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Please note that the medicines mentioned may not be available in all countries. Additionally, currently approved indications (uses) and presentations may differ between countries.

Please always consult local prescribing information and labelling text before use.

Key medicines

Alprolix® * (eftrenonacog alfa)

Alprolix® (eftrenonacog alfa) is a treatment and prophylaxis of bleeding in patients with haemophilia B (HB). Alprolix can be used for all age groups.

ALTUVOCT®* (efanesoctocog alfa)

ALTUVOCT® (efanesoctocog alfa) is indicated for the treatment and prophylaxis of bleeding in patients with haemophilia A (HA). ALTUVOCT can be used for all age groups and any disease severity.

Aspaveli®/Empaveli® ** (pegcetacoplan)

Aspaveli®/Empaveli® (pegcetacoplan) is indicated for the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (PNH) who are anaemic after treatment with a C5 inhibitor for at least 3 months.

Doptelet® (avatrombopag)

Doptelet® (avatrombopag) is indicated for the treatment of primary chronic immune thrombocytopenia (ITP) in adult patients who are refractory to other treatments, and a treatment of severe thrombocytopenia in adult patients with chronic liver disease (CLD) who are scheduled to undergo an invasive procedure.

Elocta®/Eloctate® * (efmoroctocog alfa)

Elocta®/Eloctate® (efmoroctocog alfa) is a treatment and prophylaxis of bleeding in patients with haemophilia A (HA). Elocta/Eloctate can be used for all age groups.

Gamifant® (emapalumab)

Gamifant® (emapalumab) is indicated for the treatment of adult and paediatric (newborn and older) patients with primary hemophagocytic lymphohistiocytosis (HLH) with refractory, recurrent or progressive disease or intolerance with conventional HLH therapy.

Kineret® (anakinra)

Kineret® (anakinra) is indicated for the treatment of cryopyrin-associated periodic syndrome (CAPS), rheumatoid arthritis (RA), familial Mediterranean fever (FMF), deficiency of interleukin-1 receptor antagonist (DIRA) and Still's disease including systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease.

Orfadin® (nitisinone)

Orfadin® (nitisinone) is indicated for the treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (HT-1) in combination with dietary restriction of tyrosine and phenylalanine. Orfadin is also indicated for the treatment of adult patients with alkaptonuria (AKU).

Synagis® (palivizumab)

Synagis® (palivizumab) is indicated for the prevention of serious lower respiratory tract infection caused by respiratory syncytial virus (RSV) in infants and young children at high risk of RSV disease.

VONJO® (pacritinib)

VONJO is a kinase inhibitor that is indicated in the US for the treatment of adults with intermediate or high-risk primary or secondary (post-polycythemia vera or post-essential thrombocythemia) myelofibrosis with a platelet count below 50 × 109/L. This indication is approved under accelerated approval based on spleen volume reduction. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).

Zynlonta® (loncastuximab tesirine)

Zynlonta® (loncastuximab tesirine) is a CD19-directed antibody drug conjugate (ADC). Zynlonta as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) and high-grade B-cell lymphoma (HGBL), after two or more lines of systemic therapy.

Other medicines
  • Akynzeo® (netupitant/palonosetron)
  • Aloxi® (palonosetron)
  • Jyseleca® (filgotinib maleate)
  • Kepivance® (palifermin)
  • Tegsedi® (inotersen)
  • Waylivra® (volanesorsen)sen)

*Sobi and Sanofi collaborate on the development and commercialisation of Alprolix, Elocta/Eloctate and ALTUVOCT.

**Sobi and Apellis have global co-development rights for systemic pegcetacoplan. Sobi has exclusive ex-US commercialization rights for systemic pegcetacoplan, and Apellis has exclusive US commercialisation rights for systemic pegcetacoplan.