Exenatide (Byetta) for type 2 diabetes mellitus
Published in NPS RADAR
Date published: About this date
Injectable option but with more limited data than insulin
Evidence snapshot | PBS listing | Reason for PBS listing | What is it? | Who is it for? |
How is it used? | Where does it fit? | How does it compare? | Safety issues | Dosing issues | Information for patients | References
- First injectable synthetic analogue of glucagon-like peptide 1
Exenatide has a different mechanism of action to that of other antidiabetes drugs.
- Inject subcutaneously twice daily before meals
Give within the hour before the morning and evening meals. Do not give after a meal.
- PBS listed for dual or triple therapy
Exenatide is not approved for use as monotherapy or in combination with antidiabetes drugs other than metformin and/or a sulfonylurea.
- Improves glycaemic control with metformin and/or a sulfonylurea
Exenatide reduces glycated haemoglobin levels (HbA1c) to a similar extent as insulin (glargine, aspart).
- No data on diabetes-related complications and mortality
Clinical trials have only measured HbA1c levels as a surrogate for clinical outcomes.
- Long-term effect on weight is unknown
Exenatide is associated with weight loss, but there are no data on whether this affects clinical outcomes or is maintained in the long term.
- Gastrointestinal adverse effects are common
Nausea, vomiting and diarrhoea are 2–3 times more likely with exenatide compared with insulin or placebo.
- Long-term safety profile yet to be established
There have been rare postmarketing reports of acute pancreatitis and altered kidney function with exenatide.
What is known about this drug
Adding exenatide to metformin or a sulfonylurea reduced HbA1c by about 1.0% compared with placebo. Similar reductions in HbA1c were achieved when either exenatide or insulin (glargine, aspart) were used as part of triple therapy. Nausea and vomiting are common and usually improve with continued therapy.
Areas of uncertainty
There are no data on exenatide's effect on diabetes-related complications, mortality or long-term weight. The long-term safety profile of exenatide is yet to be established: be alert for acute pancreatitis or altered kidney function.
What does NPS say?
Exenatide is an option for people who need dual or triple therapy. However, insulin is usually preferred because there are clinical outcome data, it has extensive experience of use and an established long-term safety profile.
Authority required (streamlined)
Dual therapy in combination with either metformin or a sulfonylurea for people with type 2 diabetes whose glycated haemoglobin (HbA1c) is > 7% despite use of metformin or a sulfonylurea, and for whom the combination of metformin and a sulfonylurea is contraindicated or not tolerated.
Triple therapy in combination with metformin and a sulfonylurea, for people with type 2 diabetes whose HbA1c is > 7% despite maximally tolerated doses of metformin and a sulfonylurea.
The date of the HbA1c measurement* (within the last 4 months) is required except when the person is transferring from a PBS-subsidised thiazolidinedione ('glitazone') or dipeptidyl peptide-4 inhibitor ('gliptin') to exenatide.
*Blood glucose monitoring may be accepted in some situations. Refer to www.pbs.gov.au for details.
Reason for PBS listing
The Pharmaceutical Benefits Advisory Committee (PBAC) recommended exenatide for listing on a cost-minimisation basis — that is, similar efficacy and cost — compared with a combination of rosiglitazone and insulin glargine. The equi-effective doses for the purposes of setting the listing price for dual therapy were exenatide 9.35 micrograms twice a day equivalent to insulin glargine 27.30 international units/day. For triple therapy these were exenatide 10 micrograms twice daily equivalent to rosiglitazone 8 mg once daily, and exenatide 9.07 micrograms twice daily equivalent to insulin glargine 24.93 international units/day. Special pricing arrangements apply.1 The PBAC also recommended that the listings allow people to switch from a glitazone or a gliptin to exenatide without the need for an HbA1c of > 7%. Although there is limited evidence to support switching between these drugs, the PBAC considered it unreasonable for people to require a loss of diabetes control in order to qualify for an alternative drug.
What is it?
