Oral JESDUVROQ (daprodustat) is comparable to ESA for cardiovascular outcomes1

Oral JESDUVROQ (daprodustat) is comparable to ESA for cardiovascular outcomes1

CO-PRIMARY ENDPOINT (ASCEND-D Trial)

Time to first occurrence of MACE (ITT population)2*

JESDUVROQ and ESA Cumulative Incidence graph

*ITT analyses included events on and off treatment after randomization.

Adjusted for baseline covariates.

MACE events (ITT population)1*
Co-primary composite endpoint JESDUVROQ
(n=1,487)
ESA
(n=1,477)
First occurrence of MACE, n 374 394
All-cause mortality,§ n 244 233
Nonfatal myocardial infarction,§ n 101 126
Nonfatal stroke,§ n 29 35
Hazard ratio (95% CI)|| 0.93 (0.81, 1.07)
Incidence rate per 100 PY 11 12

Noninferiority of JESDUVROQ to ESA on MACE was achieved because the upper limit of the 95% CI for the MACE hazard ratio was less than the prespecified noninferiority margin of 1.25.1

*ITT analyses included events on and off treatment after randomization.

Patients on hemodialysis received epoetin alfa; patients on peritoneal dialysis received darbepoetin alfa.

Co-primary endpoint.

§Component of composite endpoint.

Adjusted for baseline covariates.

ASCEND/D Dialysis

Robust clinical trial1

The efficacy and safety of JESDUVROQ were evaluated in adults with Anemia due to Chronic Kidney Disease (CKD) on dialysis for at least 4 months and receiving an ESA at the time of study entry in a randomized, sponsor-blind, active-controlled, global, event-driven clinical trial (N=2,964). Study co-primary endpoints were mean change in Hb from baseline to the Evaluation Period (Weeks 28-52) and time to first adjudicated MACE, using a noninferiority comparison for JESDUVROQ to ESA for both endpoints.1

REVIEW STUDY DESIGN

Oral JESDUVROQ has a well-studied safety profile1

Clinically significant adverse reactions1:
  • Increased risk of death, myocardial infarction, stroke, venous thromboembolism, and thrombosis of vascular access
  • Risk of hospitalization for heart failure
  • Hypertension
  • Gastrointestinal erosion

Please see Important Safety Information, including BOXED WARNING, and full Prescribing Information for more information on clinically significant adverse reactions.

Most common adverse reactions reported in ≥5% of patients1
Adverse reaction JESDUVROQ
(n=1,482)
%
ESA*
(n=1,474)
%
HypertensionHyperten- sion 24 24
Abdominal pain 11 8
Dizziness 7 6
Hypersen-sitivityHypersensitivity 7 7

*Patients on hemodialysis received epoetin alfa; patients on peritoneal dialysis received darbepoetin alfa.
Includes unspecified abdominal pain, upper abdominal pain, and abdominal discomfort.
Includes rash, urticaria, and dermatitis.

Thrombotic vascular events1
Adverse reaction JESDUVROQ
(n=1,482)
ESA*
(n=1,474)
Adjudicated thrombotic vascular events (fatal and nonfatal) 9.8 per 100 PY 11.7 per 100 PY

These data are not an adequate basis for comparison of rates between the study drug and the active control.
*Patients on hemodialysis received epoetin alfa; patients on peritoneal dialysis received darbepoetin alfa.

ASCEND-D, Anemia Studies in Chronic Kidney Disease: Erythropoiesis Via a Novel Prolyl Hydroxylase Inhibitor Daprodustat-Dialysis; CI, confidence interval; ESA, erythropoiesis-stimulating agent; Hb, hemoglobin; HR, hazard ratio; ITT, intent-to-treat; MACE, major adverse cardiovascular event; PY, patient years.