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Swedish Orphan Biovitrum clinical trials

Source: ClinicalTrials.gov, U.S. National Library of Medicine — current trials in our UK, USA, Ireland and India registers with Swedish Orphan Biovitrum as lead sponsor. Synced 26 Sep 2026
6Current trials
3Recruiting now
3Drugs in these trials
4Trial registers
Maintained by Sreepriya Prasannan
MSc Digital Transformation of Life Sciences (Innopharma Education / Griffith College); MSc & BSc Botany HSE Spark Ignite 2026 — Top 14 finalist
Compiled from ClinicalTrials.gov and CTIS registry records · Last verified · Editorial standards
At a glance

Swedish Orphan Biovitrum is the lead sponsor of 6 current clinical trials in our UK, USA, Ireland and India registers. 3 are recruiting patients now. The most common phase is Phase 4. The drugs named most often in its trials are Pacritinib, Pegcetacoplan and Efanesoctocog alfa. The most-studied condition is Hemophilia A.

ClinicalTrials.gov trials by status

  • Recruiting350%
  • Active, closed350%

Trials by phase

  • Phase 4233%
  • Observational233%
  • Phase 3117%
  • Phase 2117%
01

Clinical trials sponsored by Swedish Orphan Biovitrum

6 on ClinicalTrials.gov
StudyPhaseStatusStartRegisters
Long-term Study Evaluating Joint Health in People With Haemophilia A Receiving Real-world Prophylactic Treatment With Efanesoctocog Alfa
NCT06940830 · ClinicalTrials.gov ↗ · Hemophilia A
Phase 4 Recruiting 2025-05 Ireland, UK
Real-World Effectiveness and Safety of Pegcetacoplan in Patients With C3G or IC-MPG: A Multi-Country Study
NCT07746895 · ClinicalTrials.gov ↗ · C3 Glomerulopathy (C3G), Immune Complex Membranoproliferative Glomerulonephritis (IC-MPGN)
Phase 4 Recruiting 2026-08 UK
Pacritinib Effectiveness in Real-world Settings
NCT07774455 · ClinicalTrials.gov ↗ · Myelofibrosis (MF)
Observational Recruiting 2026-08 USA
A Phase 3 Study of Pacritinib in Patients With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis
NCT03165734 · ClinicalTrials.gov ↗ · Primary Myelofibrosis, Post-polycythemia Vera Myelofibrosis, Post-essential Thrombocythemia Myelofibrosis
Phase 3 Active, closed 2017-06 UK, USA, India
A Study to Assess the Effectiveness and Safety of Pacritinib in Patients With VEXAS Syndrome (PAXIS)
NCT06782373 · ClinicalTrials.gov ↗ · VEXAS, VEXAS Syndrome
Phase 2 Active, closed 2025-05 UK, USA
A Real World Effectiveness Study of Pegcetacoplan in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
NCT05776472 · ClinicalTrials.gov ↗ · Paroxysmal Nocturnal Hemoglobinuria
Observational Active, closed 2023-06 UK

Registers list studies that are recruiting, about to open, active but closed to enrolment, or enrolling by invitation. The UK and USA registers cover industry-sponsored studies only. Titles and statuses are copied from the registry as published.

02

Drugs in Swedish Orphan Biovitrum trials

3 compounds

Drugs and biologicals named as interventions in these trials, with the number of this sponsor's trials that name each one. Placebos and generic comparators are excluded.

03

Conditions in Swedish Orphan Biovitrum trials

10 conditions
Hemophilia A1Primary Myelofibrosis1Post-polycythemia Vera Myelofibrosis1Post-essential Thrombocythemia Myelofibrosis1VEXAS1VEXAS Syndrome1C3 Glomerulopathy (C3G)1Immune Complex Membranoproliferative Glomerulonephritis (IC-MPGN)1Paroxysmal Nocturnal Hemoglobinuria1Myelofibrosis (MF)1
04

By trial register

RegisterTrialsRecruiting
Clinical trials in UK52
Clinical trials in USA31
Clinical trials in Ireland11
Clinical trials in India10

A trial with sites in more than one country appears in each of those registers.

05

Other sponsors in Hemophilia A

SponsorTrials
Shanghai Xinzhi BioMed1
Shanghai RAAS Blood Products1
Gritgen Therapeutics1

Sponsors with the most current trials registered for this condition.

06

Questions about Swedish Orphan Biovitrum trials

How many clinical trials does Swedish Orphan Biovitrum sponsor?

Swedish Orphan Biovitrum is the lead sponsor of 6 current trials on ClinicalTrials.gov in our UK, USA, Ireland and India registers, as of the registry sync on 26 September 2026. Completed and withdrawn studies are not counted.

Are Swedish Orphan Biovitrum trials recruiting?

Yes. 3 of its 6 ClinicalTrials.gov trials are recruiting. Eligibility and site contacts are on each trial's record. Only the study team can confirm whether a patient is eligible.

Which drugs is Swedish Orphan Biovitrum testing?

Its current trials name 3 drugs and biologicals as interventions. The most frequent are Pacritinib (2), Pegcetacoplan (2) and Efanesoctocog alfa (1). The number in brackets is how many of its trials name each drug.

Does Swedish Orphan Biovitrum have clinical trials in Ireland?

Yes. 1 trial in our Ireland register (ClinicalTrials.gov). Some may be the same study registered in both. See the Irish clinical trials register for sites and contacts.

Where does this information come from?

Every trial, status, phase and condition on this page is copied from public ClinicalTrials.gov and EU CTIS records by a daily sync, grouped by the sponsor name each registry records. It says nothing about the organisation beyond its registered trials, and it is not medical advice.

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How this page is built

Everything on this page is copied from public registry records — it is not written from memory, and nothing here describes the organisation beyond its registered trials. Each trial links to its own record so you can check it yourself.

This page is built automatically: a daily sync job reads the registry records behind our trial registers and groups every current trial by its lead sponsor name, ignoring legal-form suffixes such as Inc. or Ltd. A small, hand-checked list joins the same organisation's different registry names (for example its EU legal entity). There is no AI drafting and no per-sponsor editorial pass. The “last verified” date above is the timestamp of that sync, not a review date. Our general editorial approach is described in our editorial standards and corrections policy. The the registries data on this page was last retrieved on 26 Sep 2026.

Please verify before you rely on this. This page is general information for life-science and pharmaceutical professionals. It is not medical advice, and it has not been reviewed by a clinician — our editorial team holds life-science qualifications, not clinical ones. It is not exhaustive and may not reflect the most recent label change. Always check the official prescribing information (US Prescribing Information or EU SmPC) and speak to your doctor or pharmacist before acting on anything here. Drugs in the same class are not automatically interchangeable, and approvals, brand names and indications differ between the US, the EU/Ireland (EMA/HPRA) and other regions. Spotted an error? Tell us — we correct promptly and log it.