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Study · Observational study · n = 1,329 · 2022

9 results

Association of Dulaglutide Initiation Timing With Treatment Patterns and Clinical Outcomes in Patients With Type 2 Diabetes Mellitus in the United States.

Hoog M, Smith JL, Yu M, Peleshok J, Mody R, Grabner M

Clinical therapeutics24 May 2022Cited by 2 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC-ND. Results still quote short attributed sentences.

Results from this study9

5 results from studies that gave the peptide. 5 results from people.

  1. 01HumanObservational studyEfficacy outcome

    In adults with ≥3 prior OAD classes, dulaglutide initiation was linked to an HbA1c reduction of -1.01%.

    In plain wordsIn adults with at least three prior oral drug classes, dulaglutide initiation was linked to lower blood sugar than baseline.

    Outcome
    DecreaseHbA1c change, at least three prior OAD classes
    Study

    n = 1,329

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg or 1.5 mg once weekly · injection · 6 monthsAs given in this study (human).

    Measurements

    HbA1c change
    −1.01%
    ≥3 OAD cohort
    95% CI lower
    −1.09%
    ≥3 OAD cohort
    95% CI upper
    −0.93%
    ≥3 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group experienced larger reductions in HbA1c levels (1 OAD: -1.39%; 95% CI, -1.50 to -1.27; 2 OADs: -1.30%; 95% CI, -1.39 to -1.20; and ≥3 OADs: -1.01%; 95% CI, -1.09 to -0.93) versus the patients in the delayed initiator group.
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.
  2. 02HumanObservational studyEfficacy outcome

    In adults with ≥3 prior OAD classes, 33% achieved HbA1c <7% after dulaglutide initiation.

    In plain wordsOne third of adults with at least three prior oral drug classes reached the blood sugar target after dulaglutide initiation.

    Outcome
    Not applicableHbA1c below 7%, at least three prior OAD classes
    Study

    n = 1,329

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg or 1.5 mg once weekly · injection · 6 monthsAs given in this study (human).

    Measurements

    HbA1c <7%
    33%
    ≥3 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group also achieved HbA1c <7% at 6-month follow-up more frequently than those in the later initiator group (1 OAD: 68%; 2 OADs: 51%; and ≥3 OADs: 33%).
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.
  3. 03HumanObservational studyEfficacy outcome

    In adults with two prior OAD classes, dulaglutide initiation was linked to an HbA1c reduction of -1.30%.

    In plain wordsIn adults with two prior oral drug classes, dulaglutide initiation was linked to lower blood sugar than baseline.

    Outcome
    DecreaseHbA1c change, two prior OAD classes
    Study

    n = 1,088

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg or 1.5 mg once weekly · injection · 6 monthsAs given in this study (human).

    Measurements

    HbA1c change
    −1.3%
    2 OAD cohort
    95% CI lower
    −1.39%
    2 OAD cohort
    95% CI upper
    −1.2%
    2 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group experienced larger reductions in HbA1c levels (1 OAD: -1.39%; 95% CI, -1.50 to -1.27; 2 OADs: -1.30%; 95% CI, -1.39 to -1.20; and ≥3 OADs: -1.01%; 95% CI, -1.09 to -0.93) versus the patients in the delayed initiator group.
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.
  4. 04HumanObservational studyEfficacy outcome

    In adults with two prior OAD classes, 51% achieved HbA1c <7% after dulaglutide initiation.

    In plain wordsAbout half of adults with two prior oral drug classes reached the blood sugar target after dulaglutide initiation.

    Outcome
    Not applicableHbA1c below 7%, two prior OAD classes
    Study

    n = 1,088

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg or 1.5 mg once weekly · injection · 6 monthsAs given in this study (human).

    Measurements

    HbA1c <7%
    51%
    2 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group also achieved HbA1c <7% at 6-month follow-up more frequently than those in the later initiator group (1 OAD: 68%; 2 OADs: 51%; and ≥3 OADs: 33%).
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.
  5. 05HumanObservational studyEfficacy outcome

    In adults with one prior OAD class, dulaglutide initiation was linked to an HbA1c change of -1.39% from baseline at 6 months.

    In plain wordsIn adults with one prior oral drug class, dulaglutide initiation was linked to lower blood sugar than baseline.

    Outcome
    DecreaseHbA1c change, one prior OAD class
    Study

    n = 761

    Outcome group
    Glycemic control · Metabolic and weight
    Studied dose
    0.75 mg or 1.5 mg once weekly · injection · 6 monthsAs given in this study (human).

