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  • Imbruvica

Imbruvica (ibrutinib)

Details

pCPA file number

20807

Manufacturer:

Janssen Inc.

Status:

Concluded with an LOI

Indication:

Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma

CDA-AMC recommendation

View CDA-AMC project page

Project ID: PC0043-000

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

    March 6, 2015

    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

    June 2, 2015

Related negotiations

Imbruvica (ibrutinib)

Status:

Concluded with an LOI

Manufacturer:

Janssen Inc.

Indication:

In combination with venetoclax for the treatment of adult patients with previously untreated chronic lymphocytic leukemia (CLL), including those with 17p deletion.

Last updated:

January 17, 2025

Imbruvica (ibrutinib)

Status:

Concluded with an LOI

Manufacturer:

Janssen Inc.

Indication:

Waldenstr�m's Macroglobulinemia

Last updated:

January 17, 2025

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Page updated: February 4, 2026

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