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Will availability of inhaled human insulin (Exubera®) improve management of type 2 diabetes? The design of the Real World trial

Trials20067:25

DOI: 10.1186/1745-6215-7-25

Received: 03 July 2006

Accepted: 10 August 2006

Published: 10 August 2006

Abstract

Background

Common deterrents to insulin therapy for both physicians and patients are the complexity and burden of daily injections. In January 2006, the first inhaled human insulin (INH, Exubera® (insulinhuman [rDNA origin])InhalationPowder) was approved for use in adult patients with type 1 diabetes mellitus (T1DM) or type 2 diabetes mellitus (T2DM) in the United States and European Union. Results from the INH clinical trial program have shown comparable efficacy of INH to subcutaneous (SC) insulin and superior efficacy versus oral antidiabetic agents; thus providing effective glycemic control in adult patients with T2DM without the requirement for preprandial injections. However, because subjects in those trials were randomized to either INH or an alternative, the studies could not estimate the effect of INH on patient acceptance of insulin therapy. Therefore, traditional study designs cannot provide answers to important and practical questions regarding real world effectiveness, which is influenced by psychological and other access barriers.

Methods

To overcome these limitations, the Real World Trial was designed to estimate the effect of the availability of INH as a treatment option for glycemic control. A total of approximately 700 patients from Canada, France, Germany, Italy, Spain, United Kingdom, and the United States with T2DM poorly controlled by oral agent therapy will be randomized to two different treatment settings. Patients and clinicians in both groups (A & B) may choose from all licensed therapies for diabetes including SC insulin delivered by pens; INH will be an additional treatment option only available in Group A. The Real World Trial (Protocol A2171018) has been registered with ClincalTrials.gov, registration id NCT00134147.

Results

The primary outcome for the trial will be the difference in mean glycosylated hemoglobin (HbA1c) at 6 months between groups. The design was based on a preceding feasibility study examining the theoretical effects of inhaled insulin availability on treatment choice in 779 patients. In that study, patients were three times more likely to choose insulin therapy when inhaled insulin was available.

Conclusion

Innovations in study designs may provide an opportunity to reveal unbiased answers to important treatment questions that are more relevant to prescribers, funding agencies, and healthcare policymakers.

1.0 Background

Diabetes mellitus constitutes a major healthcare problem globally. In the United States, 10.3 million people were reported with this disease in 1997; and an additional 5.4 million people were suspected to have diabetes, but were not diagnosed nor treated [1]. The total number of individuals with identified diabetes is expected to increase to approximately 16 million by 2010 [2], and 22 million by 2025 [3]. Most patients have type 2 diabetes mellitus (T2DM), characterized by a combination of insulin resistance and progressive loss of insulin secretion. In approximately 58% of patients with T2DM, the disease is not sufficiently controlled based on American Diabetes Association (ADA) recommendations [4]. As a result, patients experience substantial morbidity and mortality due to complications resulting from chronic exposure to hyperglycemia [59] although major clinical trials have demonstrated that improved glycemic control can significantly reduce the risk of complications [10, 11].

Oral antidiabetic agents (OAs) are the current mainstay of T2DM management, but their long-term efficacy is limited by the progressive and irreversible loss of β-cell function, whereas insulin therapy remains continually effective. However, initiation of insulin injections frequently is restricted as a "last resort" for a variety of reasons such as fear of needles, inconvenience, and technique. Indeed, several studies have shown delays of 4 years or longer in the uptake of insulin therapy by patients uncontrolled with multiple OAs [12, 13]. This delay may accelerate β-cell failure and disease progression and hasten development of complications, highlighting the need for improved patient acceptance of insulin therapy so it may be used in a timelier and appropriate manner.

