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Study · Randomized controlled trial · 2001

12 results

Effect of alendronate and MK-677 (a growth hormone secretagogue), individually and in combination, on markers of bone turnover and bone mineral density in postmenopausal osteoporotic women.

Murphy MG, Weiss S, McClung M, Schnitzer T, Cerchio K, Connor J, Krupa D, Gertz BJ

The Journal of clinical endocrinology and metabolism1 Mar 2001Cited by 60 (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 study12

9 results from studies that gave the peptide. 9 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 alone increased IGF-I from baseline, significantly versus placebo.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 alone increased IGF-I from baseline more than placebo.

    Outcome
    IncreaseIGF-I with MK-677 alone
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones
    Studied dose
    25 mg daily · oral · 12 monthsAs given in this study (human).

    Measurements

    IGF-I change from baseline
    39%
    MK-677 with or without alendronate; the source does not say which arm has 39% and which has 45%
    IGF-I change from baseline
    45%
    MK-677 with or without alendronate; the source does not say which arm has 39% and which has 45%
    P value for IGF-I
    < 0.05
    MK-677 alone versus placebo, month 12

    Source sentences

    Summary
    MK-677, with or without alendronate, increased insulin-like growth factor I levels from baseline (39% and 45%; P < 0.05 vs. placebo).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  2. 02HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 increased osteocalcin by 22%, significantly versus placebo.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 increased osteocalcin more than placebo.

    Outcome
    IncreaseOsteocalcin with MK-677 alone
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 12 monthsAs given in this study (human).

    Measurements

    Osteocalcin change
    22%
    MK-677 group versus placebo, on the average
    P value for osteocalcin
    < 0.05
    MK-677 versus placebo, month 12

    Source sentences

    Summary
    MK-677 increased osteocalcin and urinary NTx by 22% and 41%, on the average, respectively (P < 0.05 vs. placebo).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  3. 03HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 increased urinary NTx by 41%, significantly versus placebo.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 increased urinary NTx more than placebo.

    Outcome
    IncreaseUrinary NTx with MK-677 alone
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 12 monthsAs given in this study (human).

    Measurements

    Urinary NTx change
    41%
    MK-677 group versus placebo, on the average
    P value for urinary NTx
    < 0.05
    MK-677 versus placebo, month 12

    Source sentences

    Summary
    MK-677 increased osteocalcin and urinary NTx by 22% and 41%, on the average, respectively (P < 0.05 vs. placebo).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  4. 04HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, adding MK‑677 to alendronate reduced osteocalcin less than alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, adding MK‑677 to alendronate reduced osteocalcin less than alendronate alone.

    Outcome
    IncreaseOsteocalcin with combination
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 12 monthsAs given in this study (human).

    Measurements

    Osteocalcin relative change
    −40%
    MK-677 plus alendronate
    Osteocalcin relative change
    −54%
    alendronate alone
    P value for osteocalcin relative change
    < 0.05
    MK-677 plus alendronate versus alendronate alone, month 12

    Source sentences

    Summary
    MK-677 and alendronate mitigated the reduction in bone formation compared with alendronate alone based on mean relative changes in serum osteocalcin (-40% vs. -54%; P < 0.05, combination vs. alendronate)
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  5. 05HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, adding MK‑677 to alendronate reduced NTx less than alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, adding MK‑677 to alendronate reduced NTx less than alendronate alone.

    Outcome
    IncreaseNTx with combination
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 12 monthsAs given in this study (human).

    Measurements

    NTx relative change
    −52%
    MK-677 plus alendronate
    NTx relative change
    −61%
    alendronate alone
    P value for NTx relative change
    < 0.05
    MK-677 plus alendronate versus alendronate alone, month 12

    Source sentences

    Summary
    and reduced the effect of alendronate on resorption (NTx) as well (-52% vs. -61%; P < 0.05, combination vs. alendronate).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  6. 06HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 plus alendronate increased femoral neck BMD more than alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 plus alendronate increased femoral neck bone density more than alendronate alone.

    Outcome
    IncreaseFemoral neck BMD
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 18 monthsAs given in this study (human).

    Measurements

    Femoral neck BMD increase
    4.2%
    MK-677 plus alendronate
    Femoral neck BMD increase
    2.5%
    alendronate alone
    P value for femoral neck BMD increase
    < 0.05
    MK-677 plus alendronate versus alendronate alone, BMD assessment

    Source sentences

    Summary
    MK-677 plus alendronate increased BMD at the femoral neck (4.2% vs. 2.5% for alendronate; P < 0.05).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  7. 07HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly enhance lumbar spine BMD versus alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly improve lumbar spine bone density versus alendronate alone.

