Efficacy and safety of preprandial human insulin inhalation powder versus injectable insulin in patients with type 1 diabetes
- First Online:
- Cite this article as:
- Garg, S., Rosenstock, J., Silverman, B.L. et al. Diabetologia (2006) 49: 891. doi:10.1007/s00125-006-0161-3
- 721 Downloads
The efficacy and safety of human insulin inhalation powder (HIIP) plus insulin glargine were compared to subcutaneously injected insulin (SC insulin) plus insulin glargine in patients with type 1 diabetes.
This was a randomised, open-label crossover study in which one group of patients received preprandial HIIP plus insulin glargine for 12 weeks, followed by the same duration with preprandial SC insulin (lispro or regular) plus insulin glargine. Another group of patients received the reverse treatment sequence. The trial was designed as a non-inferiority comparison of the two treatments for effect on HbA1c; blood glucose levels were also monitored. Safety assessments included adverse event reporting and hypoglycaemic events.
HbA1c at endpoint was 7.95±0.12% for the HIIP treatment and 8.06±0.12% for the SC insulin treatment; mean changes from baseline to endpoint were −0.08 and 0.00%, respectively, (p=NS). The upper limit of the 95% CI of mean difference in HbA1c between the two treatments was 0.02%, indicating that HIIP was not inferior relative to SC insulin, as measured against the pre-defined margin of 0.3%. Fasting blood glucose was significantly lower for HIIP treatment (8.09±0.33 mmol/l; n=117) than for SC insulin treatment (9.05±0.33 mmol/l; n=111) (p=0.01). Safety profiles were comparable between the two treatments. The rate of any hypoglycaemia (least-squares mean adjusted for 30 days±SE) was 8.9±0.7 and 8.2±0.8 for HIIP and SC insulin treatments, respectively, (p=0.29). The rate of nocturnal hypoglycaemia was greater for HIIP (4.2±0.4) than for SC insulin (2.7±0.4; p<0.001).
HIIP was similar in efficacy to SC insulin for glycaemic control in type 1 diabetes mellitus. The two treatments had comparable safety profiles.
KeywordsDrug delivery HbA1c Hyperglycaemia Inhaled insulin Injection Pulmonary Type 1 diabetes mellitus
diffusing capacity for carbon monoxide
fasting blood glucose
forced expiratory volume in 1 s
fasting plasma glucose
human insulin inhalation powder
self-monitoring blood glucose
total lung volume
Insulin therapy in patients with diabetes often involves multiple daily injections of insulin, which, from the patient perspective, has several disadvantages including physical discomfort and inconvenience, as well as technical issues regarding drug administration [1, 2]. Many patients dislike such injection regimens , possibly resulting in poor compliance and suboptimal glycaemic control . Inhaled insulin represents a promising and practical alternative way of insulin delivery , with demonstrated proof of principle for effective pulmonary delivery in clinical trials involving patients with diabetes . Multiple studies have shown that such patients prefer inhaled to injected regimens [1, 6, 7, 8], which may lead to greater patient acceptance of daily insulin administration and improved therapeutic outcomes.
A previous study has shown that the human inhaled insulin powder (HIIP) used in the present study is well tolerated and has a good safety profile . Moreover, HIIP demonstrated a broad range of dose proportionality relative to subcutaneously injected insulin lispro, as well as comparable glucodynamic effects and intra-subject variability. Here we report safety and efficacy findings of HIIP compared to subcutaneously injected (SC) insulin in patients with type 1 diabetes. This study represents the first investigation of efficacy with a small, breath-actuated delivery device using AIR particle technology [9, 11, 12] (Alkermes, Cambridge, MA, USA). The study was designed with moderate-intensity treatment goals to ensure patient safety and a crossover design to determine treatment preference , which will be reported separately.
Subjects and methods
A total of 137 patients with type 1 diabetes of at least 24 months duration were enrolled. Diagnosis was confirmed by C-peptide concentration of <165 pmol/l. At screening, per eligibility criteria, HbA1c values were ≥7 and ≤12% and patients had been currently injecting regular human insulin or insulin lispro for at least 4 weeks prior to study entry. Patients had pulmonary function tests within the normal range, i.e. forced expiratory volume in 1 s (FEV1), forced vital capacity, and diffusing capacity for carbon monoxide (DLCO) ≥75 and ≤125% of predicted values. Patients were excluded from participation for the following reasons: history of asthma, atopy, or allergic rhinitis; upper respiratory infection within 4 weeks prior to screening; lower respiratory infection within 5 months prior to screening; chronic cough; clinical signs or symptoms of liver disease; renal dialysis, history of renal transplantation, or serum creatinine ≥0.13 mmol/l (males) or ≥0.12 mmol/l (females); history of angina, myocardial infarction, or New York Heart Association Class III/IV cardiac disease within 2 years prior to study entry; congestive heart failure requiring pharmacotherapy; advanced autonomic neuropathy; history of severe hypoglycaemia; confirmed gastroparesis; treatment for malignancy, excluding basal or squamous cell carcinoma; or systemic glucocorticoid therapy (except topical preparations). Participants had to be nonsmokers for at least 1 year, with a negative serum cotinine at screening. This phase II trial was conducted in agreement with the Declaration of Helsinki and the International Council on Harmonisation Guidelines to Good Clinical Practice. Patients signed informed consent prior to participation in the study.
