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Study · Non-randomized trial · n = 15 · 1992

5 results

Bioavailability of nafarelin in healthy volunteers.

Chaplin MD

American journal of obstetrics and gynecology1 Feb 1992Cited by 10 (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 study5

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

  1. 01HumanNon-randomized trialPharmacokinetics

    In healthy women, intravenous nafarelin reached maximum concentration at 2 minutes.

    In plain wordsIn healthy women, intravenous nafarelin reached its highest concentration at 2 minutes.

    Peptide
    Nafarelin
    Outcome
    Not applicableIntravenous Tmax
    Study

    n = 15

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    25 micrograms · intravenousAs given in this study (human).

    Measurements

    Tmax
    2 minutes
    intravenous

    Source sentences

    Summary
    After intravenous administration, time to maximum concentration (Tmax) was 2 minutes, and maximum serum concentration (Cmax) was 8.2 +/- 2.09 (SD) ng/ml.
    2 context sentences
    Summary · context
    The bioavailability of a single dose of intranasal nafarelin was evaluated in 15 healthy female volunteers.
    Summary · context
    Each subject received a 400 micrograms intranasal and a 25 micrograms intravenous dose of nafarelin separated by at least 7 days.
  2. 02HumanNon-randomized trialPharmacokinetics

    In healthy women, intravenous nafarelin had a maximum serum concentration of 8.2 +/- 2.09 ng/ml.

    In plain wordsIn healthy women, intravenous nafarelin had a maximum serum concentration of 8.2 +/- 2.09 ng/ml.

    Peptide
    Nafarelin
    Outcome
    Not applicableIntravenous Cmax
    Study

    n = 15

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    25 micrograms · intravenousAs given in this study (human).

    Measurements

    Cmax
    8.2 ng/ml
    mean
    Cmax SD
    2.09 ng/ml
    intravenous

    Source sentences

    Summary
    After intravenous administration, time to maximum concentration (Tmax) was 2 minutes, and maximum serum concentration (Cmax) was 8.2 +/- 2.09 (SD) ng/ml.
    2 context sentences
    Summary · context
    The bioavailability of a single dose of intranasal nafarelin was evaluated in 15 healthy female volunteers.
    Summary · context
    Each subject received a 400 micrograms intranasal and a 25 micrograms intravenous dose of nafarelin separated by at least 7 days.
  3. 03HumanNon-randomized trialPharmacokinetics

    In healthy women, intranasal nafarelin had mean Tmax 18.4 +/- 7.9 minutes, ranging from 5 to 40 minutes.

    In plain wordsIn healthy women, intranasal nafarelin reached its highest concentration after 18.4 minutes on average.

    Peptide
    Nafarelin
    Outcome
    Not applicableIntranasal Tmax
    Study

    n = 15

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    400 micrograms · intranasalAs given in this study (human).

    Measurements

    Tmax
    18.4 minutes
    mean
    Tmax SD
    7.9 minutes
    intranasal
    Tmax range
    5 to 40 minutes
    intranasal

    Source sentences

    Summary
    For intranasal nafarelin, mean Tmax was 18.4 +/- 7.9 minutes (range, 5 to 40 minutes), and Cmax was 2.04 +/- 1.29 ng/ml (range, 0.49 to 5.7 ng/ml).
    2 context sentences
    Summary · context
    The bioavailability of a single dose of intranasal nafarelin was evaluated in 15 healthy female volunteers.
    Summary · context
    Each subject received a 400 micrograms intranasal and a 25 micrograms intravenous dose of nafarelin separated by at least 7 days.
  4. 04HumanNon-randomized trialPharmacokinetics

    In healthy women, intranasal nafarelin had mean Cmax 2.04 +/- 1.29 ng/ml, ranging from 0.49 to 5.7 ng/ml.

    In plain wordsIn healthy women, intranasal nafarelin reached a maximum concentration of 2.04 ng/ml on average.

    Peptide
    Nafarelin
    Outcome
    Not applicableIntranasal Cmax
    Study

    n = 15

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    400 micrograms · intranasalAs given in this study (human).

    Measurements

    Cmax
    2.04 ng/ml
    mean
    Cmax SD
    1.29 ng/ml
    intranasal
    Cmax range
    0.49 to 5.7 ng/ml
    intranasal

    Source sentences

    Summary
    For intranasal nafarelin, mean Tmax was 18.4 +/- 7.9 minutes (range, 5 to 40 minutes), and Cmax was 2.04 +/- 1.29 ng/ml (range, 0.49 to 5.7 ng/ml).
    2 context sentences
    Summary · context
    The bioavailability of a single dose of intranasal nafarelin was evaluated in 15 healthy female volunteers.
    Summary · context
    Each subject received a 400 micrograms intranasal and a 25 micrograms intravenous dose of nafarelin separated by at least 7 days.
  5. 05HumanNon-randomized trialPharmacokinetics

    In healthy women, nafarelin bioavailability averaged 2.82% +/- 1.23%, ranging from 1.15% to 5.62%.

    In plain wordsIn healthy women, an average of 2.82% of intranasal nafarelin reached the circulation.

    Peptide
    Nafarelin
    Outcome
    Not applicableSystemic bioavailability
    Study

    n = 15

    Outcome group
    Pharmacokinetics · Pharmacology
    Studied dose
    400 micrograms · intranasalAs given in this study (human).

    Measurements

    Bioavailability
    2.82%
    mean
    Bioavailability SD
    1.23%
    intranasal
    Bioavailability range
    1.15 to 5.62%
    intranasal

    Source sentences

    Summary
    Systemic bioavailability of nafarelin ranged from 1.15% to 5.62% and averaged 2.82% +/- 1.23%.
    2 context sentences
    Summary · context
    The bioavailability of a single dose of intranasal nafarelin was evaluated in 15 healthy female volunteers.
    Summary · context
    Each subject received a 400 micrograms intranasal and a 25 micrograms intravenous dose of nafarelin separated by at least 7 days.

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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, 16:36 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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