    Measurements

    HbA1c change
    −1.39%
    1 OAD cohort
    95% CI lower
    −1.5%
    1 OAD cohort
    95% CI upper
    −1.27%
    1 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group experienced larger reductions in HbA1c levels (1 OAD: -1.39%; 95% CI, -1.50 to -1.27; 2 OADs: -1.30%; 95% CI, -1.39 to -1.20; and ≥3 OADs: -1.01%; 95% CI, -1.09 to -0.93) versus the patients in the delayed initiator group.
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.

Studies that did not test the peptide alone4

In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Dulaglutide (Trulicity).

  1. 06HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyOther

    In US adults with diabetes, most dulaglutide initiators started at 0.75 mg.

    In plain wordsMost adults in the claims study started dulaglutide at the lower dose.

    Outcome
    Not applicableInitial dose
    Study

    n = 18,121

    Outcome group
    Patterns of use · Pharmacology

    Measurements

    Initiation at 0.75 mg
    67 to 70%
    cohorts

    Source sentences

    Summary
    Most patients (67%-70%) initiated treatment with dulaglutide 0.75 mg.
    3 context sentences
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  2. 07HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyOther

    In US adults with diabetes, dulaglutide dose escalation was uncommon but trended higher with more prior OAD classes.

    In plain wordsDose escalation was uncommon and tended to be higher among adults with more prior oral diabetes drug classes.

    Outcome
    IncreaseDose escalation
    Study

    n = 18,121

    Comparator
    Cohorts with fewer prior OAD classes
    Outcome group
    Patterns of use · Pharmacology

    Measurements

    Dose escalation
    15 to 20%
    to 1.5 mg

    Source sentences

    Summary
    Dose escalation to 1.5 mg was uncommon (15%-20%) but trended higher in the ≥3 OAD cohort.
    3 context sentences
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  3. 08HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyOther

    In US adults with diabetes, dulaglutide adherence at follow-up increased with higher baseline OAD use.

    In plain wordsHigher prior oral diabetes drug use was linked to higher dulaglutide adherence.

    Outcome
    IncreaseAdherence
    Study

    n = 18,121

    Comparator
    Lower baseline OAD use
    Outcome group
    Treatment adherence and retention · Pharmacology

    Measurements

    Adherence
    61 to 67%
    6-month follow-up

    Source sentences

    Summary
    Adherence to dulaglutide at 6-month follow-up (61%-67%) increased with higher baseline OAD use.
    3 context sentences
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

  4. 09HumanNot a test of Dulaglutide (Trulicity) aloneObservational studyEfficacy outcome

    In adults with one prior OAD class, early dulaglutide initiation was linked to more frequent HbA1c target achievement than later initiation.

    In plain wordsEarlier dulaglutide initiation was linked to more frequent blood sugar target achievement than later initiation.

    Outcome
    IncreaseHbA1c below 7%, one prior OAD class
    Study

    n = 761

    Comparator
    Later initiator cohorts
    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    HbA1c <7%
    68%
    1 OAD cohort

    Source sentences

    Summary
    Patients in the early dulaglutide therapy initiator group also achieved HbA1c <7% at 6-month follow-up more frequently than those in the later initiator group (1 OAD: 68%; 2 OADs: 51%; and ≥3 OADs: 33%).
    4 context sentences
    Summary · context
    The HbA1c assessment (n = 3178) included 761 patients in the 1 OAD cohort, 1088 patients in the 2 OADs cohort, and 1329 patients in the ≥3 OADs cohort.
    Summary · context
    This retrospective, claims-based analysis evaluated adults with type 2 diabetes, ≥1 claim for dulaglutide 0.75 mg or 1.5 mg once-weekly injection (between November 2014 and August 2019), and no prior use of glucagon-like peptide 1 receptor agonists or insulin.
    Summary · context
    Cohorts were defined based on the number of oral antidiabetic drug (OAD) classes used within the 24-month baseline period before dulaglutide therapy initiation: 1 OAD, 2 OADs, or ≥3 OADs.
    Summary · context
    Six-month follow-up outcomes, including change in glycosylated hemoglobin (HbA1c) and treatment patterns, were descriptively assessed within each cohort.

    In this study, Dulaglutide (Trulicity) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Dulaglutide (Trulicity).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    22 Oct 2026, 02:25 UTC

    Study results updated

  2. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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