Effect on Acetaminophen Metabolism by Liquid Formulations

NCT ID: NCT01246713

Last Updated: 2017-05-08

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

15 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-12-31

Study Completion Date

2012-07-31

Brief Summary

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The purpose of this study is to determine whether excipients in the liquid formulation of acetaminophen prevent the formation of the toxic metabolites of acetaminophen.

Detailed Description

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Acetaminophen (APAP) poisoning is the most frequent cause of acute hepatic failure in the United States. Toxicity requires cytochrome P-450 bioactivation of APAP. Children are less susceptible to APAP toxicity; the current theory is that they have different metabolism than adults. However, children's liquid preparations of APAP contain excipients which have been shown to inhibit APAP bioactivation in vitro and in rodents. Children tend to ingest liquid preparations, which could potentially explain their decreased susceptibility instead of an intrinsically different metabolism. Further, our review of Poison Center epidemiologic data shows that liquid preparations are less toxic in adults. Our hypothesis is that excipients in liquid preparations inhibit the bioactivation of APAP. The design is a pharmacokinetic cross-over study in humans. Healthy adult subjects will be recruited for administration of therapeutic doses of APAP in capsule and liquid formulations. Plasma via a heplock will be collected at serial time points up to 8 hours and assayed for APAP and its metabolites. After a washout period, subjects will receive the same dose of APAP in the alternate preparation. The pattern of metabolites, indicating the activity of the bioactivating enzymes, will be compared. A significant difference in P-450 metabolites will support the hypothesis and provide preliminary data for studies in patients who have ingested potentially toxic doses of APAP. Ultimately, this work could support development of novel antidotal therapy for APAP overdose.

Conditions

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Acetaminophen Metabolism Acetaminophen Poisoning Drug Metabolism by Excipients

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Acetaminophen solid formulation

Subjects in this arm will receive a 15mg/kg dose of a solid acetaminophen formulation.

Group Type PLACEBO_COMPARATOR

Acetaminophen solid formulation

Intervention Type DRUG

Subjects in this arm will receive a 15mg/kg dose of a solid acetaminophen formulation.

Acetaminophen liquid formulation

Subjects in this arm will receive a 15mg/kg dose of a liquid acetaminophen formulation.

Group Type ACTIVE_COMPARATOR

Acetaminophen liquid formulation

Intervention Type DRUG

Subjects in this arm will receive a 15mg/kg dose of a solid acetaminophen formulation.

Interventions

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Acetaminophen liquid formulation

Subjects in this arm will receive a 15mg/kg dose of a solid acetaminophen formulation.

Intervention Type DRUG

Acetaminophen solid formulation

Subjects in this arm will receive a 15mg/kg dose of a solid acetaminophen formulation.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Healthy volunteer ages 18-40
* Not taking any chronic medications

Exclusion Criteria

* Pregnancy
* Any history of liver disease
* Frequent alcohol use (2 or more drinks more than 4 times per week)
* Unable to provide informed consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Harvard University

OTHER

Sponsor Role collaborator

National Center for Research Resources (NCRR)

NIH

Sponsor Role collaborator

Beth Israel Deaconess Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Michael Ganetsky

Assistant Professor of Emergency Medicine

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Michael Ganetsky, MD

Role: PRINCIPAL_INVESTIGATOR

Beth Israel Deaconess Medical Center

Locations

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Harvard - Thorndike Clinical Research Center at Beth Israel Deaconess Medical Center

Boston, Massachusetts, United States

Site Status

Countries

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United States

References

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Ganetsky M, Bohlke M, Pereira L, Williams D, LeDuc B, Guatam S, Salhanick SD. Effect of excipients on acetaminophen metabolism and its implications for prevention of liver injury. J Clin Pharmacol. 2013 Apr;53(4):413-20. doi: 10.1002/jcph.24. Epub 2013 Feb 22.

Reference Type DERIVED
PMID: 23436315 (View on PubMed)

Other Identifiers

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UL1RR025758

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2010P000135

Identifier Type: -

Identifier Source: org_study_id

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