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.
The following trials have been conducted for products in the diabetes/endocrine therapeutic area.
| Drug |
Disease/Device |
Trial ID |
Trial Title |
Trial
Phase |
| Byetta for Diabetes |
Byetta |
Diabetes |
8243 |
A Study by Scintigraphy to Evaluate the Effect of Exenatide on Gastric Emptying in Subjects with Type 2 Diabetes |
1 |
Byetta |
Diabetes |
8372 |
Muliple Dose Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of LY2148568 Administered Subcutaneously to Japanese Subjects with Type 2 Diabetes |
1 |
Byetta |
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 |
Byetta |
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 |
Byetta |
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 |
Byetta |
Diabetes |
8075 |
Safety and Efficacy of Exenatide in Patients with Type 2 Diabetes Using Thiazolidinediones or Thiazolidinediones and Metformin |
3 |
Byetta |
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 |
Byetta |
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 |
Byetta |
Diabetes |
9697 |
Safety and Efficacy of Exenatide in Patients with Type 2 Diabetes Using Metformin or Sulfonylureas and Metformin |
3 |
Byetta |
Diabetes |
9698 |
Safety and Efficacy of Exenatide as Monotherapy in Drug-Naïve Patients with Type 2 Diabetes |
3 |
Byetta |
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 |
Byetta |
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 |
| Cialis for Diabetic Complications |
Cialis |
Diabetic Complications |
4979 |
A Randomized, Double-Blind, Placebo-Controlled, Parallel Study of Tadalafil in Patients with Diabetic Gastroparesis |
2 |
| Cymbalta for Diabetic Peripheral Neuropathic Pain (DPNP) |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4098a |
A Dose Response Study of Duloxetine versus Placebo in Patients with Painful Diabetic Neuropathy |
2 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4098b |
A Dose Response Study of Duloxetine versus Placebo in Patients with Painful Diabetic Neuropathy
|
2 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4097aa |
Duloxetine versus Placebo in the Treatment of Patients with Painful Diabetic Neuropathy
|
3 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4097ab |
Duloxetine versus Routine Care in the Treatment of Patients with Painful Diabetic Neuropathy (Diabetic Peripheral Neuropathic Pain)
|
3 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4097ba |
Duloxetine versus Placebo in the Treatment of Patients with Painful Diabetic Neuropathy
|
3 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
4097bb |
Duloxetine versus Routine Care in the Treatment of Patients with Painful Diabetic Neuropathy (Diabetic Peripheral Neuropathic Pain)
|
3 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
5110 |
An Open-Label Safety Study of Duloxetine in Patients with Painful Diabetic Neuropathy
|
3 |
Cymbalta |
Diabetic Peripheral Neuropathic Pain (DPNP) |
8952 |
A Comparison of Strategies for Switching Patients from Amitriptyline to Duloxetine for the Management of Diabetic Peripheral Neuropathic Pain
|
4 |
| Glucagon for Hypoglycemia |
Glucagon |
Hypoglycemia |
1316 |
Comparison of Pharmacokinetic Parameters of Recombinant and Animal-Source Glucagon After IV, IM, and SC Injection |
1 |
Glucagon |
Hypoglycemia |
1317 |
Safety and Immunogenicity of Recombinant DNA Glucagon in Comparison with Animal-Source Glucagon |
1 |
| Humalog Devices |