Non-invasive methods of insulin delivery, such as inhaled insulins, may increase the acceptance, and thus earlier initiation, of insulin therapy. The first inhaled human insulin (INH, Exubera® (insulinhuman [rDNA origin]) Inhalation Powder) was recently approved by the European Commission and the US Food and Drug Administration to deliver effective glycemic control in adult patients with type 1 or type 2 diabetes. Phase 3 trials have demonstrated that INH is as efficacious as subcutaneously (SC) injected regular human insulin in type 1 diabetes (T1DM) [14, 15] or T2DM [16], and superior to OAs in T2DM [1720]. INH offers a number of potential advantages [1429], including a time-action profile that is more suited for mealtime insulin administration compared with SC regular human insulin [21, 22]. Another advantage of INH is that patients with T2DM who are poorly controlled with OAs are able to attain good glycemic control by simply adding INH to their oral regimen [18, 19]. In a 12-week study by Rosenstock and colleagues, adjusted treatment group differences from baseline (9.5–9.6%) in glycosylated hemoglobin (HbA1c) of -1.2% and -1.7% were observed when INH was substituted for combination OA therapy or added to combination therapy, respectively [18]. Furthermore, Phase 3 trial results indicate that INH lowers HbA1c to ADA target levels (HbA1c < 7%) in more than one third of patients after only 3 months of treatment [16, 18, 20].

Evidence from completed Phase 2 and 3 studies up to 4 years in duration support that insulin administration via the lung is generally well tolerated in patients with T1DM or T2DM [1220, 23, 24]. A slight, but clinically insignificant, decline in lung function was observed to a greater extent in patients treated with INH compared with control patients; this decline was nonprogressive and reversed after discontinuation of INH therapy [1416, 19, 23, 24]. The only significant clinical adverse effect associated with INH was cough, which was generally characterized as mild to moderate in severity, decreased over time, and was not associated with decline in lung function [1416, 19]. In extensions of several Phase 2 studies, patients appear to be satisfied with INH, as evidenced by more than 85% of subjects choosing to remain on INH [29]. Subjects also demonstrated a preference for INH to SC insulin or OAs when offered the choice [2528].

This combination of attributes suggests that INH may be a valuable addition to the treatment options available to patients and physicians in attaining glycemic control. However, these data on efficacy and safety cannot address the overall health benefits and pharmacoeconomic impact of INH in society. No randomized trials have examined the potential advantages of increased uptake of insulin due to avoidance of injections.

This paper describes the Real World Trial of INH, which was designed to overcome the limitations associated with traditional study design. The Real World Trial has adopted a novel design in order to estimate the effects of the availability of INH on physician and patient acceptance of insulin, health status (e.g. glycemic control), and health economic parameters.

2.0 Methods

2.1 Study population

Approximately 700 patients with T2DM, aged 35 to 80 years with poor glycemic control despite treatment with two or more OAs. Abstinence from smoking is required because smoking greatly increases insulin absorption [30, 31].

2.2 Study design

The study is a 52-week, open label, randomized (1:1), parallel, multicenter study consisting of a 6-month core phase to assess change in HbA1c, and a 6-month extension phase to assess persistence of effects observed during the initial trial phase. The study design is summarized in Figure 1. Patients will be randomized to one of two experimental groups. In Group A, subjects will be given the option to choose from all appropriate treatment options including SC insulin delivered by either syringe or pen, oral agents, and INH treatment. Study subjects randomized to Group B will have the same treatment options except INH will not be available. In both groups, irrespective of the availability of INH, patients may choose to remain on their current treatment or start any other marketed treatment. Patients and physicians are not under any obligation to use INH in Group A. Choices made at the beginning of the study can be revisited and changed midway through the study.
Figure 1

Real World Trial Study Design.

2.3 Outcomes

This trial will provide an estimate of the effect of availability of INH in general practice. The primary end point is change from baseline HbA1c (%) after 6 months of treatment between groups. Secondary efficacy end points include:

  • HbA1c at Week 52

  • Proportion of patients achieving adequate glycemic control (HbA1c ≤ 6.5%, ≤ 7.0%)

  • Time-to-insulin therapy initiation

  • Change from baseline in fasting plasma glucose level

  • Incidence and severity of hypoglycemia

  • Change from baseline in body weight and body mass index

  • Change from baseline in fasting lipid profile

  • Proportion of different treatment categories: INH, SC insulin, changed OAs, no treatment change

  • Treatment satisfaction

  • Health status

Usual laboratory and clinical monitoring of adverse events will assess safety.

