A Phase I Study to Assess Cardiac and General Safety and Pharmacokinetics of 60 mg MGN1703

NCT ID: NCT01982747

Last Updated: 2014-05-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 14 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-11-30
• Study Completion Date: 2013-12-31

Brief Summary

MGN1703 is being developed for use in treating cancerous tumors effecting the colon, skin, kidneys and lungs. The dosage form of MGN1703 under investigation is an injection.

The goal of this study is to evaluate the effects of MGN1703 on the electrical activity of the heart in healthy subjects and to look at general safety.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

MGN - Placebo

Subjects of the MGN-Placebo arm will receive 60mg MGN1703 as 2 s.c. injections of 2 ml each during period 1 and physiological saline solution as Placebo as 2 s.c. injections of 2 ml each during period 2

Group Type: OTHER

MGN-Placebo

Intervention Type: DRUG

Placebo-MGN

Subjects of the Placebo-MGN arm will receive physiological saline solution as Placebo as 2 s.c. injections of 2 ml each during period 1 and 60mg MGN1703 as 2 s.c. injections of 2 ml each during period 2

Group Type: OTHER

Placebo-MGN

Intervention Type: DRUG

Interventions

MGN-Placebo

Intervention Type: DRUG

Placebo-MGN

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. The subject signs an IRB/IEC-approved informed consent prior to any study-related procedures.

2. Subject is male or female with no less than 6 subjects per sex in the study.

3. Subject is 18 to 65 years of age.

4. Subject's BMI is ≤32 kg/m2.

5. Female subjects of childbearing potential must not be pregnant or lactating with a negative serum HCG pregnancy test result at Screening and a negative urine HCG pregnancy test result on Days -1 and 14 prior to receiving study medication.

6. Female subjects of childbearing potential and male subjects must use an adequate method of contraception from Screening until completion of the study. Acceptable methods of contraception are barrier methods (male condom, female condom, diaphragm, cervical cap, spermicide or IUD), surgical sterility (documented doctor's report of vasectomy, hysterectomy and/or bilateral oophorectomy) and/or postmenopausal status (defined as at least 1 year without menses as demonstrated by medical history or subject report).

7. Subject is in good health as determined by vital signs, medical history, physical exam, and safety laboratory analyses at Screening and during the study.

Exclusion Criteria

1. Subject has used an investigational product within 30 days prior to screening or during the study.

2. Subject has used prescription or non-prescription drugs (including vitamins, minerals, and herbal/plant-derived preparations) within 2 weeks of Screening (excluding oral contraceptives, hormonal IUD, hormone replacement therapy and acetaminophen) unless deemed acceptable by the Investigator in consultation with the Sponsor.

3. Subject has a positive drug and/or alcohol test at Screening, Day -1 or Day 14.

4. The subject has a history of drug or alcohol abuse within 2 years before Screening.

5. The subject is unable to abstain from ingesting alcohol, caffeine, grapefruit or Grapefruit juice for 72 hour prior to dosing.

6. The subject has a clinically significant history of cardiovascular, endocrinologic, hematologic, hepatic, immunologic, metabolic, urologic, pulmonary, neurologic, dermatologic, psychiatric, renal, and/or other major diseases or malignancy.

7. Subject has a history of cardiac disease or any risk factors for TdP including (but not limited to) unexplained syncope, cardiac arrest, unexplained cardiac arrhythmia, structural heart disease and family history of Long QT syndrome.

8. Subject has evidence of any of the following cardiac conduction abnormalities at Screening, Day -1 or Day 1 prior to receiving any study medication:

1. QTcF interval >430 msec for males and >450 msec for females

2. PR interval >240 msec or <110 msec

3. Evidence of second- or third-degree AVB

4. Electrocardiographic evidence of complete LBBB, complete RBBB or incomplete LBBB

5. Intraventricular conduction delay with QRS duration >120 msec

6. Heart rate <40 bpm or >90 bpm

7. Pathological Q waves (defined as >40 msec or depth >0.4-0.5 mV)

8. Evidence of ventricular pre-excitation

9. The safety laboratory analyses at Screening are outside the normal limits and considered by the Investigator as clinically significant.

10. Any acute or chronic condition that, in the opinion of the Investigator, would limit the subject's ability to complete and/or participate in this clinical study, a history of noncompliance to medical regimens, or subjects who are considered to be potentially unreliable.

1. The subject has a positive test result for HIV antibody.

2. The subject has a positive test result for the hepatitis C antibody or the HBsAg.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Mologen AG

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Carlos R Sanabria, MD

Role: PRINCIPAL_INVESTIGATOR

Spaulding Clinical

Locations

Spaulding Clinical

West Bend, Wisconsin, United States

Countries

United States

Other Identifiers

MGN1703-C04

Identifier Type: -

Identifier Source: org_study_id