Determining a Tolerable Dose of Primaquine in G6PD-deficient Persons Without Malaria in Mali

Malaria Clinical Trial

— PQSAFETY  

Official title:

Determining a Tolerable Dose of Primaquine in G6PD-deficient Persons Without Malaria in Mali

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02535767
• Other study ID #: 14-14495
• Status: Completed
• Phase: Phase 1/Phase 2
• First received: August 7, 2015
• Last updated: February 2, 2017
• Start date: August 2015
• Est. completion date: January 2016

Study information

• Verified date: February 2017
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the highest tolerable dose of primaquine within 0.75 mg/kg. A tolerable dose is defined as one in which:

• Two or fewer participants (< 30%) experience hemolysis;

• No participant experiences a drug-related serious adverse event; and

• No participant requires a blood transfusion.

Description:

Purpose: The purpose of this study is to determine the highest tolerable dose of primaquine within 0.75 mg/kg. A tolerable dose is defined as one in which:

• Two or fewer participants (< 30%) experience hemolysis;

• No participant experiences a drug-related serious adverse event; and

• No participant requires a blood transfusion.

Design:

• This is an open-label, phase 2, dose-adjustment study.

• The initial primaquine dose will be 0.40 mg/kg. Subsequent dose groups will be selected depending on the occurrence of adverse events in the previous dose group. Once the highest tolerable dose in G6PD-deficient (G6PDd) individuals is established, a control group of G6PD normal malaria-free men will be enrolled and evaluated under the highest tolerable dose of primaquine.

Study Population:

• Malian men aged 18-50 years without malaria infection.

• The majority of study participants will be G6PDd.

Study Size: This study will enroll 7 participants per dose group. If all dose groups are tested, this study will enroll approximately 28 participants.

Study visit and duration:

• Each participant will be followed for 28 days.

• Participants will be evaluated for hemolysis and adverse events on Days 1-10, 14, and 28 following their assigned primaquine dose.

Primary objective:

To measure the change in hemoglobin among G6PD deficient west-African men following a single low-dose of primaquine not to exceed 0.75 mg/kg.

Secondary objectives:

1. To measure the occurrence of adverse events, graded by severity, at each primaquine dose among G6PD deficient men

2. To measure the occurrence of markers of acute hemolytic anemia (AHA), at each primaquine dose among G6PD deficient men. AHA markers will include:

• Absolute and fractional change in hemoglobin on day 7 vs. baseline

• Urine color

• Reticulocyte count

• Bilirubin (both total and direct)

• Methemoglobin concentration

• Development of physical signs or symptoms of hemolytic anemia

3. To compare the change in hemoglobin, frequency and severity of adverse events, and occurrence of markers of AHA between G6PD deficient and non-deficient participants receiving the highest tolerable primaquine dose

4. To measure G6PD enzyme activity (semiquantitative testing, U / gHb)

5. To measure the pharmacokinetics of primaquine, carboxyprimaquine, and other metabolites according to plasma concentrations.

6. To genotype participant blood samples for cytochrome P450 2D6 (CYP2D6) single nucleotide polymorphisms (SNPs), to determine if potential hemolysis in G6PDd individuals is affected by CYP2D6 metabolizer status (e.g. weak metabolizers and/or intermediate metabolizers)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 28
• Est. completion date: January 2016
• Est. primary completion date: January 2016
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 50 Years

Eligibility

Inclusion Criteria:

• Males ages 18- 50 (inclusive)

• Ability to swallow oral medication

• Informed consent

• Willing and able to participate in the study for 28 days

For the G6PDd participants:

• G6PDd defined by Carestart 3 rapid diagnostic test or

• The OSMMR2000 G6PD qualitative test

For the G6PDn participants:

• G6PDn defined by Carestart 3 rapid diagnostic test or

• The OSMMR2000 G6PD qualitative test

Exclusion Criteria:

• Moderate to severe anemia (Hb < 10 g/dL)

• Malaria infection by blood smear

• Individuals with known positive HIV test

• Individuals with known positive hepatitis B test.

