Safety and Pharmacokinetics of Oral PRX-112 in Gaucher Disease Patients

Gaucher Disease Clinical Trial

Official title:

An Exploratory, Open-label Study to Evaluate the Safety of PRX-112 and Pharmacokinetics of Oral prGCD (Plant Recombinant Human Glucocerebrosidase) in Gaucher Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01747980
• Other study ID #: PB-112-01
• Status: Completed
• Phase: Phase 1
• First received: December 5, 2012
• Last updated: April 4, 2014
• Start date: March 2013
• Est. completion date: March 2014

Study information

• Verified date: April 2014
• Source: Protalix
• Contact: n/a
• Is FDA regulated: No
• Health authority: Israel: Ministry of Health
• Study type: Interventional

Clinical Trial Summary

Absorption of therapeutic proteins taken orally has remained the major hurdle for treatment in humans. The proteins are generally degraded by enzymes in the stomach and intestine and the intestine lining that prevents absorption into the circulation. Administration of PRX-112, a plant recombinant human glucocerebrosidase (prGCD) using plant cells as carrier vehicle, may help overcome many of these hurdles. The plant cell wall protects the protein from degradation in its transport through the upper GI and allows release in the lower intestine. Studies in animals have shown that prGCD delivered in this way can be found in the blood stream in an active form.

Description:

This exploratory, open-label safety and pharmacokinetic (PK) study is designed to assess the delivery of prGCD after oral administration of PRX-112 in Gaucher subjects. Subjects will receive an oral dose of PRX-112 in a single administration and followed by 3 consecutive daily administrations at the same dose. prGCD levels in plasma will be determined at selected time points. Safety parameters will also be assessed at selected time points. Enrollment will proceed into the next dosage cohort after the pharmacokinetic and safety data of the previous cohort have been reviewed. A different dosage may be selected based on the pharmacokinetic results of the first cohort.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 16
• Est. completion date: March 2014
• Est. primary completion date: January 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Males and females, 18 years or older.

• Historical diagnosis of Gaucher disease with leukocyte GCD activity level =3 nmol/mg*hr (=30 % of the mean activity of the reference range)

• Subjects who have not received enzyme replacement therapy (ERT) or substrate replacement therapy (SRT) in the past or patients who have not received ERT in the past twelve months

• Body Mass Index (BMI) 19 to 25 kg/m2 (inclusive).

• Non-smoking (by declaration) for a period of at least 6 months prior to screening visit.

• Subjects in generally good health in the opinion of the investigator as determined by medical history, vital signs and a physical examination.

• Negative hepatitis B or hepatitis C serology tests at screening.

• Ability to provide a written informed consent

• Female subjects of child-bearing potential or male subjects with female partners of child-bearing potential must agree to use two methods of contraception, one of which must be a barrier method. Acceptable methods of contraception include hormonal products, intrauterine device, or male or female condoms.

Exclusion Criteria:

• Presence of any co-morbidity other than Gaucher Disease

• Presence of any GIT disease or symptomatology suspected to be GIT related using a study specific GI questionnaire

• Subjects with any history of allergic response to drugs or other allergies deemed clinically significant or exclusionary for the study, including known food allergies

• History of alcohol or drug abuse

• Subjects who donated blood in the three months, or received blood or plasma derivatives in the six months, preceding study drug administration.

• Use of any investigational drug at screening or within 3 months of dosing.

• Subjects with an inability to communicate well with the investigators and study staff (i.e., language problem, poor mental development or impaired cerebral function).

• Subjects who are non-cooperative or unwilling to sign the consent form.

• Pregnant or nursing or planning to be pregnant during the study period.

• Have used any medication (excluding paracetamol), within 7 days of study drug administration including laxatives or other drugs, teas or food additives known to be used to treat constipation or diarrhea.

• Presence of any medical, emotional, behavioral or psychological condition that in the judgment of the investigator would interfere with the subject's compliance with the requirements of the study.

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Gaucher Disease

Intervention

Drug:
• PRX-112
Single dose level, four doses per cohort

Locations

Country	Name	City	State
Israel	Rambam Medical Center	Haifa
Israel	Shaare Zedek Medical Center	Jerusalem

Sponsors (1)

Lead Sponsor	Collaborator
Protalix

Country where clinical trial is conducted

Israel, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adverse Events	Spontaneous reports of adverse events, or events identified during physical examination or clinical laboratory testing	3 days after the last dose	Yes
Secondary	Area Under the Curve (AUC)	Area under the GCD level curve 0-30 hours (AUC0-30h)	From start of infusion to 30 hours after infusion	No
Secondary	Maximum Concentration (Cmax)		From start of infusion to 30 hours after infusion	No
Secondary	Time of maximum prGCD concentration (Tmax)		From start of infusion to 30 hours after infusion	No