Exenatide is the first injectable synthetic analogue of the incretin hormone glucagon-like peptide 1 (GLP-1). Exenatide is an ‘incretin mimetic’: it mimics the action of GLP-1. Incretin mimetics increase glucose-dependent insulin secretion, suppress inappropriate glucagon secretion, delay gastric emptying (which reduces the rate of glucose absorption) and reduce appetite.2,3
The action of incretin mimetics is different from that of ‘incretin enhancers’, such as the gliptins, which inhibit the breakdown of incretins. For more information about the pharmacological action of gliptins, refer to the NPS RADAR review Dipeptidyl peptidase-4 inhibitors (‘gliptins’) for type 2 diabetes mellitus.4
Exenatide is a treatment option for people with type 2 diabetes mellitus who require:
- dual therapy but for whom a combination of metformin and a sulfonylurea is contraindicated or not tolerated, or
- triple therapy for people who are already taking metformin and a sulfonylurea.
Exenatide is given as a subcutaneous injection twice a day (see Dosing issues). It is used in combination with metformin and/or a sulfonylurea.
Exenatide improves glycaemic control in combination with metformin and/or a sulfonylurea. It is not approved by the Therapeutic Goods Administration (TGA) or PBS listed for monotherapy or for use in combination with acarbose, a gliptin, a glitazone, insulin or repaglinide.
Other options for dual or triple therapy include insulin or an oral antidiabetes drug (Table 1). Insulin is usually the preferred option, as there are data on its effect on diabetes-related complications and mortality, it has extensive experience of use and an established long-term safety profile.
Table 1: Other antidiabetes drugs for dual or triple therapy†
Glitazones (pioglitazone or rosiglitazone)
Gliptins (sitagliptin or vildagliptin)
† Repaglinide is not listed on the PBS: refer to www.pbs.gov.au for details about PBS restrictions for other drugs.
Other factors may influence the choice of antidiabetes drug, including dosage form (oral or injectable), frequency of administration, what other drugs can be co-prescribed, titrated versus fixed dose, and potential adverse effects such as weight gain and hypoglycaemia.
There are no data on the effects of exenatide on diabetes-related complications or mortality. Clinical trials have been small (n = 150–733), relatively short (16–82 weeks) and have measured HbA1c levels as a surrogate for clinical outcomes. Some trial data suggest that exenatide may not affect lipids.5 Exenatide’s effects on blood pressure and cardiovascular events are unknown.
In contrast, some other antidiabetes drugs have known effects on clinical outcomes. Metformin reduces the incidence of diabetes-related complications and mortality.6 Sulfonylureas and insulin have been shown to reduce the incidence of microvascular complications.7
Exenatide reduces HbA1c levels with metformin and/or a sulfonylurea
Two trials have assessed the efficacy of exenatide as dual therapy with either metformin or a sulfonylurea.8–11 Exenatide 10 micrograms twice a day reduced HbA1c by about 1.0% after 30 weeks compared with placebo. The proportion of people who achieved an HbA1c ≤ 7% (34–40%, compared with placebo 8–11%) was maintained over the following year in unblinded extension trials.8,10
Exenatide has been compared with placebo and insulin (glargine, aspart) for use as triple therapy (with metformin and a sulfonylurea).12–14 Reductions in HbA1c were comparable between exenatide and insulin (average insulin dose studied was about 25 units daily) and a similar proportion in each treatment group achieved an HbA1c ≤ 7% (Table 2). However, more people receiving exenatide stopped treatment, mostly because of gastrointestinal adverse effects (see Safety issues).
Table 2: Exenatide compared with insulin (glargine, aspart) as triple therapy with metformin and a sulfonylurea‡13,14
Change in HbA1c
Trial 1 (26 weeks)
Trial 2 (52 weeks)
‡ Sulfonylureas used in the 26-week trial were not reported13
Long-term effect on weight is not known
Exenatide is associated with weight loss and thus may be a useful option for people who are overweight. However, whether weight loss with exenatide improves clinical outcomes, or is maintained in the long term, is currently unknown.
In trials of up to 30 weeks, people who had exenatide added to their oral therapy lost an average of 1.4 kg more than those who received oral therapy alone.5 Weight loss continued during the following year, although this observation came from uncontrolled unblinded extension studies (n = 150, n = 401).9,11 Weight loss also occurred with exenatide (2.3 kg loss) compared with insulin glargine (1.8 kg gain) in a 26-week trial; similarly, in a 52-week trial, exenatide led to a 2.5 kg weight loss compared with a 2.9 kg gain with insulin aspart.13,14
The effect on weight loss should be interpreted cautiously: no trial has studied weight loss with exenatide as a primary outcome, and the available data are limited to 1 year of unblinded treatment.
