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Metabolic DiseasePhase 4NCT01443806

Characterisation of the Human Carboxylesterase 1 (CES1) Mutations in Thailand

A Phase 4 study testing Oseltamivir in people with Metabolic Disease, run by University of Oxford at 1 site in Thailand.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The aim of this study is to evaluate the conversion of OP to OC in individual X and the family member of individual X. The investigators hypothesize that one or more of the single nucleoprotein polymorphisms (SNPs) of the CES1 gene represent a clinically important functional polymorphism. Read more about this study

Who is it for?
Any ageHealthy volunteers can take part
Conditions the study is for
Metabolic Disease
What is being tested?
Oseltamivir
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1 participants
Where
1 siteThailand
Study dates
Jul 2011to Dec 2012
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Who may be able to join

  • Signed informed consent
  • Healthy family member of individual X and individual X
  • Aged between 18 and 70, inclusive.

Who cannot join

  • known allergy to oseltamivir
  • any underlying illness that is considered a risk to the health of the individual
  • pregnant
  • breast feeding
  • creatinine clearance < 30 mL/min calculated by the Cockcroft Gault formula: CrCl (ml/min) = (140-age) x Wt in kg / creatinine mg/dL x 72, for females, the result is multiplied by 0.85.

Trial locations and contacts

1 site in 1 country.

Thailand1 site
  • The Faculty of Tropical medicine,Mahidol University

    Bangkok, 10400

Other trials in Thailand

About this study

Official title: Characterisation of the Human Carboxylesterase 1 (CES1) Mutation(s) Which May be Responsible for Markedly Reduced Conversion of Oseltamivir Phosphate to Oseltamivir Carboxylate

The aim of this study is to evaluate the conversion of OP to OC in individual X and the family member of individual X. The investigators hypothesize that one or more of the single nucleoprotein polymorphisms (SNPs) of the CES1 gene represent a clinically important functional polymorphism.

Read the detailed description

Oseltamivir is beneficial in the treatment of mild influenza. When given by mouth, oseltamivir phosphate (OP), the parent drug, is rapidly absorbed and rapidly converted to oseltamivir carboxylate (OC) by carboxylesterase enzymes (CES1) in the gut, plasma and liver. The mean time to maximum concentration of OP is 2 hours and OC is about 4. Plasma protein binding is ~42% for OP and <3% for OC. The latter has a volume of distribution at steady state after an IV dose of 23 to 26 L which is similar to extracellular water, consistent with its polar nature and low protein binding. OC and OP are renally excreted via glomerular filtration and active secretion via the organic anion transporter in the proximal renal tubules. In healthy subjects, oseltamivir carboxylate has a half life of 6-11 hours, achieves steady-state within 3 days (bd dosing) and has a higher AUC on Day 7 compared to Day 1.

Oseltamivir was associated with bizarre behaviour and acute confusion. Since these reports, similar events have also been associated with inhaled zanamivir, suggesting that the influenza rather than the drugs were responsible.

Because OP is more lipophilic than OC, it should cross the blood brain barrier more easily than OC. However, plasma to CSF ratios in 4 healthy volunteers were low for both substances, just over two and just under 3.5% for OP and OC, respectively. The low OP ratio is probably due to the actively export of OC from the brain by P-glycoprotein pump. In vitro and mice studies demonstrate that OP but not OC is a substrate for the glycoprotein P (P-gp) transporter and that the brain distribution of OC is affected by P-gp activity. PK simulations predict levels of OP that would be within the range of exposures observed in clinical studies without neuropsychiatric adverse effects.

One individual subject (individual X) from SEA004 "Long Term Influenza Prophylaxis with Inhaled Zanamivir or Oral Oseltamivir" had carboxylesterase 1 (CES1) gene mutation which may affect oseltamivir phosphate conversion. This means that the conversion of OP to OC in this subject can be substantially lower than the normal population.

This is a very important finding relevant both to antiviral efficacy and also potentially to toxicity because OP has no antiviral activity and may play a role in toxicity as a potentially neuroexcitatory compound. On the basis of in vitro data, the risk of cardiac toxicity should be not existent at therapeutic doses. OP had a variable effect on the hERG (human ether a go go K+ channel in cardiac muscle) but only at concentrations far in excess of those achieved with therapeutic doses; OC has no proarrhythmic effect.

Given that OP penetrates the blood brain barrier and is pumped out by P-glycoprotein, high plasma concentrations of OP could result in increased CNS concentrations in individuals with either reduced carboxylesterase activity, such as infants and the volunteer in this study and/or reduced P-glycoprotein activity.

Human carboxylesterase 1 (CES1) polymorphisms CES1 is a member of a multigene family of serine esterases that is involved in drug metabolism and activation as well as in other biological processes. The study from Shi et al reported the correlation between oseltamivir hydrolysis from OP to OC and the concentration of CES1.

The gene encoding CES1 is on the long arm of chromosome 16 (16q13-22.1), and consists of 14 exons spanning 30kb. Several studies have identified the CES1 gene polymorphisms in the promoter and coding region and have tried to relate these polymorphisms with variation in the hydrolysis activity of this protein. A study from Zhu HJ et al presented potentially 2 functional polymorphisms locating in exon 4 (Gly143Glu) and 6 (Asp260fs) that can impair the CES1 hydrolytic activity to methylphenidate in vitro. However, some CES1 variants (V21I, and R182H) have a higher rate of oseltamivir metabolism compared to wild-type.

All subjects from these reports were recruited from Japanese and European populations. Therefore, it would be important to investigate the CES1 gene in the Thai population.

Oseltamivir efficacy may well be compromised in individuals who do not convert OP to OC but there are no data on the prevalence of this mutation/polymorphism and, therefore, the number of individuals who may not benefit form oseltamivir is unknown.

It will be important to study further the carboxylesterase gene in order to characterise its inheritance in the family of individual X and then to conduct prevalent studies in e.g. stored serum banks and as part of PK studies of oseltamivir in patients.

Being tested
Oseltamivir
Keywords
oseltamivir metabolism, Carboxylesterase 1
Medical subject headings
Metabolic Diseases

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • OseltamivirDrug

    Also called Tamiflu

    75 mg, one time

Study groups in NCT01443806
Study groupRoleWhat they receive
Oseltamivir, genetic testingExperimentalNot described
Receives: Drug: Oseltamivir

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Tmax

    Conversion of Oseltamivir at 2 and 4 hours post dose

    Measured: 2 and 4 hours

Secondary outcomes (1)
  1. Conversion of oseltamivir phosphate to oseltamivir carboxylate

    Document the sequence of all 14 exons of CES1 from individual X and the family members of individual X.

    Measured: one year (anticipate)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted30 Sep 2011 (estimated)
  2. Study startJul 2011
  3. Primary completionDec 2012
  4. Study completionDec 2012

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Basic science
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
1 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01443806
Sponsor's protocol ID
SEA 026
Status last verified
Jun 2018
First submitted
12 Jul 2011
Last updated
27 Jun 2018
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Oseltamivir in people with Metabolic Disease, run by University of Oxford at 1 site in Thailand.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Jun 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Thailand. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Tmax (time frame: 2 and 4 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Jun 2018.

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