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  • Listing 3 - Actual negotiations

Listing 3 - Actual negotiations

Search by drug, manufacturer, or indication

Displaying 201 - 210 of 1165

Pemazyre (pemigatinib)

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

Rezurock (belumosudil)

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

Blincyto (blinatumomab)

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

Blincyto (blinatumomab)

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

Noyada (Captopril)

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

Ojjaara (momelotinib)

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

Obodence (denosumab)

Status:

Concluded with an LOI

Manufacturer:

Samsung Bioepis Co., Ltd.

Indication:

Multiple Indications

Last updated September 16, 2025

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Page updated: February 12, 2026

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