Common adverse effects with exenatide include gastrointestinal adverse effects (nausea, vomiting, diarrhoea, dyspepsia, gastro-oesophageal reflux disease and abdominal pain), headache, dizziness, jitteriness and injection-site reactions. Hypoglycaemia may also occur, mainly when exenatide is used with a sulfonylurea.2
Pancreatitis, allergic reactions and altered kidney function have been reported rarely with exenatide.2,15 Avoid exenatide in people with severe renal impairment or end-stage kidney disease.15,16 Be cautious about starting or increasing the dose of exenatide in people with moderate renal impairment (creatinine clearance 30–50 mL/minute).16
Report suspected adverse reactions to the TGA online or by using the 'Blue Card' distributed three times a year with Australian Prescriber. For information about reporting adverse reactions, see the TGA website.
Nausea and vomiting are common and usually improve with continued therapy
A meta-analysis of trials found that about one in two people experienced nausea, and about one in five experienced vomiting when exenatide was added to oral therapy.5 People receiving exenatide were about three times more likely to experience nausea or vomiting and twice as likely to experience diarrhoea than those using placebo or insulin.5 Nausea and vomiting usually improve with continued therapy.2
Hypoglycaemia mostly occurs in combination with a sulfonylurea
The risk of hypoglycaemia appears to increase with exenatide when it is combined with a sulfonylurea.5 In one trial 36% of people experienced hypoglycaemia when exenatide 10 micrograms was added to a sulfonylurea (incidence for a sulfonylurea alone: 3%).10 In another trial 28% of people experienced hypoglycaemia when exenatide 10 micrograms was added to metformin with a sulfonylurea (metformin with sulfonylurea alone: 13%).12 In contrast, there was no increased risk of hypoglycaemia when exenatide was added to metformin, compared with placebo or insulin, unless used as triple therapy.
Risk of hypoglycaemia appears similar to that with insulin
Trials found a similar incidence of self-reported hypoglycaemia between exenatide and insulin (glargine, aspart) at the insulin doses studied (average about 25 units daily).13,14 However, the comparative risk in people who frequently experience severe episodes of hypoglycaemia is unknown, because those who had more than three recent severe episodes were excluded from trials. The risk of hypoglycaemia for exenatide compared with other insulins (e.g. isophane) and escalating insulin doses is also unknown.
Development of anti-exenatide antibodies is common
Exenatide is derived from a non-mammalian source — from the venom of the Gila monster lizard (Heloderma suspectum) — and may be recognised as an antigen by the human immune system.17,18 Up to 50% of people in clinical trials developed anti-exenatide antibodies8,10,12–14,19, but only about 3% of these people had no apparent glycaemic response to exenatide.17 Consider alternative antidiabetic therapy for people in whom exenatide therapy does not reduce HbA1c.20
Stop exenatide and check serum amylase level if severe abdominal pain occurs
Be alert for pancreatitis in anyone taking exenatide who complains of persistent, severe unexplained abdominal pain (with or without nausea and/or vomiting). Stop exenatide (and any other suspect drugs)15 and check amylase. Consider other antidiabetic drugs for people with a history of pancreatitis (avoid gliptins: for more information refer to the NPS RADAR review of gliptins4).21
Postmarketing reports of acute pancreatitis, including fatal haemorrhagic or necrotising pancreatitis, have occurred with exenatide in the US, UK, Europe and Australia.21–24 A causal association has not been confirmed and some of these cases may have involved other risk factors such as concomitant use of other suspect drugs, obesity, gallstones, severe hypertriglyceridaemia and alcohol use.
