Status:
Concluded with an LOI
Manufacturer:
Jamp Pharma Corporation
Indication:
Febrile neutropenia in non-myeloid malignancies
Last updated June 17, 2025
Status:
Concluded with an LOI
Manufacturer:
Novartis Pharmaceuticals Canada Inc.
Indication:
Follicular lymphoma (FL), Relapsed or refractory, grade 1, 2 or 3a, in adult patients after two or more lines of systemic therapy
Last updated June 12, 2025
Status:
Concluded with an LOI
Manufacturer:
Medison Pharma Canada Inc.
Indication:
Leptin deficiency in lipodystrophy
Last updated June 10, 2025
Status:
Concluded with an LOI
Manufacturer:
Mirum Pharmaceuticals Inc.
Indication:
Alagille syndrome
Last updated June 10, 2025
Status:
Concluded without agreement
Manufacturer:
Boehringer Ingelheim (Canada) Ltd.
Indication:
Adjunct to standard of care therapy for the treatment of chronic heart failure in adults
Last updated June 9, 2025
Breyanzi (lisocabtagene maraleucel)
Status:
Concluded with an LOI
Manufacturer:
Bristol Myers Squibb Canada Inc.
Indication:
Treatment of adult patients with diffuse large B-cell lymphoma (DLBCL) not otherwise specified (NOS), primary mediastinal large B-cell lymphoma (PMBCL), high-grade B-cell lymphoma (HGBCL), and DLBCL arising from follicular lymphoma, who have refractory disease to first-line chemoimmunotherapy or relapse within 12 months of first-line chemoimmunotherapy, and who are candidates for autologous hematopoietic stem cell transplant (HSCT)
Last updated June 6, 2025
Ryaltris (olopatadine hydrochloride and mometasone)
Status:
Negotiations were not pursued
Manufacturer:
Bausch Health, Canada Inc.
Indication:
Seasonal allergic rhinitis
Last updated June 6, 2025
Status:
Concluded with an LOI
Manufacturer:
Pfizer Canada ULC
Indication:
In combination with pembrolizumab, for the treatment of adult patients with unresectable locally advanced or metastatic urothelial cancer (mUC) with no prior systemic therapy for mUC.
Last updated June 6, 2025
Status:
Concluded with an LOI
Manufacturer:
Servier Canada Inc.
Indication:
In combination with azacitidine is indicated for the treatment of adult patients with newly diagnosed acute myeloid leukemia (AML) with an isocitrate dehydrogenase-1 (IDH1) R132 mutation who are not eligible to receive intensive induction chemotherapy
Last updated May 30, 2025
Status:
Concluded with an LOI
Manufacturer:
Rhythm Pharmaceuticals, Inc.
Indication:
Bardet-Biedl syndrome
Last updated May 29, 2025