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NCT Number: NCT05086575

Observatory of Patients With Haemophilia B Treated by IdElvion®

OrPHEe is a non-interventional, prospective and national study which aim is to record real life data in haemophilia B French patients treated with Idelvion® to confirm the efficacy and safety of this product established in clinical development studies.

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This study is active but is not currently recruiting participants.

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Key information

About this study

Haemophilia B is a congenital coagulation disorder caused by a deficiency or anomaly of coagulation factor IX (FIX).

The severity of the haemophilia depends on the extent of the FIX deficiency with clinical manifestations differing depending on the location of the bleed.

Treatment of this disease involves the administration of the deficient factor, i.e. FIX, to patients. Depending on the severity of the disease and context, a range of treatment regimens are available (long-term prophylactic treatment for the prevention of non-surgical bleeds, short-term prophylactic treatment for high-risk periods, treatment for the prevention of surgical bleeds or on-demand curative treatment).

CSL Behring has developed a long-acting recombinant FIX, i.e. rIX-FP (Idelvion®), to extend the intervals between the administrations of treatment while also providing a therapeutic benefit. Data from clinical studies clearly confirm the therapeutic benefit of Idelvion® in adult and paediatric patients with haemophilia B previously receiving an on-demand treatment for bleeding episodes, for long-term prophylaxis, as well as in patients undergoing surgery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have agreed to participate in the observatory after receiving written information on the purpose of the study and the personal data to be collected (agreement of parents for under-age patients);
  • Present with haemophilia B and are currently being treated or have previously been treated with Idelvion® as a long-term prophylactic treatment, on-demand treatment or short-term treatment for surgical procedures or to cover periods with a high-risk of bleeding.
  • Do not have FIX targeted antibodies at the time of the inclusion visit

Exclusion criteria

  • Refusal by the patient or his/her legal representative to participate in the study;
  • Existence of a contraindication to the use of Idelvion® treatment (known hypersensitivity to FIX or hamster proteins);
  • Simultaneous participation in an interventional clinical study on a drug

Treatment and study plan

Primary outcomes

  1. Annual bleeding rates (overall, spontaneous and traumatic) under the scope of long-term prophylaxis or on-demand treatment of non-surgical bleeding events

    Time frame: Up to 36 months

  2. Number of spontaneous bleeding events per patient

    Time frame: Up to 36 months

  3. Number of Idelvion® infusions and doses injected by infusion required to prevent and resolve non-surgical bleeding episodes

    Time frame: Up to 36 months

  4. Incidence of non-surgical bleeding episodes

    Time frame: Up to 36 months

Secondary outcomes

  1. The number of infusions and total dose of Idelvion® (in IU/kg) required to prevent or treat surgical bleeding episodes

    Time frame: up to 36 months

  2. Incidence of surgical bleeding episodes

    Time frame: up to 36 months

  3. The number of infusions and total dose of Idelvion® (in IU/kg) required to cover a high risk of bleeding

    Time frame: up to 36 months

  4. The number of infusions and total dose of Factor IX consumed in the year prior to taking Idelvion®

    Time frame: up to 36 months

  5. The number of infusions and total dose of Idelvion®

    Time frame: up to 36 months

  6. The type and incidence of adverse events (AE) in particular severe AE,and AE related to Idelvion®

    Time frame: up to 36 months

  7. Completion of the following questionnaire: EQ-5D-3L for adults

    Time frame: up to 36 months

  8. Completion of the following questionnaire: EQ-5D-Y for children from 8 to 12 years

    Time frame: up to 36 months

Sponsors and collaborators

Lead sponsor

CSL Behring

Industry

Registry information

Acronym: OrPHEe

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Oct 21, 2021
Registry last updated
Jan 8, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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