Avandia™ + Amaryl™ or Avandamet™ Compared With Metformin (AVALANCHE™ Study)

Canadian Heart Research Centre

Status and phase: Completed; Phase 3

Conditions: Type 2 Diabetes Mellitus

Treatments: Drug: Metformin; Drug: Avandamet; Drug: Avandia and Amaryl

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT00131664

AVM103436

Details and patient eligibility

About

The incidence of type 2 diabetes is on the increase. According to recent Canadian Diabetes Association guidelines glucose control, based on the A1C measurement, needs to be achieved within a 6-12 month period of time after the initial diagnosis of type 2 diabetes. The guidelines on the use of antihyperglycemic agents identify the potential benefits of sub-maximal oral combination therapy in order to achieve more rapid and improved glycemic control compared with higher dose monotherapy. Furthermore, many patients on prolonged oral antihyperglycemic monotherapy who then start on combination therapy may not achieve the required target glycemic control. Indeed early initiation of combination therapies may be necessary to achieve and maintain glycemic targets because of the progressive deterioration of pancreatic β cell function and glycemic control.

Full description

AvandametTM combines two oral antihyperglycemic agents, rosiglitazone maleate and metformin hydrochloride, with different but complementary mechanisms of action to improve glycemic control while reducing circulating insulin levels in patients with type 2 diabetes. AvandiaTM and AmarylTM combine two antidiabetic agents, rosiglitazone maleate and glimepiride. Glimepiride is an effective antihyperglycemic agent which has a low incidence of hypoglycemia, symptomatic hypoglycemia, severe hypoglycemia, and confirmed hypoglycemia. Subjects in this study who are inadequately controlled on diet, exercise and a submaximal dose of metformin or sulfonylurea (SU) will be randomized to either a combination of metformin plus rosiglitazone (AvandametTM) or a combination of AvandiaTM + AmarylTM or a Metformin monotherapy arm. As per the Canadian Diabetes Association (CDA) guidelines, their fasting plasma glucose and A1C to be 7 (mmol/L / percent) or less throughout the study. If the subject does not achieve the target then either AvandametTM or AvandiaTM and AmarylTM or Metformin will be up-titrated in an effort to reach this CDA recommended target. This study will attempt to demonstrate that the either combination arm of rosiglitazone plus metformin (AvandametTM) or the other combination arm of AvandiaTM + AmarylTM will provide greater glycemic control while avoiding the side-effects associated with the use of maximal dose metformin.

Enrollment: 391 patients

Sex: All

Ages: 18 to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Type 2 diabetes patients

2. 18 - 75 years old

3. Type 2 diabetes mellitus (DM) drug naïve or on submaximal oral monotherapy < 3 years

4. A1C criteria at screening:

   1. 7.1-10% for drug naïve patients after failure of diet control and life-style modification
   2. 7.1 - 9% on single therapy (e.g. not more 10 mg of Glyburide or 4 mg of Amaryl™ or 1000mg of Metformin) who will start after 2 weeks wash-out. During wash out the following will be done: i) diet and life style modification ii) Angiotensin converting enzyme inhibitor (ACE), aspirin (80 mg), and statin if appropriate

5. Signed informed consent

Exclusion criteria

1. Type 1 diabetes
2. Subjects currently treated with insulin
3. Subject treated for previous 3 month with any thiazolidinedione (TZD)
4. Evidence of clinically significant concomitant illnesses which are not controlled by medication and/or may limit participation in the study as judged by the investigator
5. Subjects who have hypersensitivity to any components of study drugs
6. Participation in a clinical trial and/or intake of an investigational drug within 30 days prior to screening.
7. Pregnant or nursing females
8. Females of childbearing potential who are not on adequate birth control
9. Liver enzymes (Alanine Aminotransferase (ALT) > 2.5 times upper limit of normal)
10. Renal impairment: serum creatinine ≥ 136umol/L (males) and ≥ 124 umol/L (females)
11. Congestive Heart Failure (CHF class III/IV)
12. Weight >160 kg

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

391 participants in 3 patient groups

Avandamet

Active Comparator group

Description:

Avandamet 2 mg / 500 mg twice daily titration up to 4 mg / 1000 mg twice daily over 6 months

Treatment:

Drug: Avandamet

Avandia and Amaryl

Active Comparator group

Description:

Avandia + Amaryl 4 mg + 1 mg once daily titration up to 8 mg + 2 mg once daily over 6 months

Treatment:

Drug: Avandia and Amaryl

Metformin

Active Comparator group

Description:

Metformin 500 mg twice daily titration up to 1000 mg twice daily over 6 months

Treatment:

Drug: Metformin