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Purpose

The main aims of this study are to understand why adults with Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) chose a certain treatment, why they changed to HyQvia from another therapy, how satisfied they are with HyQvia and their previous treatment, how their work productivity and activity is impacted and learn about their CIDP signs and symptoms. Other aims are to collect information on any medical problems or side effects during the treatment with HyQvia, learn how effective treatment of CIDP with HyQvia is and understand details on the use of HyQvia in standard clinical routine as well on the need for healthcare intervention (such as emergency room visits or hospital visits or stays). During the study, data will be collected from medical records already available, interviews with participants at study start and study completion and via questionnaires completed by participants. Participants will be treated as per the doctor's or the clinic's routine.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participants aged 18 years or older. - Investigator-confirmed documented diagnosis of CIDP of any type (e.g., typical, multifocal, focal, motor, sensory, or distal) according to the revised European Academy of Neurology and Peripheral Nerve Society (EAN/PNS) 2021 guidelines on the diagnosis and treatment of CIDP. - Participants must currently have a stable disease course (as per physician judgment) for at least 12 weeks. - Is considered a new user or current user of HyQvia- - New users (Cohort A) are participants on a CIDP treatment as of the date of enrollment, who intend to switch to HyQvia within 6 weeks after enrollment. - Current users (Cohort B) are participants on HyQvia as of the date of enrollment, who switched to HyQvia within the 6 weeks preceding the date of enrollment (the 6-week window may be extended depending on the recruitment progress). - Has provided written informed consent (for the main study). - Participant is willing to comply with the protocol requirement of non-standard of care (non-SOC) assessments (e.g., adjusted inflammatory neuropathy cause and treatment (INCAT) assessment). - Participants must be able to communicate fluently in their local language (if they participate in the optional qualitative participant interview [sub-study].

Exclusion Criteria

  • Had any HyQvia use, defined as - any record of HyQvia use prior to enrollment for new users of HyQvia (Cohort A), and - any record of HyQvia use more than 6 weeks preceding the enrollment date (the 6-week window may be extended depending on the recruitment progress) for current users of HyQvia (Cohort B). - Without any prior treatment for CIDP. - Pregnant or breastfeeding. - Participants with known hypersensitivity to any component of HyQvia. - Has participated in an interventional clinical study within 30 days prior to enrollment or was scheduled to participate in an interventional clinical study during this study. - Has had major surgery within 12 weeks prior to enrollment, or has surgery planned during the time the participant is expected to participate in the study. Note: Participants with planned surgical procedures to be conducted under local anesthesia may participate. Kyphoplasty or vertebroplasty are not considered major surgeries. - Received induction treatment for CIDP during the past 12 weeks. - Participant is identified by the investigator as being unable or unwilling to cooperate with the study procedures. - (Cohort A) only: Participants who do not initiate HyQvia treatment within 6 weeks after enrollment.

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Cohort A: New Users of HyQvia Participants with CIDP who intend to switch to HyQvia within 6 weeks after enrollment will be interviewed and data from medical records will be reviewed for 12 months.
  • Other: No Intervention
    This is a non-interventional study.
Cohort B: Current Users of HyQvia Participants with CIDP who switched to HyQvia within 6 weeks prior to enrollment will be interviewed and data from medical records will be reviewed for 12 months.
  • Other: No Intervention
    This is a non-interventional study.

Recruiting Locations

University of Kansas Medical Center Research Institute, Inc.
Kansas City 4273837, Kansas 4273857 66160
Contact:
Site Contact
913-588-6922
mpasnoor@kumc.edu

More Details

Status
Recruiting
Sponsor
Takeda

Study Contact

Takeda Contact
+1-877-825-3327
medinfoUS@takeda.com

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.