[No standalone website (unbranded, no questionnaire)] A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness of Adalimumab Introduction Compared With Methotrexate Dose Escalation (CONTROL)

How to apply

Determine if a study site for this clinical trial is near you. Contact the study to apply.

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Study’s contact

Call center

+358401585669

Email address

sigrid.booms@herantis.com

Condition

Brain Diseases,Movement Disorders,Nervous System Diseases,Neuro-Degenerative Disease,Parkinson Disease

Treatment type

Interventional

Investigational product

Renishaw Drug Delivery System

Phase

Phase 1/Phase 2

Sponsor

Herantis Pharma Plc.

ClinicalTrials.gov identifier

NCT03775538

Study number

HP-CD-CL-2003

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About the study

This study is an extension to the HP-CD-CL-2002 clinical study. It evaluates the long-term safety and tolerability of CDNF in patients with Parkinson's disease when dosed directly into the brain using an implanted investigational drug delivery system (DDS). Long-term safety of the DDS is also being evaluated. All patients will receive monthly infusions of either mid- or high-dose of CDNF for a period of 6 months.

Who can take part?

You may be eligible to participate in the study if you meet the following criteria:

Inclusion criteria
  1. 2002) including End-of-Study assessment 2. Negative pregnancy test at study entry for females of childbearing potential. Willingness of using a highly effective form of contraception until 30 days after end of study. Males: willingness to use condom and not to donate sperm for 3 months following DAT-PET. Willingness of female partners of male study participants to use highly effective form of contraception until 30 days after their male partner's end of the study. 3. At least one functioning catheter in each putamen 4. Provision of informed consent
Exclusion criteria

For a full list of inclusion/exclusion criteria, please visit ClinicalTrials.gov

Study locations

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How to apply

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