Humalog |
Device |
6159 |
Functionality and Safety of the Humapen Memoir in Patients with Type 1 or Type 2 Diabetes |
3 |
Humalog |
Device |
9673 |
Complaints Associated with Use of the Prefilled Pen B When Used by Patients with Type 2 Diabetes on Twice-Daily Insulin Therapy |
3 |
| Humalog for Diabetes |
Humalog |
Diabetes |
Z011 |
LY275585 vs. Humulin® R: Premeal Therapy in Type I Diabetes |
2 |
Humalog |
Diabetes |
Z012 |
LY275585 vs. Humulin® R: Premeal Therapy in Type II Diabetes |
2 |
Humalog |
Diabetes |
Z013 |
LY275585 vs. Humulin® R: Premeal Therapy in Type I Diabetes |
2 |
Humalog |
Diabetes |
Z014 |
LY275585 vs. Humulin® R: Premeal Therapy in Type II Diabetes |
2 |
Humalog |
Diabetes |
Z015 |
LY275585 vs. Humulin® R: Premeal Therapy in New Patients with Type 1 Diabetes |
3 |
Humalog |
Diabetes |
Z016 |
LY275585 vs. Humulin® R: Premeal Therapy in New Patients with Type 2 Diabetes |
3 |
Humalog |
Diabetes |
Z017 |
LY275585 vs. Humulin® R: Premeal Therapy in Type 1 Diabetes |
3 |
Humalog |
Diabetes |
Z018 |
LY275585 vs. Humulin® R: Premeal Therapy in Type 2 Diabetes |
3 |
Humalog |
Diabetes |
4269 |
Insulin Lispro Low Mixture Administered Twice Daily In Insulin-Requiring Patients With Type 1 Or Type 2 Diabetes |
3 |
Humalog |
Diabetes |
7354 |
Comparison Of The Insulin Therapies: Insulin Lispro Low Mix (25%) And Insulin Glargine In Patients With Diabetes Mellitus Type 2 |
3 |
Humalog |
Diabetes |
9537 |
Comparison of 2-Hour Postprandial Blood Glucose Excursion in Response to a Standard Test Meal in Insulin-Requiring Diabetic Patients Treated Twice Daily with Either Insulin Lispro Mix 50/50 or Human Insulin Mix 50/50 |
3 |
Humalog |
Diabetes |
4050 |
Efficacy and Safety of Twice-Daily Insulin Lispro Low Mixture Compared to Once-Daily Insulin Glargine in Patinets who Have Been Using One or More Oral Antihyperglycemic Agents Without Insulin |
3 / 4 |
Humalog |
Diabetes |
4286 |
Insulin Lispro Mid Mixture And Insulin Lispro Low Mixture, Administered Twice Daily In Insulin Requiring Patients With Type 1 And 2 Diabetes |
3 / 4 |
Humalog |
Diabetes |
4011 |
Efficacy and Safety of Twice-Daily Insulin Lispro Low Mixture Compared to Once-Daily Insulin Glargine in Patients With Type 2 Diabetes on NPH Alone or Combination Therapy of Insulin and Oral Agents
|
4 |
Humalog |
Diabetes |
4957 |
Pilot Study Investigating the Effects of Insulin Lispro Low Mixture Compared with Insulin Glargine on Perceived Mood Symptoms in Patients with Type 2 Diabetes Mellitus
|
4 |
Humalog |
Diabetes |
5881 |
Comparison of Intensive Mixture Therapy Vs Basal Insulin Therapy in Patients with Type 2 Diabetes Receiving Oral Antidiabetes Agents |
4 |
Humalog |
Diabetes |
6071 |
Non-Inferiority Of Morning Administration Of Insulin Lispro -Lispro-Protamine 50% Versus Bedtime Insulin NPH In Type 2 Diabetic Patients Treated With Oral Antidiabetic Drugs |
4 |
Humalog |
Diabetes |
6107 |
Characterization of Postprandial Events Associated With Regimens of Premeal Insulin Lispro or Twice-Daily NPH in Patients With Type 2 Diabetes |
4 |
Humalog |
Diabetes |
6146 |
Long-Term Effects of Insulin plus Metformin Regimens on the Overall and Postprandial Glycemic Control of Patients with Type 2 Diabetes: A Comparison of Premeal Insulin Lispro Mixtures to Once-Daily Insulin Glargine |
4 |
Humalog |
Diabetes |
6722 |
Glycemic control and quality of life with Insulin Lispro Mix75/25 Twice Daily versus NPH Human Insulin Twice Daily in Type 2 Diabetes |
