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Study on Two Different Formulations of 6-mercaptopurine. Tablet Versus Oral Liquid

Primary Purpose

Acute Lymphoblastic Leukemia, 6-mercaptopurine Therapy

Status
Unknown status
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
Xaluprine
Puri-Nethol
Sponsored by
Kjeld Schmiegelow
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Acute Lymphoblastic Leukemia focused on measuring 6-mercaptopurine, Drug formulation

Eligibility Criteria

undefined - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Childhood acute lymphoblastic leukemia patients, age 0-18 years at diagnosis, treated at the department of pediatrics and adolescent medicine, Rigshospitalet.
  • Informed consent

Exclusion Criteria:

  • None

Sites / Locations

  • Juliane Marie Centret, RigshospitaletRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Puri-Nethol

Xaluprine

Arm Description

Tablet formulation of 6-mercaptopurine

Oral liquid formulation of 6-mercaptopurine

Outcomes

Primary Outcome Measures

Time to maximum concentration (Tmax)
Time to maximum concentration (Tmax)

Secondary Outcome Measures

Area under curve(AUC)
Area under curve(AUC)
Maximum concentration (Cmax)
Maximum concentration (Cmax)
Time to half-life (T½)
Time to half-life (T½)

Full Information

First Posted
July 16, 2013
Last Updated
April 19, 2018
Sponsor
Kjeld Schmiegelow
Collaborators
Danish Cancer Society
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1. Study Identification

Unique Protocol Identification Number
NCT01906671
Brief Title
Study on Two Different Formulations of 6-mercaptopurine. Tablet Versus Oral Liquid
Official Title
Plasma Kinetics of Tablet and Liquid Formulations of 6-mercaptopurine in Childhood Acute Lymphoblastic Leukemia.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 2013 (Actual)
Primary Completion Date
September 2018 (Anticipated)
Study Completion Date
November 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Kjeld Schmiegelow
Collaborators
Danish Cancer Society

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute lymphoblastic leukemia (ALL) accounts for 30 % of all childhood malignancies. The patients undergo four phases of treatment, finishing with a late maintenance phase in which 6-mercaptopurine and Methotrexate are essential components. Insufficient treatment intensity in this phase is associated with increased risk of relapse. Excessive variation in the bioavailability of 6-mercaptopurine has been observed which can cause both risks of undertreatment/relapse as well as overtreatment with severe side effects. In the attempt to achieve individualized 6-mercaptopurine dosing different approaches have been pursued. Nonetheless variation in bioavailability remains a problem. Earlier, oral tablets of 50 mg (Purinethol) were the only administration form of 6-mercaptopurine and it was primarily designed for adult patients. Challenges with accurate dosing and getting the children to swallow the tablets have been a widespread problem, forcing the caregivers to divide or crush the tablets as well as having to administer different dosages over 2-3 days. Due to these problems, an oral liquid formulation of 6-mercaptopurine (Xaluprine) has been developed. However this oral liquid has only been tested on healthy adult volunteers, and not on the target group, childhood patients. This project will assess the bioavailability and plasma kinetics of oral liquid and tablet formulation of 6-mercaptopurine in children with acute lymphoblastic leukemia. The investigators hypothesize to observe comparable plasma kinetics, in children with acute lymphoblastic leukemia when treated with 6-mercaptopurine in the form of a tablet and oral liquid formulation, as previously observed in healthy adults.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Lymphoblastic Leukemia, 6-mercaptopurine Therapy
Keywords
6-mercaptopurine, Drug formulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
16 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Puri-Nethol
Arm Type
Experimental
Arm Description
Tablet formulation of 6-mercaptopurine
Arm Title
Xaluprine
Arm Type
Experimental
Arm Description
Oral liquid formulation of 6-mercaptopurine
Intervention Type
Drug
Intervention Name(s)
Xaluprine
Intervention Description
Comparison of plasma kinetics after administration of 6-mercaptopurine in the form of a tablet (Puri-Nethol) and in the form of an oral liquid formulation (Xaluprine). Each patient will be included in both arms of the study, because of the cross-over design.
Intervention Type
Drug
Intervention Name(s)
Puri-Nethol
Intervention Description
Comparison of plasma kinetics after administration of 6-mercaptopurine in the form of a tablet (Puri-Nethol) and in the form of an oral liquid formulation (Xaluprine). Each patient will be included in both arms of the study, because of the cross-over design.
Primary Outcome Measure Information:
Title
Time to maximum concentration (Tmax)
Description
Time to maximum concentration (Tmax)
Time Frame
Will be measured within a six months after collection of the blood samples
Secondary Outcome Measure Information:
Title
Area under curve(AUC)
Description
Area under curve(AUC)
Time Frame
Will be measured within six months after collection of the blood samples
Title
Maximum concentration (Cmax)
Description
Maximum concentration (Cmax)
Time Frame
Will be measured within six months after collection of the blood samples
Title
Time to half-life (T½)
Description
Time to half-life (T½)
Time Frame
Will be measured within six months after collection of the blood samples

10. Eligibility

Sex
All
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Childhood acute lymphoblastic leukemia patients, age 0-18 years at diagnosis, treated at the department of pediatrics and adolescent medicine, Rigshospitalet. Informed consent Exclusion Criteria: None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kjeld Schmiegelow, Professor
Organizational Affiliation
Pediatric Clinic II, Rigshospitalet, Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Juliane Marie Centret, Rigshospitalet
City
Copenhagen
State/Province
DK-
ZIP/Postal Code
2100
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Kjeld Schmiegelow, Professor
Phone
+45 35451357
Email
kjeld.schmiegelow@regionh.dk
First Name & Middle Initial & Last Name & Degree
Rikke Hebo Larsen, MD
Phone
+45 35457932
Email
rikke.hebo.larsen.01@regionh.dk
First Name & Middle Initial & Last Name & Degree
Kjeld Schmiegelow, Professor
First Name & Middle Initial & Last Name & Degree
Rikke Hebo Larsen, MD

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32519032
Citation
Larsen RH, Hjalgrim LL, Grell K, Kristensen K, Pedersen LG, Brunner ED, Als-Nielsen B, Schmiegelow K, Nersting J. Pharmacokinetics of tablet and liquid formulations of oral 6-mercaptopurine in children with acute lymphoblastic leukemia. Cancer Chemother Pharmacol. 2020 Jul;86(1):25-32. doi: 10.1007/s00280-020-04097-x. Epub 2020 Jun 9.
Results Reference
derived

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Study on Two Different Formulations of 6-mercaptopurine. Tablet Versus Oral Liquid

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