Use the search bar to search by drug, manufacturer, or indication. You can also filter your search results by drug, manufacturer, or negotiation status.
To learn more about a specific file, click on a drug name. It will open its product card, which includes information about the manufacturer, indication (the approved use of a drug by Health Canada), and negotiation milestones.
There are 6 negotiation statuses, which reflect where the drug file is in the pCPA process:
Under consideration for negotiation
We’re considering the evidence and gathering other information to inform the negotiation approach, including eligibility for expedited negotiation pathways.
Active negotiation
Negotiation activities are underway for the drug, with our negotiation team and the manufacturer meeting regularly.
Concluded with an LOI
Negotiations ended successfully with mutually agreed-upon terms, and these terms are outlined in a letter of intent (LOI).
Concluded without agreement
Negotiating parties couldn’t agree on terms. Negotiations have ended without a pricing agreement for the drug.
Negotiation not pursued
It has been decided, in partnership with our member drug plans, not to engage in a negotiation. Typically, this is because the drug’s health technology (HTA) assessment reimbursement recommendations were negative, or “do not reimburse.” Other reasons, like the manufacturer declining to negotiate or a lack of supply of the drug in Canada, may be reflected in an accompanying status note.
Negotiation on hold
We began negotiation activities for the drug, but they’ve since been paused. An accompanying status note indicates whether the pause was requested by the manufacturer or the pCPA.
Learn more
To learn more about our negotiation processes, or where the pCPA fits into the Canadian drug reimbursement system, consult these pages:
Status:
Under consideration for negotiation
Manufacturer:
Incyte Biosciences Canada Corporation
Indication:
in combination with carboplatin and paclitaxel by public drug plans for the first-line treatment of adult patients with metastatic or inoperable locally recurrent squamous cell carcinoma of the anal canal (SCAC).
Last updated October 27, 2026
Status:
Under consideration for negotiation
Manufacturer:
Regeneron
Indication:
For the treatment of patients with cutaneous squamous cell carcinoma (CSCC) at high risk of recurrence after surgery and radiation
Last updated October 27, 2026
Status:
Concluded with an LOI
Manufacturer:
Jamp Pharma Corporation
Indication:
Multiple Indications
Last updated October 27, 2026
Status:
Concluded with an LOI
Manufacturer:
Jamp Pharma Corporation
Indication:
Multiple Indications
Last updated October 27, 2026
Status:
Concluded with an LOI
Manufacturer:
AbbVie Corporation
Indication:
Giant Cell Arteritis
Last updated October 26, 2026
Talvey (Active ENP) (talquetamab)
Status:
Concluded without agreement
Manufacturer:
Janssen Inc.
Indication:
For the treatment of adult patients with relapsed or refractory multiple myeloma who have received at least three prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody, and have demonstrated disease progression on or after the last therapy.
Last updated October 23, 2026
Jatenzo (testosterone undecanoate)
Status:
Concluded without agreement
Manufacturer:
Tolmar International
Indication:
Testosterone replacement therapy
Last updated October 22, 2026
Status:
Concluded without agreement
Manufacturer:
Recordati Rare Diseases Canada Inc.
Indication:
For the treatment of adult patients with Cushing's disease who have persistent or recurrent hypercortisolism after primary pituitary surgery and/or irradiation, or for whom pituitary surgery is not an option.
Last updated October 22, 2026
Status:
Active negotiation
Manufacturer:
Hoffmann-La Roche Ltd.
Indication:
Zepzelca, in combination with atezolizumab, for the first-line maintenance treatment of extensive-stage small cell lung cancer in adult patients whose disease has not progressed following induction therapy with atezolizumab, carboplatin and etoposide
Last updated October 20, 2026
Elahere (mirvetuximab soravtansine)
Status:
Concluded with an LOI
Manufacturer:
AbbVie Corporation
Indication:
For the treatment of adults with folate receptor-alpha positive, platinum-resistant epithelial ovarian, fallopian tube, or primary peritoneal cancer, who have received one to three prior systemic treatment regimens
Last updated October 20, 2026