjects who have received any prescribed systemic or topical medication
• Subjects who have received aspirin, anti-platelet therapy, anticoagulant therapy and prophylactic and therapeutic LMWH or un-fractioned heparin.
• Subjects who have used any non-prescribed systemic or topical medication (including herbal remedies)
• Subjects who have received any medications known to chronically alter drug absorption or elimination processes
• Subjects who are still participating in a clinical study
• Subjects who have donated any blood, plasma or platelets
• Subjects with a significant history of drug allergy
• Subjects who have any clinically significant allergic disease
• Subjects who have a supine blood pressure and supine pulse rate higher than 140/90 mmHg and 100 beats per minute (bpm), respectively, or lower than 90/50 mmHg and 40 bpm, respectively
• Subjects who have an abnormality in the 12-lead ECG that, in the opinion of the investigator, increases the risk of participating in the study, such as QTcF interval > 470 ms, or with sinus rhythm with PR interval <110 ms or >210 ms, confirmed by a repeat ECG.
• Screening transaminases (AST, ALT, GGT) ≥ 1.5 times the ULN; estimated glomerular filtration rate (GFR, MDRD equation) < 60 mL/min; APTT above the normal range, INR above 1.4; absolute platelet count <150,000/μL.
• Male subjects who consume more than 3 units of alcohol per day. Female subjects who consume more than 2 units of alcohol per day.
• Subjects with a positive urine drug screen/alcohol test result
• Subjects who smoke more than 6 cigarettes
• Subjects who have positive hepatitis B or hepatitis C antibody or HIV antibodies.
• Subjects who test positive for HIT antibodies at Screening.
• Any relevant condition, behavior, laboratory value or concomitant medication which, in the opinion of the investigator, makes the subject unsuitable for entry into the study.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Dose cohort 9 mg/kg sevuparin	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.
Dose cohort 3 mg/kg sevuparin	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.
Dose cohort 6 mg/kg sevuparin	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.

Primary Outcome Measures

Name	Time	Method
To determine the safety and tolerability of single ascending subcutaneous doses of sevuparin in healthy male and female subjects.	From baseline until day 28	Number of participants with treatment-related adverse events as assessed by CTCAE

Secondary Outcome Measures

Name	Time	Method
PK characteristics of sevuparin during and after administration of sevuparin as a single subcutanous injection (3 dose co-horts).	Pre dose until day 3	Area Under the Curve \[AUC\]).

Trial Locations

Locations (1)

Clinical Pharmacology of Miami (CPMI); 🇺🇸 Miami, Florida, United States