Status:
Negotiations were not pursued
Manufacturer:
Incyte Biosciences Canada Corporation
Indication:
In combination with lenalidomide for the treatment of adult patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL) not otherwise specified, including DLBCL arising from low grade lymphoma, who are not eligible for autologous stem cell transplant (ASCT).
Last updated September 21, 2026
Status:
Concluded with an LOI
Manufacturer:
Ipsen Biopharmaceuticals Canada, Inc.
Indication:
Primary biliary cholangitis
Last updated September 21, 2026
Status:
Active negotiation
Manufacturer:
Hoffmann-La Roche Ltd.
Indication:
As monotherapy for the treatment of adult patients with relapsed or refractory follicular lymphoma (Grades 1 – 3a) who have received at least two prior lines of systemic therapy.
Last updated September 18, 2026
Status:
Active negotiation
Manufacturer:
Hoffmann-La Roche Ltd.
Indication:
As monotherapy for the treatment of adult patients with relapsed or refractory follicular lymphoma (Grades 1 – 3a) who have received at least two prior lines of systemic therapy.
Last updated September 18, 2026
Status:
Negotiations were not pursued
Manufacturer:
Janssen Inc.
Indication:
An add-on to standard therapy for the treatment of Generalized myasthenia gravis (gMG) in adult and adolescent patients aged 12 years and older who are anti-AChR or anti-MuSK antibody positive.
Last updated September 18, 2026
Blenrep (belantamab mafodotin) (in combination with bortezomib and dexamethasone)
Status:
Concluded with an LOI
Manufacturer:
GlaxoSmithKline Inc.
Indication:
For the treatment of multiple myeloma in combination with bortezomib and dexamethasone (BVd) in adult patients who have received at least one prior therapy.
Last updated September 18, 2026
Blenrep (belantamab mafodotin) (in combination with pomalidomide and dexamethasone)
Status:
Concluded with an LOI
Manufacturer:
GlaxoSmithKline Inc.
Indication:
For the treatment of multiple myeloma in combination with pomalidomide and dexamethasone (Bpd) in adult patients who have received at least one prior therapy including lenalidomide.
Last updated September 18, 2026
Status:
Concluded with an LOI
Manufacturer:
Merck Canada Inc.
Indication:
Keytruda (pembrolizumab), for the treatment of adult patients with muscle-invasive bladder cancer (MIBC) who are ineligible for cisplatin containing chemotherapy, in combination with enfortumab vedotin (Padcev), as neoadjuvant treatment and then continued after radical cystectomy as adjuvant treatment.
Last updated September 17, 2026
Status:
Active negotiation
Manufacturer:
Hoffmann-La Roche Ltd.
Indication:
Active lupus nephritis
Last updated September 17, 2026
Status:
Concluded without agreement
Manufacturer:
Bayer Inc.
Indication:
As an adjunct to standard of care in adults with heart failure with left ventricular ejection fraction (LVEF) ≥ 40% to reduce the risk of cardiovascular death, hospitalization for heart failure, and urgent heart failure visits.
Last updated September 17, 2026