DrugLib.com — Drug Information Portal

Rx drug information, pharmaceutical research, clinical trials, news, and more



Pharmacokinetics (PK) of Liquid Hydroxyurea in Pediatric Patients With Sickle Cell Anemia

Information source: Children's Mercy Hospital Kansas City
ClinicalTrials.gov processed this data on August 23, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Sickle Cell Anemia

Intervention: Hydroxyurea (Drug)

Phase: Phase 1

Status: Completed

Sponsored by: Children's Mercy Hospital Kansas City

Official(s) and/or principal investigator(s):
Kathleen Neville, MD, MS, Principal Investigator, Affiliation: Children's Mercy Hosptials and Clinics

Summary

Hydroxyurea (HU) is approved by the United States Food and Drug Administration (FDA) to treat adults with sickle cell anemia. Hydroxyurea has also been tested and used with children with sickle cell anemia. However, there are not many studies describing the disposition of drug in children less than 5 years old. The FDA has requested this study to better understand how children ages 2 to 17 years with sickle anemia absorb and eliminate the drug (this is called pharmacokinetics). The investigators will measure how much Hydroxyurea (HU) gets into the bloodstream at different time points after taking this medication.

Clinical Details

Official title: Pharmacokinetics and Relative Bioavailability of a Liquid Formulation of Hydroxyurea in Pediatric Patients With Sickle Cell Anemia

Study design: Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Open Label

Primary outcome:

Composite of Pharmacokinetics

Pharmacokinetics of HU

Secondary outcome: Bioavailability of HU

Eligibility

Minimum age: 2 Years. Maximum age: 17 Years. Gender(s): Both.

Criteria:

For Both Arms: Pharmacokinetics and Relative Bioavailability of a Liquid Formulation of Hydroxyurea in Pediatric Patients with Sickle Cell

- The study participant will be a pediatric (male or female) participant with sickle

cell anemia with laboratory (i. e. electrophoretic, chromatographic or DNA) confirmation of the diagnosis of Hemoglobin SS or Sβ0thalassemia.

- Weight ≥ 10 kg.

- Participants may or may not be currently receiving hydroxyurea. If participants are

taking hydroxyurea, the last dose must be no less than 24 hours prior to the start of the study.

- Participant is in the "well" state (i. e. at least 2 weeks since the last

vaso-occlusive crisis, acute chest syndrome episode, or splenic sequestration episode).

- Clinical evidence of normal gastrointestinal function and structure.

- No clinical evidence of hepatic compromise including transaminases no more than 3

times the upper limit of normal.

- A glomerular filtration rate (GFR--estimated from serum creatinine using

age-appropriate, validated equations such as the Schwartz equation) > 70 ml/min/1. 73m2 and no known renal impairment (creatinine no more than 1. 5 times the upper limit of normal for age in the screening laboratory).

- Body mass index (BMI) ≥5th and ≤ 95th percentile as per CDC growth charts.

- The parent or guardian is willing and able to provide a signed and dated written

informed consent form prior to any study related procedures. When appropriate, the participant has signed an assent to participate according to local IRB guidelines.

- The participants and/or participant's parents are able to understand and comply with

protocol requirements, instructions, and protocol-stated restrictions such that the participant is likely to complete the study as planned.

- Based on the opinion of the physicians providing patient care and those conducting

the study, there are no apparent contraindications for inclusion as a participant in a pharmacokinetic study.

- For the Pharmacokinetic Study (Arm 1):

- Participant is ≥ 2 years and ≤ 5 years of age.

- The participant is able to consume a minimum of 30 ml of water following ingestion of

the study article.

- For the Relative Bioavailability Study:

- Participant is > 5 years and < 17 years of age.

- All females of child-bearing potential must be found to have a negative serum

pregnancy test prior to initial dosing and be willing to practice appropriate contraceptive measures, including abstinence, from the time of the initial pregnancy testing through the remainder of the study (30 days after last administration of investigational agents).

- The participant is able to ingest both capsule and liquid study articles and consume

a minimum of 30 ml of water following ingestion of medication. EXCLUSION CRITERIA

- A participant will not be eligible for inclusion in this study if any of the

following criteria apply:

- Chronic transfusion therapy, or transfused within 3 months of study participation.

- Known renal impairment (creatinine greater than 1. 5 times the upper limit of normal

for age in the screening laboratory).

- Known hepatic impairment or elevated transaminases (greater than 3 times normal).

- Known presence of malignancy.

- The participant is unwilling and/or unable to abstain from use of tobacco- or

nicotine-containing products for 24 hours prior to screening and for 24 hours prior to dosing until collection of the final PK sample during each treatment period.

- Diagnoses other than sickle cell anemia or sickle beta-zero thalassemia (i. e., other

sickle cell variants or sickle hereditary persistence of fetal hemoglobin).

- Blood count parameters as follows: Hemoglobin less than 6. 0 gm/dL, absolute

reticulocyte count less than 80,000 mm-3, neutrophil count less than 1200 mm-3, platelet count less than 150,000 mm-3.

- The participant has used opiates, H2 blockers, proton pump inhibitors, antacids,

other GI motility agents or any other medication that, in the opinion of the investigator and/or sponsor, will interfere with the study procedures or affect the interpretation of the results of the study for 3 days prior to the first dose of study.

- Use of over the counter non-steroidal anti-inflammatory agent or narcotic analgesic

within 3 days.

- Participant has received an investigational drug within the past 30 days.

- Use of any illicit or illegal substances.

- The parent or guardian is unwilling or unable to provide a signed and dated written

informed consent form prior to any study related procedures, or, when appropriate, the participant has refused to sign an assent to participate according to local IRB guidelines.

- Any other condition or chronic illness, which in the opinion of the Principal

Investigator makes participation unadvised or unsafe.

- The caregiver is unwilling or unable to provide a completed study diary for a

participant in the steady-state subset.

Locations and Contacts

Children's Hospital of Alabama, Birmingham, Alabama 35233, United States

Children's Memorial Hospital (Northwestern University), Chicago, Illinois 60614-3363, United States

Columbia University Medical Center, New York, New York 10032, United States

Duke University Medical Center, Durham, North Carolina 27710, United States

UT Southwestern University Hospital, Dallas, Texas 75390-9063, United States

Children's Hospital of Wisconsin, Wauwatosa, Wisconsin 53226, United States

Additional Information

Starting date: December 2011
Last updated: December 10, 2014

Page last updated: August 23, 2015

-- advertisement -- The American Red Cross
 
Home | About Us | Contact Us | Site usage policy | Privacy policy

All Rights reserved - Copyright DrugLib.com, 2006-2017