2.4 Sample size and analysis plan

A minimum sample size of approximately 279 patients per group will be required to provide 90% power to detect a difference between groups in the primary end point HbA1c of at least 0.33% assuming that the standard deviation does not exceed 1.2%. To protect against a possible drop-out rate as high as 10%, approximately 650 patients need to be enrolled.

The primary outcome will be analyzed by intention to treat, using a mixed model. The primary analysis will include treatment and number of OAs as fixed effects. It also will include study centers as random effects due to the large number of anticipated sites (approximately 90), and baseline HbA1c (defined as the Week -1 HbA1c) will be a patient-level covariate. A similar approach will be used for other continuous outcome measures. Analogous nonlinear mixed models will be used to estimate the effect of random allocation on dichotomous outcomes, incorporating study centers as random effects. An unstratified Cox Proportional Hazards model will be used to estimate the effect of random allocation on time-to-insulin initiation.

2.5 Study organization

The study has been accepted by regulatory authorities and IRBs/IECs where the study is being conducted without request for change. All laboratory data are handled by a central contract laboratory. Quality assurance is being provided by a global contract research organization. A standing external advisory committee has provided input into the design and conduct of the study since inception of the aforementioned feasibility study.

3.0 Discussion

Estimating the potential benefits of INH on improved insulin acceptance and glycemic control requires adaptation of conventional randomized trial designs. The Real World Trial will estimate the effects of insulin acceptance on glycemic control while preserving the benefits of randomization to reduce bias. Its design takes into account the need for internal and external validity that the results are attributable to the intervention (i.e. INH availability) and that they may be applied to general practice. This design is practical because patients and physicians have real life choices that are normally "designed out" and removed in a "classical" clinical trial. In this trial, physicians are able to freely use the new treatment without some of the restrictions of a traditional trial; physicians and patients can interact normally in discussing, designing, and optimizing treatment regimens. The study also will encompass a variety of clinical practices including community specialist and primary care to better reflect the expected post-marketing use of the product. The findings from the Real World Trial will provide important information that can be generalized for clinicians and healthcare policymakers in distinguishing the role of INH by identifying the association between INH availability/acceptability and glycemic control, and establishing the effects on resource use. Recruitment for the Real World Trial concluded in spring 2006 after recruitment of 739 patients, and results are expected in 2007.

A questionnaire-based feasibility study examining the theoretical effects of the availability of inhaled insulin on treatment in 779 patients with T2DM who were not achieving target glycemic control with their current therapy was recently completed [32]. This randomized, controlled trial provided supportive insight into the design of the Real World Trial, as well as evidence that inhaled insulin may lead to improved uptake of insulin. Treatment preferences expressed by subjects of the feasibility study, by number of OAs, are described in Table 1. In each group, 77% of patients had HbA1c values greater than 10%, and the majority of patients were receiving treatment with one or more OA along with dietary and lifestyle advice. Patients were three times more likely to choose insulin therapy when inhaled insulin was available (odds ratio [OR]: 4.16; 95% confidence interval [CI]: 2.93 to 5.95, p < 0.0001) and significantly fewer patients in the group offered inhaled insulin chose to make no change to their therapy compared with patients offered standard treatments only (OR: 0.49; 95% CI: 0.36 to 0.67, p < 0.0001). The proportion of patients choosing insulin in both groups increased with the number of OAs currently being taken, and inhaled insulin was the most frequently chosen treatment option. Aversion to incorporating SC insulin into therapy remained strong, despite high HbA1c levels, and the availability of insulin pens in some countries. The enhanced willingness of those offered the option of inhaled insulin treatment to change to a more appropriate therapy increases the potential for achieving improved glycemic control and reducing complications, associated morbidity, premature mortality, and increased cost of diabetes.
Table 1

Results from the Real World Feasibility Study [32].

