Keytruda vs Opdivo
both PD-1 checkpoint inhibitors reviewed across overlapping tumor types
Keytruda(pembrolizumab)
Merck & Co., Inc. ยท 24441 cited findings โ
Opdivo(nivolumab)
Bristol-Myers Squibb Company ยท 17346 cited findings โ
What the regulatory reviews say
Keytruda (pembrolizumab) and Opdivo (nivolumab) are both PD-1 checkpoint inhibitors that have been reviewed by regulatory bodies for various cancer indications. Keytruda is indicated for the first-line treatment of patients with metastatic nonsquamous non-small cell lung cancer (NSCLC) in combination with pemetrexed and platinum chemotherapy, and for resectable locally advanced head and neck squamous cell carcinoma whose tumors express PD-L1 (CPSโฅ1). Opdivo is indicated for the first-line treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) whose tumors express PD-L1 (โฅ1%) in combination with ipilimumab, and for MSI-H or dMMR metastatic colorectal cancer that has progressed following prior treatment.
Keytruda's review documents highlight an Objective Response Rate of 74.4% in the pembrolizumab arm compared to 51.9% in the placebo arm, with a Complete Response Rate of 11.3% versus 3.1%, respectively, and a Median Duration of Response of 10.6 months versus 9.5 months. Opdivo's review documents report an Overall Response Rate (ORR) of 31.7%, a Median Progression-free Survival of 3.5 months, and a Median Overall Survival of 15.7 months.
It is crucial to note that these drugs were studied in separate clinical trials with distinct designs, patient populations, and timepoints. The endpoints, comparator arms, and specific patient characteristics varied between the studies. Therefore, the figures presented for each drug are not directly comparable, and no implication of superiority or inferiority between the two drugs should be drawn from these data.
Each drug's own results โ cited
| Keytruda | Opdivo | |
|---|---|---|
| Objective Response Rate | 74.4 pembrolizumab arm Keytruda FDA Review, p.132 | 31.7% Overall Response Rate (ORR) BRISTOL MYERS SQUIBB โ Opdivo FDA Summary Review (NDA/BLA 12, p.3 |
Explore the full evidence
Every cited finding behind both drugs is in the Oncology research library โ
Figures are as stated in the cited regulatory review documents. Educational reference only โ not medical or investment advice.