This site is intended for UK healthcare professionals only and contains promotional information.UK Flag Please visit the MHRA Yellowcard site to report an Adverse Event.

INVOKANA® (canagliflozin) cardiovascular (CV) protection in T2D

Prescribing Information can be found under Useful Links

Invokana®(canagliflozin) is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:

  • as monotherapy when metformin is considered inappropriate due to intolerance or contraindications
  • in addition to other medicinal products for the treatment of diabetes

For study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, please refer to section 4.4, 4.5 and 5.1 of the Invokana SmPC.

The addition of INVOKANA to standard of care reduced the risk of major adverse cardiovascular events (MACE) vs placebo.4,5

CANVAS Program5

The CANVAS Program consisted of two double-blind randomised trials, that assessed canagliflozin vs placebo in participants with T2D who were at high risk of CV events. Canagliflozin 100mg to 300mg daily on a background of standard of care treatments for glycaemic management and control of other risk factors, e.g. atherosclerotic cardiovascular disease.

CREDENCE4

CREDENCE is the first study involving an SGLT2 inhibitor, dedicated to renal outcomes patients with T2D. Canagliflozin 100mg daily on a background of standard of care treatments for glycaemic management, control of other risk factors, and stable maximally tolerated RAS-blockade (e.g. angiotensin converting enzyme or angiotensin receptor blockers).

Invokana-Diagram-11

MACE (composite endpoint)

Major
Averse
Cardiovascular
Event

CANVAS Program5

(HR 0.86; 95% Cl,0.75-0.97; P<0.001 for non-inferiority, P=0.02 for superiority) NNT (3.0 years): 79 (95% CI, not stated)5


CREDENCE4

(HR 0.80; 95% Cl, 0.67-0.95; P=0.01) NNT (2.5 years): 40 (95% CI, 23-165)4

-20%-Blue-Circle

Invokana-Diagram-12

CANVAS Program5

(HR 0.67; 95% Cl, 0.52-0.87; nominal significance; exploratory endpoint) NNT (3 years): 106 (95% CI, not stated)5

CREDENCE4

(HR 0.61; 95% Cl, 0.47-0.80; P<0.001) NNT (2.5 years): 46(95% CI, 29-124) 4

-33%-Red-Circle

Abbreviations:
CI – Confidence Interval
HR – Hazard Ratio
MACE – Major adverse cardiovascular events
NNT – Number Needed to Treat
CV-Cardiovascular
RRR - Relative Risk Reduction

 

Invokana-Arrow-2

PP-IN-UK-0237 July 2023

Adverse events should be reported. Reporting forms and information can be found at www.yellowcard.mhra.gov.uk or search for MHRA Yellow Card in Google Play or Apple App Store.

Adverse events should also be reported to A. Menarini Farmaceutica Internazionale SRL.

Phone 0800 085 8678