Phase 2 Type 1 Diabetes Trial, Terminated NCT01113801 Sponsor: Eli Lilly and Company Condition: Type 1 Diabetes
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Trial results

AI generated results summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

According to the results reported on ClinicalTrials.gov, this trial enrolled 417 people across four groups: one group received a placebo (a dummy treatment with no active ingredient), and the other three groups received different doses of an experimental drug called LY2382770 — either 2 mg, 10 mg, or 50 mg. The trial ran for 12 months and was primarily looking at changes in kidney function over time, measured through a blood marker called serum creatinine (a waste product the kidneys filter out — higher levels can suggest the kidneys are working less well). Around 62–66 people in each group completed the full study, with roughly 37–41 in each group not completing it. The reported data shows that for the primary measure — the change in serum creatinine levels from the start to the 12-month mark — all four groups showed a small increase over time. The placebo group's figure was 0.13 (on a mathematical scale used to analyse the data), while the three LY2382770 groups each recorded figures of 0.17–0.18. For the secondary measures, the reported data shows changes in a urine protein ratio (another marker linked to kidney health) were similarly small across all groups: 0.06 for placebo, 0.05 for the 2 mg and 10 mg groups, and −0.01 for the 50 mg group. The rate at which kidney filtration capacity (eGFR — a standard measure of how well kidneys filter the blood) changed per month was reported as −0.37 for placebo, −0.37 for the 2 mg group, −0.56 for the 10 mg group, and −0.40 for the 50 mg group. Drug exposure levels in the blood were also measured and increased with higher doses, though no placebo figure applies for that measure. These are the results as reported to ClinicalTrials.gov. They are not medical advice — always discuss what they mean for you with your doctor.

These are the results as reported to ClinicalTrials.gov, not medical advice. Verify independently with the trial site and discuss what they mean for you with your doctor.

Phase 2 Type 1 Diabetes Trial, Terminated

NCT01113801
Terminated Phase 2 🇦🇺 Australian site

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You have chronic kidney disease that is believed to be caused by Type 1 or Type 2 diabetes
  • Your kidney function falls within a specific range, based on blood test results measuring creatinine levels or an estimated kidney function score (confirm with trial site for your exact numbers)
  • A urine test shows that your kidneys are leaking a significant amount of protein (confirm with trial site for your exact levels)
  • You are already taking a stable dose of a common blood pressure/kidney-protecting medication (ACE inhibitor or ARB), or you are unable to take these types of medications

Who may not be able to join:

  • Women who are pregnant, breastfeeding, or who are able to become pregnant
  • People who have a long-term inflammatory or autoimmune condition (such as lupus or rheumatoid arthritis)
  • People whose kidney disease is caused by something other than diabetes
  • People who have received an organ transplant
  • People with blood pressure that is too high
  • People who have Hepatitis B, Hepatitis C, cirrhosis, or another serious liver condition
  • People who have had recent bleeding in their stomach or intestines
  • People who had a serious kidney injury in the 3 months before joining the study
  • People who had major surgery in the 3 months before joining, or who plan to have major surgery during the study
  • People who are living with HIV
  • People with an unstable heart condition
  • People with a recent cancer diagnosis or a condition that significantly raises the risk of cancer (confirm with trial site)
  • People who need to take medications that affect the immune system

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 14 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST), Eli Lilly and Company

Australian sites

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Camperdown, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Concord, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Gosford, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Liverpool, New South Wales
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Adelaide, South Australia
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Launceston, Tasmania
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Box Hill, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Fitzroy, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Heidelberg, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Melbourne, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Parkville, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Reservoir, Victoria
For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician., Nedlands, Western Australia

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Terminated
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
1 July 2010
Est. completion
1 May 2014

Where this trial is recruiting

🇦🇺 Australia 🇨🇿 Czechia 🇫🇷 France 🇭🇺 Hungary 🇮🇱 Israel Puerto Rico 🇺🇸 United States

13 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Change in Log Transformed (In) Serum Creatinine From Baseline to 12 Month Endpoint

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov