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Study · Not a test of the peptide alone · 2005

11 results

Rh/IGF-I/rhIGFBP-3 administration to patients with type 2 diabetes mellitus reduces insulin requirements while also lowering fasting glucose.

Clemmons DR, Moses AC, Sommer A, Jacobson W, Rogol AD, Sleevi MR, Allan G

Growth hormone & IGF research : official journal of the Growth Hormone Research Society and the International IGF Research Society1 Aug 2005Cited by 55 (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: Publisher copyright. Results still quote short attributed sentences.

Results from this study11

No result from this study comes from a test of the peptide.

Studies that did not test the peptide alone11

In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  1. 01HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialEfficacy outcome

    In insulin-treated type 2 diabetes, rhIGF-I/rhIGFBP-3 reduced insulin requirements by 54% to 82% across four regimens.

    In plain wordsIn type 2 diabetes, the complex reduced insulin requirements across four regimens.

    Outcome
    DecreaseInsulin requirements
    Study

    n = 52

    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    Insulin requirement decrease
    54 to 82%
    across the four dosage groups

    Source sentences

    Summary
    Across these four groups rhIGF-I/rhIGFBP-3 decreased insulin requirements between 54% and 82%.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  2. 02HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialEfficacy outcome

    In insulin-treated type 2 diabetes, fasting glucose decreased by 32-37% during rhIGF-I/rhIGFBP-3 treatment.

    In plain wordsIn type 2 diabetes, fasting glucose decreased during complex treatment.

    Outcome
    DecreaseFasting glucose
    Study

    n = 52

    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    Fasting glucose decrease
    32 to 37%
    across the four dosage groups

    Source sentences

    Summary
    Fasting glucose decreased by 32-37%.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  3. 03HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialEfficacy outcome

    In insulin-treated type 2 diabetes, mean daily glucose decreased by 9-23% across all rhIGF-I/rhIGFBP-3 groups.

    In plain wordsIn type 2 diabetes, daily glucose decreased in all complex treatment groups.

    Outcome
    DecreaseMean daily blood glucose
    Study

    n = 52

    Outcome group
    Glycemic control · Metabolic and weight

    Measurements

    Mean daily blood glucose decrease
    9 to 23%
    range across the four groups

    Source sentences

    Summary
    Mean daily blood glucose (4 determinations per day) declined in all 4 groups (range 9-23% decrease).
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  4. 04HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialPharmacokinetics

    In type 2 diabetes, total IGF-I rose 4.0-4.8-fold and peaked at 16-24 h during complex treatment.

    In plain wordsIn type 2 diabetes, the complex increased total IGF-I concentrations.

    Outcome
    IncreasePeak total IGF-I
    Study

    n = 52

    Outcome group
    Pharmacokinetics · Endocrine and hormones

    Measurements

    Peak total IGF-I increase
    4 to 4.8 fold
    peak total IGF-I
    Time of peak total IGF-I
    16 to 24 h
    peak total IGF-I

    Source sentences

    Summary
    The peak total IGF-I values were increased to 4.0-4.8-fold at 16-24 h.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  5. 05HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialPharmacokinetics

    In type 2 diabetes, free IGF-I rose 7.1 to 8.2-fold and peaked at 16-20 h after complex administration.

    In plain wordsIn type 2 diabetes, the complex increased free IGF-I concentrations.

    Outcome
    IncreasePeak free IGF-I
    Study

    n = 52

    Outcome group
    Pharmacokinetics · Endocrine and hormones

    Measurements

    Peak free IGF-I increase
    7.1 to 8.2 fold
    free IGF-I
    Time of peak free IGF-I
    16 to 20 h
    after administration

    Source sentences

    Summary
    For free IGF-I the increase varied between 7.1 and 8.2-fold and peak values were attained at 16-20 h after administration.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  6. 06HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialPharmacokinetics

    In type 2 diabetes, free IGF-I Tmax with the complex was lower than in published lower-dose IGF-I-alone studies.

    In plain wordsIn type 2 diabetes, the complex produced an earlier free IGF-I peak than published IGF-I-alone studies.

    Outcome
    DecreaseFree IGF-I Tmax
    Study

    n = 52

    Comparator
    Previously published IGF-I-alone studies
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    Both the time to maximum concentration (Tmax) and the maximum free IGF-I levels (Cmax) on day 1 for all groups were substantially less than previously published studies, wherein lower doses of rhIGF-I were given without IGFBP-3.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  7. 07HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialPharmacokinetics

    In type 2 diabetes, free IGF-I Cmax with the complex was lower than in published lower-dose IGF-I-alone studies.

