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

Intradermal Injections Clinical Trial

— MicronJet  

Official title:

An Open Label Study in Healthy Volunteers and Diabetes Mellitus Type II Subjects to Determine the Safety, Pharmacokinetics and Pharmacodynamics Profile of Insulin Injected by the MicronJet Device

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00602914
• Other study ID #: NP-1-001
• Status: Completed
• Phase: Phase 0
• First received: December 30, 2007
• Last updated: May 8, 2013
• Start date: March 2008
• Est. completion date: July 2009

Study information

• Verified date: April 2008
• Source: NanoPass Technologies Ltd
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ethics CommissionIsrael: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

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

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 23
• Est. completion date: July 2009
• Est. primary completion date: December 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 70 Years

Eligibility

A. Healthy volunteers

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.

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

Inclusion Criteria:

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

Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics/Dynamics Study, Intervention Model: Crossover Assignment, Masking: Open Label

Related Conditions & MeSH terms

• Intradermal Injections

Intervention

Device:
• 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.
• MicronJet
MicronJet, Intradermal Injection

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
NanoPass Technologies Ltd

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Blood samples for PK and PD will be collected		pre dose and up to 360 minutes post dose of administration	No
Secondary	Feedback from study participants and staff on their overall impression with the MicronJet device, using questionnaires		All study duration	No