Study of IRX4204 for Treatment of Early Parkinson's Disease

Completed · Phase 1

Conditions studied: Parkinson's Disease

In brief

This is a single site, open-label study designed to examine dopamine transporter density using \[123I\]β-CIT SPECT imaging before and following treatment with IRX4204 for a 30-day period in early Parkinson's disease patients. In addition, clinical evaluations will be performed to evaluate the effect of IRX4204 treatment on the motor and cognitive symptoms of PD.

Key facts

Study ID

NCT02438215

Run by

Io Therapeutics

People needed

15

Starts

2014-08-01

Expected to finish

2015-05-01

Last updated by the study team

2015-05-12

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Participant is 40-80 years of age, inclusive.
• Participant has a clinical diagnosis of PD based on the UK Brain Bank Criteria.
• Participant has Hoehn and Yahr stage < 3.
• Participant may be treated with PD symptomatic therapy on a stable dose for at least 30 days prior to the Screening Visit. Dose levels of PD symptomatic therapies will remain stable through the patient's participation in the study, unless a change of dose level is indicated because of adverse events.
• Participant must be willing and able to provide informed consent.
• Females must be of either non-child bearing potential based on:
• post-menopausal for at least 2 years, or
• surgically sterilized If of child bearing potential, must be neither pregnant or breastfeeding at Screening, and must be willing to avoid pregnancy by using medically accepted contraception (use of an intrauterine device or use of a double barrier method when engaging in sexual intercourse with a male partner) for 4 weeks prior to and 4 weeks following the last dose of study medication.

You may not qualify if…

• Has any form of parkinsonism other than idiopathic PD
• Are currently experiencing motor fluctuations (end of dose wearing off or dyskinesias) reflective of later stage PD
• Has evidence of dementia or significant cognitive dysfunction
• Has clinically significant abnormal laboratory value and/or clinically significant unstable medical or psychiatric illness.
• The subject has any disorder that may interfere with drug absorption, distribution, metabolism or excretion.
• The subject has evidence of clinically significant gastrointestinal, cardiovascular, hepatic, renal, hematological, neoplastic, endocrine, alternative neurological, immunodeficiency, pulmonary, or other disorder or disease.
• Pregnancy or breastfeeding

Where it is running

• Molecular NeuroImaging, [MNI] — New Haven, Connecticut, United States

Full record on ClinicalTrials.gov

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