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Completed

NCT Number: NCT02205905

An Open-label, Single-dose, Non-randomized Study of IV 14C-labeled PER977 in Healthy Male Subjects

This is an open-label, single-dose, non-randomized study in healthy male subjects to characterize the mass balance, metabolic disposition, and identification of the metabolites and general metabolic pathways following administration of a single dose of IV solution containing 200 mg of PER977 plus a tracer amount of 14C PER977 in health male subjects.

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Key information

Conditions

Age range

15 year–55 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 1

Primary location

Worldwide Clinical Trials Early Phase Services

San Antonio, Texas, 78217, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male
  • 18-55 years of age (inclusive)
  • Body mass index 18-32 kg/m2 (inclusive) and a minimum of 50 kg (110 lbs)
  • voluntarily consent to participate and provide written informed consent prior to start of study specific procedures
  • Willing and able to remain in the study unit for the entire duration of the confinement period
  • Willing to collect all urine and fecal samples for the duration of the study period as required
  • Will to eat entire meals and snacks provided during confinement at the research facility, and understand diet will include foods with high fiber content and possibly prune juice
  • Willing to use a waterless commode located in a designated dry room for urine and feces collection for the duration of the study period as required
  • Willing to abstain from showering for the first 72 hours following study drug administration. After the restriction is lifted, willing to provide a urine sample prior to showering for the remainder of the confinement period.

Exclusion criteria

  • History or presence of clinically significant cardiovascular, pulmonary, hepatic, renal, hematologic, gastrointestinal, endocrine, immunologic, dermatologic, neurologic, oncologic, or psychiatric disease or any condition which, in the opinion of the investigator, would jeopardize the safety of the subject or the validity of the study results
  • Clinically significant abnormal finding on the physical exam, medical history, electrocardiogram or clinical laboratory resutls at screening
  • History or presence of allergic or adverse response to anticoagulant reversal agents or related drugs
  • Significantly abnormal diet within 4 weeks
  • Donated blood or plasma within 30 days
  • Participated in another clinical trial (randomized subjects only) within 30 days
  • Participated in a radiolabeled clinical trial within the last 12 months
  • Used any over-the-counter medication, including nutritional supplements, within 7 days
  • Used any prescription medication within 14 days prior
  • Treated with any known drugs that are moderate or strong inhibitors/inducers of CYP enzymes such as barbiturates,phenothiazines, cimetidine, carbamazepine, etc. within 30 days
  • Smoked or used tobacco products within 60 days
  • History of substance abuse or treatment (including alcohol ) within the past 2 years
  • Positive urine screen for drugs of abuse (amphetamines, barbiturates, benzodiazepines, cocaine, cannabinoids, opiates) or cotinine at screening or check-in
  • Positive test for hepatitis B surface antigen, hepatitis C antibody or human immunodeficiency virus at screening or has previously been treated for hepatitis B, hepatitis C or HIV infection
  • Has irregular bowel habits
  • Has had significant radiation exposure within the prior 12 months

Treatment and study plan

14C PER977

Drug

Open-label, single dose

Other names: ciraprantag

Primary outcomes

  1. Mass balance of PER977 and metabolite

    Time frame: 3 weeks

    To characterize the mass balance, metbaolic disposition, and identification of the metabolites and general metabolic pathways following administration of a single dose of IV solution containing 200 mg of PER977 plus a tracer amount of 14C PER977 to healthy male subjects

Secondary outcomes

  1. Number of subjects with adverse events

    Time frame: 3 weeks

    To assess the safety and tolerability of a single intravenous dose of 200 mg PER977

Sponsors and collaborators

Lead sponsor

Perosphere Pharmaceuticals Inc, a wholly owned subsidiary of AMAG Pharmaceuticals, Inc.

Industry

Collaborators

  • World Wide Clinical Trials Early Phase Services, LLC

Registry information

Official study title

An Open-label, Single-dose, Non-randomized Study of the Absorption, Metabolism, and Excretion of Intravenously Administered 14C-labeled PER977 in Healthy Male Subjects

Important dates

Study start
2014
Primary completion
2014
Study completion
2014
First posted
Aug 1, 2014
Registry last updated
May 20, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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