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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT05872620
Registration number
NCT05872620
Ethics application status
Date submitted
15/05/2023
Date registered
24/05/2023
Titles & IDs
Public title
A Study of Orforglipron in Adult Participants With Obesity or Overweight and Type 2 Diabetes
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Scientific title
A Phase 3, Randomized, Double-Blind Study to Investigate the Efficacy and Safety of Once-Daily Oral LY3502970 Compared With Placebo in Adult Participants With Obesity or Overweight and Type 2 Diabetes (ATTAIN-2)
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Secondary ID [1]
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J2A-MC-GZGQ
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Secondary ID [2]
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18560
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Universal Trial Number (UTN)
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Trial acronym
ATTAIN-2
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Obesity
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Overweight
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Type 2 Diabetes
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Condition category
Condition code
Metabolic and Endocrine
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Diabetes
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Diet and Nutrition
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Obesity
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Metabolic and Endocrine
0
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Other metabolic disorders
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - Orforglipron
Treatment: Drugs - Placebo
Experimental: Orforglipron Dose 1 - Participants will receive orforglipron administered orally.
Experimental: Orforglipron Dose 2 - Participants will receive orforglipron administered orally.
Experimental: Orforglipron Dose 3 - Participants will receive orforglipron administered orally.
Placebo comparator: Placebo - Participants will receive placebo
Treatment: Drugs: Orforglipron
Administered orally
Treatment: Drugs: Placebo
Administered orally
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Mean Percent Change from Baseline in Body Weight
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Assessment method [1]
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Timepoint [1]
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Baseline, Week 72
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Secondary outcome [1]
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Mean Change from Baseline in Waist Circumference
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Assessment method [1]
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Timepoint [1]
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Baseline, Week 72
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Secondary outcome [2]
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Mean Change from Baseline in Hemoglobin A1c (HbA1c) %
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Assessment method [2]
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Timepoint [2]
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Baseline, Week 72
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Secondary outcome [3]
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Mean Change from Baseline in Fasting Glucose
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Assessment method [3]
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Timepoint [3]
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Baseline, Week 72
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Secondary outcome [4]
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Mean Change from Baseline in Systolic Blood Pressure (SBP)
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Assessment method [4]
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Timepoint [4]
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Baseline, Week 72
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Secondary outcome [5]
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Mean Change from Baseline in Fasting Triglycerides
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Assessment method [5]
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Timepoint [5]
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Baseline, Week 72
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Secondary outcome [6]
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Mean Percent Change from Baseline in Fasting non-High-Density Lipoprotein (HDL) Cholesterol
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Assessment method [6]
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Timepoint [6]
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Baseline, Week 72
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Secondary outcome [7]
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Mean Percent Change from Baseline in Fasting Insulin
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Assessment method [7]
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Timepoint [7]
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Baseline, Week 72
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Secondary outcome [8]
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Mean Change from Baseline in Diastolic Blood Pressure (DBP)
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Assessment method [8]
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Timepoint [8]
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Baseline, Week 72
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Secondary outcome [9]
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Mean Change from Baseline in Short Form 36 Version 2 Health Survey Acute Form (SF-36v2) Domain Scores
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Assessment method [9]
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Timepoint [9]
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Baseline, Week 72
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Eligibility
Key inclusion criteria
* Have a body mass index (BMI) =27.0 kilogram/square meter (kg/m²).
* Have a history of at least 1 self-reported unsuccessful dietary effort to lose body weight.
* Have a diagnosis of Type 2 Diabetes (T2D), with HbA1c =7% (=53 mmol/mol) to =10% (86 mmol/mol) and are on stable treatment for T2D for at least 90 days prior to screening, consisting of:
* either diet/exercise alone or
* up to 3 oral antihyperglycemic medications (excluding dipeptidyl peptidase IV inhibitors (DPP-4i) or glucagon-like peptide-1 (GLP-1) receptor agonists (RA).
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Have Type 1 Diabetes (T1D), history of ketoacidosis or hyperosmolar state/coma, or any other types of diabetes except T2D.
* Have a self-reported change in body weight >5 kg (11 pounds) within 90 days prior to screening.
* Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema (for example, laster photocoagulation or intravitreal injections of anti-vascular endothelial growth factor inhibitors).
* Have family (first-degree relative) or personal history of medullary thyroid cancer (MTC) or multiple endocrine neoplasia 2 (MEN2) syndrome.
* Have had a history of chronic or acute pancreatitis.
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Study design
Purpose of the study
Treatment
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
The people receiving the treatment/s
The people analysing the results/data
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Intervention assignment
Parallel
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Other design features
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Phase
Phase 3
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Active, not recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
5/06/2023
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
1/06/2025
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Actual
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Sample size
Target
1500
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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Optimus Clinical Research - Botany
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Recruitment hospital [2]
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The AIM Centre / Hunter Diabetes Centre - Merewether
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Royal Brisbane and Women's Hospital - Brisbane
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Core Research Group - Brisbane
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Logan Hospital - Meadowbrook
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Southern Adelaide Diabetes & Endocrine Services - Oaklands Park
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Box Hill Hospital - Box Hill
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Emeritus Research - Camberwell
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Austin Health - Repatriation Hospital - Heidelberg West
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Baker IDI Heart and Diabetes Institute - Melbourne - Melbourne
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Recruitment hospital [11]
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GenesisCare - Joondalup
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2019 - Botany
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2291 - Merewether
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4029 - Brisbane
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4064 - Brisbane
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4131 - Meadowbrook
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5046 - Oaklands Park
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3128 - Box Hill
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3124 - Camberwell
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3081 - Heidelberg West
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3004 - Melbourne
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Recruitment postcode(s) [11]
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6027 - Joondalup
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Recruitment outside Australia
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Bayamón
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Guaynabo
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Eli Lilly and Company
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Address
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Ethics approval
Ethics application status
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Summary
Brief summary
This study will investigate the safety and efficacy of once daily oral treatment with orforglipron compared with placebo on body weight in adult participants with obesity or overweight and type 2 diabetes. The study will last about 77 weeks and may include up to 22 visits.
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Trial website
https://clinicaltrials.gov/study/NCT05872620
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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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)
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Address
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Eli Lilly and Company
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Yes
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What data in particular will be shared?
Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.
Supporting document/s available: Study protocol, Statistical analysis plan (SAP), Clinical study report (CSR)
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When will data be available (start and end dates)?
Time Frame:
Data are available 6 months after the primary publication and approval of the indication studied in the US and European Union (EU), whichever is later. Data will be indefinitely available for requesting.
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Available to whom?
A research proposal must be approved by an independent review panel and researchers must sign a data sharing agreement.
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Available for what types of analyses?
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How or where can data be obtained?
IPD available at link: http://vivli.org/
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT05872620