Current treatment

Percentage of study patients (%)

Treatment preferences (%)

   

"I will NOT change my current treatment"

"I am willing to consider new oral agents"

"I am willing to consider SC insulin"

"I am willing to consider inhaled insulin"

 

Inhaled insulin available

Inhaled insulin NOT available

Inhaled insulin available

Inhaled human insulin NOT available

Inhaled insulin available

Inhaled insulin NOT available

Inhaled insulin available

Inhaled insulin NOT available

Inhaled insulin available

Inhaled insulin NOT available

Diet/exercise

5.4

7.2

28.6

39.3

47.6

60.7

4.8

0

4.8

N/A

1 oral agent

32.5

36.6

26.0

41.5

33.9

43.0

5.5

14.1

30.7

N/A

2 oral agents

52.4

46.1

28.8

45.3

19.0

35.8

8.3

17.9

38.5

N/A

3 oral agents

9.7

10.1

23.7

43.6

5.3

33.3

15.3

20.5

50.0

N/A

One of the key decisions that required consideration in the design of the Real World Trial was the question of the appropriateness of patient- or cluster-level randomization. Rather than allocating patients between treatment groups using a random process, cluster-level randomized trials allocate patients in groups [33]. The rationale for cluster-level randomized trials is apparent when treatments cannot be applied to individuals, for example in a trial of fluoridation of water supplies. Similarly, a cluster trial would be appropriate when there is a risk of contamination of treatments between groups, for example where a healthcare professional was expected to provide different levels of healthcare promotion advice to different patients.

Thus, cluster-level randomized trials are necessary in certain circumstances, but they are associated with a certain disadvantage – we cannot consider patients allocated in this way to be independent of each other. This lack of independence must be addressed in the analysis. The degree to which clustering affects the design of a study depends upon the extent to which patients are clustered within their units of allocation and the number of patients per unit. However, patient per patient, a clustered trial always will be less efficient than an individual patient randomized trial. In addition, there are potential problems associated with the implementation of cluster-level randomized trials. For example, when a trial intervention is considered particularly attractive or of interest to investigating clinicians, the disappointment engendered from being allocated to the control rather than experimental condition may affect the behavior of the investigator. Thus, control group investigators may recruit fewer patients or different patients from those recruited by the experimental group investigators, or they may experience greater loss to follow up. The treatment of interest in the Real World Trial may be applied to individual patients without the risk of contamination; at the time of the study enrollment INH was available only as an investigational product. Thus, there is no requirement to move to a cluster design and the associated issues regarding trial quality and loss of efficiency.

4.0 Conclusion

The novel design of the Real World Trial, randomizing patients to scenarios where different treatment options are available for the management of their condition, is necessary in order to provide an estimate of the potential utility of the intervention in standard practice. Trials required for the registration of a new product generally do not provide such information, which is increasingly necessary for healthcare policymakers and clinicians in an environment where healthcare resources are limited. It is very likely that we will see many more such trials in the future.

