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  • Opdivo-Yervoy

Opdivo-Yervoy (nivolumab-ipilimumab)

Details

pCPA file number

23060

Manufacturer:

Bristol Myers Squibb Canada Inc.

Status:

Concluded with an LOI

Indication:

In combination, for the first-line treatment of adult patients with advanced (unresectable or metastatic) melanoma when patients progress during or within 6 months of adjuvant PD-1 therapy.

CDA-AMC recommendation

View CDA-AMC project page

Project ID: PX0347-000

Negotiation Timeline

  • Initiation

    A drug is identified and brought into a pCPA process (see standard negotiation process or expedited negotiation pathways).

  • Consideration

    The pCPA considers the evidence (including HTA reimbursement recommendations) and gathers other data to inform the negotiation approach, in alignment with the needs of public drug plans. This phase concludes when the pCPA sends a letter of engagement to the manufacturer. 

    Letter of engagement sent to manufacturer

    February 6, 2025

    This lets the manufacturer know the pCPA is ready to start negotiating.

  • Negotiation

    The pCPA negotiation team reaches out to the manufacturer to outline next steps, then we exchange offers to try to reach an agreement on terms and funding conditions.

  • Completion

    The pCPA creates a letter of intent outlining negotiated terms. If the negotiation ended without an agreement, the pCPA sends a letter letting the manufacturer know that the negotiation is closed. 

    Negotiation process concluded

    February 21, 2025

Related negotiations

Opdivo-Yervoy (nivolumab-ipilimumab)

Status:

Concluded with an LOI

Manufacturer:

Bristol Myers Squibb Canada Inc.

Indication:

Metastatic Melanoma

Last updated:

March 20, 2019

Opdivo-Yervoy (nivolumab-ipilimumab)

Status:

Concluded with an LOI

Manufacturer:

Bristol Myers Squibb Canada Inc.

Indication:

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Last updated:

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Opdivo-Yervoy (nivolumab-ipilimumab)

Status:

Concluded with an LOI

Manufacturer:

Bristol Myers Squibb Canada Inc.

Indication:

Unresectable malignant pleural mesothelioma (MPM) in adult patients who have not received prior systemic therapy for MPM (in combination with ipilimumab)

Last updated:

January 18, 2022

Opdivo-Yervoy (nivolumab-ipilimumab)

Status:

Concluded with an LOI

Manufacturer:

Bristol Myers Squibb Canada Inc.

Indication:

Metastatic or recurrent NSCLC with no EGFR or ALK genomic tumor aberrations, first-line treatment (in combination with ipilimumab and 2 cycles of platinum-based chemotherapy)

Last updated:

January 18, 2022

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Page updated: April 9, 2026

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