A Phase I, Randomized, Single-Blind, Four-Period Cross-Over, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of Single Oral Doses of GR181413A/AT1001 in Healthy Japanese Subjects

Fabry Disease Clinical Trial

Official title:

A Phase I, Randomized, Single-Blind, Four-Period Cross-Over, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety and Pharmacokinetics of Single Oral Doses of GR181413A/AT1001 in Healthy Japanese Subjects

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01853852
• Other study ID #: 115806
• Status: Completed
• Phase: Phase 1
• First received: November 10, 2011
• Last updated: December 17, 2013
• Start date: September 2011
• Est. completion date: December 2011

Study information

• Verified date: December 2013
• Source: Amicus Therapeutics
• Contact: n/a
• Is FDA regulated: No
• Health authority: Australia: Therapeutic Goods Administration
• Study type: Interventional

Clinical Trial Summary

GR181413A/AT1001 (migalastat hydrochloride) is a low molecular weight iminosugar, an analog of the terminal galactose group that is cleaved from the substrate GL-3. This compound was researched and developed as a drug for treatment of Fabry disease. This study, MGM115806, will be the first administration of GR181413A/AT1001 to Japanese subjects to investigate the safety, tolerability and pharmacokinetics of single oral doses in healthy Japanese adult subjects. Approximately 12 subjects will receive three treatments of 50, 150 and 450 mg GR181413A/AT1001 under fasted conditions plus placebo in a dose ascending crossover design. Serial pharmacokinetic samples will be collected and safety assessments will be performed following each dose. The pharmacokinetics and dose proportionality of GR181413A/AT1001 after single oral doses of GR181413A/AT1001 at the dose levels of 50, 150 and 450 mg under fasted conditions will be assessed.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 14
• Est. completion date: December 2011
• Est. primary completion date: December 2011
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 20 Years to 55 Years

Eligibility

Inclusion Criteria:

1. Healthy as determined by a responsible and experienced physician, based on a medical evaluation including medical history, physical examination, laboratory tests and cardiac monitoring. A subject with a clinical abnormality or laboratory parameters outside the reference range for the population being studied may be included only if the Investigator and the GSK Medical Monitor agree that the finding is unlikely to introduce additional risk factors and will not interfere with the study procedures.

2. Male or female between 20 and 55 years of age inclusive, at the time of signing the informed consent.

3. A female subject is eligible to participate if she is of: Non-childbearing potential defined as pre-menopausal female.

4. Male subjects with female partners of child-bearing potential must agree to use one of the contraception methods. This criterion must be followed from the time of the first dose of study medication until 5 terminal half-lives post-last dose.

5. Body weight >=50 kg and BMI within the range 18.5 - 29.0 kg/m2 (inclusive).

6. Capable of giving written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.

7. AST, ALT, alkaline phosphatase and bilirubin > 1.5xULN (isolated bilirubin >1.5xULN is acceptable if bilirubin is fractionated and direct bilirubin <35%).

8. Single QTcB or QTcF < 450 msec; or QTc < 480 msec in subjects with Bundle Branch Block.

9. Japanese defined being born in Japan, having four ethnic Japanese grandparents, holding a Japanese passport or identity papers and being able to speak Japanese. Japanese subjects should be also have lived outside Japan for less than 10 years.

Exclusion Criteria:

1. A positive pre-study Hepatitis B surface antigen or positive Hepatitis C antibody result within 3 months of screening.

2. A positive pre-study drug/alcohol screen.

3. A positive test for HIV antibody.

4. History of regular alcohol consumption within 6 months of the study

5. The subject has participated in a clinical trial and has received an investigational product within the following time period prior to the first dosing day in the current study: 30 days, 5 half-lives or twice the duration of the biological effect of the investigational product (whichever is longest).

6. Exposure to more than four new chemical entities within 12 months prior to the first dosing day.

7. Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St Johns Wort) within 7 days (or 14 days if the drug is a potential enzyme inducer) or 5 half-lives (whichever is longer) prior to the first dose of study medication, unless in the opinion of the Investigator and GSK Medical Monitor the medication will not interfere with the study procedures or compromise subject safety.

8. History of sensitivity to any of the study medications, or components thereof or a history of drug or other allergy that, in the opinion of the investigator or GSK Medical Monitor, contraindicates their participation.

9. Where participation in the study would result in donation of blood or blood products in excess of 500 mL within a 56 day period.

10. History or regular use of tobacco- or nicotine-containing products within 6 months prior to screening.

11. Pregnant females as determined by positive serum or urine hCG test at screening or prior to dosing.

12. Lactating females.

13. Unwillingness or inability to follow the procedures outlined in the protocol.

14. Subject is mentally or legally incapacitated.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject)

Related Conditions & MeSH terms

• Fabry Disease

Intervention

Drug:
• GR181413A/AT1001 solution
Powder for reconstitution
• GR181413A/AT1001 capsule
Size 2, hard gelatin capsule, white opaque / blue opaque

Other:
• Potable water
Matched, Size 2, hard gelatin capsule, white opaque/blue opaque

Drug:
• Placebo capsule
Solution matched

Locations

Country	Name	City	State
Australia	GSK Investigational Site	Randwick	New South Wales

Sponsors (1)

Lead Sponsor	Collaborator
Amicus Therapeutics

Country where clinical trial is conducted

Australia, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Profile of plasma pharmacokinetics	AUC, Cmax, tmax, Tlast , t1/2, CL/F, Vz/F	0, 0.5, 1, 1.5, 2, 3, 3.5, 4, 5, 6, 8, 10, 12h post dose	No
Primary	Number of Participants with adverse events		up to 24 hr	Yes
Primary	Change from baseline in clinical laboratory tests (hematology, chemistry and urinalysis)		0, 24h post dose	Yes
Primary	Change from baseline in vital signs (blood pressure and heart rate)		0 ,1 , 2, 3, 4, 5, 6, 24h post dose	Yes
Primary	Change from baseline in 12-lead ECG		0, i, 2, 3, 6, 24h post dose	Yes
Primary	Profile of urine pharmacokinetics	Ae, CLr, %Fx	0-4, 4-10, 10-12, 12-24h post dose	No