4 |
Humalog |
Diabetes |
7505 |
Twenty-Four-Hour Plasma Glucose Profiles Observed in Patients with Type 2 Diabetes During Therapy Consisting of Oral Agent(s) Plus Twice-Daily Insulin Lispro Low Mixture or Once-Daily Insulin Glargine
|
4 |
Humalog |
Diabetes |
9057 |
A Comparison of Prandial Insulin Lispro Mixtures Therapy to Glargine Basal-Bolus Therapy With Insulin Lispro on the Overall Glycemic Control of Patients With Type 2 Diabetes Previously Treated With Oral Agents Combined With Insulin Glargine
|
4 |
| Humatrope for Achondroplasia |
Humatrope |
Achondroplasia |
Z019 |
Evaluation of Growth Promoting Effect and Safety of Growth Hormone in Achondroplasia |
3 |
| Humatrope for Adult Replacement Growth Hormone Deficiency |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
Z007 |
Investigation of the Safety and Efficacy of Growth Hormone Replacement Therapy in Adults with Growth Hormone Deficiency Arising in Adult Life |
3 |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
818 |
Investigation of the Safety and Efficacy of Growth Hormone Replacement Therapy in Adults with Previously Treated Childhood Growth Hormone Deficiency |
3 |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
2889 |
Placebo-Controlled Double Blind Study Of LY137998 [Somatropin Recombinant DNA Origin] In Adults With Growth Hormone Deficiency |
3 |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
5300 |
Long-Term Clinical Study Of LY137998 [Somatropin Recombinant DNA Origin] In Adults With Growth Hormone Deficiency |
3 |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
6018 |
Extended Clinical Study of LY137998 [Somatropin (Recombinant DNA Origin)] In Adults with Growth Hormone Deficiency |
3 / 4 |
Humatrope |
Adult Replacement Growth Hormone Deficiency |
883 |
The Effect of Chronic Somatropin Treatment on Bone Mineral Density in Patients Diagnosed with Adult-Onset Growth Hormone Deficiency |
4 |
| Humatrope for Chronic Renal Insufficiency |
Humatrope |
Chronic Renal Insufficiency |
824 |
Use of Biosynthetic Human Growth Hormone (Humatrope®) in Short Children with Chronic Renal Failure |
3 |
| Humatrope for Growth Hormone Deficiency |
Humatrope |
Growth Hormone Deficiency |
5123 |
The Genetics and Neuroendocrinology in Children with GHD: A Part of GeNeSIS
|
4 |
| Humatrope for Idiopathic Short Stature |
Humatrope |
Idiopathic Short Stature |
843 |
Humatrope® in Non-Growth Hormone-Deficient Children with Short Stature |
3 |
| Humatrope |
Idiopathic Short Stature |
843b |
Humatrope® in Non-Growth Hormone-Deficient Children with Short Stature
|
3 |
Humatrope |
Idiopathic Short Stature |
Z009 |
The Efficacy and Safety of Biosynthetic Authentic Human Growth Hormone in Short Prepubertal Children with Normal Growth Hormone Response to Standard Provocation Tests |
3 |
| Humatrope for SHOX Deficiency |
Humatrope |
SHOX Deficiency |
2704 |
Efficacy and Safety of Somatropin Treatment in Pediatric Subjects with SHOX Disorder and SHOX-Deficient Turner Syndrome
|
3 |
| Humatrope for Small for Gestational Age |
Humatrope |
Small for Gestational Age |
6581 |
Optimization of Growth Hormone Treatment in Short Children Born Small for Gestational Age Based on a Growth Prediction Model: The OPTIMA Trial
|
3 |
| Humatrope for Turner Syndrome |
Humatrope |
Turner Syndrome |
2878 |
The Effect Of Recombinant Human Growth Hormone Treatment On The Growth Of Infants And Toddlers With Turner Syndrome
|
3 / 4 |