Be alert for changes in kidney function
Look out for signs and symptoms including increased serum creatinine, changes in urine (such as colour, frequency and amount), unexplained swelling in the extremities, increased blood pressure, lethargy or changes in appetite and/or digestion.16
There have been postmarketing reports of altered kidney function (including acute renal failure, increased serum creatinine concentration) in the US, the UK and Europe.16,23,26 A causal association has not been confirmed and some of these cases occurred in people with pre-existing kidney disease or in people with risk factors such as other diseases (e.g. hypertension, heart failure) or using other drugs (e.g. nonsteroidal anti-inflammatory drugs, diuretics). Some cases reported nausea, vomiting and diarrhoea, which may have contributed to the development of altered kidney function.
Start with a subcutaneous injection of 5 micrograms twice a day for at least a month. Give within 1 hour before the morning and evening meals (or before two main meals at least 6 hours apart). Do not inject after a meal. If an injection is missed, continue with the next scheduled injection.15
If the initial dose is tolerated, after 1 month the dose can be increased to 10 micrograms twice a day.15 Stop exenatide if improved glycaemic control is not achieved after 3–4 months of therapy.
When adding exenatide to a sulfonylurea, consider reducing the dose of sulfonylurea to reduce the risk of hypoglycaemia (see Safety issues).15 The dose of metformin does not need to be modified in combination with exenatide.
Information for patients
Provide patients or carers with instructions on how to inject and dispose of exenatide, including the timing of the dose (not after meals).
Nausea, vomiting and diarrhoea commonly occur with exenatide. Inform patients or carers that the initial dose titration aims to improve tolerability to gastrointestinal adverse effects.
Exenatide delays stomach emptying, which can slow the absorption of oral medicines. Advise on what medicines should be taken separately from exenatide (at least 1 hour before or 4 hours after an injection) to prevent the medicine from causing gastric irritation or having a delayed effect.
Recommend that patients promptly seek medical attention if they experience persistent or severe unexplained abdominal pain (with or without nausea and/or vomiting) or changes in urine (such as colour, frequency and amount) or dehydration.
Discuss the Byetta consumer medicine information (CMI) leaflet with the patient.
An NPS Medicine Update leaflet on exenatide is available for consumers. Medicine Update helps consumers to ask the right questions about new medicines, and helps them compare the potential benefits and harms of a new medicine with those of other medicines.
- Department of Health and Ageing. Therapeutic relativity sheets: ATC A10 — drugs used in diabetes. Canberra, 2010. http://pbs.gov.au/info/industry/pricing/pbs-items/therapeutic-relativity-sheets (accessed 15 November 2010).
- Rossi S, ed. Australian Medicines Handbook. Adelaide: Australian Medicines Handbook Pty Ltd, 2010.
- Prins JB. Incretin mimetics and enhancers: mechanisms of action. Aust Prescr 2008;31:102–4. http://www.australianprescriber.com/magazine/31/4/102/4/
- National Prescribing Service. Dipeptidyl peptidase-4 inhibitors ('gliptins') for type 2 diabetes mellitus. NPS RADAR August 2010. Sydney: National Prescribing Service, 2010. http://www.nps.org.au/health_professionals/publications/nps_radar/2008/august_2008/gliptins (accessed 4 August 2010).
- Amori RE, Lau J, Pittas AG. Efficacy and safety of incretin therapy in type 2 diabetes: systematic review and meta-analysis. JAMA 2007;298:194–206. [PubMed]
- UK Prospective Diabetes Study (UKPDS) Group. Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34). Lancet 1998 352:854–65. [PubMed]
- 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;352:837–53. [PubMed]
- DeFronzo RA, Ratner RE, Han J, et al. Effects of exenatide (Exendin-4) on glycemic control and weight over 30 weeks in metformin-treated patients with type 2 diabetes. Diabetes Care 2005;28:1092–100. [PubMed]
- Ratner RE, Maggs D, Nielsen LL, et al. Long-term effects of exenatide therapy over 82 weeks on glycaemic control and weight in over-weight metformin-treated patients with type 2 diabetes mellitus. Diabetes Obes Metab 2006;8:419–28. [PubMed]
- Buse JB, Henry RR, Kim DD, et al. Effects of exenatide (Exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes. Diabetes Care 2004;27:2628–35. [PubMed]
- Riddle MC, Henry RP, Poon TH, et al. Exenatide elicits sustained glycaemic control and progressive reduction of body weight in patients with type 2 diabetes inadequately controlled by sulphonylureas with or without metformin. Diabetes Metab Res Rev 2006;22:483–91. [PubMed]
- Kendall DM, Riddle MC, Rosenstock J, et al. Effects of exenatide (Exendin-4) on glycemic control over 30 weeks in patients with type 2 diabetes treated with metformin and a sulfonylurea. Diabetes Care 2005;28:1083–91. [PubMed]
- Heine RJ, Van Gaal LF, Johns D, et al. Exenatide versus insulin glargine in patients with suboptimally controlled type 2 diabetes: a randomized trial. Ann Intern Med 2005;143:559–69. [PubMed]
- Nauck MA, Duran S, Kim D, et al. A comparison of twice-daily exenatide and biphasic insulin aspart in patients with type 2 diabetes who were suboptimally controlled with sulfonylurea and metformin: a non-inferiority study. Diabetologia 2007;50:259–67. [PubMed]
- Eli Lilly Australia Pty Ltd. Byetta product information. 22 March 2010.
