Ready for the Road Ahead

Impact report 2025–26

Five white lines on a blue background extending away from us on a horizontal plane, then changing direction upward and forming the shape of an upward arrow.,

Making headway

Every journey has milestones that signal meaningful progress. In 2025–26, we reached several. Even with significant resources devoted to major organizational initiatives like new or expanded expedited negotiation pathways, the pCPA delivered results at a record pace, and saved public drug plans an estimated $5.36 billion.  

Graph depicting cumulative savings totals by fiscal year, separated by brand-name drugs and generic drugs. Click for accessible text.

Estimated savings

  • $4.4B from brand-name drugs
  • $940M from generic drugs
  • $34+B in cumulative savings

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A record-breaking year for brand-name negotiations

In 2025–26, negotiation volumes reached another record high, resulting in more agreements than we’d ever completed in a year before.

125 negotiations undertaken – up 11%; 124 negotiations concluded – up 20%; 107 agreements reached – up 15%
Bar graph labeled Among our 2025-26 agreements: 48 Cancer drugs, 36 drugs for rare diseases, 20 biosimilar drugs
Stacked bar graph depicting median business days by fiscal year showing files in consideration versus files in active negotiation, showing all files as well as oncology files. Click for accessible text.

Timelines

Our timelines across all files — and especially time under consideration — continued to improve.

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45 business days under consideration, down 40%; 121 business days total timeline, down 19%

Reliable progress for generic drugs

The number of generics files remained consistently high, with a slight increase in market entries. 

695 pricing assessments completed – up 0.3%, 287 generic drugs entered the market – up 1.8%

What is a pricing assessment?

It’s the process we use to determine the applicable pricing tier and pan-Canadian list price under the tiered pricing framework (TPF) when a new generic drug is entering the market. An assessment is also done to confirm a new price when increasing or declining numbers of competitor products result in a tier change.

Top 5 therapeutic areas represented: #1 Central nervous system (CNS) and neurology (Nervous system), 79;  #2 Gastroenterology and metabolism (Digestive system and metabolism), 50; #3. Cardiology (Cardiovascular system), 39; #4 Oncology and immunology (Cancer and immune system), 30; #5 Hematology (Blood health), 25

Nearly 2x more agreements for drugs for rare diseases (DRDs)

In 2025–26, we successfully negotiated 36 drugs for rare diseases — nearly double the number achieved the previous year. 

This included several drugs that were added to Health Canada’s common list of drugs for rare diseases:

  • Winrevair (sotatercept) for pulmonary arterial hypertension (high blood pressure in the lungs)
  • Livmarli (maralixibat) for cholestatic pruritus (severe itching) in patients with Alagille syndrome (genetic liver disease)
  • Breyanzi (lisocabtagene maraleucel) for 2nd line treatment of diffuse large B-cell lymphoma (cancer of the lymph nodes and immune system)
  • Enhertu (trastuzumab deruxtecan) for 2nd line treatment of HER2-positive gastric or gastroesophageal junction cancer (stomach or upper digestive tract cancer)
  • Evkeeza (evinacumab) for homozygous familiar hypercholesterolemia (inherited condition that affects cholesterol levels)
  • Imcivree (setmelanotide) for Bardet-Biedl syndrome (genetic disorder affecting multiple body systems)
  • Hemgenix (etranacogene dezaparvovec) for hemophilia B (inherited bleeding disorder affecting clotting)
36 agreements for drugs for rare diseases, up 89%; Top 5 medical conditions treated (*Beyond a diverse range of rare diseases that don’t fall within a single disease category): #1 Leukemia (cancer of the blood and bone marrow), 5; #2 Lung cancer, 5; #3 Lymphoma (cancer of the lymph nodes and immune system), 4; #4. Gastrointestinal cancer (cancer of the digestive system), 3; #5 Gastrointestinal disorders (digestive system disorders), 3

Year-over-year improvements

  • 89% more agreements
  • 16% faster total timeline
    (148 business days)
  • 45% less time under consideration
    (51 business days)

1.3x more biosimilar drug agreements, reached faster

Last fiscal year, we successfully negotiated 20 biosimilar drugs representing 8 reference biologic drugs, and 90% of these negotiations included multiple indications.

Year-over-year improvements

  • 33% more agreements
  • 27% faster total timeline
    (99 business days)
  • 19% less time under consideration
    (59 business days)
20 agreements for biosimilar drugs, up 33%; Top treatment areas represented: Oncology and immunology (cancer and immune system), 9; Hematology (blood health), 7; Ophthalmology (eyes), 6; Gastroenterology (digestive system), 4; Rheumatology and bone health (bones and skeletal system), 4; #6 Endocrinology (hormone health), 4

Cancer drug agreements up and time under consideration cut in half

In 2025–26, we reached agreement for 48 cancer drugs and completed these negotiations 20% faster than non-cancer drugs.

48 agreements for cancer drugs, up 17%; Top 5 medical conditions treated: #1 Genitourinary cancer (Cancer of the urinary and reproductive system),8 #2 Leukemia (cancer of the blood and bone marrow), 8; #3 Gastrointestinal cancer (Cancer of the digestive system), 7; #4 Lung cancer, 7; #5 Lymphoma (cancer of the lymph nodes and immune system), 7

Year-over-year improvements

  • 17% more agreements 
  • 15% faster total timeline
    (105 business days)
  • 54% less time under consideration
    (25 business days)