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Bristol Myers' (BMY) Opdivo Label Expansion Gets Priority Review

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Zacks Equity Research
·3 min read
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Bristol Myers Squibb BMY announced that the FDA has accepted its supplemental biologics license application (sBLA), seeking approval for a further label expansion of immuno-oncology drug, Opdivo (nivolumab).

The company is seeking approval of the drug in combination with fluoropyrimidine- and platinum-containing chemotherapy, for the treatment of patients with advanced or metastatic gastric cancer, gastroesophageal junction cancer (GEJC) or esophageal adenocarcinoma (EAC).

The FDA has granted the application a Priority Review and assigned a Prescription Drug User Fee Act (PDUFA) goal date of May 25, 2021.

The application was based on positive results from the CheckMate -649 study, which showed that first-line treatment with Opdivo plus leucovorin, 5-fluorouracil and oxaliplatin (FOLFOX) or capecitabine and oxaliplatin (CapeOX) led to a statistically significant improvement in overall survival (OS) and progression-free survival (PFS) for patients with unresectable advanced or metastatic gastric cancer, GEJC or EAC whose tumors express PD-L1 with a combined positive score (CPS) ≥ 5, compared to treatment with chemotherapy alone.

Concurrently, the FDA also accepted its sBLA for Opdivo for the treatment of patients with resected esophageal or gastroesophageal junction (GEJ) cancer in the adjuvant setting, after neoadjuvant chemoradiation therapy (CRT). The FDA granted the application a Priority Review and assigned a PDUFA goal date of May 20, 2021.

Gastric cancer or stomach cancer is the fifth most common cancer and esophageal cancer is the seventh most common cancer.

Potential label expansions of the drug will boost sales.

Earlier in the month, the European Medicines Agency (EMA) validated its Marketing Authorization Application (MAA) for Opdivo as an adjuvant treatment for GEJ cancer in adult patients with residual pathologic disease after neoadjuvant CRT and resection.

Opdivo is approved in several countries for various indications — unresectable or metastatic melanoma, metastatic non-small cell lung cancer (NSCLC) with progression on or after platinum-based chemotherapy, metastatic small cell lung cancer (SCLC) with progression after platinum-based chemotherapy, advanced renal cell carcinoma (RCC), adult patients with classical Hodgkin lymphoma (cHL), and recurrent or metastatic squamous cell carcinoma of the head and neck (SCCHN), among others. It is also approved for various indications in combination with Yervoy.

Shares of Bristol-Myers have decreased 1.8% in the past year against the industry’s growth of 13.9%.

 

Approval of additional indications should boost Opdivo’s sales, which were not impressive in 2020. Notably, the drug faces stiff competition from Merck’s MRK Keytruda and Roche’s RHHBY Tecentriq, particularly for the NSCLC indication.

Bristol-Myers currently carries a Zacks Rank #3 (Hold). A better-ranked stock in the biotech space is Alkermes ALKS, which sports a Zacks Rank #1 (Strong Buy), presently. You can see the complete list of today’s Zacks #1 Rank stocks here.

Earnings estimates for Alkermes have increased 4 cents in the past 60 days for 2021.

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Alkermes plc (ALKS) : Free Stock Analysis Report
 
Roche Holding AG (RHHBY) : Free Stock Analysis Report
 
Merck & Co., Inc. (MRK) : Free Stock Analysis Report
 
Bristol Myers Squibb Company (BMY) : Free Stock Analysis Report
 
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