Declarations

Acknowledgements

The Real World Trial is funded by Pfizer Inc

Authors’ Affiliations

(1)
University of Birmingham
(2)
Pfizer Inc

References

  1. American Diabetes Association: Economic consequences of diabetes mellitus in the U.S. in 1997. Diabetes Care. 1998, 21: 296-309.View ArticleGoogle Scholar
  2. Amos AF, McCarty DJ, Zimmet P: The rising burden of diabetes and its complications: Estimates and projections to the year 2010. Diabet Med. 1997, 14: S7-S85. 10.1002/(SICI)1096-9136(199712)14:5+<S7::AID-DIA522>3.3.CO;2-I.View ArticleGoogle Scholar
  3. King H, Aubert RE, Herman WH: Global burden of diabetes, 1995–2025: prevalence, numerical estimates, and projection. Diabetes Care. 1998, 21: 1414-1431.View ArticlePubMedGoogle Scholar
  4. Harris MI: Health care and health status and outcomes for patients with type 2 diabetes. Diabetes Care. 2000, 23: 754-801.View ArticlePubMedGoogle Scholar
  5. Klein R: The epidemiology of diabetic retinopathy: Findings from the Wisconsin Epidemiologic Study of Diabetic Retinopathy. Int Ophthalmol Clin. 1987, 27: 230-238.View ArticlePubMedGoogle Scholar
  6. Klein R, Moss SE, Klein BEK, Davis MD, DeMets DL: The Wisconsin Epidemiologic Study of Diabetic Retinopathy. XI. The incidence of macular edema. Ophthalmology. 1989, 96: 1501-1510.View ArticlePubMedGoogle Scholar
  7. Consensus statement: Proceedings from the International Symposium on Preventing the Kidney Disease of Diabetes Mellitus: public health perspectives. Am J Kidney Dis. 1989, 13: 2-6.View ArticleGoogle Scholar
  8. Diabet Neuropathy. Edited by: Dyck PJ, Thomas PK, Asbury AK, Winegard AI, Porte D Jr. 1987, Philadelphia: WB SaundersGoogle Scholar
  9. Kannel WB, McGee DL: Diabetes and cardiovascular disease: the Framingham Study. JAMA. 1979, 241: 2035-2038. 10.1001/jama.241.19.2035.View ArticlePubMedGoogle Scholar
  10. Rubino A, McQuay L, Kvasz M, Tennis P: Population-based study of time to insulin after failure or oral antidiabetic (OA) therapy in type 2 diabetes (T2DM) in the UK. Diabetes. 2006, 55 (suppl 1): A76-Google Scholar
  11. Nichols G, Koo Y, Menditto L: Delay in treatment escalation when glycemic control is not maintained on oral combination therapy. Diabetes. 2006, 55 (suppl 1): A12-Google Scholar
  12. The Diabetes Control and Complications Trial Research Group: The effect of intensive treatment of diabetes on the development and progression of long-term complications in insulin-dependent diabetes mellitus. N Engl J Med. 1993, 329: 977-986. 10.1056/NEJM199309303291401.View ArticleGoogle Scholar
  13. UK Prospective Diabetes Study (UKPDS) Group: Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33). Lancet. 1998, 352: 837-835. 10.1016/S0140-6736(98)07019-6.View ArticleGoogle Scholar
  14. Quattrin T, Belanger A, Bohannon NJ, Schwartz SL: Efficacy and safety of inhaled insulin (Exubera) compared with subcutaneous insulin therapy in patients with type 1 diabetes. Diabetes Care. 2004, 27: 2622-2627.View ArticlePubMedGoogle Scholar
  15. Skyler JS, Weinstock RS, Raskin P, Yale JF, Barrett E, Gerich JE, Gerstein HC: Use of inhaled insulin in a basal/bolus insulin regimen in subjects with type 1 diabetes: a 6-month randomized, comparative trial. Diabetes Care. 2005, 28: 1630-1635.View ArticlePubMedGoogle Scholar
  16. Hollander P, Blonde L, Rowe R, Mehta AE, Milburn JL, Hershon KS, Chiasson JL, Levin SR: Efficacy and safety of inhaled insulin (Exubera) compared with subcutaneous insulin therapy in patients with type 2 diabetes: results of a 6-month, randomized, comparative trial. Diabetes Care. 2004, 27: 2356-2362.View ArticlePubMedGoogle Scholar
  17. Cefalu WT, Skyler JS, Kourides IA, Landschulz WH, Balagtas CC, Cheng S, Gelfand RA: Inhaled human insulin treatment of patients with type 2 diabetes mellitus. Ann Intern Med. 2001, 134: 203-207.View ArticlePubMedGoogle Scholar
  18. Rosenstock J, Zinman B, Murphy LJ, Clement SC, Moore P, Bowering CK, Hendler R, Lan SP, Cefalu WT: Inhaled insulin (Exubera®) improves glycemic control when substituted for or added to oral combination therapy in type 2 diabetes: a randomized controlled trial. Ann Intern Med. 2005, 143: 549-558.View ArticlePubMedGoogle Scholar
