FDA approves additional doses of Trulicity (dulaglutide) for the treatment of type 2 diabetes
AWARD-11 showed 3.0 mg and 4.5 mg doses led to additional blood sugar control; as a secondary endpoint, both doses also led to weight
INDIANAPOLIS,?Sept. 3, 2020?/PRNewswire/ --?The?U.S. Food and Drug Administration (FDA) today approved two additional doses of Eli Lilly and Company's?(NYSE:?LLY) Trulicity??(dulaglutide). The approval expands the label of once-weekly Trulicity to include 3.0 mg and 4.5 mg doses based on data from AWARD-11. The phase 3 trial showed the additional doses led to further benefits in A1C and body weight reduction when compared to Trulicity 1.5 mg in people with type 2 diabetes.
"The FDA's decision to approve the additional doses of Trulicity is a positive step forward for people living with type 2 diabetes and their care teams," said Juan Pablo Frias,?M.D., Medical Director and Principal Investigator, National Research Institute. "This progressive condition can require different treatment approaches over time, and findings from AWARD-11 showed the additional doses of Trulicity can lead to further A1C and weight reductions for people with type 2 diabetes whose current treatment may no longer be meeting their needs."
The AWARD-11 trial evaluated the safety and efficacy of additional doses of Trulicity (3.0 mg and 4.5 mg) compared to Trulicity 1.5 mg, using two different statistical approaches[i]. The efficacy estimand, which analyzes participants who remained on treatment throughout the trial, showed both doses led to significant reductions in A1C and weight:
Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. We were founded more than a century ago by a man committed to creating high-quality medicines that meet real needs, and today we remain true to that mission in all our work. Across the globe, Lilly employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism. To learn more about Lilly, please visit us at?lilly.com?and?lilly.com/newsroom. P-LLY Trulicity??is a registered trademark owned or licensed by Eli Lilly and Company, its subsidiaries, or affiliates. This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about dulaglutide 3.0 mg and/or 4.5 mg as a potential treatment for people with type 2 diabetes and reflects Lilly's current belief. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of development and commercialization. Among other things, there can be no guarantee that future study results will be consistent with the results to date or that dulaglutide 3 mg and/or 4.5 mg will receive additional regulatory approvals.?For further discussion of these and other risks and uncertainties, see Lilly's most recent Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release. 1?Centers for Disease Control and Prevention. National Diabetes Statistics Report, 2020.?Atlanta, GA: Centers for Disease Control and Prevention, U.S. Dept. of Health and Human Services; 2020. 2?International Diabetes Federation. IDF Diabetes Atlas, 9th?edn.?Brussels, Belgium: International Diabetes Federation, 2019. Available at:?http://diabetesatlas.org.
i?The efficacy estimand was used to evaluate results in participants who stayed on treatment and did not start another diabetes medicine throughout the trial. The treatment-regimen estimand, conducted based on regulatory guidance, includes data from all participants through the end of the trial, which may include confounding effects of rescue medication or discontinuation from the study drug or the trial. In the treatment-regimen estimand, which was conducted based on regulatory guidance, each dose led to clinically meaningful A1C and body weight reductions but only the 4.5 mg dose showed superiority compared to Trulicity 1.5 mg.
SOURCE Eli Lilly and Company
- 4.5 mg?(A1C: -1.9 percent, weight: -10.4 pounds)
- 3.0 mg?(A1C: -1.7 percent; weight: -8.8 pounds)
- 1.5 mg?(A1C: -1.5 percent; weight: -6.8 pounds)
- Trulicity is given through an injection (needle). You take it once a week by injecting it under the skin of your stomach, thigh, or upper arm. Use Trulicity together with the diet and exercise that your doctor recommends.
- Do not use Trulicity if you or any of your family have ever had a type of thyroid cancer called medullary thyroid carcinoma (MTC).
- Do not use Trulicity if you have Multiple Endocrine Neoplasia syndrome type 2 (MEN 2).
- Do not use Trulicity if you are allergic to dulaglutide or other ingredients in Trulicity.
- Your healthcare provider should show you how to use Trulicity before you use it for the first time.
- Before?you?use?Trulicity,?talk?to?your?doctor?about?low?blood?sugar?and?how?to?manage?it.
- Do you have other medical conditions, including problems with your pancreas, kidneys, liver, or stomach, or have a history of diabetic retinopathy (vision problems related to diabetes)?
- Do you take other diabetes medicines, such as insulin or sulfonylureas?
- Do you take any other prescription medicines or over-the-counter drugs, vitamins or herbs?
- You are pregnant or plan to become pregnant or breastfeeding or plan to breastfeed.
- You have type 1 diabetes.
- You have or have had an inflamed pancreas (pancreatitis).
- You have severe intestinal or stomach problems, such as slowed emptying or problems with digesting food.
- You are a child under 18 years old.
- Read the Instructions for Use that come with Trulicity.
- Use Trulicity exactly as your doctor says.
- Do not share your Trulicity pen, syringe or needles with another person.
- Do not give Trulicity to other people.
- If you take too much Trulicity, call your healthcare provider or seek medical advice promptly.
Lilly is a global healthcare leader that unites caring with discovery to make life better for people around the world. We were founded more than a century ago by a man committed to creating high-quality medicines that meet real needs, and today we remain true to that mission in all our work. Across the globe, Lilly employees work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to communities through philanthropy and volunteerism. To learn more about Lilly, please visit us at?lilly.com?and?lilly.com/newsroom. P-LLY Trulicity??is a registered trademark owned or licensed by Eli Lilly and Company, its subsidiaries, or affiliates. This press release contains forward-looking statements (as that term is defined in the Private Securities Litigation Reform Act of 1995) about dulaglutide 3.0 mg and/or 4.5 mg as a potential treatment for people with type 2 diabetes and reflects Lilly's current belief. However, as with any pharmaceutical product, there are substantial risks and uncertainties in the process of development and commercialization. Among other things, there can be no guarantee that future study results will be consistent with the results to date or that dulaglutide 3 mg and/or 4.5 mg will receive additional regulatory approvals.?For further discussion of these and other risks and uncertainties, see Lilly's most recent Form 10-K and Form 10-Q filings with the United States Securities and Exchange Commission. Except as required by law, Lilly undertakes no duty to update forward-looking statements to reflect events after the date of this release. 1?Centers for Disease Control and Prevention. National Diabetes Statistics Report, 2020.?Atlanta, GA: Centers for Disease Control and Prevention, U.S. Dept. of Health and Human Services; 2020. 2?International Diabetes Federation. IDF Diabetes Atlas, 9th?edn.?Brussels, Belgium: International Diabetes Federation, 2019. Available at:?http://diabetesatlas.org.
i?The efficacy estimand was used to evaluate results in participants who stayed on treatment and did not start another diabetes medicine throughout the trial. The treatment-regimen estimand, conducted based on regulatory guidance, includes data from all participants through the end of the trial, which may include confounding effects of rescue medication or discontinuation from the study drug or the trial. In the treatment-regimen estimand, which was conducted based on regulatory guidance, each dose led to clinically meaningful A1C and body weight reductions but only the 4.5 mg dose showed superiority compared to Trulicity 1.5 mg.
Refer to: ???????? ??????????? |
Dani Barnhizer;?dbarnhizer@lilly.com; 317-607-6119 (Lilly Diabetes) |
Kevin Hern;?hern_kevin_r@lilly.com?; 317-277-1838 (Investors)?????????????? ? ? |