An Ascending Dose Study to Evaluate M281 Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD)

NCT ID: NCT02828046

Last Updated: 2019-10-14

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-05-09
• Study Completion Date: 2017-08-08

Brief Summary

The purpose of this study is to evaluate safety, tolerability, and PK/PD of M281 after single and multiple doses in healthy volunteers.

Conditions

Healthy Volunteers

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: DOUBLE

Study Groups

Placebo

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

M281

M281

Group Type: EXPERIMENTAL

M281

Intervention Type: BIOLOGICAL

Interventions

M281

Intervention Type: BIOLOGICAL

Placebo

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Healthy male or female subjects between 18 and 55 years, inclusive.

2. Good health

3. Body weight between 50 and 110 kg inclusive

Exclusion Criteria

1. History of any drug allergy, hypersensitivity, or intolerance to any drug product that in the opinion of the Investigator would place the subject at particular risk and compromise the safety of the subject in the study.

2. History or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, psychiatric disease, or any other condition, that in the opinion of the Investigator would jeopardize the safety of the subject or the validity of the study results.

3. History or current diagnosis of substance dependence (except nicotine and caffeine) or alcohol abuse over the past 2 years, according to the criteria of DSM-IV-TR.

4. Smokes or has smoked more than 5 cigarettes per day in the last 90 days and is unable to stop smoking during in-patient observation period in clinic.

5. Unwillingness to abstain from alcohol for at least 24 hours prior to dosing with study medication until the time of discharge from the study unit and at least 24 hours prior to each ambulatory visit.

6. Plans to participate in another clinical trial while enrolled in this study and/or received an investigational drug and/or device within 60 days prior to admission.

7. Donation or significant loss of whole blood (480 mL or more) within 30 days or plasma within 14 days prior to admission.

8. History of splenectomy, asthma (with the exception of childhood asthma that has resolved), COPD, recurrent or current GI or respiratory infections.

9. On fluid restriction.

10. Systemic steroids within 3 months prior to the start of study drug administration, or any prescription medication(s) within 14 days of dose administration or any non-prescribed systemic or topical medication (including any herbal product) within 7 days prior to dose administration.

11. Vaccination within 1 month before dosing, or plans to receive vaccination during the study.

12. Any illness within 5 days, or clinically significant airway infections within 30 days, prior to first study drug dosing.

13. Positive urine drug screen (UDS) at screening.

14. Positivity for human immunodeficiency virus (HIV), hepatitis B, or hepatitis C at screening.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Momenta Pharmaceuticals, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John Hogan, MPM

Role: STUDY_DIRECTOR

Momenta Director of Clinical Operations

Tjerk Bosji, MD

Role: PRINCIPAL_INVESTIGATOR

PRA Research Physician

Locations

PRA Health Sciences

Zuidlaren, , Netherlands

Countries

Netherlands

Other Identifiers

MOM-M281-001

Identifier Type: -

Identifier Source: org_study_id