- US Food and Drug Administration — Center for Drug Evaluation and Research. Reports of altered kidney function in patients using exenatide (marketed as Byetta). Information for Healthcare Professionals Silver Spring, MD: US Department of Health and Human Services, 2009; 1. http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/DrugSafetyInformationforHeathcareProfessionals/ucm188656.htm (accessed 29 July 2010).
- European Medicines Evaluation Agency. Byetta European Public Assessment Report. London: EMEA, 2006. http://www.emea.europa.eu/humandocs/Humans/EPAR/byetta/byetta.htm (accessed 29 July 2010).
- Eng J, Kleinman WA, Singh L, et al. Isolation and characterization of exendin-4, an exendin-3 analogue, from Heloderma suspectum venom: further evidence for an exendin receptor on dispersed acini from guinea pig pancreas. J Biol Chem 1992;267:7402–5. [PubMed]
- Zinman B, Hoogwerf BJ, Garcia SD, et al. The effect of adding exenatide to a thiazolidinedione in suboptimally controlled type 2 diabetes. Ann Intern Med 2007;146:477–85. [PubMed]
- Amylin Pharmaceuticals Inc. Byetta product information. USA, 2007. http://www.fda.gov/cder/foi/label/2008/021773s012lbl.pdf (accessed 29 July 2010).
- US Food and Drug Administration — Center for Drug Evaluation and Research. Information for healthcare professionals: exenatide (marketed as Byetta). Silver Spring, MD: US Department of Health and Human Services, 2008. http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm124713.htm (accessed 15 November 2010).
- Medicines and Healthcare products Regulatory Agency and the Commission on Human Medicines. Exenatide (Byetta): risk of acute pancreatitis. Drug Safety Update London: MHRA, 2008;1:5. http://www.mhra.gov.uk/Publications/Safetyguidance/DrugSafetyUpdate/CON015025 (accessed 15 November 2010).
- Medicines and Healthcare Products Regulatory Agency and the Commission on Human Medicines. Exenatide (Byetta): risk of severe pancreatitis and renal failure. Drug Safety Update London: MHRA, 2009;2:6–7. http://www.mhra.gov.uk/Publications/Safetyguidance/DrugSafetyUpdate/CON041211 (accessed 29 July 2010).
- Therapeutic Goods Administration. Drug-induced pancreatitis and exenatide (Byetta). Medicine Safety Update 2010;3:3–4. http://www.australianprescriber.com/upload/pdf/articles/1098.pdf (accessed 29 July 2010).
- US Food and Drug Administration — Center for Drug Evaluation and Research. Exenatide (marketed as BYETTA): acute pancreatitis. FDA Drug Safety Newsletter Silver Spring, MD: US Department of Health and Human Services, 2008;1. http://www.fda.gov/Drugs/DrugSafety/DrugSafetyNewsletter/ucm109165.htm (accessed 15 November 2010).
- Anonymous. Exenatide: renal failure. Prescrire 2009;18:124.
Updated 1 March 2012 to reflect addition of 'streamlined' to authority PBS listing. Evidence since the original release date has not been reviewed.
First released November 2010.