  19. Barnett AH, Dreyer M, Lange P, Serdarevic-Pehar M: An open, randomized, parallel-group study to compare the efficacy and safety profile of inhaled human insulin (Exubera) with metformin as adjunctive therapy in patients with type 2 diabetes poorly controlled on a sulfonylurea. Diabetes Care. 2006, 29: 1282-1287. 10.2337/dc05-1879.View ArticlePubMedGoogle Scholar
  20. DeFronzo RA, Bergenstal RM, Cefalu WT, Cefalu WT, Pullman J, Lerman S, Bode BW, Phillips LS, for the Exubera Phase 3 Study Group: Efficacy of inhaled insulin in patients with type 2 diabetes not controlled with diet and exercise: a 12-week, randomized, comparative trial. Diabetes Care. 2005, 28: 1922-1928.View ArticlePubMedGoogle Scholar
  21. Rave K, Bott S, Heinemann L, Sha S, Becker RH, Willavize SA, Heise T: Time-action profile of inhaled insulin in comparison with subcutaneously injected insulin lispro and regular human insulin. Diabetes Care. 2005, 28: 1077-1082.View ArticlePubMedGoogle Scholar
  22. Gelfand RA, Schwartz SL, Horton M: Pharmacological reproducibility of inhaled human insulin dosed pre-meal in patients with type 2 DM. Diabetologia. 2000, 43 (Suppl 1): A202-Google Scholar
  23. Skyler J, for the Exubera® Phase 2 Study Group: Long-term, sustained efficacy, and safety of inhaled insulin after 4 years of continuous therapy. Diabetologia. 2004, 47 (Suppl 1): A311-Google Scholar
  24. Dumas R, England RD, Riese RJ, Teeter JG, for the Exubera® Phase 3 Study Group: Exubera® is well tolerated and achieves tight glycemic control in patients with type 1 diabetes. Diabetes. 2005, 54 (Suppl 1): A87-Google Scholar
  25. Gerber RA, Cappelleri JC, Kourides IA, Gelfand RA: Treatment satisfaction with inhaled insulin in patients with type 1 diabetes: a randomized controlled trial. Diabetes Care. 2001, 24: 1556-1559.View ArticlePubMedGoogle Scholar
  26. Gerber RA, Cappelleri JC, Bell-Farrow AD: Improved patient satisfaction with inhaled insulin in patients with type 1 diabetes mellitus after one year: results from a multicenter extension trial [abstract]. Diabetes. 2000, 49 (Suppl 1): A108-Google Scholar
  27. Cappelleri JC, Nadkarni S, Petrie CD: Balancing compliance, patient satisfaction and improved glycemic control in patients with type 1 and type 2 diabetes mellitus: long-term studies with inhaled insulin (Exubera®) [abstract 751]. Diabetologia. 2002, 45 (Suppl 1):
  28. Cappelleri JC, Cefalu WT, Rosenstock J, Kourides IA, Gerber RA: Treatment satisfaction with inhaled insulin in patients with type 2 diabetes: a randomized controlled trial. Clin Ther. 2002, 24: 552-564. 10.1016/S0149-2918(02)85131-1.View ArticlePubMedGoogle Scholar
  29. Rosenstock J, Cappelleri JC, Bolinder B, Gerber RA: Patient satisfaction and glycemic control after 1 year with inhaled insulin (Exubera) in patients with type 1 or type 2 diabetes. Diabetes Care. 2005, 27: 1318-1323.View ArticleGoogle Scholar
  30. Becker RHA, Sha S, Frick AD, Fountaine RJ: The effect of smoking cessation and subsequent resumption on absorption of inhaled insulin. Diabetes Care. 2006, 29: 277-282. 10.2337/diacare.29.02.06.dc05-1913.View ArticlePubMedGoogle Scholar
  31. Himmelmann A, Jendle J, Mellen A, Petersen AH, Dahl UL, Wollmer P: The impact of smoking on inhaled insulin. Diabetes Care. 2003, 26: 677-682.View ArticlePubMedGoogle Scholar
  32. Freemantle N, Blonde L, Duhot D, Hompesch M, Eggertsen R, Hobbs FD, Martinez L, Ross S, Bolinder B, Stridde E: Availability of inhaled insulin promotes greater perceived acceptance of insulin therapy in patients with type 2 diabetes. Diabetes Care. 2005, 28: 427-428.View ArticlePubMedGoogle Scholar
  33. Moore H, Summerbell CD, Vail A, Greenwood DC, Adamson AJ: The design features and practicalities of conducting a pragmatic cluster randomized trial of obesity management in primary care. Stat Med. 2001, 20: 331-340. 10.1002/1097-0258(20010215)20:3<331::AID-SIM795>3.0.CO;2-K.View ArticlePubMedGoogle Scholar

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© Freemantle et al; licensee BioMed Central Ltd. 2006

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.