Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action
Home
Summary
Relativity-047 Study
Efficacy Data
Safety Profile
Dosing
Mechanism of Action

 

PrOPDUALAG®: A FIXED-DOSE COMBINATION*
FOR PATIENTS WITH UNRESECTABLE OR METASTATIC MELANOMA1 

 

At the primary analysis, 13.2-month median follow-up:1†

 

Statistically significant PFS benefit
Overall survival
Objective response rate shown

 

4-year exploratory analysis: Demonstrated consistent PFS,
OS, and ORR results vs. nivolumab alone1,3†

 

Statistically significant PFS benefit
Overall survival
Objective response rate shown
The safety of OPDUALAG remains manageable with no new signal and a favorable benefit/risk profile
OPDUALAG is a fixed-dose combination* of nivolumab + relatlimab administered as a 30-minute infusion every 4 weeks

 

 

CI: confidence interval; HR: hazard ratio; ORR: objective response rate; OS: overall survival; PFS: progression-free survival.

* Comparative clinical significance unknown.

† Relativity-047 is a phase 2/3, randomized, double-blinded trial in 714 patients with previously untreated metastatic or unresectable Stage III or IV melanoma. Patients received OPDUALAG (nivolumab 480 mg and relatlimab 160 mg, n=355) or nivolumab 480 mg (n=359) by IV infusion every 4 weeks until disease progression or unacceptable toxicity. Patients were allowed to have received prior adjuvant or neoadjuvant melanoma therapy: anti-PD-1 therapy, anti-CTLA-4 therapy, or BRAFMEK inhibitors were allowed if there was at least 6 months between the last dose of therapy and date of  recurrence; interferon therapy was allowed if the last dose was at least 6 weeks prior to randomization.

‡ Clinical significance unknown.