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Completed

NCT Number: NCT02716610

Dose-Response and Variability of Inhaled Insulin in Type 2 Diabetes

Pharmacokinetic (PK) and Pharmacodynamic (PD) dose-response investigation of Dance-501 inhaled human insulin

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Key information

Age range

18 year–74 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1 / Phase 2

About this study

This study investigated the pharmacokinetic (PK) and pharmacodynamic (PD) properties of Dance-501, a novel inhaled human insulin liquid formulation (INH) and device. Twenty-four subjects with type 2 diabetes (T2DM) received 3 INH doses: low (69 units), medium (139 units) and high (208 units) and 1 equivalent medium dose (18 units) of subcutaneous insulin lispro (LIS).

The medium dose was repeated to determine within subject variability. PD was investigated during a 12 hour euglycemic clamp.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Type 2 diabetes mellitus treated with insulin injections at a total daily dose less than 1.2 U/kg/day.
  • Body mass index 25-40 kg/m2
  • Hemoglobin A1c 6.5-9.5%
  • Forced vital capacity and forced expiratory volume in 1 second at least 75% of predicted normal values.
  • Fasting c-peptide less than 1 nmol/L

Exclusion criteria

  • Any condition possibly affecting drug absorption from the lung, in particular subjects with decreased lung function or subjects taking bronchodilators or subjects who smoke.
  • Active or chronic pulmonary disease.
  • Any major disorder other than type 2 diabetes.
  • Decompensated heart failure or myocardial infarction at any time or angina pectoris within the last 12 months.
  • Proliferative retinopathy or maculopathy or severe neuropathy.

Treatment and study plan

INH 69 U (low)

Drug

inhaled human insulin

Other names: Dance-501

INH 69 U (high)

Drug

inhaled human insulin

Other names: Dance-501

INH 139 U

Drug

inhaled human insulin

Other names: Dance-501

INH 208 U

Drug

inhaled human insulin

Other names: Dance-501

LIS 18 U

Drug

subcutaneous insulin lispro

Other names: subcutaneous insulin lispro

Primary outcomes

  1. Area under the curve for insulin from 0-8 hours (AUCins0-8h)

    Time frame: 0 to 8 hours following each dose

    Assessment of the linearity of the dose-response curves

  2. Maximum concentration of insulin (CMaxIns)

    Time frame: up to 12 hours following each dose

    Assessment of the linearity of the dose-response curves

  3. Area under the curve for glucose infusion rate from 0-12 hours (AUGgir0-12h)

    Time frame: 0 to 8 hours following each dose

    Assessment of the linearity of the dose-response curves

  4. Maximum glucose infusion rate (GIRmax)

    Time frame: up to 12 hours following each dose

    Assessment of the linearity of the dose-response curves

Secondary outcomes

  1. Bioavailability

    Time frame: 0 to 8 hours following each dose

    Relative delivery efficiency (FREL) of inhaled human insulin (INH) compared to subcutaneous injected insulin lispro (LIS)

Sponsors and collaborators

Lead sponsor

Dance Biopharm Inc.

Industry

Registry information

Official study title

Samba-02: An Investigation of the Dose-Response and Subject Variability of Inhaled Insulin in Subjects With Type 2 Diabetes

Acronym: Samba-02

Important dates

Study start
2013
Primary completion
2014
Study completion
2014
First posted
Mar 23, 2016
Registry last updated
Mar 23, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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