Safety, Tolerability and PK of a Single iv Infusion of 10, 40, and 80 µg/kg XG-102 Administered to Healthy Volunteers

NCT01570205 | Completed Phase 1

• 1 other identifier: SDD-1002-024
• Study Type: interventional
• Target: 24
• Locations: 1 country
• Sites: 1

Brief Summary

The objective of the study is to investigate safety, tolerability, and pharmacokinetics of XG-102 following iv infusion of single escalating dose of 10, 40, and 80 µg/kg XG-102 to healthy male volunteers

Conditions

Inflammation

Outcome Measures

Primary Outcomes (1)

• Safety of XG-102

  Safety of XG-102 assessed by incidence and intensity of adverse events, clinical laboratory evaluations, vital signs, ECG, phaysical examination, ocular examination

  1 month

Secondary Outcomes (1)

• Pharmacokinetics

  16 time-points up to 24 hours

Study Arms (4)

XG-102 10 µg/kg

EXPERIMENTAL

Drug: XG-102

XG-102 40 µg/kg

EXPERIMENTAL

Drug: XG-102

XG-102 80 µg/kg

EXPERIMENTAL

Drug: XG-102

placebo

PLACEBO COMPARATOR

Drug: XG-102

Interventions

XG-102 DRUG

single intravenous infusion

XG-102 10 µg/kg; XG-102 40 µg/kg; XG-102 80 µg/kg; placebo

Eligibility Criteria

• Age: 18 Years - 45 Years
• Sex: male
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Healthy male volunteers
• Age ≥ 18 to ≤ 45 years
• BP: 100 - 150 mm Hg systolic, 50 - 95 mm Hg diastolic and pulse rate: 50 - 100 bpm.
• Body mass index between 18.5 and 30.0 kg/m2 and body weight in the 50 - 100 kg range.
• Are able to communicate and co-operate with the Investigator and his/her staff
• Healthy on the basis of medical history, physical examination findings, clinical laboratory test results, vital sign measurements, and digital 12 lead ECG readings
• Written informed consent obtained
• Male subjects with partners of childbearing potential have to use adequate contraception during, and for at least the four weeks after administration of study medication.

You may not qualify if:

• Heavy smokers, i.e. more than 10 cigarettes per day
• Participation in a clinical trial during the previous 4 weeks
• Loss of 500 mL blood or more during the 3 month period before the screening visit of the study
• Existence of any surgical or medical condition which might relevantly interfere with the subject safety, the distribution, metabolism or excretion of the drug or the study assessments, i.e. impaired renal or hepatic function, diabetes mellitus, thyroid function abnormalities including abnormal thyroid hormone values in the Screening evaluation, cardiovascular abnormalities, chronic symptoms of pronounced constipation or diarrhea or conditions associated with total or partial obstruction of the urinary tract.
• History of alcohol or drug abuse in the last 3 years.
• Positive results of the drug Screening.
• Clinically significant abnormal laboratory values at the Screening or baseline evaluation.
• A history of any serious adverse reaction or hypersensitivity to any drug or other medicines
• Presence or history of any allergy requiring acute or chronic treatment (seasonal allergic rhinitis which requires no treatment may be tolerated).
• Positive results from serology examination for HBV, HCV, HIV or tuberculosis
• History of serious mental disorders.
• Need of any prescription medication within 30 days prior to the administration of the drug and/or nonprescription medication within 7 days prior to the administration of the drug or anticipated need for any concomitant medication during the study.
• Volunteers who are unwilling to comply with the provisions of this protocol
• Symptoms of a significant (upon Investigator's medical judgment) somatic or mental illness in the two week period preceding drug administration.

Sponsors & Collaborators

• Xigen SA: lead

Study Sites (1)

Covance Clinical Research

Allschwil, Canton of Basel-City, 4123, Switzerland

Location

MeSH Terms

Conditions

Inflammation

Interventions

D-JNKI-1

Condition Hierarchy (Ancestors)

Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Officials

• Michael Seiberling, MD

  Covance Clinical Research

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: RANDOMIZED
• Masking: QUADRUPLE
• Who Masked: PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: March 29, 2012
• First Posted: April 4, 2012
• Study Start: July 1, 2011
• Primary Completion: November 1, 2011
• Study Completion: February 1, 2012
• Last Updated: April 4, 2012

Record last verified: 2012-04

Locations

CH (1)