The study was an open-label, 2-period crossover study conducted at 24 centres in the USA. During the 1-week lead-in period patients were instructed to inject regular human insulin or insulin lispro, as used prior to study entry, before meals, and insulin glargine at bedtime. Patients were randomised to one of two treatment sequences. One group received 12 weeks of preprandial HIIP plus insulin glargine daily, followed by 12 weeks of preprandial injectable insulin (SC insulin, i.e. regular human insulin or insulin lispro) plus insulin glargine daily. The other group received the same treatments in reverse order.
HIIP (of recombinant DNA origin) was formulated as a dry powder (AIR particle technology; Alkermes, Cambridge, MA, USA). Capsules were available in 2 dose strengths, low and medium. The low-dose capsules were filled with 0.9 mg of insulin, equivalent to 2 U of SC insulin. Medium-dose capsules were filled with 2.6 mg of insulin, equivalent to 6 U of SC insulin . Capsules were loaded into a breath-actuated inhaler (pre-commercial model), which contained a puncturing mechanism to allow release and dispersal of insulin from the capsule without requiring an external energy source. Patients requiring preprandial insulin doses above 6 U performed multiple inhalations to achieve the required dosage.
Administration and dose adjustments
Patients were instructed to follow these guidelines for timing of insulin administration: regular human insulin, 30–60 min before meals; insulin lispro 0 to 15 min before meals; HIIP 0 to 15 min before meals. Insulin glargine (subcutaneous) was administered at bedtime.
Fasting and preprandial ≤7.8 mmol/l (140 mg/dl)
2-h postprandial ≤8.9 mmol/l (160 mg/dl)
Insulin dose (both preprandial and insulin glargine) was dependent upon the individual requirements of the patient and could be adjusted at any time during the study.
Efficacy and safety measurements
A central laboratory was used to analyse laboratory samples. HbA1c levels were measured by high performance liquid chromatography (Bio-Rad Variant II; BioRad, Hercules, CA, USA), as certified by the National Glycohaemoglobin Standardisation Program . Seven-point self-monitoring of blood glucose (SMBG) profiles were performed by the patient using a blood glucose meter (Accu-Chek Compact; Roche Diagnostics, Indianapolis, IN, USA) provided for the study. Patients were instructed to perform the test before breakfast, lunch, and evening meals; 2 h after breakfast, lunch, and evening meals; and at bedtime before injecting insulin glargine. The values and times of SMBG were recorded in patient diaries; insulin doses and times of administration, episodes of hypoglycaemia, illnesses, and concomitant medications were also recorded.
Safety assessments consisted of adverse event reporting; laboratory abnormalities; vital signs and body weight; hypoglycaemic episodes; and tests of pulmonary function. Adverse events were coded with a MedDRA dictionary. Hypoglycaemic episodes were defined by either (1) symptoms of hypoglycaemia as reported by the patient, or (2) SMBG of <3.5 mmol/l (63 mg/dl), regardless of the presence of hypoglycaemic signs or symptoms. Nocturnal hypoglycaemia was defined as any hypoglycaemic event that occurred between bedtime, after insulin glargine administration, and the following morning before administration of the prandial insulin. Severe hypoglycaemia was defined as an episode in which the patient required the assistance of another person and which was associated with either a blood glucose level <2.8 mmol/l (50 mg/dl) or prompt recovery after oral carbohydrate, glucagon or intravenous glucose. Data regarding hypoglycaemic episodes were drawn from patient diaries, in which patients were instructed to record symptoms, SMBG levels, and treatment.
Pulmonary function tests were reviewed by a central quality-assurance monitor and assessed for compliance with American Thoracic Society testing standards .
