A Pilot Study to Assess the Safety, PK and PD of Insulin Injected Via MicronJet or Conventional Needle

NCT ID: NCT00602914

Last Updated: 2013-05-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: EARLY_PHASE1
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-03-31
• Study Completion Date: 2009-07-31

Brief Summary

The purpose of this study is to compare glucose pharmacokinetics and insulin pharmacodynamics injected via the MicronJet in comparison with a conventional needle.

Detailed Description

Administration of insulin to the skin has many potential advantages including improved kinetics and reduced pain. Today, insulin is injected to the SQ space, using, in most cases, various devices incorporating standard metal needles and usually causing considerable pain and discomfort to the patients. NanoPass has developed a microneedle based needle substitute for intradermal injections. This device requires minimal expertise and is expected to cause minimal or no pain during injections.

The objective of this study is to compare the pharmacokinetics and pharmacodynamics of insulin Novorapid® (Novo Nordisk) injected via the MicronJet device intradermally, to a conventional needle injected to the SQ space.

Conditions

Intradermal Injections

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: NONE

Study Groups

1

10 healthy volunteers will receive 0.1 U/kg. Once administered with a conventional needle (SQ) and then with MicronJet needle (ID) in a randomized order

Group Type: EXPERIMENTAL

MicronJet

Intervention Type: DEVICE

The micronJet is a microneedle injection device designed for intradermal delivery of drugs (i.e. delivery into the skin). In this study the MicronJet will be used to inject insulin vs. a convention needle injection.

MicronJet

Intervention Type: DEVICE

MicronJet, Intradermal Injection

2

10 Type II DM subject will receive 0.2 U/kg. Once administered with a conventional needle (SQ) and then with MicronJet needle (ID) in a randomized order

Group Type: EXPERIMENTAL

MicronJet

Intervention Type: DEVICE

The micronJet is a microneedle injection device designed for intradermal delivery of drugs (i.e. delivery into the skin). In this study the MicronJet will be used to inject insulin vs. a convention needle injection.

MicronJet

Intervention Type: DEVICE

MicronJet, Intradermal Injection

Interventions

MicronJet

The micronJet is a microneedle injection device designed for intradermal delivery of drugs (i.e. delivery into the skin). In this study the MicronJet will be used to inject insulin vs. a convention needle injection.

Intervention Type: DEVICE

MicronJet

MicronJet, Intradermal Injection

Intervention Type: DEVICE

Other Intervention Names

Microneedles

Eligibility Criteria

Inclusion Criteria

1. Men ranging in age from 18-40 years.

2. In good general health as determined by medical history, physical examination, ECG and clinical laboratory tests obtained with 14 days prior to the start of the study.

3. BMI<30 or the volunteer is not considered obese by the Principal Investigator with a written statement at screening.

4. Willing and able to abide by the dietary requirements of the study.

5. Willing and able to give written informed consent in a manner approved by the Institutional Review Board or Ethics Committee.

1. Type 2 male patients and post-menopausal females aged 30-70 years.

2. HA1c 6.5-10%

3. Naïve or treated with Metformin only

4. BMI< 35

5. Willing and able to abide by the dietary requirements of the study.

6. Willing and able to give written informed consent in a manner approved by the Institutional Review Board or Ethics Committee.

Exclusion Criteria

1. History of known or suspected clinically significant hypersensitivity to any drug.

2. History or presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.

3. Clinically significant cardiovascular, hepatic, gastrointestinal, metabolic, neurological, pulmonary, endocrine, psychiatric, coagulation or neoplastic disorders.

4. Participation in radiologic studies involving parenteral administration of iodinated contrast materials within two weeks prior to screening.

5. Subjects with history of recent alcohol abuse (defined as consumption of more than 21- ml of alcohol per week; or the equivalent of fourteen 4-oz glasses of wine, fourteen 12 oz can/bottle of beer or wine cooler) or other substance abuse.

6. Any protocol-required laboratory test abnormality that is considered clinically significant.

7. Participation in another investigational drug study within 90 days before the first day of dosing.

8. History of non-compliance to medical regimens, or subjects who are considered potentially unreliable.

9. Blood or plasma donation within the past 90 days.

10. Mentally unstable or incompetent.

11. Positive hepatitis C screen or positive hepatitis B screen.

12. HIV positive

B. Type 2 diabetic patients

1. History of known or suspected clinically significant hypersensitivity to any drug.

2. History or presence of any disease or condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.

3. Clinically significant cardiovascular, hepatic, gastrointestinal, metabolic, neurological, pulmonary, endocrine, psychiatric, coagulation or neoplastic disorders.

4. Participation in radiologic studies involving parenteral administration of iodinated contrast materials within two weeks prior to screening.

5. Subjects with history of recent alcohol abuse (defined as consumption of more than 21- ml of alcohol per week; or the equivalent of fourteen 4-oz glasses of wine, fourteen 12 oz can/bottle of beer or wine cooler) or other substance abuse.

6. Any protocol-required laboratory test abnormality that is considered clinically significant.

7. Participation in another investigational drug study within 90 days before the first day of dosing.

8. History of non-compliance to medical regimens, or subjects who are considered potentially unreliable.

9. Blood or plasma donation within the past 90 days.

10. Mentally unstable or incompetent.

11. Positive hepatitis C screen or positive hepatitis B screen.

12. HIV positive

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

NanoPass Technologies Ltd

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Itamar Raz, MD

Role: PRINCIPAL_INVESTIGATOR

Head, Diabetes Unit, Hadassah Medical Organization, Jerusalem, Israel

Other Identifiers

NP-1-001

Identifier Type: -

Identifier Source: org_study_id