CIDP07 Rozanolixizumab Post Trial Access Program (the PTA)

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Brief Title

CIDP07 Rozanolixizumab Post Trial Access Program (the PTA)

Official Title

CIDP07 Rozanolixizumab Post Trial Access Program (the PTA)

Brief Summary

      This Post Trial Access (PTA) Program enables access to rozanolixizumab for eligible patients
      who have taken part in the CIDP04 trial (NCT04051944) and are continuing to derive benefit
      from treatment.
    



Study Type

Expanded Access




Condition

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Intervention

Rozanolixizumab


Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Drug





Eligibility Criteria

        Inclusion Criteria:

          -  Patient who has taken part in the CIDP04 (NCT04051944) study

          -  Patient who derives continued benefit from treatment

          -  All required safety information has been reported as per local laws/regulations,
             reported to Bionical, as appropriate, and documented in the patient's medical records

          -  Patient is not pregnant

        Exclusion Criteria:
      

Gender

All

Ages

18 Years - N/A


Contacts

UCB Cares, 0018445992273, [email protected]



Administrative Informations


NCT ID

NCT05014724

Organization ID

CIDP07


Responsible Party

Sponsor

Study Sponsor

UCB Biopharma SRL


Study Sponsor

UCB Cares, Study Director, 001 844 599 2273 (UCB)


Verification Date

September 2022