The primary objective of this study was to test noninferiority of HIIP compared to SC insulin treatment. The analysis was based on an intent-to-treat sample, which included all randomised patients. The primary efficacy variable was HbA1c at the end of each treatment period. Noninferiority of HIIP to SC insulin treatment was demonstrated if the upper limit of the one-sided 95% CI of treatment difference was less than 0.3% as defined in the protocol. The CI was derived from ANOVA model for crossover study design. For other continuous efficacy and safety variables, a similar ANOVA model was performed to compare treatment differences. Fisher’s exact test was used for crossover analyses of categorical variables. For missing post-baseline measurements, endpoint was defined by the last observation carried forward within each period. No carry-over effects were observed for the analyses described here.
Patient characteristics and disposition
Subgroup analyses were conducted to examine possible effects of type of SC insulin on treatment outcome. For patients whose SC insulin was regular human insulin, the LSM±SE at endpoint was 8.34±0.21 and 8.32±0.21% for the HIIP (n=40) and SC insulin groups (n=37), respectively, (p=0.90; upper limit of 95% CI 0.24) (Fig. 3), with similar changes from baseline (means±SD: 0.08±0.78 and 0.00±0.79%, respectively). For patients whose SC insulin was insulin lispro, the LSM±SE at endpoint was 7.89±0.16 and 8.05±0.16% for the HIIP (n=87) and SC insulin (n=82) groups, respectively, (p=0.08; upper limit of 95% CI −0.01), with similar changes from baseline (0.16±0.80 and 0.00±0.69%, respectively).
Daily insulin requirements
Insulin dose requirements
SC insulin [n=109]
Bolus insulin dose
Basal (glargine) dose
Total daily insulin dose
The incidence of treatment-emergent adverse events did not differ significantly between HIIP (79/133; 59.4%) and SC insulin treatments (79/126; 62.7%) (p=0.99). Cough was the most frequently reported adverse event during HIIP treatment and was the only adverse event whose incidence differed significantly between treatments (13.5 and 4.0% of patients during the HIIP and SC insulin treatments, respectively; p=0.005). Three serious treatment-emergent adverse events were reported during treatment with SC insulin, one of which was due to hypoglycaemia. Two patients discontinued the study due to adverse events: one patient discontinued during the HIIP phase because of hypoglycaemia and another patient discontinued during the SC insulin phase because of viral encephalitis. Only small changes in weight were observed from baseline to endpoint for the two treatments (0.18 kg for both HIIP and SC insulin).
The rate of nocturnal hypoglycaemia was significantly higher during HIIP treatment than during SC insulin treatment (LSM±SE: 4.2±0.4 vs. 2.7±0.4 events per 30 days), both overall and at each timepoint (Fig. 5b). Differences between the two treatments remained statistically significant at all timepoints in the insulin lispro subgroup (Fig. 5c), but were not statistically significant for any of the timepoints in the regular insulin group (Fig. 5d).
At endpoint, insulin-specific antibody titre (LSM±SE) was 1.7±0.4% for the HIIP treatment period and 0.6±0.4% for the SC insulin treatment period (p<0.001 between treatments), with mean changes from baseline of 1.3 and 0.03%, respectively.
Pulmonary function tests by treatment
Pulmonary function test
Baseline, mean (SD)
Endpoint, mean (SD)
p value for treatment difference
SC insulin (n=124)
SC insulin (n=123)
DLCO (ml min−1 mmHg−1)
SC insulin (n=123)
SC insulin (n=123)
This was the first study to compare the use of inhaled insulin with that of subcutaneous insulin in type 1 diabetic patients on either insulin lispro or regular human insulin at mealtimes and insulin glargine for basal coverage. Our primary finding was that inhaled insulin+insulin glargine was not inferior to standard treatment with subcutaneous insulin+insulin glargine with respect to endpoint HbA1c. Similar results were obtained, i.e. equivalent glycaemic control with respect to HbA1c, for subgroup analyses of patients on insulin lispro or regular human insulin. These results are consistent with those reported previously in randomised, parallel-group studies of 12-weeks  and 24-weeks duration [7, 17], in which reductions in HbA1c were comparable for groups treated with mealtime inhaled insulin or subcutaneously injected regular human insulin. The results of these two previous studies [7, 17], however, are difficult to interpret since different basal insulins were used in the two treatment groups.
FBG values were significantly lower during HIIP treatment than during the SC insulin treatment, a finding which is similar to those of previous trials of a dry-powder insulin formulation, in which FPG was significantly lower after 24 weeks of treatment in the inhaled insulin group than in the SC insulin group [7, 17]. Lower FBG was not attributable to mean differences in insulin or glargine dosage. Although morning 2-h excursion blood glucose levels were significantly higher during HIIP treatment than during SC insulin treatment (due to significantly lower FBG before breakfast), all postprandial daily blood glucose values were similar between treatments. Furthermore, average daily values for the 2-h excursion blood glucose levels were not significantly different between treatments. Together with the comparability of insulin dosing requirements between the two treatments, these results suggest that HIIP provided equivalent glycaemic control to that of SC insulin.
