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Study · Randomized controlled trial · n = 24 · 2005

14 results

LH suppression following different low doses of the GnRH antagonist ganirelix in polycystic ovary syndrome.

Hohmann FP, Laven JS, Mulders AG, Oberyé JJ, Mannaerts BM, de Jong FH, Fauser BC

Journal of endocrinological investigation1 Dec 2005Cited by 4 (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 study14

14 results from studies that gave the peptide. 14 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In PCOS patients, significant LH suppression with repeated ganirelix was comparable between the different doses.

    In plain wordsIn PCOS patients, LH suppression with repeated ganirelix was comparable between the different doses.

    Peptide
    Ganirelix
    Outcome
    Direction not reportedLH suppression across doses
    Study

    n = 24

    Comparator
    other ganirelix doses
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Source sentences

    Summary
    Repeated GnRH antagonist administration induced a significant suppression of LH (and to a lesser extent of FSH) serum levels, which was comparable between the different doses.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In PCOS patients, FSH suppression with repeated ganirelix was comparable between doses and less marked than LH suppression.

    In plain wordsIn PCOS patients, FSH suppression with repeated ganirelix was comparable between doses and less marked than LH suppression.

    Peptide
    Ganirelix
    Outcome
    Direction not reportedFSH suppression across doses
    Study

    n = 24

    Comparator
    other ganirelix doses
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Source sentences

    Summary
    Repeated GnRH antagonist administration induced a significant suppression of LH (and to a lesser extent of FSH) serum levels, which was comparable between the different doses.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  3. 03HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix reduced LH for 12 h, with levels returning to baseline at 24 h.

    In plain wordsIn PCOS patients, ganirelix reduced LH for 12 h, with levels returning to baseline at 24 h.

    Peptide
    Ganirelix
    Outcome
    MixedDuration of LH suppression
    Study

    n = 24

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    Duration of LH suppression
    12 h
    after drug administration
    Time to return to baseline
    24 h
    after drug administration

    Source sentences

    Summary
    The decrease in serum LH and FSH levels was transient and lasted for 12 h, after which serum levels returned to baseline levels at 24 h after drug administration.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  4. 04HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix reduced FSH for 12 h, with levels returning to baseline at 24 h.

    In plain wordsIn PCOS patients, ganirelix reduced FSH for 12 h, with levels returning to baseline at 24 h.

    Peptide
    Ganirelix
    Outcome
    MixedDuration of FSH suppression
    Study

    n = 24

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    Duration of FSH suppression
    12 h
    after drug administration
    Time to return to baseline
    24 h
    after drug administration

    Source sentences

    Summary
    The decrease in serum LH and FSH levels was transient and lasted for 12 h, after which serum levels returned to baseline levels at 24 h after drug administration.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  5. 05HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix did not significantly suppress androgen levels.

    In plain wordsIn PCOS patients, ganirelix did not significantly reduce androgen levels compared with baseline.

    Peptide
    Ganirelix
    Outcome
    No significant changeAndrogen suppression
    Study

    n = 24

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Source sentences

    Summary
    Androgen levels were not significantly suppressed using this regimen.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  6. 06HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix significantly reduced E2 levels (p < 0.001), with the strongest suppression at 0.500 mg daily.

    In plain wordsIn PCOS patients, ganirelix reduced E2 versus baseline, with the strongest suppression at 0.500 mg daily.

    Peptide
    Ganirelix
    Outcome
    DecreaseEstradiol suppression
    Study

    n = 24

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    p value
    < 0.001
    E2 decrease

    Source sentences

    Summary
    E2 levels decreased significantly (p < 0.001) and suppression was most pronounced in Group C.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  7. 07HumanNon-randomized trialEfficacy outcome

    In PCOS patients receiving ganirelix, spontaneous follicle development was not recorded during treatment.

    In plain wordsIn PCOS patients receiving ganirelix, spontaneous follicle development was not recorded during treatment.

    Peptide
    Ganirelix
    Outcome
    Not applicableSpontaneous follicle development
    Study

    n = 24

    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Source sentences

    Summary
    Spontaneous follicle development or ovulations were not recorded during the course of treatment.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  8. 08HumanNon-randomized trialEfficacy outcome

    In PCOS patients receiving ganirelix, ovulations were not recorded during treatment.

    In plain wordsIn PCOS patients receiving ganirelix, ovulations were not recorded during treatment.

    Peptide
    Ganirelix
    Outcome
    Not applicableOvulation
    Study

    n = 24

    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125, 0.250 or 0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Source sentences

    Summary
    Spontaneous follicle development or ovulations were not recorded during the course of treatment.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  9. 09HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.125 mg suppressed endogenous LH by 49% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.125 mg reduced LH by 49% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseLH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    LH suppression at 6 h
    49%
    0.125 mg group (Group A)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  10. 10HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.250 mg suppressed endogenous LH by 69% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.250 mg reduced LH by 69% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseLH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.250 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    LH suppression at 6 h
    69%
    0.250 mg group (Group B)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  11. 11HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.500 mg suppressed endogenous LH by 75% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.500 mg reduced LH by 75% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseLH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    LH suppression at 6 h
    75%
    0.500 mg group (Group C)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  12. 12HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.125 mg suppressed endogenous FSH by 23% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.125 mg reduced FSH by 23% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseFSH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.125 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    FSH suppression at 6 h
    23%
    0.125 mg group (Group A)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  13. 13HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.250 mg suppressed endogenous FSH by 19% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.250 mg reduced FSH by 19% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseFSH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.250 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    FSH suppression at 6 h
    19%
    0.250 mg group (Group B)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.
  14. 14HumanNon-randomized trialEfficacy outcome

    In PCOS patients, ganirelix 0.500 mg suppressed endogenous FSH by 25% six hours after administration.

    In plain wordsIn PCOS patients, ganirelix 0.500 mg reduced FSH by 25% six hours after administration compared with baseline.

    Peptide
    Ganirelix
    Outcome
    DecreaseFSH suppression at six hours
    Study

    n: not reported in source

    Comparator
    baseline
    Outcome group
    Sex hormones and fertility · Endocrine and hormones
    Studied dose
    0.500 mg daily · subcutaneous · 7 daysAs given in this study (human).

    Measurements

    FSH suppression at 6 h
    25%
    0.500 mg group (Group C)

    Source sentences

    Summary
    Six hours after ganirelix administration, endogenous LH was suppressed by 49, 69 and 75%, and endogenous FSH was suppressed by 23, 19 and 25%, respectively.
    1 context sentence
    Summary · context
    Twenty-four PCOS patients with elevated endogenous LH concentrations were randomized into 3 different dose groups, receiving either 0.125 mg (Group A), 0.250 mg (Group B) or 0.500 mg (Group C) ganirelix sc daily for 7 subsequent days.

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

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:35 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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