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Bristol Myers' Opdivo+Yervoy Combo Gets FDA Nod for HCC
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Bristol Myers Squibb Company (BMY - Free Report) announced that Opdivo (nivolumab) 1 mg/kg plus Yervoy (ipilimumab) 3 mg/kg (injections for intravenous use) has been approved by the FDA to treat hepatocellular carcinoma (HCC) in patients who have been previously treated with Bayer’s (BAYRY - Free Report) Nexavar (sorafenib).
The approval was granted under accelerated approval based on the results of the CheckMate -040 trial, in which Opdivo + Yervoy showed an overall response rate of 33% in the given patient population.
The continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.
HCC is an aggressive form of lung cancer and the incidence of liver cancer is rising in the United States.
The combination of Opdivo and Yervoy was granted Breakthrough Therapy designation for this indication and a Priority Review by the FDA. Opdivo plus Yervoy is the only dual immunotherapy approved by the FDA in this setting.
We note that Opdivo is currently approved in many countries, including the United States, the EU and Japan, for several cancer indications. The company continues to evaluate Opdivo alone or in combination therapies with Yervoy and other anti-cancer agents. The Opdivo and Yervoy combination is already approved for the treatment of patients with unresectable or metastatic melanoma and intermediate or poor risk, previously untreated advanced renal cell carcinoma (RCC). The combination is also indicated for the treatment of adults and pediatric patients 12 years and older with microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) metastatic colorectal cancer (CRC).
Bristol-Myers’ shares have gained 10.9% in the past year against the industry’s decline of 3.2%.
Approval of this combination for other indications should boost sales. Opdivo’s sales were sluggish in the fourth quarter as the drug faces stiff competition from Merck’s (MRK - Free Report) Keytruda and Roche’s (RHHBY - Free Report) Tecentriq.
Last year, it generated $24 billion in global revenues. By 2020, it's predicted to blast through the roof to $77.6 billion. Famed investor Mark Cuban says it will produce "the world's first trillionaires," but that should still leave plenty of money for regular investors who make the right trades early.
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Bristol Myers' Opdivo+Yervoy Combo Gets FDA Nod for HCC
Bristol Myers Squibb Company (BMY - Free Report) announced that Opdivo (nivolumab) 1 mg/kg plus Yervoy (ipilimumab) 3 mg/kg (injections for intravenous use) has been approved by the FDA to treat hepatocellular carcinoma (HCC) in patients who have been previously treated with Bayer’s (BAYRY - Free Report) Nexavar (sorafenib).
The approval was granted under accelerated approval based on the results of the CheckMate -040 trial, in which Opdivo + Yervoy showed an overall response rate of 33% in the given patient population.
The continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trials.
HCC is an aggressive form of lung cancer and the incidence of liver cancer is rising in the United States.
The combination of Opdivo and Yervoy was granted Breakthrough Therapy designation for this indication and a Priority Review by the FDA. Opdivo plus Yervoy is the only dual immunotherapy approved by the FDA in this setting.
We note that Opdivo is currently approved in many countries, including the United States, the EU and Japan, for several cancer indications. The company continues to evaluate Opdivo alone or in combination therapies with Yervoy and other anti-cancer agents. The Opdivo and Yervoy combination is already approved for the treatment of patients with unresectable or metastatic melanoma and intermediate or poor risk, previously untreated advanced renal cell carcinoma (RCC). The combination is also indicated for the treatment of adults and pediatric patients 12 years and older with microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) metastatic colorectal cancer (CRC).
Bristol-Myers’ shares have gained 10.9% in the past year against the industry’s decline of 3.2%.
Approval of this combination for other indications should boost sales. Opdivo’s sales were sluggish in the fourth quarter as the drug faces stiff competition from Merck’s (MRK - Free Report) Keytruda and Roche’s (RHHBY - Free Report) Tecentriq.
Bristol-Myers currently carries a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.
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Last year, it generated $24 billion in global revenues. By 2020, it's predicted to blast through the roof to $77.6 billion. Famed investor Mark Cuban says it will produce "the world's first trillionaires," but that should still leave plenty of money for regular investors who make the right trades early.
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