HIIP showed a satisfactory safety and tolerability profile, consistent with previous investigations of inhaled insulin in healthy volunteers [18, 19, 20], patients with type 1 diabetes [7, 16, 17] and type 2 diabetes [18, 21, 22, 23]. Cough, the most common respiratory side effect reported in previous trials of inhaled insulin , was the most frequently repeated adverse event related to treatment with HIIP. The event was judged to be mild in severity in the majority of cases (data not shown).
The rate of any hypoglycaemia was significantly higher for the HIIP group than for the SC insulin group after 2 and 4 weeks of treatment. Differences between the two treatments were transitory inasmuch as rates of hypoglycaemia were similar at endpoint. Endpoint values approached baseline values for both treatments (data not shown). These findings suggest that patients who are switched from SC insulin to HIIP learn over a few weeks of treatment to adjust their insulin dose, diet, and exercise so that the rate of hypoglycaemia returns to the baseline level. The rate of nocturnal hypoglycaemia was significantly higher in the HIIP group than in the SC insulin group throughout the study. Subgroup analyses revealed that rates of nocturnal hypoglycaemia appeared to depend on the type of mealtime insulin patients were using. Patients who were using insulin lispro had a significantly higher rate of nocturnal hypoglycaemia during their HIIP treatment phase than during treatment with their usual SC-injectable insulin. In contrast, patients on regular human insulin had similar rates of nocturnal hypoglycaemia in both treatment phases. These results are consistent with the observation that serum insulin concentration returns more slowly to baseline for HIIP compared to SC lispro users (480 and 360 min, respectively)  and indicate that dosing regimens for HIIP may require minor adjustments to minimise the risk of nocturnal hypoglycaemia without sacrificing optimal control of FBG.
Insulin-specific antibodies increased over baseline values during the HIIP treatment period, a well-known finding from previous trials with various inhaled insulin formulations . The increase in antibody binding observed here was not associated with changes in clinically meaningful variables. A recent study that pooled data from phase II and III trials showed that antibody formation from inhaled insulin (Exubera) was not associated with hypersensitivity reactions or with loss of glycaemic control or change in pulmonary function . Together with another prospectively designed trial that assessed the impact of insulin antibody formation on glucodynamic variables and clinical safety in type 1 diabetic patients receiving inhaled insulin , none of these studies showed an association between increases in insulin antibody binding and adverse clinical sequelae.
Previous phase III trials in patients with type 1 diabetes showed small, nonprogressive decreases in DLCO among patients receiving of inhaled insulin [7, 17]. We observed a similar decrease in DLCO that appeared to be reversible for patients who first received HIIP, then crossed over to SC insulin. Although long-term evaluation of pulmonary function will be necessary to assess the overall safety profile of HIIP within the lung, preliminary results have shown that lung function is maintained in patients receiving a continuous regimen of inhaled insulin for up to 4 years .
In summary, results from this crossover study suggest that HIIP provided glycaemic control equivalent to that of SC insulin in patients with type 1 diabetes. HIIP demonstrated a safety profile comparable to that of SC insulin. Together with improved fasting glucose levels during the HIIP treatment period, the increased rate of nocturnal hypoglycaemia observed in this study for HIIP treatment relative to SC insulin treatment is consistent with previous reports showing that inhaled insulin formulations have a duration of activity comparable to that of regular insulin and longer than that of insulin lispro [10, 20]. Patients with type 1 diabetes have expressed greater satisfaction with inhaled over injected insulin [1, 6, 7], suggesting that the availability of inhaled insulin may lead to better patient adherence to intensive insulin therapy. Additional studies are underway to investigate whether more intensive treatment with inhaled insulin can achieve the tight glycaemic control needed to delay or prevent diabetic complications.
This work was sponsored by Eli Lilly and Company and is related to study protocol H7U-MC-IDAI. Parts of this work were presented at the 65th Annual Meeting and Scientific Sessions of the American Diabetes Association, San Diego, June 10–14, 2005 and at the 41st Annual Meeting of the European Association for the Study of Diabetes, Athens, Greece, September 12–15, 2005. S. Garg and J. Rosenstock are consultants/speakers to Eli Lilly and Company and have also received research grants from the company. B. L. Silverman is an employee and shareholder of Alkermes, Inc. B. Sun, C. S. Konkoy, A. de la Peña, and D. B. Muchmore are employees and shareholders of Eli Lilly and Company.