    In plain wordsIn type 2 diabetes, the complex produced a lower free IGF-I peak than published IGF-I-alone studies.

    Outcome
    DecreaseFree IGF-I Cmax
    Study

    n = 52

    Comparator
    Previously published IGF-I-alone studies
    Outcome group
    Pharmacokinetics · Pharmacology

    Source sentences

    Summary
    Both the time to maximum concentration (Tmax) and the maximum free IGF-I levels (Cmax) on day 1 for all groups were substantially less than previously published studies, wherein lower doses of rhIGF-I were given without IGFBP-3.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  8. 08HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialSafety outcome

    In type 2 diabetes, side effects of rhIGF-I plus rhIGFBP-3 occurred at 4%, less often than reported in previous studies of IGF-I without IGFBP-3.

    In plain wordsIn type 2 diabetes, side effects were less frequent with IGF-I plus IGFBP-3 than in earlier studies of IGF-I alone.

    Outcome
    DecreaseSide effect frequency
    Study

    n = 52

    Comparator
    Previously published IGF-I-alone studies
    Outcome group
    Adverse events · Whole body

    Measurements

    Frequency of side effects such as edema, jaw pain and arthralgias
    4%
    combined frequency, rhIGF-I plus rhIGFBP-3

    Source sentences

    Summary
    The frequency of side effects such as edema, jaw pain and arthralgias was 4% which is less than that has been reported in previous studies wherein IGF-I was administered without IGFBP-3.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  9. 09HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialEfficacy outcome

    In insulin-treated type 2 diabetes, glucose improvement with rhIGF-I plus rhIGFBP-3 was greatest in dosage regimen groups 2 and 3.

    In plain wordsIn type 2 diabetes, glucose improved most in dosage groups 2 and 3 of the IGF-I and IGFBP-3 treatment.

    Outcome
    Not applicableGlucose improvement across regimens
    Study

    n: not reported in source

    Comparator
    Other dosage regimens
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    The improvement in glucose values and the degree of reduction in insulin requirement were the greatest in groups 2 and 3 and the patients in those groups had the highest free IGF-I levels.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  10. 10HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialEfficacy outcome

    In insulin-treated type 2 diabetes, the reduction in insulin requirement with rhIGF-I plus rhIGFBP-3 was greatest in dosage regimen groups 2 and 3.

    In plain wordsIn type 2 diabetes, insulin needs fell most in dosage groups 2 and 3 of the IGF-I and IGFBP-3 treatment.

    Outcome
    Not applicableInsulin reduction across regimens
    Study

    n: not reported in source

    Comparator
    Other dosage regimens
    Outcome group
    Glycemic control · Metabolic and weight

    Source sentences

    Summary
    The improvement in glucose values and the degree of reduction in insulin requirement were the greatest in groups 2 and 3 and the patients in those groups had the highest free IGF-I levels.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

  11. 11HumanNot a test of IGF-1 (mecasermin) aloneNon-randomized trialPharmacokinetics

    In insulin-treated type 2 diabetes, dosage regimen groups 2 and 3 of rhIGF-I plus rhIGFBP-3 had the highest free IGF-I levels.

    In plain wordsIn type 2 diabetes, free IGF-I was highest in dosage groups 2 and 3 of the IGF-I and IGFBP-3 treatment.

    Outcome
    IncreaseFree IGF-I across regimens
    Study

    n: not reported in source

    Comparator
    Other dosage regimens
    Outcome group
    Pharmacokinetics · Endocrine and hormones

    Source sentences

    Summary
    The improvement in glucose values and the degree of reduction in insulin requirement were the greatest in groups 2 and 3 and the patients in those groups had the highest free IGF-I levels.
    1 context sentence
    Summary · context
    In this study, 52 patients with insulin-treated type 2 diabetes received recombinant human IGF-I plus rhIGFBP-3 in one of four dosage regimens for 14 days.

    In this study, IGF-1 (mecasermin) 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 IGF-1 (mecasermin).

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

    14 Oct 2026, 05:02 UTC

    Study results updated

  2. Version 1

    14 Oct 2026, 01:46 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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