Byetta® (exenatide)

Consistent with the company's policy of public data disclosure, this clinical trial results section includes result summaries of completed Lilly-sponsored clinical studies conducted on Lilly marketed products since July 1, 2004. The results of all Phase I, II, and III trials conducted in support of a product’s initial registration will be disclosed regardless of outcome, no later than when the first indication is approved and the drug is commercially available for patient use anywhere in the world. The results of all subsequent Phase II, III, and IV trials conducted after initial approval will be similarly disclosed within one year of trial completion. A trial’s results, irrespective of study phase, will be disclosed as soon as possible if there are significant safety findings.

Consistent with ICH E3 guidelines, Lilly will disclose the results of primary and secondary outcome measures that are specified in the study protocol, as well as additional safety and efficacy results that impact patient care and the use of our products. Also, Lilly discloses a comprehensive description of the trial design and methodology for each study. Results will be disclosed regardless of whether they support the hypothesis being tested or are contrary to the predicted outcome. Clinical trial results will be publicly disclosed as stated above, unless posting would compromise publication in a peer reviewed medical journal or contravene national laws or regulations. Results of studies that are under review by peer-reviewed journals that prohibit pre-publication disclosure will be posted on the registry at the time of publication. Clinical trial results are also disclosed through presentations and abstract submissions at professional scientific meetings.

The registry is also populated with the results of core efficacy and safety registration trials for products first approved after July 1, 1994.

Included are trial result summaries that are completed to date. The company will continue to disclose additional summaries and publication citations as they become available.

Summaries of clinical study results are intended to report the results of the study that were known at the time of each study's completion. The information contained in these summaries is not intended to promote or otherwise commercialize (directly or indirectly) any off-label or unapproved uses of Lilly medicines, nor is it intended to provide a comprehensive analysis of all data currently available regarding a particular drug. In some cases, more current information regarding a drug, including post-hoc analyses and meta-analyses, may be available as part of the general body of scientific knowledge in forms such as manuscripts, abstracts, or posters.

Clinical studies on Lilly products may also be sponsored and reported by parties other than Lilly in other clinical trial registries.

Trial Results

The following trials have been conducted for Byetta.

Disease Trial ID Trial Title Trial
Phase
Diabetes
8243
A Study by Scintigraphy to Evaluate the Effect of Exenatide on Gastric Emptying in Subjects with Type 2 Diabetes
1
Diabetes
8372
Muliple Dose Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LY2148568 Administered Subcutaneously to Japanese Subjects with Type 2 Diabetes
1
Diabetes
8073
An Exploratory Study of the Safety of Substituting Exenatide for Insulin in Patients With Type 2 Diabetes Who Have Been Using Insulin in Combination With Oral Antidiabetic Therapy
2
Diabetes
8683
A Dose Response Study to Assess the Effect on Glucose Control and Safety and Tolerability of Exenatide in Japanese Patients with Type 2 Diabetes Who are Treated with Oral Antidiabetic(s) but Not Well Controlled
2
Diabetes
8068
Effect of AC2993 (Synthetic Exendin-4) Compared with Insulin Glargine in Patients with Type 2 Diabetes Also Using Combination Therapy with Sulfonylurea and Metformin
3
Diabetes
8075
Safety and Efficacy of Exenatide in Patients with Type 2 Diabetes Using Thiazolidinediones or Thiazolidinediones and Metformin
3
Diabetes
8078
Efficacy of Exenatide Compared with Insulin Glargine in Patients with Type 2 Diabetes Using Metformin or Sulfonylurea for Whom Insulin Is the Next Appropriate Therapy
3
Diabetes
8121
Efficacy of Exenatide (AC2993, Synthetic Exendin-4, LY2148568) Compared with Twice-Daily Biphasic Insulin Aspart in Patients with Type 2 Diabetes Using Sulfonylurea and Metformin
3
Diabetes
9697
Safety and Efficacy of Exenatide in Patients with Type 2 Diabetes Using Metformin or Sulfonylureas and Metformin
3
Diabetes
9698
Safety and Efficacy of Exenatide as Monotherapy in Drug-Naïve Patients with Type 2 Diabetes
3
Diabetes
10749
Safety and Efficacy of Exenatide Taken Before Lunch and Before Dinner Compared with Before Breakfast and Before Dinner in Patients with Type 2 Diabetes Using Oral Antidiabetic Therapy
3b
Diabetes
9693
Effect of Exenatide on 24-Hour Blood Glucose Profile Compared with Placebo in Patients with Type 2 Diabetes Using Metformin or Metformin plus a Thiazolidinedione
4