Status:
Concluded with an LOI
Manufacturer:
Incyte Biosciences Canada Corporation
Indication:
For the treatment of adults with previously treated, unresectable locally advanced or metastatic cholangiocarcinoma with a FGFR2 fusion or other rearrangement.
Last updated October 8, 2025
Status:
Concluded with an LOI
Manufacturer:
Sanofi-Aventis Canada Inc.
Indication:
Chronic graft-versus-host disease (GVHD) in adult and pediatric patients 12 years and older, after failure of at least two prior lines of systemic therapy.
Last updated October 7, 2025
Status:
Concluded with an LOI
Manufacturer:
Amgen Canada Inc.
Indication:
For the treatment of adult and pediatric patients with Philadelphia chromosome-negative CD19 positive B-cell precursor acute lymphoblastic leukemia in the consolidation phase of multiphase chemotherapy in the frontline setting.
Last updated September 29, 2025
Status:
Concluded with an LOI
Manufacturer:
Amgen Canada Inc.
Indication:
Indicated for the pediatric patients with Philadelphia chromosome negative relapsed/refractory B precursor acute lymphoblastic leukemia (ALL) who are in first relapse.
Last updated September 29, 2025
Status:
Concluded with an LOI
Manufacturer:
Ethypharm Inc.
Indication:
For the treatment of essential or renovascular hypertension; for the treatment of congestive heart failure; to improve survival, delay the onset of symptomatic heart failure and reduce hospitalizations for heart failure following myocardial infarction in clinically stable patients with left ventricular dysfunction manifested as an ejection fraction of ≤ 40%; for the treatment of diabetic nephropathy (proteinuria ≥ 500 mg/day) in patients with type I insulin-dependent diabetes mellitus and retinopathy.
Last updated September 22, 2025
Status:
Concluded with an LOI
Manufacturer:
GlaxoSmithKline Inc.
Indication:
For the treatment of splenomegaly and/or disease-related symptoms, in adult patients with intermediate or high-risk primary myelofibrosis (MF), post polycythemia vera myelofibrosis or post essential thrombocythemia MF who have moderate to severe anemia.
Last updated September 22, 2025
Hemgenix (etranacogene dezaparvovec)
Status:
Concluded with an LOI
Manufacturer:
CSL Behring Canada Inc.
Indication:
Hemophilia B
Last updated September 22, 2025
Carvykti (ciltacabtagene autoleucel)
Status:
Concluded without agreement
Manufacturer:
Janssen Inc.
Indication:
For the treatment of adult patients with multiple myeloma, who have received 1 to 3 prior lines of therapy including a proteasome inhibitor and an immunomodulatory agent, and who are refractory to lenalidomide.
Last updated September 18, 2025
Carvykti (ciltacabtagene autoleucel)
Status:
Concluded without agreement
Manufacturer:
Janssen Inc.
Indication:
Multiple myeloma (MM) in adult patients who have received at least three prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent, and an anti-CD38 antibody, and who are refractory to their last treatment.
Last updated September 18, 2025
Status:
Concluded with an LOI
Manufacturer:
Samsung Bioepis Co., Ltd.
Indication:
Multiple Indications
Last updated September 16, 2025