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Pharmacokinetics and Bioavailability of Single Subcutaneous Doses of Methylnaltrexone Versus Intravenous Dose

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Bausch Health

Status and phase

Completed
Phase 1

Conditions

Healthy Subjects

Treatments

Drug: SC Methylnaltrexone (MNTX)
Drug: IV Methylnaltrexone (MNTX)

Study type

Interventional

Funder types

Industry

Identifiers

NCT01367496
MNTX 103

Details and patient eligibility

About

This is an open-label, Phase I study. Study treatments will entail a four-way crossover among three single, ascending, subcutaneous doses and one intravenous dose of MNTX in six healthy normal male volunteers. Blood samples will be obtained to determine plasma pharmacokinetics, dose proportionality for subcutaneous doses, and absolute bioavailability versus an intravenous dose.

Enrollment

6 patients

Sex

Male

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. Subject weight between 60 and 80 kg
  2. Subject a non-smoker
  3. Subject in good physical health, based on history, physical exam, appropriate laboratory and diagnostics tests at screening with no evidence of clinically significant chronic medical condition.

Exclusion criteria

  1. Subject with known hypersensitivity to methylnaltrexone, naltrexon or other opioids
  2. Subject consuming any prescription medication within the past two weeks, over-the-counter (OTC) products within seven days, any experimental medication within 30 days prior to study screening, or of any drug with a half-life longer then three days within 10 half-lives (>30 days) of screening
  3. Subject consuming barbiturates or other inducers or inhibitors of CYP450 within 3 months of screening
  4. Subject with history or evidence of cardiovascular, gastrointestinal, hepatic, neurological, pulmonary, and renal or other significant chronic illness.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

6 participants in 4 patient groups

Arm 1
Experimental group
Treatment:
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Arm 2
Experimental group
Treatment:
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Arm 3
Experimental group
Treatment:
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Drug: SC Methylnaltrexone (MNTX)
Arm 4
Experimental group
Treatment:
Drug: IV Methylnaltrexone (MNTX)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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