• Known allergy to study drugs

• Current use of medication (for tuberculosis, HIV, or any drugs that have hemolytic potential in G6PDd individuals including sulphonamides, dapsone, nitrofurantoin, nalidixic acid, ciprofloxacin, methylene blue, toluidine blue, phenazopyridine, and co-trimoxazole)

• The individual is unwilling to abstain from the ingestion of grapefruit-containing products from 72 hours prior to the start of dosing until the study is complete

• Use of antimalarials within 2 weeks before contact with the study team as reported by the patient

• History of blood transfusion or a bleed of > 500 mLs within the last 3 months, as reported by the patient

• Reported history of high alcohol intake (> 14 units per week, each unit is equivalent to 10 g of alcohol (1 glass of wine or 1 bottle of beer or one shot of distilled spirits), within 6 months of study as reported by the patient

• Reported use of illicit drugs (marijuana, heroin, cocaine, methamphetamine) or dependence within 6 months of study, as reported by the patient

• Participants who vomit within 1 hour after administration of primaquine (will be removed from the analysis and will not count towards the total sample size, though they will be followed as any other enrolled individual)

• Already enrolled in this study.

Related Conditions & MeSH terms

• Malaria

Intervention

Drug:
• Primaquine
A single low dose of primaquine will be crushed and dissolved in water, and administered in weight-based doses.

Locations

Country	Name	City	State
Mali	Malaria Research and Training Centre	Bamako

Sponsors (5)

Lead Sponsor	Collaborator
University of California, San Francisco	Bill and Melinda Gates Foundation, Malaria Research and Training Center, Bamako, Mali, Radboud University, University of Mississippi Medical Center

Country where clinical trial is conducted

Mali, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Primary outcome: the change in hemoglobin concentration from baseline levels following a single low-dose of primaquine not to exceed 0.75 mg/kg.		Between day 0 and day 10.
Secondary	To measure the occurrence of adverse events, graded by severity, at each primaquine dose among G6PD deficient men	Severity: = mild; = moderate; = severe; = life threatening	Days 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, and 28
Secondary	To measure the occurrence of absolute and fractional change in hemoglobin concentration (g/dL) on day 7 vs. baseline at each primaquine dose among G6PD deficient men, in comparison with G6PD normal men		Days 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, and 28
Secondary	To measure the occurrence of reticulocytosis (by microscopic quantification of reticulocytes stained with brilliant cresyl blue / 1,000 RBCs) on each day of followup, at each primaquine dose, among G6PD deficient men, in comparison with G6PD normal men		Days 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, and 28
Secondary	To monitor methemoglobin levels (%) on each day of followup, at each primaquine dose among G6PD deficient men, in comparison with G6PD normal men	Use of a Masimo Rad-57 pulse oximeter that measures methemoglobin levels non-invasively, based on absorption of light through the fingertip.	Days 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 14, and 28
Secondary	To determine G6PD enzyme activity (semiquantitative testing, U/g Hb)	Semiquantitative testing will be performed on frozen blood samples to determine G6PD activity on day of enrolment	Day 0
Secondary	Area Under Curve (AUC) for primaquine	Pharmacokinetic analysis of plasma concentration of primaquine at all sampled timepoints	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Maximal concentration (Cmax) for primaquine	Pharmacokinetic analysis of plasma concentration of primaquine at all sampled timepoints	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Area Under Curve (AUC) for carboxyprimaquine	Pharmacokinetic analysis of plasma concentration of carboxyprimaquine	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Maximal concentration (Cmax) for carboxyprimaquine	Pharmacokinetic analysis of plasma concentration of carboxyprimaquine	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Area Under Curve (AUC) for select minor metabolites of primaquine	Pharmacokinetic analysis of plasma concentration of metabolites of primaquine, exact metabolites to be determined by ongoing in vivo studies (including 5-hydroxyprimaquine)	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Maximal concentration (Cmax) for select minor metabolites of primaquine	Pharmacokinetic analysis of plasma concentration of metabolites of primaquine, exact metabolites to be determined by ongoing in vivo studies (including 5-hydroxyprimaquine)	Hours 1, 2, 4, 6, 8, and 24 after primaquine administration
Secondary	Cytochrome P450 (CYP) 2D6 genotyping	To determine whether a correlation between CYP 2D6 metabolism (weak metabolizer, intermediate metabolizer, normal metabolizer, ultrarapid metabolizer) and hemolysis exists.	Day 0