Safety Study of Subcutaneously-Injected Prandial INSULIN-PH20 NP Compared to Insulin Lispro Injection in Participants With Type 1 Diabetes Mellitus
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|ClinicalTrials.gov Identifier: NCT00883558|
Recruitment Status : Completed
First Posted : April 17, 2009
Results First Posted : September 8, 2014
Last Update Posted : September 8, 2014
|Condition or disease||Intervention/treatment||Phase|
|Diabetes Mellitus, Type 1||Drug: Insulin Lispro Drug: regular human insulin Drug: recombinant human hyaluronidase PH20 Drug: Insulin glargine||Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||48 participants|
|Intervention Model:||Crossover Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase II, Randomized, Open Label, 2-Way Crossover, Safety Study of Subcutaneously Injected Prandial INSULIN-PH20 NP Compared to Insulin Analog Injection in Patients With Type 1 Diabetes|
|Study Start Date :||May 2009|
|Actual Primary Completion Date :||February 2010|
|Actual Study Completion Date :||April 2010|
Experimental: INSULIN-PH20 NP / Insulin Lispro
All enrolled participants underwent a 1-month dose titration period and received 100 units per milliliter (U/mL) insulin lispro, injected subcutaneously (SC) pre-meals, with doses titrated to each participant individually.
Next participants were randomly assigned to 1 of 2 study treatments (Treatment A or B) for the first of two, 3-month treatment cycles. Each participant then received the second treatment for the second cycle.
INSULIN-PH20 NP (Treatment A): 100 U/mL non-preserved (NP) formulation of regular human insulin with 5.0 micrograms per milliliter (µg/mL) recombinant human hyaluronidase PH20, injected SC, pre-meals, doses titrated to each participant individually.
Insulin Lispro (Treatment B): 100 U/mL insulin lispro, injected SC, pre-meals, doses titrated to each participant individually.
Throughout the study, participants requiring basal insulin used twice daily SC injections of 100 U/mL insulin glargine or maintained their usual regimen through an insulin pump.
Drug: Insulin Lispro
Other Name: Humalog
Drug: regular human insulin
Other Name: Humulin R
Drug: recombinant human hyaluronidase PH20
Drug: Insulin glargine
Other Name: Lantus
- Postprandial Glucose Excursion [ Time Frame: Week 14 and Week 26 ]A 2-hour postprandial glucose excursion was measured for 3 meals over 3 days during each treatment cycle (3 days during Week 14 of the first treatment cycle and 3 days during Week 26 of the second treatment cycle). For each of the 3 days, the mealtime (breakfast, lunch, and dinner) excursions were calculated as the post-meal glucose value minus the pre-meal value as determined by 8-point glucose monitoring. The average of all excursions over the 3 days for the corresponding treatment cycle is presented.
- Time Spent With Blood Glucose Value Outside a 71-139 Milligrams Per Deciliter (mg/dL) Range During Continuous Glucose Monitoring [ Time Frame: Week 14 and Week 26 ]Participants were provided a continuous glucose monitoring (CGM) device, consisting of a sensor, transmitter, and receiver. Total time the participant's blood glucose was outside the 71-139 mg/dL range during 3 days of CGM during each treatment cycle (3 days during Week 14 of the first treatment cycle and 3 days during Week 26 of the second treatment cycle) is presented.
- Number of Participants With Hypoglycemic Events [ Time Frame: Baseline through Week 29 ]The number of participants with at least one hypoglycemic event (HE) reported during the entire study is presented. Additionally, the number of participants with severe HEs (those that necessitated administration of carbohydrate or glucagon, or resuscitation, by another person) is also presented. A summary of serious and other non-serious adverse events regardless of causality is located in the Reported Adverse Events module.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00883558
|United States, Colorado|
|Barbara Davis Center for Childhood Diabetes|
|Aurora, Colorado, United States, 80045|
|United States, Florida|
|Diabetes Research Institute|
|Miami, Florida, United States, 33136|
|United States, Michigan|
|Henry Ford Health System|
|Detroit, Michigan, United States, 48202|
|United States, Montana|
|Mercury Street Medical|
|Butte, Montana, United States, 59701|
|United States, North Carolina|
|UNC Diabetes Care Center/Highgate Specialty Center|
|Durham, North Carolina, United States, 27713|
|United States, Ohio|
|Cleveland, Ohio, United States, 44195|
|United States, Texas|
|Texas Diabetes and Endocrinology|
|Austin, Texas, United States, 78731|
|United States, Washington|
|West Olympia Internal Medicine|
|Olympia, Washington, United States, 98502|
|Study Director:||Douglas Muchmore, M.D.||Halozyme Therapeutics|