G-PUR® for Reduced Lead Bioavailability

Not Applicable

Completed

• Conditions: Lead Exposure
• Interventions: Device: G-PUR® 2x 2.0 g oral suspension; Device: G-PUR® 1x 2.0 g oral suspension; Device: Placebo oral suspension

• Registration Number: NCT04138693
• Lead Sponsor: Glock Health, Science and Research GmbH

Brief Summary

This is a prospective, randomized, placebo-controlled, double blind, parallel-arm study in a two-staged approach that will assess the effect of two different doses of G-PUR® on enteral lead absorption in healthy adults using a stable lead isotopic tracer (204Pb).

Detailed Description

Not available

Study Timeline

• Study Start: 2019-09-24
• Study First Submitted: 2019-10-16
• Study First Submitted QC: 2019-10-23
• Study First Posted: 2019-10-24
• Primary Completion: 2020-02-12
• Study Completion: 2020-02-12
• Status Verified: 2020-06
• Last Update Submitted: 2020-06-02
• Last Update Posted: 2020-06-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

1. Healthy male and female subjects
2. Age 18-45 years
3. BMI 19-27 for males and BMI 17-25 for female
4. Blood lead (PbB) concentration < 40 μg/l
5. Serum ferritin concentration within the sex-specific normal range, i.e. ≥ 15 - 150 ng/ml for women and 30 - 400 ng/ml for men
6. Presence of scalp hair with a minimum length of 5 mm and willingness to remove 5 single hairs with hair roots at end of study visit
7. Subject is in good clinical and mental health as established by medical history and physical examination
8. Stable eating habits, within one month before the start of the study
9. Subject agrees to be compliant for study related diet schedule
10. Women of childbearing potential agree to use adequate birth control methods during the study (for all females, negative pregnancy test at screening and at Visit 3 before dosing of IMD is required. Females of childbearing potential must use adequate contraception during the entire study period. Acceptable methods of contraception include: oral contraceptives, intrauterine device, female or male condoms with spermicide, diaphragm with spermicide, contraceptive medication patch, contraceptive medication implant, contraceptive medication injection, abstinence, or surgical sterilization more than 3 months before randomization.
11. Written informed consent

Exclusion Criteria

1. Pregnancy and breastfeeding
2. Lack of willingness or capacity to co-operate appropriately
3. Regular use of medications or iron supplements in the previous 2 months except intake of contraceptives
4. Planning to shave head during study
5. History of malignancies within the past two years or on current anticancer treatment
6. History of gastrointestinal pathology such as gastritis, gastric ulcers, irritable bowel disease, inflammatory bowel disease, chronic constipation
7. History of diarrhoea within the past 14 days of screening
8. History of gastrointestinal surgery with exception of appendectomy
9. History of chronic autoimmune disease requiring treatment within the past two months of screening
10. Known diabetes mellitus I or II or Hba1c >6.5%
11. Known symptomatic food allergies
12. Any clinically relevant laboratory abnormalities in screening test
13. Alcohol, cigarette or drug abuse
14. Mental condition rendering the subject unable to understand the nature, scope and possible consequences of the study
15. Presence of any condition that impacts compliance with the study procedures
16. Use of any regular medication (prescription or over the counter) for prevention or treatment of any medical condition
17. Use of any investigational or non-registered product (drug or device) within 30 days preceding the first study product administration, or planned use during the study period
18. Employee at the study site, spouse/partner or relative of any study staff (e.g. investigator, sub-investigators, or study nurse) or relationship to the sponsor
19. IMD should not be applied to patients that suffer from aluminium and/or silicon hypersensitivity or in case of renal failure that requires dialysis.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Cohort 1: 2 x 2.0 g G-PUR® oral suspension	G-PUR® 2x 2.0 g oral suspension	-
Cohort 2: 1 x 2.0 g G-PUR® oral suspension	G-PUR® 1x 2.0 g oral suspension	-
Cohort 3: Placebo oral suspension	Placebo oral suspension	-

Primary Outcome Measures

Name	Time	Method
204PbB Cmax normalized for total PbB	216 hours	Cmax of 204PbB normalized for total natural PbB levels after intake of 204Pb-enriched water

Secondary Outcome Measures

Name	Time	Method
Incidence of (S)ADE	216 hours	Incidence of (serious) adverse device effects
Plasma PK parameters - AUC0-t of 204PbB	216 hours	The observed area under the blood concentration versus time curve between time 0 and the time point of the last quantifiable concentration, calculated using the trapezoidal rule method
Plasma PK parameters - tmax of 204PbB	216 hours	Time to reach the peak concentration: The sampling time at which Cmax was observed
204Pb concentrations in 24-hour urine	24 hours	Measurement of 204Pb isotope tracer concentrations in 24-hour urine after intake of 204Pb enriched water
204Pb in single hairs	9 days	Lead isotope tracer (204Pb) distribution and ratio in single hairs

Trial Locations

Locations (1)

Department of Clinical Pharmacology, Medical University of Vienna; 🇦🇹 Vienna, Austria