    Outcome
    No significant changeLumbar spine BMD
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 18 monthsAs given in this study (human).

    Source sentences

    Summary
    However, similar enhancement was not seen with MK-677 plus alendronate in BMD of the lumbar spine, total hip, or total body compared with alendronate alone.
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  8. 08HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly enhance total hip BMD versus alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly improve total hip bone density versus alendronate alone.

    Outcome
    No significant changeTotal hip BMD
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 18 monthsAs given in this study (human).

    Source sentences

    Summary
    However, similar enhancement was not seen with MK-677 plus alendronate in BMD of the lumbar spine, total hip, or total body compared with alendronate alone.
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD
  9. 09HumanRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly enhance total body BMD versus alendronate alone.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 plus alendronate did not similarly improve total body bone density versus alendronate alone.

    Outcome
    No significant changeTotal body BMD
    Study

    n: not reported in source

    Comparator
    Alendronate alone
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    25 mg daily · oral · 18 monthsAs given in this study (human).

    Source sentences

    Summary
    However, similar enhancement was not seen with MK-677 plus alendronate in BMD of the lumbar spine, total hip, or total body compared with alendronate alone.
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD

Studies that did not test the peptide alone3

In this study, MK-677 (ibutamoren) 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 MK-677 (ibutamoren).

  1. 10HumanNot a test of MK-677 (ibutamoren) aloneRandomized controlled trialEfficacy outcome

    In postmenopausal osteoporotic women, MK‑677 with alendronate increased IGF-I from baseline, significantly versus placebo.

    In plain wordsIn postmenopausal osteoporotic women, MK‑677 with alendronate increased IGF-I from baseline more than placebo.

    Outcome
    IncreaseIGF-I with combination
    Study

    n: not reported in source

    Comparator
    Placebo
    Outcome group
    Growth hormone and IGF-1 · Endocrine and hormones

    Measurements

    IGF-I change from baseline
    39%
    MK-677 with or without alendronate; the source does not say which arm has 39% and which has 45%
    IGF-I change from baseline
    45%
    MK-677 with or without alendronate; the source does not say which arm has 39% and which has 45%
    P value for IGF-I
    < 0.05
    MK-677 plus alendronate versus placebo, month 12

    Source sentences

    Summary
    MK-677, with or without alendronate, increased insulin-like growth factor I levels from baseline (39% and 45%; P < 0.05 vs. placebo).
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD

    In this study, MK-677 (ibutamoren) 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 MK-677 (ibutamoren).

  2. 11HumanNot a test of MK-677 (ibutamoren) aloneRandomized controlled trialSafety outcome

    In postmenopausal osteoporotic women, GH-mediated side effects occurred in pooled MK‑677-containing groups.

    In plain wordsIn postmenopausal osteoporotic women, pooled MK‑677-containing groups had growth hormone-related side effects.

    Outcome
    Not applicableGH-mediated side effects
    Study

    n: not reported in source

    Outcome group
    Adverse events · Whole body

    Source sentences

    Summary
    GH-mediated side effects were noted in the groups receiving MK-677, although adverse events resulting in discontinuation from the study were relatively infrequent.
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD

    In this study, MK-677 (ibutamoren) 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 MK-677 (ibutamoren).

  3. 12HumanNot a test of MK-677 (ibutamoren) aloneRandomized controlled trialSafety outcome

    In postmenopausal osteoporotic women, adverse-event discontinuations were relatively infrequent in pooled MK‑677-containing groups.

    In plain wordsIn postmenopausal osteoporotic women, adverse-event discontinuations were relatively infrequent in pooled MK‑677-containing groups.

    Outcome
    Not applicableAdverse-event discontinuations
    Study

    n: not reported in source

    Outcome group
    Adverse events · Whole body

    Source sentences

    Summary
    GH-mediated side effects were noted in the groups receiving MK-677, although adverse events resulting in discontinuation from the study were relatively infrequent.
    2 context sentences
    Summary · context
    We determined the individual and combined effects of MK-677 and alendronate administration on insulin-like growth factor I levels and biochemical markers of bone formation (osteocalcin and bone-specific alkaline phosphatase) and resorption [urinary N-telopeptide cross-links (NTx)] for 12 months and BMD for 18 months.
    Summary · context
    In a multicenter, randomized, double blind, placebo-controlled, 18-month study, 292 women (64-85 yr old) with low femoral neck BMD

    In this study, MK-677 (ibutamoren) 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 MK-677 (ibutamoren).

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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